HGS (hepatocyte growth factor-regulated tyrosine kinase substrate) - Rat Genome Database

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Gene: HGS (hepatocyte growth factor-regulated tyrosine kinase substrate) Homo sapiens
Analyze
Symbol: HGS
Name: hepatocyte growth factor-regulated tyrosine kinase substrate
RGD ID: 733649
HGNC Page HGNC:4897
Description: Enables protein domain specific binding activity and ubiquitin-like protein ligase binding activity. Involved in several processes, including negative regulation of signal transduction; positive regulation of exosomal secretion; and protein targeting to lysosome. Located in cytosol; early endosome; and lysosome. Part of ESCRT-0 complex.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: FLJ11421; FLJ39878; hgf-regulated tyrosine kinase substrate; HRS; human growth factor-regulated tyrosine kinase substrate; protein pp110; Vps27; ZFYVE8
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
GRCh381781,684,011 - 81,702,121 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1781,683,326 - 81,703,138 (+)EnsemblGRCh38hg38GRCh38
GRCh371779,651,041 - 79,669,151 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361777,261,425 - 77,279,553 (+)NCBINCBI36Build 36hg18NCBI36
Build 341777,261,424 - 77,279,550NCBI
Celera1776,295,942 - 76,314,294 (+)NCBICelera
Cytogenetic Map17q25.3NCBI
HuRef1775,097,132 - 75,115,050 (+)NCBIHuRef
CHM1_11779,737,183 - 79,755,370 (+)NCBICHM1_1
T2T-CHM13v2.01782,600,905 - 82,619,025 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Cellular Component

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
5. How do ESCRT proteins control autophagy? Rusten TE and Stenmark H, J Cell Sci. 2009 Jul 1;122(Pt 13):2179-83.
Additional References at PubMed
PMID:9407053   PMID:9630564   PMID:10809762   PMID:10861283   PMID:11031247   PMID:11094085   PMID:11110793   PMID:11285248   PMID:11397816   PMID:11532964   PMID:11687594   PMID:11779178  
PMID:11916981   PMID:11984006   PMID:11988743   PMID:12021262   PMID:12151521   PMID:12207904   PMID:12218189   PMID:12230472   PMID:12444101   PMID:12444102   PMID:12477932   PMID:12551915  
PMID:12554698   PMID:12750381   PMID:12802020   PMID:12847087   PMID:12900394   PMID:12900395   PMID:12953068   PMID:13679051   PMID:14519844   PMID:14602072   PMID:14702039   PMID:15071556  
PMID:15113837   PMID:15212941   PMID:15218037   PMID:15240819   PMID:15489334   PMID:15509564   PMID:15592455   PMID:15611048   PMID:15772161   PMID:15828871   PMID:15944737   PMID:16084064  
PMID:16159959   PMID:16189514   PMID:16212419   PMID:16352611   PMID:16429130   PMID:16448788   PMID:16462748   PMID:16467847   PMID:16516194   PMID:16707569   PMID:16713569   PMID:16716190  
PMID:16735510   PMID:16771824   PMID:16832584   PMID:17014699   PMID:17138565   PMID:17182674   PMID:17229889   PMID:17320394   PMID:17445799   PMID:17545595   PMID:17624298   PMID:17675298  
PMID:17686993   PMID:17714434   PMID:17804729   PMID:17853893   PMID:18029348   PMID:18187620   PMID:18362181   PMID:18445679   PMID:18508924   PMID:18626516   PMID:18675823   PMID:18767904  
PMID:18977327   PMID:19019082   PMID:19056867   PMID:19158374   PMID:19278655   PMID:19362549   PMID:19478092   PMID:19542561   PMID:19624486   PMID:19808888   PMID:19874558   PMID:19953087  
PMID:20150893   PMID:20159979   PMID:20224683   PMID:20420830   PMID:20463881   PMID:20504764   PMID:20505072   PMID:20588296   PMID:20675381   PMID:20720151   PMID:20736164   PMID:20812348  
PMID:20936779   PMID:21070952   PMID:21244100   PMID:21304933   PMID:21362618   PMID:21411634   PMID:21520210   PMID:21635887   PMID:21653829   PMID:21706016   PMID:21748597   PMID:21832049  
PMID:21873635   PMID:21988832   PMID:22046132   PMID:22138215   PMID:22458338   PMID:22479182   PMID:22658674   PMID:22706924   PMID:22800866   PMID:22832105   PMID:22863883   PMID:22939629  
PMID:23153581   PMID:23208550   PMID:23222715   PMID:23236378   PMID:23314748   PMID:23477725   PMID:23602387   PMID:23867513   PMID:24105262   PMID:24134837   PMID:24204276   PMID:24255178  
PMID:24344129   PMID:24486797   PMID:24489825   PMID:24662486   PMID:24722188   PMID:24790097   PMID:24828152   PMID:25260751   PMID:25296754   PMID:25416956   PMID:25588945   PMID:25910212  
PMID:25921289   PMID:25959826   PMID:26186194   PMID:26317613   PMID:26344197   PMID:26456826   PMID:26496610   PMID:26508657   PMID:26638075   PMID:26715116   PMID:26819309   PMID:26871637  
PMID:27008177   PMID:27107014   PMID:27684187   PMID:27764233   PMID:27880917   PMID:28190767   PMID:28218281   PMID:28514442   PMID:28581508   PMID:28718761   PMID:28867611   PMID:28959041  
PMID:29357390   PMID:29395067   PMID:29509190   PMID:29568061   PMID:29604273   PMID:29764989   PMID:29791485   PMID:29844126   PMID:29891722   PMID:29892012   PMID:29997244   PMID:30097533  
PMID:30166454   PMID:30456986   PMID:30759391   PMID:31177093   PMID:31462741   PMID:31467278   PMID:31515488   PMID:31536960   PMID:31597781   PMID:31699778   PMID:31732153   PMID:31744816  
PMID:31871319   PMID:31995728   PMID:32044971   PMID:32296183   PMID:32546618   PMID:32814053   PMID:33277362   PMID:33417871   PMID:33462405   PMID:33545068   PMID:33957083   PMID:33961781  
PMID:34079125   PMID:34273398   PMID:34349018   PMID:34373451   PMID:34535262   PMID:34591612   PMID:34672954   PMID:34702444   PMID:34709727   PMID:34761192   PMID:34831298   PMID:35140242  
PMID:35256949   PMID:35271311   PMID:35331737   PMID:35384245   PMID:35509820   PMID:35563538   PMID:35831314   PMID:35944360   PMID:36114006   PMID:36215168   PMID:36484721   PMID:36610398  
PMID:36810288   PMID:36949045   PMID:36976175   PMID:37071682   PMID:37223481   PMID:37398436   PMID:37429858   PMID:38569033   PMID:38803224   PMID:38943005   PMID:39231216   PMID:39358380  


Genomics

Comparative Map Data
HGS
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381781,684,011 - 81,702,121 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1781,683,326 - 81,703,138 (+)EnsemblGRCh38hg38GRCh38
GRCh371779,651,041 - 79,669,151 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361777,261,425 - 77,279,553 (+)NCBINCBI36Build 36hg18NCBI36
Build 341777,261,424 - 77,279,550NCBI
Celera1776,295,942 - 76,314,294 (+)NCBICelera
Cytogenetic Map17q25.3NCBI
HuRef1775,097,132 - 75,115,050 (+)NCBIHuRef
CHM1_11779,737,183 - 79,755,370 (+)NCBICHM1_1
T2T-CHM13v2.01782,600,905 - 82,619,025 (+)NCBIT2T-CHM13v2.0
Hgs
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3911120,358,431 - 120,374,810 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl11120,358,461 - 120,374,805 (+)EnsemblGRCm39 Ensembl
GRCm3811120,467,605 - 120,483,984 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl11120,467,635 - 120,483,979 (+)EnsemblGRCm38mm10GRCm38
MGSCv3711120,328,949 - 120,345,298 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3611120,283,781 - 120,300,069 (+)NCBIMGSCv36mm8
Celera11132,203,066 - 132,219,316 (+)NCBICelera
Cytogenetic Map11E2NCBI
cM Map1184.16NCBI
Hgs
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr810106,237,988 - 106,256,174 (+)NCBIGRCr8
mRatBN7.210105,739,617 - 105,757,838 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl10105,739,296 - 105,757,835 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx10110,844,188 - 110,862,000 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.010110,307,219 - 110,325,031 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.010105,660,239 - 105,678,295 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.010109,638,944 - 109,657,460 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl10109,638,767 - 109,657,456 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.010109,232,509 - 109,250,728 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.410109,861,289 - 109,869,587 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.110109,875,792 - 109,883,652 (+)NCBI
Celera10104,283,857 - 104,301,769 (+)NCBICelera
Cytogenetic Map10q32.3NCBI
Hgs
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555061,405,543 - 1,418,095 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049555061,405,543 - 1,418,095 (-)NCBIChiLan1.0ChiLan1.0
HGS
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21998,273,839 - 98,292,160 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan117103,174,297 - 103,192,557 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01776,143,212 - 76,161,469 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11781,844,379 - 81,862,335 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1781,844,379 - 81,862,335 (+)Ensemblpanpan1.1panPan2
HGS
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.19499,071 - 513,375 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl9499,116 - 514,308 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha91,101,298 - 1,115,455 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.091,092,550 - 1,106,872 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl91,092,550 - 1,107,809 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.191,117,545 - 1,131,697 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.091,244,142 - 1,258,290 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.091,323,173 - 1,337,298 (-)NCBIUU_Cfam_GSD_1.0
Hgs
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244056021,110,692 - 1,126,331 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365945,285,551 - 5,301,233 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365945,285,678 - 5,301,267 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
HGS
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl121,207,036 - 1,219,715 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1121,207,036 - 1,219,750 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
HGS
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11673,613,711 - 73,632,527 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1673,613,786 - 73,632,016 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607745,022,394 - 45,041,222 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Hgs
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462480110,620,753 - 10,634,341 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462480110,620,717 - 10,634,670 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in HGS
74 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q25.3(chr17:78901959-83086677)x3 copy number gain See cases [RCV000050934] Chr17:78901959..83086677 [GRCh38]
Chr17:76898041..81044553 [GRCh37]
Chr17:74409636..78637842 [NCBI36]
Chr17:17q25.3		 pathogenic
GRCh38/hg38 17q25.3(chr17:78092236-83086677)x3 copy number gain See cases [RCV000050685] Chr17:78092236..83086677 [GRCh38]
Chr17:76088317..81044553 [GRCh37]
Chr17:73599912..78637842 [NCBI36]
Chr17:17q25.3		 pathogenic
GRCh38/hg38 17q24.3-25.3(chr17:69209079-83086677)x3 copy number gain See cases [RCV000052486] Chr17:69209079..83086677 [GRCh38]
Chr17:67205220..81044553 [GRCh37]
Chr17:64716815..78637842 [NCBI36]
Chr17:17q24.3-25.3		 pathogenic
GRCh38/hg38 17q25.3(chr17:78918650-83021095)x3 copy number gain See cases [RCV000052497] Chr17:78918650..83021095 [GRCh38]
Chr17:76914732..80978971 [GRCh37]
Chr17:74426327..78572260 [NCBI36]
Chr17:17q25.3		 pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3		 pathogenic
GRCh38/hg38 17q25.3(chr17:80328106-83086677)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053454]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053454]|See cases [RCV000053454] Chr17:80328106..83086677 [GRCh38]
Chr17:78301906..81044553 [GRCh37]
Chr17:75916501..78637842 [NCBI36]
Chr17:17q25.3		 pathogenic
GRCh38/hg38 17q25.3(chr17:81008196-83102584)x3 copy number gain See cases [RCV000138688] Chr17:81008196..83102584 [GRCh38]
Chr17:78981996..81048189 [GRCh37]
Chr17:76596591..78653749 [NCBI36]
Chr17:17q25.3		 pathogenic
GRCh38/hg38 17q25.3(chr17:81401966-83084062)x1 copy number loss See cases [RCV000142007] Chr17:81401966..83084062 [GRCh38]
Chr17:79375766..81041938 [GRCh37]
Chr17:76990361..78635227 [NCBI36]
Chr17:17q25.3		 likely pathogenic
GRCh38/hg38 17q24.3-25.3(chr17:69916435-83102552)x3 copy number gain See cases [RCV000143342] Chr17:69916435..83102552 [GRCh38]
Chr17:67912576..81048189 [GRCh37]
Chr17:65424171..78653717 [NCBI36]
Chr17:17q24.3-25.3		 pathogenic
GRCh37/hg19 17q25.3(chr17:78514452-81041938)x1 copy number loss See cases [RCV000449416] Chr17:78514452..81041938 [GRCh37]
Chr17:17q25.3		 pathogenic
GRCh37/hg19 17q25.1-25.3(chr17:73951701-81041938)x3 copy number gain See cases [RCV000447539] Chr17:73951701..81041938 [GRCh37]
Chr17:17q25.1-25.3		 pathogenic
GRCh37/hg19 17q24.2-25.3(chr17:64241326-81041938)x3 copy number gain See cases [RCV000447577] Chr17:64241326..81041938 [GRCh37]
Chr17:17q24.2-25.3		 pathogenic
GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3 copy number gain See cases [RCV000447823] Chr17:42580684..81085615 [GRCh37]
Chr17:17q21.31-25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17q25.1-25.3(chr17:73951701-81041938)x3 copy number gain See cases [RCV000510919] Chr17:73951701..81041938 [GRCh37]
Chr17:17q25.1-25.3		 pathogenic
NM_004712.5(HGS):c.1142C>G (p.Ser381Cys) single nucleotide variant not specified [RCV004294075] Chr17:81695186 [GRCh38]
Chr17:79662216 [GRCh37]
Chr17:17q25.3		 uncertain significance
GRCh37/hg19 17q24.2-25.3(chr17:67002415-81041938)x3 copy number gain See cases [RCV000512573] Chr17:67002415..81041938 [GRCh37]
Chr17:17q24.2-25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17q24.1-25.3(chr17:63689671-81041938)x3 copy number gain not provided [RCV000683952] Chr17:63689671..81041938 [GRCh37]
Chr17:17q24.1-25.3		 pathogenic
GRCh37/hg19 17q25.3(chr17:76552611-81041938)x3 copy number gain not provided [RCV000683965] Chr17:76552611..81041938 [GRCh37]
Chr17:17q25.3		 likely pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
NM_004712.5(HGS):c.1006G>A (p.Glu336Lys) single nucleotide variant not specified [RCV004314590] Chr17:81694954 [GRCh38]
Chr17:79661984 [GRCh37]
Chr17:17q25.3		 uncertain significance
GRCh37/hg19 17q25.3(chr17:79650594-79663010)x0 copy number loss not provided [RCV000752229] Chr17:79650594..79663010 [GRCh37]
Chr17:17q25.3		 benign
NM_004712.5(HGS):c.1567-7C>T single nucleotide variant not provided [RCV000879219] Chr17:81696600 [GRCh38]
Chr17:79663630 [GRCh37]
Chr17:17q25.3		 benign
NM_004712.5(HGS):c.739C>G (p.Gln247Glu) single nucleotide variant not provided [RCV000899727] Chr17:81693579 [GRCh38]
Chr17:79660609 [GRCh37]
Chr17:17q25.3		 likely benign
NM_004712.5(HGS):c.1200G>C (p.Glu400Asp) single nucleotide variant not provided [RCV000959461] Chr17:81695806 [GRCh38]
Chr17:79662836 [GRCh37]
Chr17:17q25.3		 benign
NM_004712.5(HGS):c.1374C>T (p.Asn458=) single nucleotide variant not provided [RCV000906836] Chr17:81695980 [GRCh38]
Chr17:79663010 [GRCh37]
Chr17:17q25.3		 benign
NM_004712.5(HGS):c.1974C>T (p.Pro658=) single nucleotide variant not provided [RCV000922314] Chr17:81700558 [GRCh38]
Chr17:79667588 [GRCh37]
Chr17:17q25.3		 likely benign
NM_004712.5(HGS):c.416-9T>C single nucleotide variant not provided [RCV000925159] Chr17:81690173 [GRCh38]
Chr17:79657203 [GRCh37]
Chr17:17q25.3		 likely benign
GRCh37/hg19 17q25.3(chr17:79496613-79693150)x3 copy number gain not provided [RCV000848240] Chr17:79496613..79693150 [GRCh37]
Chr17:17q25.3		 uncertain significance
GRCh37/hg19 17q24.1-25.3(chr17:62778720-81041938)x3 copy number gain not provided [RCV000849900] Chr17:62778720..81041938 [GRCh37]
Chr17:17q24.1-25.3		 pathogenic
GRCh37/hg19 17q25.3(chr17:79663313-80197463)x3 copy number gain not provided [RCV000848219] Chr17:79663313..80197463 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1998T>A (p.Thr666=) single nucleotide variant not provided [RCV000958746] Chr17:81700582 [GRCh38]
Chr17:79667612 [GRCh37]
Chr17:17q25.3		 benign
GRCh37/hg19 17q25.3(chr17:78608912-81041938)x3 copy number gain not provided [RCV000848418] Chr17:78608912..81041938 [GRCh37]
Chr17:17q25.3		 pathogenic
GRCh37/hg19 17q25.3(chr17:79531886-79685043)x1 copy number loss not provided [RCV000846802] Chr17:79531886..79685043 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.2192A>C (p.Tyr731Ser) single nucleotide variant not specified [RCV004292662] Chr17:81701100 [GRCh38]
Chr17:79668130 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.709T>C (p.Tyr237His) single nucleotide variant not specified [RCV004293118] Chr17:81693549 [GRCh38]
Chr17:79660579 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.891G>T (p.Ser297=) single nucleotide variant not provided [RCV000962558] Chr17:81693920 [GRCh38]
Chr17:79660950 [GRCh37]
Chr17:17q25.3		 benign
NM_004712.5(HGS):c.1891A>G (p.Met631Val) single nucleotide variant not provided [RCV000955534] Chr17:81700475 [GRCh38]
Chr17:79667505 [GRCh37]
Chr17:17q25.3		 likely benign
NM_004712.5(HGS):c.1567-6G>A single nucleotide variant not provided [RCV000904940] Chr17:81696601 [GRCh38]
Chr17:79663631 [GRCh37]
Chr17:17q25.3		 likely benign
NM_004712.5(HGS):c.199-9C>T single nucleotide variant not provided [RCV000953062] Chr17:81686994 [GRCh38]
Chr17:79654024 [GRCh37]
Chr17:17q25.3		 benign
NC_000017.10:g.(?_79618104)_(79894690_?)dup duplication not provided [RCV003109580] Chr17:79618104..79894690 [GRCh37]
Chr17:17q25.3		 uncertain significance
NC_000017.10:g.(?_79618104)_(79674270_?)del deletion not provided [RCV003122585] Chr17:79618104..79674270 [GRCh37]
Chr17:17q25.3		 pathogenic
NC_000017.10:g.(?_79477716)_(80900339_?)dup duplication not provided [RCV003122586] Chr17:79477716..80900339 [GRCh37]
Chr17:17q25.3		 uncertain significance
GRCh37/hg19 17q25.1-25.3(chr17:73481509-81043199)x3 copy number gain not provided [RCV002276051] Chr17:73481509..81043199 [GRCh37]
Chr17:17q25.1-25.3		 pathogenic
NM_004712.5(HGS):c.2198C>T (p.Ala733Val) single nucleotide variant not specified [RCV004233304] Chr17:81701106 [GRCh38]
Chr17:79668136 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1028G>A (p.Arg343His) single nucleotide variant not specified [RCV004230984] Chr17:81694976 [GRCh38]
Chr17:79662006 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1163G>A (p.Gly388Asp) single nucleotide variant not specified [RCV004093238] Chr17:81695207 [GRCh38]
Chr17:79662237 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1909T>A (p.Tyr637Asn) single nucleotide variant not specified [RCV004104638] Chr17:81700493 [GRCh38]
Chr17:79667523 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1910A>G (p.Tyr637Cys) single nucleotide variant not specified [RCV004104295] Chr17:81700494 [GRCh38]
Chr17:79667524 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.2020G>A (p.Val674Met) single nucleotide variant not specified [RCV004156965] Chr17:81700698 [GRCh38]
Chr17:79667728 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.748C>G (p.Pro250Ala) single nucleotide variant not specified [RCV004201493] Chr17:81693660 [GRCh38]
Chr17:79660690 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1282A>G (p.Met428Val) single nucleotide variant not specified [RCV004150468] Chr17:81695888 [GRCh38]
Chr17:79662918 [GRCh37]
Chr17:17q25.3		 likely benign
NM_004712.5(HGS):c.1475G>A (p.Arg492Gln) single nucleotide variant not specified [RCV004143577] Chr17:81696438 [GRCh38]
Chr17:79663468 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1819G>A (p.Val607Met) single nucleotide variant not specified [RCV004153572] Chr17:81696935 [GRCh38]
Chr17:79663965 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1331A>G (p.Gln444Arg) single nucleotide variant not specified [RCV004159768] Chr17:81695937 [GRCh38]
Chr17:79662967 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1729G>A (p.Gly577Arg) single nucleotide variant not specified [RCV004152445] Chr17:81696845 [GRCh38]
Chr17:79663875 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1789G>A (p.Gly597Ser) single nucleotide variant not specified [RCV004118892] Chr17:81696905 [GRCh38]
Chr17:79663935 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1730G>T (p.Gly577Val) single nucleotide variant not specified [RCV004159461] Chr17:81696846 [GRCh38]
Chr17:79663876 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.2276C>T (p.Pro759Leu) single nucleotide variant not specified [RCV004091282] Chr17:81701560 [GRCh38]
Chr17:79668590 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.2191T>A (p.Tyr731Asn) single nucleotide variant not specified [RCV004123052] Chr17:81701099 [GRCh38]
Chr17:79668129 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.238C>T (p.His80Tyr) single nucleotide variant not specified [RCV004088411] Chr17:81687042 [GRCh38]
Chr17:79654072 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.2297C>A (p.Ala766Glu) single nucleotide variant not specified [RCV004081634] Chr17:81701581 [GRCh38]
Chr17:79668611 [GRCh37]
Chr17:17q25.3		 uncertain significance
Single allele deletion See cases [RCV003154621] Chr17:79539041..81052322 [GRCh37]
Chr17:17q25.3		 pathogenic
NM_004712.5(HGS):c.1909T>C (p.Tyr637His) single nucleotide variant not specified [RCV004281277] Chr17:81700493 [GRCh38]
Chr17:79667523 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1221G>A (p.Gln407=) single nucleotide variant not provided [RCV003422979] Chr17:81695827 [GRCh38]
Chr17:79662857 [GRCh37]
Chr17:17q25.3		 likely benign
NM_004712.5(HGS):c.1919G>T (p.Gly640Val) single nucleotide variant not specified [RCV004348453] Chr17:81700503 [GRCh38]
Chr17:79667533 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.698T>G (p.Leu233Arg) single nucleotide variant not specified [RCV004343703] Chr17:81693538 [GRCh38]
Chr17:79660568 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.851C>T (p.Ser284Phe) single nucleotide variant not specified [RCV004342546] Chr17:81693880 [GRCh38]
Chr17:79660910 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.161A>C (p.Asn54Thr) single nucleotide variant not specified [RCV004356789] Chr17:81686350 [GRCh38]
Chr17:79653380 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.304G>T (p.Val102Leu) single nucleotide variant not specified [RCV004349021] Chr17:81688716 [GRCh38]
Chr17:79655746 [GRCh37]
Chr17:17q25.3		 uncertain significance
GRCh37/hg19 17q25.3(chr17:79128754-80092824)x1 copy number loss not provided [RCV003483326] Chr17:79128754..80092824 [GRCh37]
Chr17:17q25.3		 likely pathogenic
NM_004712.5(HGS):c.1446G>A (p.Gly482=) single nucleotide variant not provided [RCV003422980] Chr17:81696409 [GRCh38]
Chr17:79663439 [GRCh37]
Chr17:17q25.3		 likely benign
NM_004712.5(HGS):c.538C>T (p.His180Tyr) single nucleotide variant not provided [RCV003421555] Chr17:81691447 [GRCh38]
Chr17:79658477 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1346T>C (p.Met449Thr) single nucleotide variant not specified [RCV004396981] Chr17:81695952 [GRCh38]
Chr17:79662982 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.251C>G (p.Ala84Gly) single nucleotide variant not specified [RCV004396982] Chr17:81687055 [GRCh38]
Chr17:79654085 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.713T>C (p.Leu238Pro) single nucleotide variant not specified [RCV004396984] Chr17:81693553 [GRCh38]
Chr17:79660583 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.724C>A (p.Leu242Met) single nucleotide variant not specified [RCV004396986] Chr17:81693564 [GRCh38]
Chr17:79660594 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.734A>C (p.Gln245Pro) single nucleotide variant not specified [RCV004396989] Chr17:81693574 [GRCh38]
Chr17:79660604 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.731A>C (p.Gln244Pro) single nucleotide variant not specified [RCV004396987] Chr17:81693571 [GRCh38]
Chr17:79660601 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.364G>A (p.Glu122Lys) single nucleotide variant not specified [RCV004396983] Chr17:81688776 [GRCh38]
Chr17:79655806 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.720C>A (p.Ser240Arg) single nucleotide variant not specified [RCV004396985] Chr17:81693560 [GRCh38]
Chr17:79660590 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.887C>T (p.Pro296Leu) single nucleotide variant not specified [RCV004396990] Chr17:81693916 [GRCh38]
Chr17:79660946 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.947C>T (p.Ala316Val) single nucleotide variant not specified [RCV004396991] Chr17:81694825 [GRCh38]
Chr17:79661855 [GRCh37]
Chr17:17q25.3		 uncertain significance
NC_000017.10:g.(?_79477716)_(80901020_?)dup duplication not provided [RCV004581372] Chr17:79477716..80901020 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1108A>G (p.Asn370Asp) single nucleotide variant not specified [RCV004630552] Chr17:81695056 [GRCh38]
Chr17:79662086 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1243G>A (p.Ala415Thr) single nucleotide variant not specified [RCV004630553] Chr17:81695849 [GRCh38]
Chr17:79662879 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1751C>T (p.Ser584Leu) single nucleotide variant not specified [RCV004630556] Chr17:81696867 [GRCh38]
Chr17:79663897 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1040C>T (p.Thr347Met) single nucleotide variant not specified [RCV004626192] Chr17:81694988 [GRCh38]
Chr17:79662018 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.2291C>T (p.Pro764Leu) single nucleotide variant not specified [RCV004630551] Chr17:81701575 [GRCh38]
Chr17:79668605 [GRCh37]
Chr17:17q25.3		 uncertain significance
GRCh37/hg19 17q25.3(chr17:79663142-81041938)x1 copy number loss not provided [RCV004819392] Chr17:79663142..81041938 [GRCh37]
Chr17:17q25.3		 pathogenic
NM_004712.5(HGS):c.1759G>T (p.Ala587Ser) single nucleotide variant not specified [RCV004925922] Chr17:81696875 [GRCh38]
Chr17:79663905 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.706G>A (p.Glu236Lys) single nucleotide variant not specified [RCV004925923] Chr17:81693546 [GRCh38]
Chr17:79660576 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1810A>G (p.Met604Val) single nucleotide variant not specified [RCV004925924] Chr17:81696926 [GRCh38]
Chr17:79663956 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1928G>T (p.Gly643Val) single nucleotide variant not specified [RCV004925925] Chr17:81700512 [GRCh38]
Chr17:79667542 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1474C>T (p.Arg492Trp) single nucleotide variant not specified [RCV004925926] Chr17:81696437 [GRCh38]
Chr17:79663467 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.944C>T (p.Ser315Leu) single nucleotide variant not specified [RCV004925927] Chr17:81694822 [GRCh38]
Chr17:79661852 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1961C>T (p.Pro654Leu) single nucleotide variant not specified [RCV004925928] Chr17:81700545 [GRCh38]
Chr17:79667575 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1502A>T (p.Glu501Val) single nucleotide variant not specified [RCV004925929] Chr17:81696465 [GRCh38]
Chr17:79663495 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.314G>A (p.Arg105His) single nucleotide variant not specified [RCV004925930] Chr17:81688726 [GRCh38]
Chr17:79655756 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1180C>T (p.Pro394Ser) single nucleotide variant not specified [RCV004925931] Chr17:81695786 [GRCh38]
Chr17:79662816 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.2158A>G (p.Ser720Gly) single nucleotide variant not specified [RCV004925932] Chr17:81701066 [GRCh38]
Chr17:79668096 [GRCh37]
Chr17:17q25.3		 likely benign
NM_004712.5(HGS):c.340G>A (p.Ala114Thr) single nucleotide variant not specified [RCV004925933] Chr17:81688752 [GRCh38]
Chr17:79655782 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.764C>T (p.Thr255Met) single nucleotide variant not specified [RCV004925934] Chr17:81693676 [GRCh38]
Chr17:79660706 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.430G>C (p.Glu144Gln) single nucleotide variant not specified [RCV004925935] Chr17:81690196 [GRCh38]
Chr17:79657226 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1730G>C (p.Gly577Ala) single nucleotide variant not specified [RCV004925936] Chr17:81696846 [GRCh38]
Chr17:79663876 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.1825A>C (p.Met609Leu) single nucleotide variant not specified [RCV004925937] Chr17:81696941 [GRCh38]
Chr17:79663971 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_004712.5(HGS):c.503G>A (p.Arg168His) single nucleotide variant not specified [RCV004925938] Chr17:81690708 [GRCh38]
Chr17:79657738 [GRCh37]
Chr17:17q25.3		 uncertain significance
miRNA Target Status (No longer updated)

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR296hsa-miR-296-5pMirtarbaseexternal_infoLuciferase reporter assay//Western blotFunctional MTI18977327
MIR296hsa-miR-296-5pMirecordsexternal_infoNANA18977327
MIR296hsa-miR-296-5pOncomiRDBexternal_infoNANA18977327

Predicted Target Of
Summary Value
Count of predictions:5651
Count of miRNA genes:1162
Interacting mature miRNAs:1492
Transcripts:ENST00000329138, ENST00000570355, ENST00000570652, ENST00000571237, ENST00000571518, ENST00000571647, ENST00000571885, ENST00000572392, ENST00000573080, ENST00000573320, ENST00000573949, ENST00000575058, ENST00000575078, ENST00000576087, ENST00000576393, ENST00000576498, ENST00000577012
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
406993410GWAS642386_Hintelligence QTL GWAS642386 (human)0.000006intelligence178170024581700246Human
597118902GWAS1214976_Hvital capacity QTL GWAS1214976 (human)2e-08vital capacity178169357981693580Human
597188124GWAS1284198_Hmitochondrial DNA measurement QTL GWAS1284198 (human)6e-19mitochondrial DNA measurement178168725581687256Human
597184141GWAS1280215_Hmitochondrial DNA measurement QTL GWAS1280215 (human)4e-13mitochondrial DNA measurement178168820281688203Human

Markers in Region
G35510  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q21UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map6pter-q22.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map11q14.2-q21UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map9p21.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map5q31-q32UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map18p11.22-p11.21UniSTS
Cytogenetic Map5q34-q35UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic MapXp22.32UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map17pUniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map20q13.33UniSTS
D11S2921  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map10q24.33UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic MapXp11.4-p11.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map18pter-p11.3UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map7q21.12UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11p13-p12UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map5q12-q13UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic MapXq25-q26.3UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map18p11.32UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map9p24.1-p23UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map12p11.22UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map9p11UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map15q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q22-qterUniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map19p13.2-cenUniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map9q33UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic MapXq26.2UniSTS
Cytogenetic Map8q13.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map5p13.1-p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map6q14.3-q16.1UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map6q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map6q11.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map10q24-q25UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map14q11.2-q21UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map5p14.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map9p13.1UniSTS
Cytogenetic Map9q34.13UniSTS


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
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_004712 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC139530 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF260566 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI365104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK021483 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097197 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294190 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303800 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC003565 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT009754 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471099 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D84064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DR001213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178467 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U43895 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000329138   ⟹   ENSP00000331201
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,684,011 - 81,702,121 (+)Ensembl
Ensembl Acc Id: ENST00000570355
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,696,601 - 81,701,127 (+)Ensembl
Ensembl Acc Id: ENST00000570652   ⟹   ENSP00000460165
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,701,215 - 81,701,929 (+)Ensembl
Ensembl Acc Id: ENST00000571237   ⟹   ENSP00000458775
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,693,870 - 81,696,987 (+)Ensembl
Ensembl Acc Id: ENST00000571518   ⟹   ENSP00000459685
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,685,605 - 81,690,234 (+)Ensembl
Ensembl Acc Id: ENST00000571647
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,695,956 - 81,698,356 (+)Ensembl
Ensembl Acc Id: ENST00000571885
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,695,681 - 81,696,383 (+)Ensembl
Ensembl Acc Id: ENST00000572392   ⟹   ENSP00000458987
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,684,052 - 81,696,529 (+)Ensembl
Ensembl Acc Id: ENST00000573080
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,691,206 - 81,693,014 (+)Ensembl
Ensembl Acc Id: ENST00000573320   ⟹   ENSP00000458789
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,701,045 - 81,702,121 (+)Ensembl
Ensembl Acc Id: ENST00000573949
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,696,186 - 81,702,115 (+)Ensembl
Ensembl Acc Id: ENST00000575058
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,693,675 - 81,695,930 (+)Ensembl
Ensembl Acc Id: ENST00000575078   ⟹   ENSP00000460130
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,700,695 - 81,701,618 (+)Ensembl
Ensembl Acc Id: ENST00000576087
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,686,267 - 81,690,830 (+)Ensembl
Ensembl Acc Id: ENST00000576393
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,983 - 81,690,604 (+)Ensembl
Ensembl Acc Id: ENST00000576498
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,984 - 81,691,830 (+)Ensembl
Ensembl Acc Id: ENST00000577012   ⟹   ENSP00000458603
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,684,108 - 81,688,827 (+)Ensembl
Ensembl Acc Id: ENST00000676462   ⟹   ENSP00000503043
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,963 - 81,701,791 (+)Ensembl
Ensembl Acc Id: ENST00000676478   ⟹   ENSP00000504482
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,684,006 - 81,702,116 (+)Ensembl
Ensembl Acc Id: ENST00000676484
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,685,274 - 81,685,689 (+)Ensembl
Ensembl Acc Id: ENST00000676546   ⟹   ENSP00000504106
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,932 - 81,702,119 (+)Ensembl
Ensembl Acc Id: ENST00000676665   ⟹   ENSP00000504079
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,700,467 - 81,700,814 (+)Ensembl
Ensembl Acc Id: ENST00000676704   ⟹   ENSP00000504565
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,696,357 - 81,700,600 (+)Ensembl
Ensembl Acc Id: ENST00000676721   ⟹   ENSP00000504783
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,684,011 - 81,688,827 (+)Ensembl
Ensembl Acc Id: ENST00000676727
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,693,870 - 81,694,424 (+)Ensembl
Ensembl Acc Id: ENST00000676729   ⟹   ENSP00000503138
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,684,047 - 81,702,116 (+)Ensembl
Ensembl Acc Id: ENST00000676879   ⟹   ENSP00000504244
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,693,503 - 81,693,752 (+)Ensembl
Ensembl Acc Id: ENST00000676898   ⟹   ENSP00000504738
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,688,704 - 81,690,234 (+)Ensembl
Ensembl Acc Id: ENST00000676963   ⟹   ENSP00000504434
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,693,870 - 81,694,853 (+)Ensembl
Ensembl Acc Id: ENST00000677012   ⟹   ENSP00000504241
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,684,067 - 81,687,095 (+)Ensembl
Ensembl Acc Id: ENST00000677044   ⟹   ENSP00000504151
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,963 - 81,702,105 (+)Ensembl
Ensembl Acc Id: ENST00000677109   ⟹   ENSP00000503405
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,963 - 81,702,116 (+)Ensembl
Ensembl Acc Id: ENST00000677129
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,690,290 - 81,690,742 (+)Ensembl
Ensembl Acc Id: ENST00000677132   ⟹   ENSP00000504147
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,693,870 - 81,694,853 (+)Ensembl
Ensembl Acc Id: ENST00000677159
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,694,749 - 81,702,110 (+)Ensembl
Ensembl Acc Id: ENST00000677161   ⟹   ENSP00000503695
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,326 - 81,702,116 (+)Ensembl
Ensembl Acc Id: ENST00000677188   ⟹   ENSP00000503993
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,696,357 - 81,700,600 (+)Ensembl
Ensembl Acc Id: ENST00000677209   ⟹   ENSP00000503175
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,684,011 - 81,687,095 (+)Ensembl
Ensembl Acc Id: ENST00000677225   ⟹   ENSP00000503479
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,684,021 - 81,702,116 (+)Ensembl
Ensembl Acc Id: ENST00000677232
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,696,824 - 81,697,191 (+)Ensembl
Ensembl Acc Id: ENST00000677243   ⟹   ENSP00000502851
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,963 - 81,702,105 (+)Ensembl
Ensembl Acc Id: ENST00000677390   ⟹   ENSP00000503349
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,693,870 - 81,695,223 (+)Ensembl
Ensembl Acc Id: ENST00000677402
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,690,825 - 81,691,571 (+)Ensembl
Ensembl Acc Id: ENST00000677463   ⟹   ENSP00000504743
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,691,447 - 81,693,581 (+)Ensembl
Ensembl Acc Id: ENST00000677466   ⟹   ENSP00000504390
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,701,045 - 81,701,929 (+)Ensembl
Ensembl Acc Id: ENST00000677472
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,692,797 - 81,693,581 (+)Ensembl
Ensembl Acc Id: ENST00000677484   ⟹   ENSP00000503188
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,963 - 81,702,116 (+)Ensembl
Ensembl Acc Id: ENST00000677511   ⟹   ENSP00000504732
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,696,607 - 81,696,747 (+)Ensembl
Ensembl Acc Id: ENST00000677639
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,690,674 - 81,691,011 (+)Ensembl
Ensembl Acc Id: ENST00000677663   ⟹   ENSP00000503376
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,701,215 - 81,701,929 (+)Ensembl
Ensembl Acc Id: ENST00000677706   ⟹   ENSP00000504348
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,700,467 - 81,700,814 (+)Ensembl
Ensembl Acc Id: ENST00000677725
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,693,400 - 81,693,581 (+)Ensembl
Ensembl Acc Id: ENST00000677728   ⟹   ENSP00000503213
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,696,607 - 81,696,998 (+)Ensembl
Ensembl Acc Id: ENST00000677805
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,689,323 - 81,690,234 (+)Ensembl
Ensembl Acc Id: ENST00000677818   ⟹   ENSP00000502990
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,690,182 - 81,693,581 (+)Ensembl
Ensembl Acc Id: ENST00000677872   ⟹   ENSP00000504691
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,691,447 - 81,693,581 (+)Ensembl
Ensembl Acc Id: ENST00000677898
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,692,888 - 81,693,965 (+)Ensembl
Ensembl Acc Id: ENST00000678055   ⟹   ENSP00000504559
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,696,357 - 81,696,747 (+)Ensembl
Ensembl Acc Id: ENST00000678096   ⟹   ENSP00000504478
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,932 - 81,703,138 (+)Ensembl
Ensembl Acc Id: ENST00000678105   ⟹   ENSP00000504789
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,684,000 - 81,702,116 (+)Ensembl
Ensembl Acc Id: ENST00000678115
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,963 - 81,702,116 (+)Ensembl
Ensembl Acc Id: ENST00000678142   ⟹   ENSP00000503319
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,695,164 - 81,696,529 (+)Ensembl
Ensembl Acc Id: ENST00000678176   ⟹   ENSP00000504798
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,696,607 - 81,696,998 (+)Ensembl
Ensembl Acc Id: ENST00000678196   ⟹   ENSP00000503545
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,963 - 81,701,929 (+)Ensembl
Ensembl Acc Id: ENST00000678218
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,691,447 - 81,692,086 (+)Ensembl
Ensembl Acc Id: ENST00000678238
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,689,360 - 81,690,234 (+)Ensembl
Ensembl Acc Id: ENST00000678271
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,689,175 - 81,690,234 (+)Ensembl
Ensembl Acc Id: ENST00000678296
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,689,856 - 81,690,234 (+)Ensembl
Ensembl Acc Id: ENST00000678313
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,690,610 - 81,692,453 (+)Ensembl
Ensembl Acc Id: ENST00000678385
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,689,035 - 81,690,234 (+)Ensembl
Ensembl Acc Id: ENST00000678387
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,932 - 81,701,348 (+)Ensembl
Ensembl Acc Id: ENST00000678406   ⟹   ENSP00000502956
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,694,815 - 81,695,067 (+)Ensembl
Ensembl Acc Id: ENST00000678428   ⟹   ENSP00000503616
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,695,164 - 81,696,747 (+)Ensembl
Ensembl Acc Id: ENST00000678478   ⟹   ENSP00000503600
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,693,654 - 81,693,965 (+)Ensembl
Ensembl Acc Id: ENST00000678485
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,691,447 - 81,691,905 (+)Ensembl
Ensembl Acc Id: ENST00000678541
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,684,047 - 81,702,116 (+)Ensembl
Ensembl Acc Id: ENST00000678550   ⟹   ENSP00000504052
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,700,467 - 81,700,814 (+)Ensembl
Ensembl Acc Id: ENST00000678565   ⟹   ENSP00000503803
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,700,467 - 81,700,600 (+)Ensembl
Ensembl Acc Id: ENST00000678607   ⟹   ENSP00000504713
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,700,695 - 81,702,121 (+)Ensembl
Ensembl Acc Id: ENST00000678658
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,685,733 - 81,702,915 (+)Ensembl
Ensembl Acc Id: ENST00000678667   ⟹   ENSP00000504194
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,696,357 - 81,696,747 (+)Ensembl
Ensembl Acc Id: ENST00000678680   ⟹   ENSP00000504409
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,693,654 - 81,694,853 (+)Ensembl
Ensembl Acc Id: ENST00000678748   ⟹   ENSP00000503483
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,693,503 - 81,694,853 (+)Ensembl
Ensembl Acc Id: ENST00000678846   ⟹   ENSP00000503372
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,685,637 - 81,696,468 (+)Ensembl
Ensembl Acc Id: ENST00000678866   ⟹   ENSP00000504854
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,684,021 - 81,702,116 (+)Ensembl
Ensembl Acc Id: ENST00000678893   ⟹   ENSP00000504821
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,688,704 - 81,693,581 (+)Ensembl
Ensembl Acc Id: ENST00000678896   ⟹   ENSP00000503714
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,696,824 - 81,700,600 (+)Ensembl
Ensembl Acc Id: ENST00000678907   ⟹   ENSP00000504806
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,693,870 - 81,695,067 (+)Ensembl
Ensembl Acc Id: ENST00000678926   ⟹   ENSP00000502989
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,694,815 - 81,695,223 (+)Ensembl
Ensembl Acc Id: ENST00000678944
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,696,064 - 81,696,529 (+)Ensembl
Ensembl Acc Id: ENST00000678979
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,688,515 - 81,688,827 (+)Ensembl
Ensembl Acc Id: ENST00000678981   ⟹   ENSP00000503275
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,695,164 - 81,695,999 (+)Ensembl
Ensembl Acc Id: ENST00000679036   ⟹   ENSP00000504505
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,696,824 - 81,700,600 (+)Ensembl
Ensembl Acc Id: ENST00000679146   ⟹   ENSP00000504113
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,693,870 - 81,695,067 (+)Ensembl
Ensembl Acc Id: ENST00000679168   ⟹   ENSP00000504810
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,691,447 - 81,694,853 (+)Ensembl
Ensembl Acc Id: ENST00000679170   ⟹   ENSP00000503359
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,949 - 81,686,387 (+)Ensembl
Ensembl Acc Id: ENST00000679191   ⟹   ENSP00000503211
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,932 - 81,703,138 (+)Ensembl
Ensembl Acc Id: ENST00000679235
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,686,902 - 81,687,095 (+)Ensembl
Ensembl Acc Id: ENST00000679275   ⟹   ENSP00000504270
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,684,021 - 81,702,086 (+)Ensembl
Ensembl Acc Id: ENST00000679336   ⟹   ENSP00000502961
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,683,963 - 81,701,929 (+)Ensembl
Ensembl Acc Id: ENST00000679340   ⟹   ENSP00000503389
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1781,701,045 - 81,701,929 (+)Ensembl
RefSeq Acc Id: NM_004712   ⟹   NP_004703
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381781,684,011 - 81,702,121 (+)NCBI
GRCh371779,650,962 - 79,669,151 (+)ENTREZGENE
Build 361777,261,425 - 77,279,553 (+)NCBI Archive
HuRef1775,097,132 - 75,115,050 (+)ENTREZGENE
CHM1_11779,737,183 - 79,755,370 (+)NCBI
T2T-CHM13v2.01782,600,905 - 82,619,025 (+)NCBI
Sequence:
RefSeq Acc Id: NP_004703   ⟸   NM_004712
- UniProtKB: Q9NR36 (UniProtKB/Swiss-Prot),   O14964 (UniProtKB/Swiss-Prot),   A0A0S2Z4R4 (UniProtKB/TrEMBL),   A0A7I2V307 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000460165   ⟸   ENST00000570652
Ensembl Acc Id: ENSP00000458775   ⟸   ENST00000571237
Ensembl Acc Id: ENSP00000459685   ⟸   ENST00000571518
Ensembl Acc Id: ENSP00000458987   ⟸   ENST00000572392
Ensembl Acc Id: ENSP00000458789   ⟸   ENST00000573320
Ensembl Acc Id: ENSP00000460130   ⟸   ENST00000575078
Ensembl Acc Id: ENSP00000458603   ⟸   ENST00000577012
Ensembl Acc Id: ENSP00000331201   ⟸   ENST00000329138
Ensembl Acc Id: ENSP00000504434   ⟸   ENST00000676963
Ensembl Acc Id: ENSP00000504244   ⟸   ENST00000676879
Ensembl Acc Id: ENSP00000504738   ⟸   ENST00000676898
Ensembl Acc Id: ENSP00000504783   ⟸   ENST00000676721
Ensembl Acc Id: ENSP00000503138   ⟸   ENST00000676729
Ensembl Acc Id: ENSP00000504565   ⟸   ENST00000676704
Ensembl Acc Id: ENSP00000504079   ⟸   ENST00000676665
Ensembl Acc Id: ENSP00000504106   ⟸   ENST00000676546
Ensembl Acc Id: ENSP00000504482   ⟸   ENST00000676478
Ensembl Acc Id: ENSP00000503043   ⟸   ENST00000676462
Ensembl Acc Id: ENSP00000503993   ⟸   ENST00000677188
Ensembl Acc Id: ENSP00000504147   ⟸   ENST00000677132
Ensembl Acc Id: ENSP00000503695   ⟸   ENST00000677161
Ensembl Acc Id: ENSP00000503405   ⟸   ENST00000677109
Ensembl Acc Id: ENSP00000504151   ⟸   ENST00000677044
Ensembl Acc Id: ENSP00000504241   ⟸   ENST00000677012
Ensembl Acc Id: ENSP00000504732   ⟸   ENST00000677511
Ensembl Acc Id: ENSP00000503188   ⟸   ENST00000677484
Ensembl Acc Id: ENSP00000504743   ⟸   ENST00000677463
Ensembl Acc Id: ENSP00000504390   ⟸   ENST00000677466
Ensembl Acc Id: ENSP00000503349   ⟸   ENST00000677390
Ensembl Acc Id: ENSP00000502851   ⟸   ENST00000677243
Ensembl Acc Id: ENSP00000503175   ⟸   ENST00000677209
Ensembl Acc Id: ENSP00000503479   ⟸   ENST00000677225
Ensembl Acc Id: ENSP00000504691   ⟸   ENST00000677872
Ensembl Acc Id: ENSP00000502990   ⟸   ENST00000677818
Ensembl Acc Id: ENSP00000503213   ⟸   ENST00000677728
Ensembl Acc Id: ENSP00000504348   ⟸   ENST00000677706
Ensembl Acc Id: ENSP00000503376   ⟸   ENST00000677663
Ensembl Acc Id: ENSP00000504559   ⟸   ENST00000678055
Ensembl Acc Id: ENSP00000504478   ⟸   ENST00000678096
Ensembl Acc Id: ENSP00000503600   ⟸   ENST00000678478
Ensembl Acc Id: ENSP00000503616   ⟸   ENST00000678428
Ensembl Acc Id: ENSP00000502956   ⟸   ENST00000678406
Ensembl Acc Id: ENSP00000503319   ⟸   ENST00000678142
Ensembl Acc Id: ENSP00000504798   ⟸   ENST00000678176
Ensembl Acc Id: ENSP00000504789   ⟸   ENST00000678105
Ensembl Acc Id: ENSP00000503545   ⟸   ENST00000678196
Ensembl Acc Id: ENSP00000503372   ⟸   ENST00000678846
Ensembl Acc Id: ENSP00000504821   ⟸   ENST00000678893
Ensembl Acc Id: ENSP00000503714   ⟸   ENST00000678896
Ensembl Acc Id: ENSP00000504854   ⟸   ENST00000678866
Ensembl Acc Id: ENSP00000503483   ⟸   ENST00000678748
Ensembl Acc Id: ENSP00000504713   ⟸   ENST00000678607
Ensembl Acc Id: ENSP00000504194   ⟸   ENST00000678667
Ensembl Acc Id: ENSP00000504409   ⟸   ENST00000678680
Ensembl Acc Id: ENSP00000504052   ⟸   ENST00000678550
Ensembl Acc Id: ENSP00000503803   ⟸   ENST00000678565
Ensembl Acc Id: ENSP00000504806   ⟸   ENST00000678907
Ensembl Acc Id: ENSP00000502989   ⟸   ENST00000678926
Ensembl Acc Id: ENSP00000503275   ⟸   ENST00000678981
Ensembl Acc Id: ENSP00000502961   ⟸   ENST00000679336
Ensembl Acc Id: ENSP00000503389   ⟸   ENST00000679340
Ensembl Acc Id: ENSP00000504270   ⟸   ENST00000679275
Ensembl Acc Id: ENSP00000503211   ⟸   ENST00000679191
Ensembl Acc Id: ENSP00000504113   ⟸   ENST00000679146
Ensembl Acc Id: ENSP00000504810   ⟸   ENST00000679168
Ensembl Acc Id: ENSP00000503359   ⟸   ENST00000679170
Ensembl Acc Id: ENSP00000504505   ⟸   ENST00000679036
Protein Domains
FYVE-type   Hepatocyte growth factor-regulated tyrosine kinase   UIM   VHS

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O14964-F1-model_v2 AlphaFold O14964 1-777 view protein structure

Promoters
RGD ID:6793746
Promoter ID:HG_KWN:27372
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000397498,   NM_001040025,   NM_004712,   UC002KBE.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361777,261,191 - 77,261,691 (-)MPROMDB
RGD ID:6811196
Promoter ID:HG_ACW:36876
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   HeLa_S3
Transcripts:HGSANDMRPL12.EAPR07,   HGSANDMRPL12.IAPR07,   HGSANDMRPL12.JAPR07-UNSPLICED,   HGSANDMRPL12.NAPR07-UNSPLICED
Position:
Human AssemblyChrPosition (strand)Source
Build 361777,262,211 - 77,262,711 (+)MPROMDB
RGD ID:6811197
Promoter ID:HG_ACW:36881
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:HGSANDMRPL12.LAPR07,   HGSANDMRPL12.PAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 361777,278,246 - 77,278,746 (+)MPROMDB
RGD ID:7236639
Promoter ID:EPDNEW_H24065
Type:initiation region
Name:HGS_1
Description:hepatocyte growth factor-regulated tyrosine kinase substrate
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381781,684,011 - 81,684,071EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:4897 AgrOrtholog
COSMIC HGS COSMIC
Ensembl Genes ENSG00000185359 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000329138 ENTREZGENE
  ENST00000329138.9 UniProtKB/Swiss-Prot
  ENST00000676546.1 UniProtKB/Swiss-Prot
Gene3D-CATH 1.20.5.1940 UniProtKB/Swiss-Prot
  1.25.40.90 UniProtKB/Swiss-Prot
  3.30.40.10 UniProtKB/Swiss-Prot
GTEx ENSG00000185359 GTEx
HGNC ID HGNC:4897 ENTREZGENE
Human Proteome Map HGS Human Proteome Map
InterPro ENTH_VHS UniProtKB/Swiss-Prot
  HRS_helical UniProtKB/Swiss-Prot
  Ubi-bd_Hrs_VPS27 UniProtKB/Swiss-Prot
  UIM_dom UniProtKB/Swiss-Prot
  VHS_dom UniProtKB/Swiss-Prot
  Znf_FYVE UniProtKB/Swiss-Prot
  Znf_FYVE-rel UniProtKB/Swiss-Prot
  Znf_FYVE_PHD UniProtKB/Swiss-Prot
  Znf_RING/FYVE/PHD UniProtKB/Swiss-Prot
KEGG Report hsa:9146 UniProtKB/Swiss-Prot
NCBI Gene 9146 ENTREZGENE
OMIM 604375 OMIM
PANTHER HEPATOCYTE GROWTH FACTOR-REGULATED TYROSINE KINASE SUBSTRATE UniProtKB/Swiss-Prot
  PTHR46275 UniProtKB/Swiss-Prot
Pfam FYVE UniProtKB/Swiss-Prot
  Hrs_helical UniProtKB/Swiss-Prot
  VHS UniProtKB/Swiss-Prot
PharmGKB PA29271 PharmGKB
PIRSF Hrs_Vps27 UniProtKB/Swiss-Prot
PROSITE UIM UniProtKB/Swiss-Prot
  VHS UniProtKB/Swiss-Prot
  ZF_FYVE UniProtKB/Swiss-Prot
SMART FYVE UniProtKB/Swiss-Prot
  VHS UniProtKB/Swiss-Prot
Superfamily-SCOP SSF48464 UniProtKB/Swiss-Prot
  SSF57903 UniProtKB/Swiss-Prot
UniProt A0A0S2Z4Q4_HUMAN UniProtKB/TrEMBL
  A0A0S2Z4R4 ENTREZGENE, UniProtKB/TrEMBL
  A0A7I2V2D8_HUMAN UniProtKB/TrEMBL
  A0A7I2V2K1_HUMAN UniProtKB/TrEMBL
  A0A7I2V2K2_HUMAN UniProtKB/TrEMBL
  A0A7I2V2M1_HUMAN UniProtKB/TrEMBL
  A0A7I2V2M4_HUMAN UniProtKB/TrEMBL
  A0A7I2V2R9_HUMAN UniProtKB/TrEMBL
  A0A7I2V2W5_HUMAN UniProtKB/TrEMBL
  A0A7I2V307 ENTREZGENE, UniProtKB/TrEMBL
  A0A7I2V310_HUMAN UniProtKB/TrEMBL
  A0A7I2V319_HUMAN UniProtKB/TrEMBL
  A0A7I2V331_HUMAN UniProtKB/TrEMBL
  A0A7I2V363_HUMAN UniProtKB/TrEMBL
  A0A7I2V3A5_HUMAN UniProtKB/TrEMBL
  A0A7I2V3C3_HUMAN UniProtKB/TrEMBL
  A0A7I2V3E9_HUMAN UniProtKB/TrEMBL
  A0A7I2V3F9_HUMAN UniProtKB/TrEMBL
  A0A7I2V3I8_HUMAN UniProtKB/TrEMBL
  A0A7I2V3J3_HUMAN UniProtKB/TrEMBL
  A0A7I2V3L0_HUMAN UniProtKB/TrEMBL
  A0A7I2V3N6_HUMAN UniProtKB/TrEMBL
  A0A7I2V3Q7_HUMAN UniProtKB/TrEMBL
  A0A7I2V3Z1_HUMAN UniProtKB/TrEMBL
  A0A7I2V468_HUMAN UniProtKB/TrEMBL
  A0A7I2V4J7_HUMAN UniProtKB/TrEMBL
  A0A7I2V4M9_HUMAN UniProtKB/TrEMBL
  A0A7I2V4X6_HUMAN UniProtKB/TrEMBL
  A0A7I2V4Z5_HUMAN UniProtKB/TrEMBL
  A0A7I2V558_HUMAN UniProtKB/TrEMBL
  A0A7I2V569_HUMAN UniProtKB/TrEMBL
  A0A7I2V5A2_HUMAN UniProtKB/TrEMBL
  A0A7I2V5A3_HUMAN UniProtKB/TrEMBL
  A0A7I2V5B7_HUMAN UniProtKB/TrEMBL
  A0A7I2V5C4_HUMAN UniProtKB/TrEMBL
  A0A7I2V5D6_HUMAN UniProtKB/TrEMBL
  A0A7I2V5E5_HUMAN UniProtKB/TrEMBL
  A0A7I2V5E7_HUMAN UniProtKB/TrEMBL
  A0A7I2V5L9_HUMAN UniProtKB/TrEMBL
  A0A7I2V5N3_HUMAN UniProtKB/TrEMBL
  A0A7I2V5V1_HUMAN UniProtKB/TrEMBL
  A0A7I2V5W6_HUMAN UniProtKB/TrEMBL
  A0A7I2V5X2_HUMAN UniProtKB/TrEMBL
  A0A7I2V605_HUMAN UniProtKB/TrEMBL
  A0A7I2V611_HUMAN UniProtKB/TrEMBL
  A0A7I2V616_HUMAN UniProtKB/TrEMBL
  A0A7I2V628_HUMAN UniProtKB/TrEMBL
  A0A7I2V637_HUMAN UniProtKB/TrEMBL
  A0A7I2V674_HUMAN UniProtKB/TrEMBL
  A0A7I2V6E0_HUMAN UniProtKB/TrEMBL
  A0A7I2YQD1_HUMAN UniProtKB/TrEMBL
  A0A7I2YQH7_HUMAN UniProtKB/TrEMBL
  A0A7I2YQM4_HUMAN UniProtKB/TrEMBL
  A0A7I2YQM9_HUMAN UniProtKB/TrEMBL
  A0A7I2YQP0_HUMAN UniProtKB/TrEMBL
  A0A7I2YQS8_HUMAN UniProtKB/TrEMBL
  A0A7I2YQU5_HUMAN UniProtKB/TrEMBL
  A0A7I2YQY0_HUMAN UniProtKB/TrEMBL
  HGS_HUMAN UniProtKB/Swiss-Prot
  I3L165_HUMAN UniProtKB/TrEMBL
  I3L1E3_HUMAN UniProtKB/TrEMBL
  I3L1F1_HUMAN UniProtKB/TrEMBL
  I3L1P5_HUMAN UniProtKB/TrEMBL
  I3L2H4_HUMAN UniProtKB/TrEMBL
  I3L326_HUMAN UniProtKB/TrEMBL
  I3L346_HUMAN UniProtKB/TrEMBL
  O14964 ENTREZGENE
  Q9NR36 ENTREZGENE
UniProt Secondary Q9NR36 UniProtKB/Swiss-Prot