DMTN (dematin actin binding protein) - Rat Genome Database

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Gene: DMTN (dematin actin binding protein) Homo sapiens
Analyze
Symbol: DMTN
Name: dematin actin binding protein
RGD ID: 1322873
HGNC Page HGNC:3382
Description: Enables actin binding activity; signaling receptor binding activity; and spectrin binding activity. Involved in several processes, including actin filament bundle assembly; cellular response to cAMP; and regulation of plasma membrane bounded cell projection assembly. Located in several cellular components, including cytoskeleton; cytosol; and platelet dense tubular network membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: dematin; dematin actin-binding protein; DMT; EPB49; erythrocyte membrane protein band 4.9 (dematin); FLJ78462; FLJ98848
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38822,048,931 - 22,082,525 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl822,048,995 - 22,082,527 (+)EnsemblGRCh38hg38GRCh38
GRCh37821,906,442 - 21,940,036 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36821,972,680 - 21,995,982 (+)NCBINCBI36Build 36hg18NCBI36
Build 34821,972,679 - 21,995,982NCBI
Celera820,873,144 - 20,902,318 (+)NCBICelera
Cytogenetic Map8p21.3NCBI
HuRef820,453,493 - 20,482,734 (+)NCBIHuRef
CHM1_1822,112,744 - 22,141,695 (+)NCBICHM1_1
T2T-CHM13v2.0822,322,887 - 22,356,487 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:7615546   PMID:8341682   PMID:8608138   PMID:10565303   PMID:11856323   PMID:12011427   PMID:12477932   PMID:14623284   PMID:14660664   PMID:14702039   PMID:15489334   PMID:16169070  
PMID:16344560   PMID:16472756   PMID:16697408   PMID:18029348   PMID:18273904   PMID:18347014   PMID:18541383   PMID:19030997   PMID:19241372   PMID:19953087   PMID:20396930   PMID:21084299  
PMID:21832049   PMID:21873635   PMID:22456662   PMID:22658674   PMID:22927433   PMID:23060452   PMID:23355471   PMID:23973789   PMID:24255178   PMID:25416956   PMID:26186194   PMID:28514442  
PMID:30652415   PMID:32296183   PMID:33961781   PMID:34079125   PMID:35013218   PMID:35063084   PMID:35561787   PMID:36526897   PMID:36931259   PMID:37689310  


Genomics

Comparative Map Data
DMTN
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38822,048,931 - 22,082,525 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl822,048,995 - 22,082,527 (+)EnsemblGRCh38hg38GRCh38
GRCh37821,906,442 - 21,940,036 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36821,972,680 - 21,995,982 (+)NCBINCBI36Build 36hg18NCBI36
Build 34821,972,679 - 21,995,982NCBI
Celera820,873,144 - 20,902,318 (+)NCBICelera
Cytogenetic Map8p21.3NCBI
HuRef820,453,493 - 20,482,734 (+)NCBIHuRef
CHM1_1822,112,744 - 22,141,695 (+)NCBICHM1_1
T2T-CHM13v2.0822,322,887 - 22,356,487 (+)NCBIT2T-CHM13v2.0
Dmtn
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391470,839,624 - 70,873,488 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1470,838,703 - 70,873,418 (-)EnsemblGRCm39 Ensembl
GRCm381470,602,184 - 70,636,048 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1470,601,263 - 70,636,048 (-)EnsemblGRCm38mm10GRCm38
MGSCv371471,003,477 - 71,029,961 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361469,338,750 - 69,365,234 (-)NCBIMGSCv36mm8
Celera1468,145,198 - 68,173,371 (-)NCBICelera
Cytogenetic Map14D2NCBI
cM Map1436.32NCBI
Dmtn
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81552,087,667 - 52,111,956 (-)NCBIGRCr8
mRatBN7.21545,677,974 - 45,702,261 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1545,677,977 - 45,705,601 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1549,795,828 - 49,820,113 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01550,907,337 - 50,931,630 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01547,766,648 - 47,790,933 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01552,292,762 - 52,320,385 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1552,292,765 - 52,320,385 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01556,016,279 - 56,043,902 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41551,004,498 - 51,032,118 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11551,021,363 - 51,047,921 (-)NCBI
Celera1545,356,046 - 45,383,646 (-)NCBICelera
Cytogenetic Map15p11NCBI
Dmtn
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540345,566,180 - 45,578,079 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495540345,566,180 - 45,579,062 (+)NCBIChiLan1.0ChiLan1.0
DMTN
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2740,550,804 - 40,584,490 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1816,275,936 - 16,309,702 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0821,293,759 - 21,327,600 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1818,238,541 - 18,267,291 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl818,251,886 - 18,266,229 (+)Ensemblpanpan1.1panPan2
DMTN
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12535,163,867 - 35,188,761 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2535,165,876 - 35,176,754 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2535,752,999 - 35,778,392 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02535,374,965 - 35,400,383 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2535,375,297 - 35,400,794 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12535,320,204 - 35,345,608 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02535,177,036 - 35,200,175 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02535,332,536 - 35,355,698 (-)NCBIUU_Cfam_GSD_1.0
Dmtn
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494312,659,342 - 12,685,809 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365555,896,471 - 5,910,098 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365555,884,746 - 5,911,171 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
DMTN
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl146,321,870 - 6,346,865 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1146,315,643 - 6,346,722 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2146,757,571 - 6,788,163 (+)NCBISscrofa10.2Sscrofa10.2susScr3
DMTN
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1820,120,054 - 20,154,368 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl820,125,703 - 20,152,985 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605222,082,446 - 22,116,979 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Dmtn
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462475817,655,803 - 17,671,666 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462475817,640,938 - 17,672,709 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in DMTN
22 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 8p23.1-11.21(chr8:12609975-42085703)x3 copy number gain See cases [RCV000050294] Chr8:12609975..42085703 [GRCh38]
Chr8:12467484..41943221 [GRCh37]
Chr8:12511855..42062378 [NCBI36]
Chr8:8p23.1-11.21		 pathogenic
GRCh38/hg38 8p23.3-21.1(chr8:2475295-27504279)x1 copy number loss See cases [RCV000050297] Chr8:2475295..27504279 [GRCh38]
Chr8:2292235..27361796 [GRCh37]
Chr8:2121457..27417713 [NCBI36]
Chr8:8p23.3-21.1		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12728904-43673207)x3 copy number gain See cases [RCV000050912] Chr8:12728904..43673207 [GRCh38]
Chr8:12586413..43528350 [GRCh37]
Chr8:12630784..43647507 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-12(chr8:12383584-36370018)x3 copy number gain See cases [RCV000051145] Chr8:12383584..36370018 [GRCh38]
Chr8:12241093..36227536 [GRCh37]
Chr8:12285464..36347088 [NCBI36]
Chr8:8p23.1-12		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3 copy number gain See cases [RCV000051206] Chr8:241530..145049449 [GRCh38]
Chr8:191530..146274835 [GRCh37]
Chr8:181530..146245639 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.1-11.21(chr8:12728904-41928741)x3 copy number gain See cases [RCV000051110] Chr8:12728904..41928741 [GRCh38]
Chr8:12586413..41786259 [GRCh37]
Chr8:12630784..41905416 [NCBI36]
Chr8:8p23.1-11.21		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12609975-43336172)x3 copy number gain See cases [RCV000053630] Chr8:12609975..43336172 [GRCh38]
Chr8:12467484..43191315 [GRCh37]
Chr8:12511855..43310472 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12609975-43255410)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053631]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053631]|See cases [RCV000053631] Chr8:12609975..43255410 [GRCh38]
Chr8:12467484..43110553 [GRCh37]
Chr8:12511855..43229710 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12750796-43532444)x3 copy number gain See cases [RCV000053632] Chr8:12750796..43532444 [GRCh38]
Chr8:12608305..43387587 [GRCh37]
Chr8:12652676..43506744 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-12(chr8:12750796-29445409)x3 copy number gain See cases [RCV000053633] Chr8:12750796..29445409 [GRCh38]
Chr8:12608305..29302926 [GRCh37]
Chr8:12652676..29358845 [NCBI36]
Chr8:8p23.1-12		 pathogenic
GRCh38/hg38 8p22-q11.21(chr8:14940110-47929925)x3 copy number gain See cases [RCV000053635] Chr8:14940110..47929925 [GRCh38]
Chr8:14797619..48842485 [GRCh37]
Chr8:14841990..49005038 [NCBI36]
Chr8:8p22-q11.21		 pathogenic
GRCh38/hg38 8p21.3(chr8:21654619-23001935)x3 copy number gain See cases [RCV000053636] Chr8:21654619..23001935 [GRCh38]
Chr8:21512131..22859448 [GRCh37]
Chr8:21556411..22915393 [NCBI36]
Chr8:8p21.3		 pathogenic
GRCh38/hg38 8p23.1-11.23(chr8:12609975-37892000)x3 copy number gain See cases [RCV000053629] Chr8:12609975..37892000 [GRCh38]
Chr8:12467484..37749518 [GRCh37]
Chr8:12511855..37868676 [NCBI36]
Chr8:8p23.1-11.23		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000053602] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|See cases [RCV000053604] Chr8:244417..145054775 [GRCh38]
Chr8:194417..146280161 [GRCh37]
Chr8:184417..146250965 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.3-12(chr8:96310-30614703)x3 copy number gain See cases [RCV000053599] Chr8:96310..30614703 [GRCh38]
Chr8:46310..30472220 [GRCh37]
Chr8:36310..30591762 [NCBI36]
Chr8:8p23.3-12		 pathogenic
GRCh38/hg38 8p21.3(chr8:21482945-22853239)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054236]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054236]|See cases [RCV000054236] Chr8:21482945..22853239 [GRCh38]
Chr8:21340456..22710752 [GRCh37]
Chr8:21384736..22766697 [NCBI36]
Chr8:8p21.3		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12609975-43673207)x3 copy number gain See cases [RCV000135786] Chr8:12609975..43673207 [GRCh38]
Chr8:12467484..43528350 [GRCh37]
Chr8:12511855..43647507 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12383584-43673207)x3 copy number gain See cases [RCV000135566] Chr8:12383584..43673207 [GRCh38]
Chr8:12241093..43528350 [GRCh37]
Chr8:12285464..43647507 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-11.21(chr8:12728904-40169194)x3 copy number gain See cases [RCV000136516] Chr8:12728904..40169194 [GRCh38]
Chr8:12586413..40026713 [GRCh37]
Chr8:12630784..40145870 [NCBI36]
Chr8:8p23.1-11.21		 pathogenic
GRCh38/hg38 8p23.3-21.2(chr8:241605-24656971)x3 copy number gain See cases [RCV000136026] Chr8:241605..24656971 [GRCh38]
Chr8:191605..24514484 [GRCh37]
Chr8:181605..24570374 [NCBI36]
Chr8:8p23.3-21.2		 pathogenic
GRCh38/hg38 8p23.3-21.3(chr8:241530-23198398)x3 copy number gain See cases [RCV000135967] Chr8:241530..23198398 [GRCh38]
Chr8:191530..23055911 [GRCh37]
Chr8:181530..23111856 [NCBI36]
Chr8:8p23.3-21.3		 pathogenic
GRCh38/hg38 8p23.1-12(chr8:12725750-30180521)x3 copy number gain See cases [RCV000136825] Chr8:12725750..30180521 [GRCh38]
Chr8:12583259..30038037 [GRCh37]
Chr8:12627630..30157579 [NCBI36]
Chr8:8p23.1-12		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12182421-43673207)x3 copy number gain See cases [RCV000137249] Chr8:12182421..43673207 [GRCh38]
Chr8:12039930..43528350 [GRCh37]
Chr8:12077339..43647507 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-12(chr8:12698495-35476082)x3 copy number gain See cases [RCV000138058] Chr8:12698495..35476082 [GRCh38]
Chr8:12556004..35333600 [GRCh37]
Chr8:12600375..35453142 [NCBI36]
Chr8:8p23.1-12		 pathogenic
GRCh38/hg38 8p23.3-11.23(chr8:226452-38021728)x3 copy number gain See cases [RCV000137807] Chr8:226452..38021728 [GRCh38]
Chr8:176452..37879246 [GRCh37]
Chr8:166452..37998403 [NCBI36]
Chr8:8p23.3-11.23		 pathogenic|likely pathogenic
GRCh38/hg38 8p23.3-12(chr8:241605-31091074)x3 copy number gain See cases [RCV000138831] Chr8:241605..31091074 [GRCh38]
Chr8:191605..30948590 [GRCh37]
Chr8:181605..31068132 [NCBI36]
Chr8:8p23.3-12		 pathogenic
GRCh38/hg38 8p23.1-21.1(chr8:12382844-28625564)x3 copy number gain See cases [RCV000138244] Chr8:12382844..28625564 [GRCh38]
Chr8:12240353..28483081 [GRCh37]
Chr8:12284724..28539000 [NCBI36]
Chr8:8p23.1-21.1		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3 copy number gain See cases [RCV000138643] Chr8:241605..145054781 [GRCh38]
Chr8:191605..146280167 [GRCh37]
Chr8:181605..146250971 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.1-11.22(chr8:7141697-38695546)x3 copy number gain See cases [RCV000139891] Chr8:7141697..38695546 [GRCh38]
Chr8:6999219..38553064 [GRCh37]
Chr8:6986629..38672221 [NCBI36]
Chr8:8p23.1-11.22		 pathogenic
GRCh38/hg38 8p23.1-11.22(chr8:12729023-39235934)x3 copy number gain See cases [RCV000139770] Chr8:12729023..39235934 [GRCh38]
Chr8:12586532..39093453 [GRCh37]
Chr8:12630903..39212610 [NCBI36]
Chr8:8p23.1-11.22		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12646123-43686843)x3 copy number gain See cases [RCV000139796] Chr8:12646123..43686843 [GRCh38]
Chr8:12503632..43541986 [GRCh37]
Chr8:12548003..43661143 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.1-11.23(chr8:11851113-37216333)x3 copy number gain See cases [RCV000139549] Chr8:11851113..37216333 [GRCh38]
Chr8:11708622..37073851 [GRCh37]
Chr8:11746031..37193009 [NCBI36]
Chr8:8p23.1-11.23		 pathogenic
GRCh38/hg38 8p23.3-12(chr8:226452-34491890)x3 copy number gain See cases [RCV000141410] Chr8:226452..34491890 [GRCh38]
Chr8:176452..34349408 [GRCh37]
Chr8:166452..34468950 [NCBI36]
Chr8:8p23.3-12		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3 copy number gain See cases [RCV000141808] Chr8:208048..145070385 [GRCh38]
Chr8:158048..146295771 [GRCh37]
Chr8:148048..146266575 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.1-12(chr8:12383584-29033946)x1 copy number loss See cases [RCV000142516] Chr8:12383584..29033946 [GRCh38]
Chr8:12241093..28891463 [GRCh37]
Chr8:12285464..28947382 [NCBI36]
Chr8:8p23.1-12		 pathogenic
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3 copy number gain See cases [RCV000142021] Chr8:21291522..145070385 [GRCh38]
Chr8:21149033..146295771 [GRCh37]
Chr8:21193313..146266575 [NCBI36]
Chr8:8p21.3-q24.3		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3 copy number gain See cases [RCV000142858] Chr8:226452..145068712 [GRCh38]
Chr8:176452..146294098 [GRCh37]
Chr8:166452..146264902 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p22-12(chr8:18972996-33619264)x1 copy number loss See cases [RCV000142747] Chr8:18972996..33619264 [GRCh38]
Chr8:18830506..33476782 [GRCh37]
Chr8:18874786..33596324 [NCBI36]
Chr8:8p22-12		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000148092] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.1-11.21(chr8:12633490-40685533)x3 copy number gain See cases [RCV000143508] Chr8:12633490..40685533 [GRCh38]
Chr8:12490999..40543052 [GRCh37]
Chr8:12535370..40662209 [NCBI36]
Chr8:8p23.1-11.21		 pathogenic
GRCh38/hg38 8p23.1-11.1(chr8:12728904-43673207)x3 copy number gain See cases [RCV000148237] Chr8:12728904..43673207 [GRCh38]
Chr8:12586413..43528350 [GRCh37]
Chr8:12630784..43647507 [NCBI36]
Chr8:8p23.1-11.1		 pathogenic
GRCh38/hg38 8p23.2-21.1(chr8:2475295-27504279)x1 copy number loss See cases [RCV000148252] Chr8:2475295..27504279 [GRCh38]
Chr8:2292235..27361796 [GRCh37]
Chr8:2121457..27417713 [NCBI36]
Chr8:8p23.2-21.1		 pathogenic
GRCh38/hg38 8p23.1-11.21(chr8:12609975-42085703)x3 copy number gain See cases [RCV000148249] Chr8:12609975..42085703 [GRCh38]
Chr8:12467484..41943221 [GRCh37]
Chr8:12511855..42062378 [NCBI36]
Chr8:8p23.1-11.21		 pathogenic
GRCh37/hg19 8p21.3-12(chr8:20478546-28986438)x3 copy number gain See cases [RCV000203434] Chr8:20478546..28986438 [GRCh37]
Chr8:8p21.3-12		 pathogenic
GRCh37/hg19 8p23.1-11.22(chr8:12528482-39593802)x3 copy number gain See cases [RCV000511325] Chr8:12528482..39593802 [GRCh37]
Chr8:8p23.1-11.22		 pathogenic
GRCh37/hg19 8p23.1-21.2(chr8:12580132-26774307)x3 copy number gain See cases [RCV000239945] Chr8:12580132..26774307 [GRCh37]
Chr8:8p23.1-21.2		 pathogenic
NM_001387751.1(DMTN):c.896G>C (p.Ser299Thr) single nucleotide variant not specified [RCV004287957] Chr8:22080240 [GRCh38]
Chr8:21937751 [GRCh37]
Chr8:8p21.3		 uncertain significance
GRCh37/hg19 8p23.1-21.2(chr8:12580104-25947329) copy number gain Autism [RCV000626542] Chr8:12580104..25947329 [GRCh37]
Chr8:8p23.1-21.2		 pathogenic
GRCh37/hg19 8p23.3-12(chr8:158048-30262760)x3 copy number gain See cases [RCV000449225] Chr8:158048..30262760 [GRCh37]
Chr8:8p23.3-12		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3 copy number gain See cases [RCV000447507] Chr8:158991..146280828 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p22-21.2(chr8:13091530-24483615) copy number loss See cases [RCV000447428] Chr8:13091530..24483615 [GRCh37]
Chr8:8p22-21.2		 pathogenic
GRCh37/hg19 8p23.3-11.1(chr8:158048-43786723)x3 copy number gain See cases [RCV000447909] Chr8:158048..43786723 [GRCh37]
Chr8:8p23.3-11.1		 pathogenic
GRCh37/hg19 8p23.1-11.1(chr8:12580132-43388233)x3 copy number gain See cases [RCV000447913] Chr8:12580132..43388233 [GRCh37]
Chr8:8p23.1-11.1		 pathogenic
GRCh37/hg19 8p21.3(chr8:21521340-22492009)x4 copy number gain See cases [RCV000510404] Chr8:21521340..22492009 [GRCh37]
Chr8:8p21.3		 uncertain significance
GRCh37/hg19 8p22-12(chr8:16992973-32612724)x1 copy number loss not provided [RCV000509389] Chr8:16992973..32612724 [GRCh37]
Chr8:8p22-12		 not provided
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771) copy number gain See cases [RCV000510234] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.1-12(chr8:12528482-33684786)x3 copy number gain See cases [RCV000510571] Chr8:12528482..33684786 [GRCh37]
Chr8:8p23.1-12		 pathogenic
GRCh37/hg19 8p23.1-11.1(chr8:11935023-43824035)x3 copy number gain See cases [RCV000511028] Chr8:11935023..43824035 [GRCh37]
Chr8:8p23.1-11.1		 pathogenic
GRCh37/hg19 8p23.1-12(chr8:11945855-34875355)x3 copy number gain See cases [RCV000510899] Chr8:11945855..34875355 [GRCh37]
Chr8:8p23.1-12		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3 copy number gain See cases [RCV000511095] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
Single allele duplication not provided [RCV000768452] Chr8:12546855..35816855 [GRCh37]
Chr8:8p23.1-12		 likely pathogenic
NM_001387751.1(DMTN):c.1095G>A (p.Met365Ile) single nucleotide variant not specified [RCV004319957] Chr8:22081184 [GRCh38]
Chr8:21938695 [GRCh37]
Chr8:8p21.3		 uncertain significance
GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3 copy number gain See cases [RCV000512169] Chr8:12490999..146295771 [GRCh37]
Chr8:8p23.1-q24.3		 pathogenic
GRCh37/hg19 8p23.1-21.2(chr8:8770948-27079636)x3 copy number gain not provided [RCV000683041] Chr8:8770948..27079636 [GRCh37]
Chr8:8p23.1-21.2		 pathogenic
GRCh37/hg19 8p23.1-12(chr8:12552775-35935825)x3 copy number gain not provided [RCV000683043] Chr8:12552775..35935825 [GRCh37]
Chr8:8p23.1-12		 pathogenic
GRCh37/hg19 8p23.3-21.2(chr8:1825200-24533193)x3 copy number gain not provided [RCV000683042] Chr8:1825200..24533193 [GRCh37]
Chr8:8p23.3-21.2		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3 copy number gain not provided [RCV000747254] Chr8:164984..146293414 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3 copy number gain not provided [RCV000747248] Chr8:10213..146293414 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.1-12(chr8:12556004-34374150)x3 copy number gain not provided [RCV000762735] Chr8:12556004..34374150 [GRCh37]
Chr8:8p23.1-12		 likely pathogenic
GRCh37/hg19 8p21.3-21.2(chr8:21662847-24199218)x1 copy number loss not provided [RCV000849161] Chr8:21662847..24199218 [GRCh37]
Chr8:8p21.3-21.2		 pathogenic
GRCh37/hg19 8p21.3(chr8:21077580-22144930)x1 copy number loss not provided [RCV000846265] Chr8:21077580..22144930 [GRCh37]
Chr8:8p21.3		 uncertain significance
GRCh37/hg19 8p21.3(chr8:20564910-22629124)x3 copy number gain not provided [RCV000847279] Chr8:20564910..22629124 [GRCh37]
Chr8:8p21.3		 uncertain significance
GRCh37/hg19 8p21.3(chr8:21840451-22037635)x3 copy number gain not provided [RCV000846785] Chr8:21840451..22037635 [GRCh37]
Chr8:8p21.3		 uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not provided [RCV000848478] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p21.3(chr8:21717395-22395625)x3 copy number gain not provided [RCV000846113] Chr8:21717395..22395625 [GRCh37]
Chr8:8p21.3		 uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771) copy number gain Polydactyly [RCV002280629] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.1-12(chr8:12528482-29886483)x3 copy number gain not provided [RCV001260030] Chr8:12528482..29886483 [GRCh37]
Chr8:8p23.1-12		 likely pathogenic
NC_000008.10:g.(?_21900440)_(23564111_?)dup duplication Conotruncal heart malformations [RCV003107885]|not provided [RCV001928022] Chr8:21900440..23564111 [GRCh37]
Chr8:8p21.3-21.2		 uncertain significance|no classifications from unflagged records
GRCh37/hg19 8p21.3(chr8:21303187-22230498) copy number gain not specified [RCV002053755] Chr8:21303187..22230498 [GRCh37]
Chr8:8p21.3		 uncertain significance
Single allele complex See cases [RCV002292428] Chr8:6999114..11935023 [GRCh37]
Chr8:8p23.3-11.21		 pathogenic
GRCh37/hg19 8p21.3-21.2(chr8:19779604-26531980)x4 copy number gain not provided [RCV002279745] Chr8:19779604..26531980 [GRCh37]
Chr8:8p21.3-21.2		 pathogenic
Single allele complex 8p inverted duplication/deletion syndrome [RCV002280753] Chr8:158048..43019304 [GRCh37]
Chr8:8p23.3-11.21		 pathogenic
GRCh37/hg19 8p23.3-12(chr8:158048-30187456)x1 copy number loss See cases [RCV002286343] Chr8:158048..30187456 [GRCh37]
Chr8:8p23.3-12		 pathogenic
NM_001387751.1(DMTN):c.673G>A (p.Asp225Asn) single nucleotide variant not specified [RCV004092032] Chr8:22072394 [GRCh38]
Chr8:21929905 [GRCh37]
Chr8:8p21.3		 uncertain significance
NM_001387751.1(DMTN):c.707G>T (p.Arg236Leu) single nucleotide variant not specified [RCV004188910] Chr8:22072428 [GRCh38]
Chr8:21929939 [GRCh37]
Chr8:8p21.3		 uncertain significance
NM_001387751.1(DMTN):c.281C>A (p.Pro94Gln) single nucleotide variant not specified [RCV004098734] Chr8:22069047 [GRCh38]
Chr8:21926558 [GRCh37]
Chr8:8p21.3		 uncertain significance
NM_001387751.1(DMTN):c.975G>T (p.Arg325Ser) single nucleotide variant not specified [RCV004086710] Chr8:22080822 [GRCh38]
Chr8:21938333 [GRCh37]
Chr8:8p21.3		 uncertain significance
NM_001387751.1(DMTN):c.634C>T (p.Arg212Trp) single nucleotide variant not specified [RCV004083157] Chr8:22072355 [GRCh38]
Chr8:21929866 [GRCh37]
Chr8:8p21.3		 uncertain significance
NM_001387751.1(DMTN):c.803G>A (p.Arg268His) single nucleotide variant not specified [RCV004230629] Chr8:22073803 [GRCh38]
Chr8:21931314 [GRCh37]
Chr8:8p21.3		 uncertain significance
NM_001387751.1(DMTN):c.1097G>A (p.Arg366Gln) single nucleotide variant not specified [RCV004253931] Chr8:22081186 [GRCh38]
Chr8:21938697 [GRCh37]
Chr8:8p21.3		 uncertain significance
GRCh38/hg38 8p23.3-21.2(chr8:449893-23854904)x1 copy number loss Neurodevelopmental disorder [RCV003327729] Chr8:449893..23854904 [GRCh38]
Chr8:8p23.3-21.2		 pathogenic
GRCh38/hg38 8p23.1-12(chr8:12721809-30183737)x1 copy number loss Microcephaly [RCV003327707] Chr8:12721809..30183737 [GRCh38]
Chr8:8p23.1-12		 pathogenic
GRCh37/hg19 8p23.1-21.1(chr8:12490999-28150620)x1 copy number loss not provided [RCV003483018] Chr8:12490999..28150620 [GRCh37]
Chr8:8p23.1-21.1		 pathogenic
Single allele duplication not provided [RCV003448693] Chr8:12530550..43483193 [GRCh37]
Chr8:8p23.1-11.1		 pathogenic
GRCh37/hg19 8p23.2-11.21(chr8:2201405-41723095)x3 copy number gain not provided [RCV003484713] Chr8:2201405..41723095 [GRCh37]
Chr8:8p23.2-11.21		 pathogenic
Single allele duplication not provided [RCV003448690] Chr8:20868762..22701502 [GRCh37]
Chr8:8p21.3		 uncertain significance
GRCh37/hg19 8p23.1-11.23(chr8:11945856-37902453)x3 copy number gain not provided [RCV003484722] Chr8:11945856..37902453 [GRCh37]
Chr8:8p23.1-11.23		 pathogenic
GRCh37/hg19 8p22-11.1(chr8:14240573-43824035)x3 copy number gain not provided [RCV003484725] Chr8:14240573..43824035 [GRCh37]
Chr8:8p22-11.1		 pathogenic
GRCh37/hg19 8p23.1-11.22(chr8:12560782-38748763)x3 copy number gain not provided [RCV003484724] Chr8:12560782..38748763 [GRCh37]
Chr8:8p23.1-11.22		 pathogenic
NM_001387751.1(DMTN):c.295-2A>T single nucleotide variant not provided [RCV003436788] Chr8:22069417 [GRCh38]
Chr8:21926928 [GRCh37]
Chr8:8p21.3		 uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not specified [RCV003986742] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.3-11.21(chr8:158048-41600696)x3 copy number gain not specified [RCV003986756] Chr8:158048..41600696 [GRCh37]
Chr8:8p23.3-11.21		 pathogenic
GRCh37/hg19 8p21.3-11.1(chr8:20136266-43786723)x3 copy number gain not specified [RCV003986767] Chr8:20136266..43786723 [GRCh37]
Chr8:8p21.3-11.1		 pathogenic
NM_001387751.1(DMTN):c.107A>T (p.Asn36Ile) single nucleotide variant not specified [RCV004368597] Chr8:22067540 [GRCh38]
Chr8:21925051 [GRCh37]
Chr8:8p21.3		 uncertain significance
NM_001387751.1(DMTN):c.79C>T (p.Pro27Ser) single nucleotide variant not specified [RCV004368601] Chr8:22067145 [GRCh38]
Chr8:21924656 [GRCh37]
Chr8:8p21.3		 uncertain significance
NM_001387751.1(DMTN):c.449G>A (p.Arg150Lys) single nucleotide variant not specified [RCV004368598] Chr8:22069935 [GRCh38]
Chr8:21927446 [GRCh37]
Chr8:8p21.3		 uncertain significance
NM_001387751.1(DMTN):c.70C>T (p.Pro24Ser) single nucleotide variant not specified [RCV004368600] Chr8:22067136 [GRCh38]
Chr8:21924647 [GRCh37]
Chr8:8p21.3		 uncertain significance
NM_001387751.1(DMTN):c.950G>A (p.Gly317Asp) single nucleotide variant not specified [RCV004368602] Chr8:22080618 [GRCh38]
Chr8:21938129 [GRCh37]
Chr8:8p21.3		 uncertain significance
NM_001387751.1(DMTN):c.622C>T (p.Arg208Trp) single nucleotide variant not specified [RCV004368599] Chr8:22072343 [GRCh38]
Chr8:21929854 [GRCh37]
Chr8:8p21.3		 uncertain significance
NM_001387751.1(DMTN):c.457G>A (p.Val153Met) single nucleotide variant not specified [RCV004340863] Chr8:22070187 [GRCh38]
Chr8:21927698 [GRCh37]
Chr8:8p21.3		 likely benign
GRCh37/hg19 8p23.3-11.1(chr8:176814-43396776) copy number gain Abnormal fetal cardiovascular morphology [RCV001291977] Chr8:176814..43396776 [GRCh37]
Chr8:8p23.3-11.1		 pathogenic
GRCh37/hg19 8p21.3-21.2(chr8:21925038-26372195)x1 copy number loss not provided [RCV003223292] Chr8:21925038..26372195 [GRCh37]
Chr8:8p21.3-21.2		 likely pathogenic
NM_001387751.1(DMTN):c.788T>C (p.Ile263Thr) single nucleotide variant not specified [RCV004608868] Chr8:22073788 [GRCh38]
Chr8:21931299 [GRCh37]
Chr8:8p21.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:12494
Count of miRNA genes:997
Interacting mature miRNAs:1253
Transcripts:ENST00000265800, ENST00000358242, ENST00000381470, ENST00000415253, ENST00000432128, ENST00000443491, ENST00000517305, ENST00000517418, ENST00000517600, ENST00000517804, ENST00000518816, ENST00000519333, ENST00000519850, ENST00000519907, ENST00000519959, ENST00000520174, ENST00000520856, ENST00000522148, ENST00000522340, ENST00000523266, ENST00000523300, ENST00000523623, ENST00000523782
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1298482BP2_HBlood pressure QTL 2 (human)1.8Blood pressurediastolic8695325632953256Human
406923205GWAS572181_Hapolipoprotein B measurement QTL GWAS572181 (human)5e-13apolipoprotein B measurementblood apoliprotein B level (CMO:0000522)82207071622070717Human
1558703SCL6_HSerum cholesterol level QTL 1 (human)1.2Lipid levelHDL cholesterol81246863538468635Human

Markers in Region
DXS8056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X25,234,657 - 25,234,813UniSTSGRCh37
GRCh37821,923,268 - 21,923,650UniSTSGRCh37
Build 36X25,144,578 - 25,144,734RGDNCBI36
CeleraX29,358,206 - 29,358,362RGD
Celera820,885,541 - 20,885,923UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map8p21.3UniSTS
HuRefX22,973,528 - 22,973,684UniSTS
HuRef820,465,679 - 20,466,022UniSTS
Marshfield Genetic MapX29.76UniSTS
Marshfield Genetic MapX29.76RGD
Genethon Genetic MapX40.6UniSTS
RH70272  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37821,939,726 - 21,939,984UniSTSGRCh37
Build 36821,995,672 - 21,995,930RGDNCBI36
Celera820,902,008 - 20,902,266RGD
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map8p21.3UniSTS
HuRef820,482,424 - 20,482,682UniSTS
GeneMap99-GB4 RH Map889.42UniSTS
NCBI RH Map8265.7UniSTS
WI-20118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37821,939,699 - 21,939,980UniSTSGRCh37
Build 36821,995,645 - 21,995,926RGDNCBI36
Celera820,901,981 - 20,902,262RGD
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map8p21.3UniSTS
HuRef820,482,397 - 20,482,678UniSTS
GeneMap99-GB4 RH Map863.51UniSTS
Whitehead-RH Map892.5UniSTS
NCBI RH Map8274.3UniSTS
D8S1951  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37821,939,857 - 21,939,980UniSTSGRCh37
Build 36821,995,803 - 21,995,926RGDNCBI36
Celera820,902,139 - 20,902,262RGD
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map8p21.3UniSTS
HuRef820,482,555 - 20,482,678UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
1204 2433 2788 2236 4961 1722 2345 4 622 1875 465 2263 7223 6393 51 3730 849 1735 1611 172

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001114135 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001114136 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001114137 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001114138 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001114139 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001302816 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001302817 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323378 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323379 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323381 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323383 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323385 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323387 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323388 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323390 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323391 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323393 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323394 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323395 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323396 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323397 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323398 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323400 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001323401 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387723 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387726 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387727 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387728 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387730 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387732 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387734 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387735 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387736 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387737 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387742 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387743 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387744 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387745 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387750 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387751 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387752 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387753 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387754 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387755 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387756 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387757 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001978 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011544435 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013190 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013191 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013194 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013198 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421496 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421497 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421498 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421499 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421500 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421501 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421504 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421505 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421506 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421507 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421510 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421511 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360011 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360012 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360013 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360014 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360015 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360017 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360018 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360020 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360023 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360024 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360025 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360026 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054360027 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956604 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956605 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956606 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956607 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956608 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956609 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956610 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956611 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956612 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956613 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956614 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956615 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956616 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956617 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956620 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB209718 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC091171 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055842 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK289650 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295452 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308807 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC006318 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC017445 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC052805 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF448882 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI222385 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI547589 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM547218 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT007396 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471080 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA131656 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA141491 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA170493 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA261872 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA267327 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA372459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA383880 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA521027 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA634148 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY024046 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L19713 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U28389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000265800   ⟹   ENSP00000265800
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,057,865 - 22,082,527 (+)Ensembl
Ensembl Acc Id: ENST00000358242   ⟹   ENSP00000350977
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,056,814 - 22,082,525 (+)Ensembl
Ensembl Acc Id: ENST00000381470   ⟹   ENSP00000370879
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,053,570 - 22,082,524 (+)Ensembl
Ensembl Acc Id: ENST00000415253   ⟹   ENSP00000401291
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,059,348 - 22,082,518 (+)Ensembl
Ensembl Acc Id: ENST00000432128   ⟹   ENSP00000416111
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,054,817 - 22,082,524 (+)Ensembl
Ensembl Acc Id: ENST00000443491   ⟹   ENSP00000397904
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,054,902 - 22,082,524 (+)Ensembl
Ensembl Acc Id: ENST00000517305   ⟹   ENSP00000430609
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,054,907 - 22,082,506 (+)Ensembl
Ensembl Acc Id: ENST00000517418   ⟹   ENSP00000429948
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,057,888 - 22,070,334 (+)Ensembl
Ensembl Acc Id: ENST00000517600   ⟹   ENSP00000430618
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,054,931 - 22,081,686 (+)Ensembl
Ensembl Acc Id: ENST00000517804   ⟹   ENSP00000428415
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,056,966 - 22,070,334 (+)Ensembl
Ensembl Acc Id: ENST00000518816
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,054,907 - 22,070,305 (+)Ensembl
Ensembl Acc Id: ENST00000519333   ⟹   ENSP00000478536
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,066,516 - 22,069,060 (+)Ensembl
Ensembl Acc Id: ENST00000519850   ⟹   ENSP00000430600
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,053,570 - 22,069,456 (+)Ensembl
Ensembl Acc Id: ENST00000519907   ⟹   ENSP00000429377
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,059,223 - 22,082,524 (+)Ensembl
Ensembl Acc Id: ENST00000519959
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,053,555 - 22,066,819 (+)Ensembl
Ensembl Acc Id: ENST00000520174   ⟹   ENSP00000430382
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,056,905 - 22,072,450 (+)Ensembl
Ensembl Acc Id: ENST00000520856
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,054,953 - 22,069,262 (+)Ensembl
Ensembl Acc Id: ENST00000522148   ⟹   ENSP00000428063
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,048,995 - 22,069,056 (+)Ensembl
Ensembl Acc Id: ENST00000522340   ⟹   ENSP00000477684
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,066,498 - 22,067,648 (+)Ensembl
Ensembl Acc Id: ENST00000523266   ⟹   ENSP00000427866
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,059,206 - 22,082,518 (+)Ensembl
Ensembl Acc Id: ENST00000523300   ⟹   ENSP00000429116
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,049,149 - 22,070,292 (+)Ensembl
Ensembl Acc Id: ENST00000523623   ⟹   ENSP00000428733
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,055,457 - 22,070,249 (+)Ensembl
Ensembl Acc Id: ENST00000523782   ⟹   ENSP00000429234
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl822,054,943 - 22,082,518 (+)Ensembl
RefSeq Acc Id: NM_001114135   ⟹   NP_001107607
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,057,864 - 22,082,525 (+)NCBI
GRCh37821,906,660 - 21,940,036 (+)NCBI
HuRef820,453,493 - 20,482,734 (+)ENTREZGENE
CHM1_1822,117,038 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,331,828 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001114136   ⟹   NP_001107608
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
GRCh37821,906,660 - 21,940,036 (+)NCBI
HuRef820,453,493 - 20,482,734 (+)ENTREZGENE
CHM1_1822,113,991 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001114137   ⟹   NP_001107609
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
GRCh37821,906,660 - 21,940,036 (+)NCBI
HuRef820,453,493 - 20,482,734 (+)ENTREZGENE
CHM1_1822,112,729 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001114138   ⟹   NP_001107610
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,059,080 - 22,082,525 (+)NCBI
GRCh37821,906,660 - 21,940,036 (+)NCBI
HuRef820,453,493 - 20,482,734 (+)ENTREZGENE
CHM1_1822,118,319 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,333,044 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001114139   ⟹   NP_001107611
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
GRCh37821,906,660 - 21,940,036 (+)NCBI
HuRef820,453,493 - 20,482,734 (+)ENTREZGENE
CHM1_1822,113,991 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001302816   ⟹   NP_001289745
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,059,080 - 22,082,525 (+)NCBI
CHM1_1822,118,319 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,333,044 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001302817   ⟹   NP_001289746
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
CHM1_1822,113,991 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323378   ⟹   NP_001310307
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
CHM1_1822,113,991 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323379   ⟹   NP_001310308
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,059,080 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,333,044 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323380   ⟹   NP_001310309
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,056,814 - 22,082,525 (+)NCBI
CHM1_1822,116,080 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,330,778 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323381   ⟹   NP_001310310
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,066,516 - 22,082,525 (+)NCBI
CHM1_1822,125,682 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,340,472 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323382   ⟹   NP_001310311
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,048,931 - 22,082,525 (+)NCBI
CHM1_1822,108,129 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,322,887 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323383   ⟹   NP_001310312
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
CHM1_1822,113,991 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323384   ⟹   NP_001310313
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
CHM1_1822,113,991 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323385   ⟹   NP_001310314
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,066,516 - 22,082,525 (+)NCBI
CHM1_1822,125,682 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,340,472 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323387   ⟹   NP_001310316
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,056,814 - 22,082,525 (+)NCBI
CHM1_1822,116,080 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,330,778 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323388   ⟹   NP_001310317
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
CHM1_1822,113,991 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323389   ⟹   NP_001310318
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
CHM1_1822,113,991 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323390   ⟹   NP_001310319
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
CHM1_1822,113,991 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323391   ⟹   NP_001310320
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
CHM1_1822,113,991 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323392   ⟹   NP_001310321
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,059,080 - 22,082,525 (+)NCBI
CHM1_1822,118,319 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,333,044 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323393   ⟹   NP_001310322
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
CHM1_1822,113,991 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323394   ⟹   NP_001310323
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,059,080 - 22,082,525 (+)NCBI
CHM1_1822,118,319 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,333,044 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323395   ⟹   NP_001310324
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,056,814 - 22,082,525 (+)NCBI
CHM1_1822,116,080 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,330,778 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323396   ⟹   NP_001310325
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,057,864 - 22,082,525 (+)NCBI
CHM1_1822,117,038 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,331,828 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323397   ⟹   NP_001310326
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,048,931 - 22,082,525 (+)NCBI
CHM1_1822,108,129 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,322,887 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323398   ⟹   NP_001310327
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
CHM1_1822,113,991 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323399   ⟹   NP_001310328
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
CHM1_1822,113,991 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323400   ⟹   NP_001310329
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,066,516 - 22,082,525 (+)NCBI
CHM1_1822,125,682 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,340,472 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001323401   ⟹   NP_001310330
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,056,814 - 22,082,525 (+)NCBI
CHM1_1822,116,080 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,330,778 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387723   ⟹   NP_001374652
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,048,931 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,322,887 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387726   ⟹   NP_001374655
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,048,931 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,322,887 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387727   ⟹   NP_001374656
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,048,931 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,322,887 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387728   ⟹   NP_001374657
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387730   ⟹   NP_001374659
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387732   ⟹   NP_001374661
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387734   ⟹   NP_001374663
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387735   ⟹   NP_001374664
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387736   ⟹   NP_001374665
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387737   ⟹   NP_001374666
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,054,907 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,328,871 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387742   ⟹   NP_001374671
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,056,814 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,330,778 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387743   ⟹   NP_001374672
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,056,814 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,330,778 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387744   ⟹   NP_001374673
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,056,814 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,330,778 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387745   ⟹   NP_001374674
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,056,814 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,330,778 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387750   ⟹   NP_001374679
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,056,814 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,330,778 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387751   ⟹   NP_001374680
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,056,814 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,330,778 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387752   ⟹   NP_001374681
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,057,864 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,331,828 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387753   ⟹   NP_001374682
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,057,864 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,331,828 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387754   ⟹   NP_001374683
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,057,864 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,331,828 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387755   ⟹   NP_001374684
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,057,864 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,331,828 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387756   ⟹   NP_001374685
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,059,205 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,333,169 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387757   ⟹   NP_001374686
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,059,205 - 22,082,525 (+)NCBI
T2T-CHM13v2.0822,333,169 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001978   ⟹   NP_001969
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,059,080 - 22,082,525 (+)NCBI
GRCh37821,906,660 - 21,940,036 (+)NCBI
Build 36821,972,680 - 21,995,982 (+)NCBI Archive
HuRef820,453,493 - 20,482,734 (+)ENTREZGENE
CHM1_1822,118,319 - 22,141,697 (+)NCBI
T2T-CHM13v2.0822,333,044 - 22,356,487 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017013194   ⟹   XP_016868683
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,056,814 - 22,082,525 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047421496   ⟹   XP_047277452
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421497   ⟹   XP_047277453
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421498   ⟹   XP_047277454
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421499   ⟹   XP_047277455
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,056,814 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421500   ⟹   XP_047277456
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421501   ⟹   XP_047277457
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421502   ⟹   XP_047277458
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421503   ⟹   XP_047277459
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421504   ⟹   XP_047277460
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421505   ⟹   XP_047277461
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421506   ⟹   XP_047277462
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,056,814 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421507   ⟹   XP_047277463
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421508   ⟹   XP_047277464
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421509   ⟹   XP_047277465
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421510   ⟹   XP_047277466
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_047421511   ⟹   XP_047277467
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38822,053,555 - 22,082,525 (+)NCBI
RefSeq Acc Id: XM_054360011   ⟹   XP_054215986
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360012   ⟹   XP_054215987
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360013   ⟹   XP_054215988
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360014   ⟹   XP_054215989
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,330,778 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360015   ⟹   XP_054215990
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360016   ⟹   XP_054215991
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360017   ⟹   XP_054215992
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360018   ⟹   XP_054215993
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360019   ⟹   XP_054215994
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360020   ⟹   XP_054215995
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360021   ⟹   XP_054215996
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,330,778 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360022   ⟹   XP_054215997
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360023   ⟹   XP_054215998
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360024   ⟹   XP_054215999
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360025   ⟹   XP_054216000
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,330,778 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360026   ⟹   XP_054216001
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
RefSeq Acc Id: XM_054360027   ⟹   XP_054216002
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0822,327,511 - 22,356,487 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001107607 (Get FASTA)   NCBI Sequence Viewer  
  NP_001107608 (Get FASTA)   NCBI Sequence Viewer  
  NP_001107609 (Get FASTA)   NCBI Sequence Viewer  
  NP_001107610 (Get FASTA)   NCBI Sequence Viewer  
  NP_001107611 (Get FASTA)   NCBI Sequence Viewer  
  NP_001289745 (Get FASTA)   NCBI Sequence Viewer  
  NP_001289746 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310307 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310308 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310309 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310310 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310311 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310312 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310313 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310314 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310316 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310317 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310318 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310319 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310320 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310321 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310322 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310323 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310324 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310325 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310326 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310327 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310328 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310329 (Get FASTA)   NCBI Sequence Viewer  
  NP_001310330 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374652 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374655 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374656 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374657 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374659 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374661 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374663 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374664 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374665 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374666 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374671 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374672 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374673 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374674 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374679 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374680 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374681 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374682 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374683 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374684 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374685 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374686 (Get FASTA)   NCBI Sequence Viewer  
  NP_001969 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868683 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277452 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277453 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277454 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277455 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277456 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277457 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277458 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277459 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277460 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277461 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277462 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277463 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277464 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277465 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277466 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277467 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215986 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215987 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215988 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215989 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215990 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215991 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215992 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215993 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215994 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215995 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215996 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215997 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215998 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215999 (Get FASTA)   NCBI Sequence Viewer  
  XP_054216000 (Get FASTA)   NCBI Sequence Viewer  
  XP_054216001 (Get FASTA)   NCBI Sequence Viewer  
  XP_054216002 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA58438 (Get FASTA)   NCBI Sequence Viewer  
  AAC50223 (Get FASTA)   NCBI Sequence Viewer  
  AAH06318 (Get FASTA)   NCBI Sequence Viewer  
  AAH17445 (Get FASTA)   NCBI Sequence Viewer  
  AAH52805 (Get FASTA)   NCBI Sequence Viewer  
  AAP36060 (Get FASTA)   NCBI Sequence Viewer  
  BAD92955 (Get FASTA)   NCBI Sequence Viewer  
  BAF82339 (Get FASTA)   NCBI Sequence Viewer  
  BAG51582 (Get FASTA)   NCBI Sequence Viewer  
  BAG52385 (Get FASTA)   NCBI Sequence Viewer  
  BAG58387 (Get FASTA)   NCBI Sequence Viewer  
  EAW63724 (Get FASTA)   NCBI Sequence Viewer  
  EAW63725 (Get FASTA)   NCBI Sequence Viewer  
  EAW63726 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000265800
  ENSP00000265800.5
  ENSP00000350977
  ENSP00000350977.3
  ENSP00000370879
  ENSP00000370879.3
  ENSP00000397904
  ENSP00000397904.2
  ENSP00000401291
  ENSP00000401291.1
  ENSP00000416111
  ENSP00000416111.1
  ENSP00000427866
  ENSP00000427866.1
  ENSP00000428063.1
  ENSP00000428415.2
  ENSP00000428733.1
  ENSP00000429116.2
  ENSP00000429234
  ENSP00000429234.2
  ENSP00000429377
  ENSP00000429377.1
  ENSP00000429948.2
  ENSP00000430382.2
  ENSP00000430600.1
  ENSP00000430609
  ENSP00000430609.2
  ENSP00000430618
  ENSP00000430618.1
  ENSP00000477684.1
  ENSP00000478536.2
GenBank Protein Q08495 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001107609   ⟸   NM_001114137
- Peptide Label: isoform 2
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001107611   ⟸   NM_001114139
- Peptide Label: isoform 3
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001107608   ⟸   NM_001114136
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001107607   ⟸   NM_001114135
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001969   ⟸   NM_001978
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001107610   ⟸   NM_001114138
- Peptide Label: isoform 2
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001289746   ⟸   NM_001302817
- Peptide Label: isoform 4
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001289745   ⟸   NM_001302816
- Peptide Label: isoform 2
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310326   ⟸   NM_001323397
- Peptide Label: isoform 6
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310311   ⟸   NM_001323382
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310307   ⟸   NM_001323378
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310313   ⟸   NM_001323384
- Peptide Label: isoform 2
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310318   ⟸   NM_001323389
- Peptide Label: isoform 5
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310320   ⟸   NM_001323391
- Peptide Label: isoform 6
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310327   ⟸   NM_001323398
- Peptide Label: isoform 7
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310312   ⟸   NM_001323383
- Peptide Label: isoform 2
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310319   ⟸   NM_001323390
- Peptide Label: isoform 5
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310322   ⟸   NM_001323393
- Peptide Label: isoform 6
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310317   ⟸   NM_001323388
- Peptide Label: isoform 4
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310328   ⟸   NM_001323399
- Peptide Label: isoform 7
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310316   ⟸   NM_001323387
- Peptide Label: isoform 3
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310330   ⟸   NM_001323401
- Peptide Label: isoform 7
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310309   ⟸   NM_001323380
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310324   ⟸   NM_001323395
- Peptide Label: isoform 6
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310325   ⟸   NM_001323396
- Peptide Label: isoform 6
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310321   ⟸   NM_001323392
- Peptide Label: isoform 6
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310323   ⟸   NM_001323394
- Peptide Label: isoform 6
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310310   ⟸   NM_001323381
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310314   ⟸   NM_001323385
- Peptide Label: isoform 2
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310329   ⟸   NM_001323400
- Peptide Label: isoform 7
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016868683   ⟸   XM_017013194
- Peptide Label: isoform X5
- UniProtKB: Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001310308   ⟸   NM_001323379
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000430618   ⟸   ENST00000517600
Ensembl Acc Id: ENSP00000429948   ⟸   ENST00000517418
Ensembl Acc Id: ENSP00000428415   ⟸   ENST00000517804
Ensembl Acc Id: ENSP00000430609   ⟸   ENST00000517305
Ensembl Acc Id: ENSP00000478536   ⟸   ENST00000519333
Ensembl Acc Id: ENSP00000429377   ⟸   ENST00000519907
Ensembl Acc Id: ENSP00000430600   ⟸   ENST00000519850
Ensembl Acc Id: ENSP00000401291   ⟸   ENST00000415253
Ensembl Acc Id: ENSP00000430382   ⟸   ENST00000520174
Ensembl Acc Id: ENSP00000428063   ⟸   ENST00000522148
Ensembl Acc Id: ENSP00000477684   ⟸   ENST00000522340
Ensembl Acc Id: ENSP00000397904   ⟸   ENST00000443491
Ensembl Acc Id: ENSP00000429116   ⟸   ENST00000523300
Ensembl Acc Id: ENSP00000427866   ⟸   ENST00000523266
Ensembl Acc Id: ENSP00000429234   ⟸   ENST00000523782
Ensembl Acc Id: ENSP00000428733   ⟸   ENST00000523623
Ensembl Acc Id: ENSP00000416111   ⟸   ENST00000432128
Ensembl Acc Id: ENSP00000370879   ⟸   ENST00000381470
Ensembl Acc Id: ENSP00000265800   ⟸   ENST00000265800
Ensembl Acc Id: ENSP00000350977   ⟸   ENST00000358242
RefSeq Acc Id: NP_001374656   ⟸   NM_001387727
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001374655   ⟸   NM_001387726
- Peptide Label: isoform 2
RefSeq Acc Id: NP_001374652   ⟸   NM_001387723
- Peptide Label: isoform 6
RefSeq Acc Id: NP_001374664   ⟸   NM_001387735
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001374663   ⟸   NM_001387734
- Peptide Label: isoform 2
RefSeq Acc Id: NP_001374661   ⟸   NM_001387732
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001374659   ⟸   NM_001387730
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001374657   ⟸   NM_001387728
- Peptide Label: isoform 2
RefSeq Acc Id: NP_001374666   ⟸   NM_001387737
- Peptide Label: isoform 8
RefSeq Acc Id: NP_001374665   ⟸   NM_001387736
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001374679   ⟸   NM_001387750
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001374680   ⟸   NM_001387751
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001374674   ⟸   NM_001387745
- Peptide Label: isoform 8
RefSeq Acc Id: NP_001374673   ⟸   NM_001387744
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001374671   ⟸   NM_001387742
- Peptide Label: isoform 2
RefSeq Acc Id: NP_001374672   ⟸   NM_001387743
- Peptide Label: isoform 5
RefSeq Acc Id: NP_001374684   ⟸   NM_001387755
- Peptide Label: isoform 2
RefSeq Acc Id: NP_001374681   ⟸   NM_001387752
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001374683   ⟸   NM_001387754
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001374682   ⟸   NM_001387753
- Peptide Label: isoform 1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001374686   ⟸   NM_001387757
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001374685   ⟸   NM_001387756
- Peptide Label: isoform 3
RefSeq Acc Id: XP_047277454   ⟸   XM_047421498
- Peptide Label: isoform X1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047277453   ⟸   XM_047421497
- Peptide Label: isoform X1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047277458   ⟸   XM_047421502
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047277456   ⟸   XM_047421500
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047277460   ⟸   XM_047421504
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047277466   ⟸   XM_047421510
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047277464   ⟸   XM_047421508
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047277452   ⟸   XM_047421496
- Peptide Label: isoform X1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047277459   ⟸   XM_047421503
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047277457   ⟸   XM_047421501
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047277461   ⟸   XM_047421505
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047277467   ⟸   XM_047421511
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047277465   ⟸   XM_047421509
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047277463   ⟸   XM_047421507
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047277455   ⟸   XM_047421499
- Peptide Label: isoform X1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047277462   ⟸   XM_047421506
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054215988   ⟸   XM_054360013
- Peptide Label: isoform X1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054215987   ⟸   XM_054360012
- Peptide Label: isoform X1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054215992   ⟸   XM_054360017
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054215990   ⟸   XM_054360015
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054215994   ⟸   XM_054360019
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054216001   ⟸   XM_054360026
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054215998   ⟸   XM_054360023
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054215986   ⟸   XM_054360011
- Peptide Label: isoform X1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054215993   ⟸   XM_054360018
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054215991   ⟸   XM_054360016
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054215995   ⟸   XM_054360020
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054216002   ⟸   XM_054360027
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054215999   ⟸   XM_054360024
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054215997   ⟸   XM_054360022
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054215989   ⟸   XM_054360014
- Peptide Label: isoform X1
- UniProtKB: Q13215 (UniProtKB/Swiss-Prot),   Q08495 (UniProtKB/Swiss-Prot),   E9PEJ0 (UniProtKB/Swiss-Prot),   B4DI75 (UniProtKB/Swiss-Prot),   B3KRH3 (UniProtKB/Swiss-Prot),   B3KP70 (UniProtKB/Swiss-Prot),   A8K0T5 (UniProtKB/Swiss-Prot),   Q9BRE3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054215996   ⟸   XM_054360021
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054216000   ⟸   XM_054360025
- Peptide Label: isoform X5
Protein Domains
HP   Putative adherens-junction anchoring

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q08495-F1-model_v2 AlphaFold Q08495 1-405 view protein structure

Promoters
RGD ID:6813386
Promoter ID:HG_ACW:76139
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   HeLa_S3,   Lymphoblastoid,   NB4
Transcripts:EPB49.MAPR07,   EPB49.PAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 36821,962,251 - 21,962,751 (+)MPROMDB
RGD ID:6806730
Promoter ID:HG_KWN:60869
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   K562,   NB4
Transcripts:UC010LTR.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36821,980,039 - 21,980,539 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:3382 AgrOrtholog
COSMIC DMTN COSMIC
Ensembl Genes ENSG00000158856 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000265800 ENTREZGENE
  ENST00000265800.9 UniProtKB/Swiss-Prot
  ENST00000358242 ENTREZGENE
  ENST00000358242.6 UniProtKB/Swiss-Prot
  ENST00000381470 ENTREZGENE
  ENST00000381470.7 UniProtKB/Swiss-Prot
  ENST00000415253 ENTREZGENE
  ENST00000415253.5 UniProtKB/Swiss-Prot
  ENST00000432128 ENTREZGENE
  ENST00000432128.6 UniProtKB/Swiss-Prot
  ENST00000443491 ENTREZGENE
  ENST00000443491.6 UniProtKB/Swiss-Prot
  ENST00000517305 ENTREZGENE
  ENST00000517305.5 UniProtKB/Swiss-Prot
  ENST00000517418.5 UniProtKB/TrEMBL
  ENST00000517600 ENTREZGENE
  ENST00000517600.5 UniProtKB/Swiss-Prot
  ENST00000517804.5 UniProtKB/TrEMBL
  ENST00000519333.6 UniProtKB/TrEMBL
  ENST00000519850.5 UniProtKB/TrEMBL
  ENST00000519907 ENTREZGENE
  ENST00000519907.5 UniProtKB/Swiss-Prot
  ENST00000520174.5 UniProtKB/TrEMBL
  ENST00000522148.5 UniProtKB/TrEMBL
  ENST00000522340.5 UniProtKB/TrEMBL
  ENST00000523266 ENTREZGENE
  ENST00000523266.5 UniProtKB/Swiss-Prot
  ENST00000523300.5 UniProtKB/TrEMBL
  ENST00000523623.5 UniProtKB/TrEMBL
  ENST00000523782 ENTREZGENE
  ENST00000523782.6 UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.950.10 UniProtKB/Swiss-Prot
GTEx ENSG00000158856 GTEx
HGNC ID HGNC:3382 ENTREZGENE
Human Proteome Map DMTN Human Proteome Map
InterPro AbLIM_anchor UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Actin-binding_LIM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Villin_headpiece UniProtKB/Swiss-Prot
  Villin_headpiece_dom_sf UniProtKB/Swiss-Prot
KEGG Report hsa:2039 UniProtKB/Swiss-Prot
NCBI Gene 2039 ENTREZGENE
OMIM 125305 OMIM
PANTHER ACTIN-BINDING LIM PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DEMATIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam AbLIM_anchor UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VHP UniProtKB/Swiss-Prot
PharmGKB PA27815 PharmGKB
PROSITE PS51089 UniProtKB/Swiss-Prot
SMART VHP UniProtKB/Swiss-Prot
Superfamily-SCOP SSF47050 UniProtKB/Swiss-Prot
UniProt A0A087WT94_HUMAN UniProtKB/TrEMBL
  A0A087WUC0_HUMAN UniProtKB/TrEMBL
  A0A979HLS0_HUMAN UniProtKB/TrEMBL
  A8K0T5 ENTREZGENE
  B3KP70 ENTREZGENE
  B3KRH3 ENTREZGENE
  B4DI75 ENTREZGENE
  DEMA_HUMAN UniProtKB/Swiss-Prot
  E5RFK4_HUMAN UniProtKB/TrEMBL
  E5RFK6_HUMAN UniProtKB/TrEMBL
  E5RGQ0_HUMAN UniProtKB/TrEMBL
  E5RGQ7_HUMAN UniProtKB/TrEMBL
  E5RJ61_HUMAN UniProtKB/TrEMBL
  E5RJC0_HUMAN UniProtKB/TrEMBL
  E9PEJ0 ENTREZGENE
  Q08495 ENTREZGENE
  Q13215 ENTREZGENE
  Q9BRE3 ENTREZGENE
UniProt Secondary A8K0T5 UniProtKB/Swiss-Prot
  B3KP70 UniProtKB/Swiss-Prot
  B3KRH3 UniProtKB/Swiss-Prot
  B4DI75 UniProtKB/Swiss-Prot
  E5RIG5 UniProtKB/TrEMBL
  E9PEJ0 UniProtKB/Swiss-Prot
  Q13215 UniProtKB/Swiss-Prot
  Q9BRE3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2013-06-04 DMTN  dematin actin binding protein  EPB49  erythrocyte membrane protein band 4.9 (dematin)  Symbol and/or name change 5135510 APPROVED