ERGIC3 (ERGIC and golgi 3) - Rat Genome Database

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Gene: ERGIC3 (ERGIC and golgi 3) Homo sapiens
Analyze
Symbol: ERGIC3
Name: ERGIC and golgi 3
RGD ID: 1317746
HGNC Page HGNC:15927
Description: Involved in endoplasmic reticulum to Golgi vesicle-mediated transport and positive regulation of intracellular protein transport. Located in membrane. Part of retrograde transporter complex, Golgi to ER. Biomarker of lung adenocarcinoma.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: C20orf47; C2orf47; CGI-54; dJ477O4.2; endoplasmic reticulum-Golgi intermediate compartment protein 3; endoplasmic reticulum-localized protein ERp43; Erv46; NY-BR-84; PRO0989; SDBCAG84; serologically defined breast cancer antigen 84; serologically defined breast cancer antigen NY-BR-84
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
GRCh382035,542,078 - 35,557,634 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2035,542,038 - 35,557,634 (+)EnsemblGRCh38hg38GRCh38
GRCh372034,129,827 - 34,145,405 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362033,593,192 - 33,608,819 (+)NCBINCBI36Build 36hg18NCBI36
Build 342033,593,191 - 33,608,818NCBI
Celera2030,878,102 - 30,893,718 (+)NCBICelera
Cytogenetic Map20q11.22NCBI
HuRef2030,907,313 - 30,922,911 (+)NCBIHuRef
CHM1_12034,031,121 - 34,046,732 (+)NCBICHM1_1
T2T-CHM13v2.02037,262,891 - 37,278,470 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Endoplasmic reticulum-Golgi intermediate compartment protein 3 knockdown suppresses lung cancer through endoplasmic reticulum stress-induced autophagy. Hong SH, etal., Oncotarget. 2016 Oct 4;7(40):65335-65347. doi: 10.18632/oncotarget.11678.
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
5. Suppression subtractive hybridization identified differentially expressed genes in lung adenocarcinoma: ERGIC3 as a novel lung cancer-related gene. Wu M, etal., BMC Cancer. 2013 Feb 1;13:44. doi: 10.1186/1471-2407-13-44.
Additional References at PubMed
PMID:10810093   PMID:11780052   PMID:12477932   PMID:12747765   PMID:14702039   PMID:15308636   PMID:15489334   PMID:16303743   PMID:17020792   PMID:17207965   PMID:19946888   PMID:20686565  
PMID:21873635   PMID:22190034   PMID:22939629   PMID:23212913   PMID:24097068   PMID:26177443   PMID:26186194   PMID:26638075   PMID:26939788   PMID:27375898   PMID:28298427   PMID:28514442  
PMID:28986522   PMID:29117863   PMID:29180619   PMID:30442662   PMID:31091453   PMID:31142615   PMID:31536960   PMID:32149426   PMID:32296183   PMID:32409323   PMID:32513696   PMID:32788342  
PMID:32994395   PMID:33001583   PMID:33545068   PMID:33961781   PMID:34079125   PMID:34189442   PMID:34837059   PMID:35216969   PMID:35256949   PMID:35271311   PMID:35337019   PMID:35602902  
PMID:35696571   PMID:36180527   PMID:36215168   PMID:36949045   PMID:37317656   PMID:37774976   PMID:38569033   PMID:39468006  


Genomics

Comparative Map Data
ERGIC3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382035,542,078 - 35,557,634 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2035,542,038 - 35,557,634 (+)EnsemblGRCh38hg38GRCh38
GRCh372034,129,827 - 34,145,405 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362033,593,192 - 33,608,819 (+)NCBINCBI36Build 36hg18NCBI36
Build 342033,593,191 - 33,608,818NCBI
Celera2030,878,102 - 30,893,718 (+)NCBICelera
Cytogenetic Map20q11.22NCBI
HuRef2030,907,313 - 30,922,911 (+)NCBIHuRef
CHM1_12034,031,121 - 34,046,732 (+)NCBICHM1_1
T2T-CHM13v2.02037,262,891 - 37,278,470 (+)NCBIT2T-CHM13v2.0
Ergic3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm392155,849,948 - 155,860,199 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl2155,849,965 - 155,860,199 (+)EnsemblGRCm39 Ensembl
GRCm382156,008,028 - 156,018,279 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl2156,008,045 - 156,018,279 (+)EnsemblGRCm38mm10GRCm38
MGSCv372155,833,861 - 155,844,015 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv362155,699,558 - 155,709,720 (+)NCBIMGSCv36mm8
Celera2161,941,989 - 161,952,143 (+)NCBICelera
Cytogenetic Map2H1NCBI
cM Map277.32NCBI
Ergic3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr83164,985,108 - 164,994,897 (+)NCBIGRCr8
mRatBN7.23144,525,059 - 144,534,813 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl3144,525,092 - 144,534,813 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx3148,390,685 - 148,400,411 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.03157,007,963 - 157,017,689 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.03154,747,487 - 154,757,213 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.03151,553,567 - 151,563,318 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl3151,553,578 - 151,563,364 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.03157,918,091 - 157,927,936 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.43146,416,599 - 146,426,325 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.13146,322,101 - 146,331,944 (+)NCBI
Celera3143,246,844 - 143,256,571 (+)NCBICelera
Cytogenetic Map3q42NCBI
Ergic3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495542225,884,080 - 25,893,236 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495542225,884,138 - 25,893,237 (-)NCBIChiLan1.0ChiLan1.0
ERGIC3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22141,272,567 - 41,288,267 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12041,265,670 - 41,281,370 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02031,867,571 - 31,883,181 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12032,986,131 - 33,001,737 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2032,986,131 - 33,001,737 (+)Ensemblpanpan1.1panPan2
ERGIC3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12424,494,494 - 24,508,114 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2424,494,524 - 24,508,113 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2424,139,705 - 24,153,330 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02425,187,036 - 25,200,658 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2425,187,082 - 25,200,658 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12424,473,444 - 24,487,049 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02424,568,398 - 24,582,205 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02425,007,842 - 25,021,464 (+)NCBIUU_Cfam_GSD_1.0
Ergic3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024408640173,479,456 - 173,493,099 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365615,256,417 - 5,270,344 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365615,256,450 - 5,270,073 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ERGIC3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1738,885,117 - 38,899,138 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11738,884,830 - 38,899,140 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21744,006,025 - 44,020,021 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ERGIC3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1256,474,811 - 56,482,788 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_0236660872,718,121 - 2,822,817 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ergic3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248423,872,518 - 3,881,937 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248423,872,518 - 3,881,994 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ERGIC3
28 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 20q11.22-12(chr20:34541747-39663219)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052766]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052766]|See cases [RCV000052766] Chr20:34541747..39663219 [GRCh38]
Chr20:33129551..38291861 [GRCh37]
Chr20:32593212..37725275 [NCBI36]
Chr20:20q11.22-12		 pathogenic
GRCh38/hg38 20q11.22-13.11(chr20:34249453-43359749)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053002]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053002]|See cases [RCV000053002] Chr20:34249453..43359749 [GRCh38]
Chr20:32837259..41988389 [GRCh37]
Chr20:32300920..41421803 [NCBI36]
Chr20:20q11.22-13.11		 pathogenic
GRCh38/hg38 20p12.2-q12(chr20:9811433-39316956)x3 copy number gain See cases [RCV000052999] Chr20:9811433..39316956 [GRCh38]
Chr20:9792081..37945599 [GRCh37]
Chr20:9740081..37379013 [NCBI36]
Chr20:20p12.2-q12		 pathogenic
NR_119376.1:n.6239G>A single nucleotide variant Malignant melanoma [RCV000072604] Chr20:35559402 [GRCh38]
Chr20:34147172 [GRCh37]
Chr20:33610586 [NCBI36]
Chr20:20q11.22		 not provided
GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3 copy number gain See cases [RCV000135859] Chr20:99557..64277321 [GRCh38]
Chr20:80198..62908674 [GRCh37]
Chr20:28198..62379118 [NCBI36]
Chr20:20p13-q13.33		 pathogenic
GRCh38/hg38 20q11.21-11.23(chr20:33432363-36821881)x1 copy number loss See cases [RCV000135440] Chr20:33432363..36821881 [GRCh38]
Chr20:32020169..35450284 [GRCh37]
Chr20:31483830..34883698 [NCBI36]
Chr20:20q11.21-11.23		 pathogenic
GRCh38/hg38 20q11.22(chr20:35285724-35744837)x1 copy number loss See cases [RCV000141309] Chr20:35285724..35744837 [GRCh38]
Chr20:33873527..34332759 [GRCh37]
Chr20:33336941..33796173 [NCBI36]
Chr20:20q11.22		 pathogenic
GRCh38/hg38 20q11.22-13.12(chr20:35237946-47631818)x1 copy number loss See cases [RCV000140816] Chr20:35237946..47631818 [GRCh38]
Chr20:33825749..46260562 [GRCh37]
Chr20:33289165..45693969 [NCBI36]
Chr20:20q11.22-13.12		 pathogenic
GRCh38/hg38 20q11.21-11.23(chr20:32062768-35906606)x3 copy number gain See cases [RCV000141833] Chr20:32062768..35906606 [GRCh38]
Chr20:30650571..34494528 [GRCh37]
Chr20:30114232..33957942 [NCBI36]
Chr20:20q11.21-11.23		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)x3 copy number gain See cases [RCV000510832] Chr20:61569..62915555 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
NM_015966.3(ERGIC3):c.686-664G>A single nucleotide variant not specified [RCV004296419] Chr20:35554380 [GRCh38]
Chr20:34142151 [GRCh37]
Chr20:20q11.22		 uncertain significance
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555) copy number gain See cases [RCV000512450] Chr20:61569..62915555 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62961294)x3 copy number gain not provided [RCV000741059] Chr20:63244..62961294 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62912463)x3 copy number gain not provided [RCV000741057] Chr20:63244..62912463 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62948788)x3 copy number gain not provided [RCV000741058] Chr20:63244..62948788 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
GRCh37/hg19 20q11.21-11.23(chr20:29833608-35087952)x3 copy number gain not provided [RCV000849735] Chr20:29833608..35087952 [GRCh37]
Chr20:20q11.21-11.23		 pathogenic
NM_015966.3(ERGIC3):c.370C>G (p.Leu124Val) single nucleotide variant not specified [RCV004289264] Chr20:35547414 [GRCh38]
Chr20:34135165 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.718-4A>G single nucleotide variant not provided [RCV000958031] Chr20:35556029 [GRCh38]
Chr20:34143800 [GRCh37]
Chr20:20q11.22		 benign
NM_015966.3(ERGIC3):c.885G>A (p.Leu295=) single nucleotide variant not provided [RCV000958032] Chr20:35556978 [GRCh38]
Chr20:34144749 [GRCh37]
Chr20:20q11.22		 benign
NM_015966.3(ERGIC3):c.717+1G>A single nucleotide variant See cases [RCV001374376] Chr20:35555076 [GRCh38]
Chr20:34142847 [GRCh37]
Chr20:20q11.22		 uncertain significance
NC_000020.10:g.(?_31189994)_(34287210_?)del deletion not provided [RCV001956104] Chr20:31189994..34287210 [GRCh37]
Chr20:20q11.21-11.22		 pathogenic
GRCh37/hg19 20q11.21-11.23(chr20:29833535-34815537)x3 copy number gain not provided [RCV002474532] Chr20:29833535..34815537 [GRCh37]
Chr20:20q11.21-11.23		 likely pathogenic
NM_015966.3(ERGIC3):c.877G>C (p.Glu293Gln) single nucleotide variant not specified [RCV004210697] Chr20:35556269 [GRCh38]
Chr20:34144040 [GRCh37]
Chr20:20q11.22		 uncertain significance
GRCh37/hg19 20q11.21-11.23(chr20:29652122-35603726)x3 copy number gain not provided [RCV002475651] Chr20:29652122..35603726 [GRCh37]
Chr20:20q11.21-11.23		 likely pathogenic
NM_015966.3(ERGIC3):c.619G>A (p.Val207Ile) single nucleotide variant not specified [RCV004139156] Chr20:35548666 [GRCh38]
Chr20:34136419 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.389C>T (p.Thr130Met) single nucleotide variant not specified [RCV004085152] Chr20:35547433 [GRCh38]
Chr20:34135184 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.571A>G (p.Met191Val) single nucleotide variant not specified [RCV004278203] Chr20:35548618 [GRCh38]
Chr20:34136371 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.829C>T (p.Gln277Ter) single nucleotide variant Developmental disorder [RCV003441161] Chr20:35556221 [GRCh38]
Chr20:34143992 [GRCh37]
Chr20:20q11.22		 likely pathogenic
NM_015966.3(ERGIC3):c.487C>T (p.Arg163Trp) single nucleotide variant not specified [RCV004380585] Chr20:35548534 [GRCh38]
Chr20:34136287 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.931G>T (p.Gly311Trp) single nucleotide variant not specified [RCV004380590] Chr20:35557024 [GRCh38]
Chr20:34144795 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.713A>G (p.Asp238Gly) single nucleotide variant not specified [RCV004380589] Chr20:35555071 [GRCh38]
Chr20:34142842 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.1004C>G (p.Thr335Arg) single nucleotide variant not specified [RCV004380582] Chr20:35557097 [GRCh38]
Chr20:34144868 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.1091C>T (p.Ser364Leu) single nucleotide variant not specified [RCV004380583] Chr20:35557443 [GRCh38]
Chr20:34145214 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.208A>G (p.Ile70Val) single nucleotide variant not specified [RCV004380584] Chr20:35542561 [GRCh38]
Chr20:34130310 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.557G>T (p.Gly186Val) single nucleotide variant not specified [RCV004380586] Chr20:35548604 [GRCh38]
Chr20:34136357 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.1022T>G (p.Phe341Cys) single nucleotide variant not specified [RCV004617964] Chr20:35557199 [GRCh38]
Chr20:34144970 [GRCh37]
Chr20:20q11.22		 uncertain significance
NC_000020.10:g.(?_31368130)_(34287210_?)del deletion Glutathione synthetase deficiency with 5-oxoprolinuria [RCV004579432] Chr20:31368130..34287210 [GRCh37]
Chr20:20q11.21-11.22		 pathogenic
NM_015966.3(ERGIC3):c.403G>C (p.Asp135His) single nucleotide variant not specified [RCV004617965] Chr20:35547447 [GRCh38]
Chr20:34135198 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.404A>G (p.Asp135Gly) single nucleotide variant not specified [RCV004617963] Chr20:35547448 [GRCh38]
Chr20:34135199 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.499C>T (p.Arg167Cys) single nucleotide variant not specified [RCV004907637] Chr20:35548546 [GRCh38]
Chr20:34136299 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.797A>G (p.Asn266Ser) single nucleotide variant not specified [RCV004923082] Chr20:35556112 [GRCh38]
Chr20:34143883 [GRCh37]
Chr20:20q11.22		 uncertain significance
NM_015966.3(ERGIC3):c.538G>C (p.Glu180Gln) single nucleotide variant not specified [RCV004923083] Chr20:35548585 [GRCh38]
Chr20:34136338 [GRCh37]
Chr20:20q11.22		 uncertain significance
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR490hsa-miR-490-3pMirtarbaseexternal_infoGFP reporter assayFunctional MTI23212913
MIR490hsa-miR-490-3pOncomiRDBexternal_infoNANA23212913

Predicted Target Of
Summary Value
Count of predictions:5868
Count of miRNA genes:1044
Interacting mature miRNAs:1303
Transcripts:ENST00000279052, ENST00000348547, ENST00000357394, ENST00000411577, ENST00000413587, ENST00000416206, ENST00000438317, ENST00000442139, ENST00000447986, ENST00000451605, ENST00000461043, ENST00000465298, ENST00000475211, ENST00000476926, ENST00000482338, ENST00000486268, ENST00000488384, ENST00000488935, ENST00000489071, ENST00000492184, ENST00000496172
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
597061846GWAS1157920_Htotal cholesterol measurement QTL GWAS1157920 (human)5e-10total cholesterol measurementblood total cholesterol level (CMO:0000051)203555550735555508Human
597127829GWAS1223903_Hlow density lipoprotein cholesterol measurement QTL GWAS1223903 (human)2e-08low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)203555532135555322Human
597061845GWAS1157919_Htotal cholesterol measurement QTL GWAS1157919 (human)4e-10total cholesterol measurementblood total cholesterol level (CMO:0000051)203555550735555508Human
597495417GWAS1591491_Htriglyceride measurement QTL GWAS1591491 (human)7e-17triglyceride measurementblood triglyceride level (CMO:0000118)203554364735543648Human
597065936GWAS1162010_Hlow density lipoprotein cholesterol measurement QTL GWAS1162010 (human)0.0000007low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)203555550735555508Human
597070654GWAS1166728_HBMI-adjusted hip circumference QTL GWAS1166728 (human)0.0000004BMI-adjusted hip circumferencehip circumference (CMO:0000014)203555072235550723Human
597312624GWAS1408698_Htotal cholesterol measurement QTL GWAS1408698 (human)3e-20total cholesterol measurementblood total cholesterol level (CMO:0000051)203555448635554487Human
597328694GWAS1424768_Hsexual dimorphism measurement QTL GWAS1424768 (human)1e-10sexual dimorphism measurement203554979135549792Human
597336884GWAS1432958_Htotal cholesterol measurement QTL GWAS1432958 (human)2e-09total cholesterol measurementblood total cholesterol level (CMO:0000051)203555451635554517Human
597140580GWAS1236654_Hlow density lipoprotein cholesterol measurement QTL GWAS1236654 (human)6e-14low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)203555448635554487Human
597580075GWAS1636935_Hlow density lipoprotein cholesterol measurement QTL GWAS1636935 (human)4e-19low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)203555550735555508Human
597337091GWAS1433165_Hhigh density lipoprotein cholesterol measurement QTL GWAS1433165 (human)2e-08high density lipoprotein cholesterol measurementblood high density lipoprotein cholesterol level (CMO:0000052)203555038635550387Human
597065935GWAS1162009_Hlow density lipoprotein cholesterol measurement QTL GWAS1162009 (human)0.0000009low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)203555550735555508Human
597471335GWAS1567409_Htotal cholesterol measurement QTL GWAS1567409 (human)2e-19total cholesterol measurementblood total cholesterol level (CMO:0000051)203554364735543648Human
597398055GWAS1494129_Hnon-high density lipoprotein cholesterol measurement QTL GWAS1494129 (human)2e-31non-high density lipoprotein cholesterol measurementblood non-high density lipoprotein cholesterol level (CMO:0003967)203554903835549039Human
597580291GWAS1637151_Hlow density lipoprotein cholesterol measurement QTL GWAS1637151 (human)2e-18low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)203555550735555508Human
597275367GWAS1371441_Hbeverage consumption measurement QTL GWAS1371441 (human)1e-12beverage consumption measurementdrink intake measurement (CMO:0000771)203554787635547877Human
597409765GWAS1505839_Hnon-high density lipoprotein cholesterol measurement QTL GWAS1505839 (human)3e-43non-high density lipoprotein cholesterol measurementblood non-high density lipoprotein cholesterol level (CMO:0003967)203554903835549039Human
597324388GWAS1420462_HBMI-adjusted hip circumference QTL GWAS1420462 (human)6e-16BMI-adjusted hip circumferencehip circumference (CMO:0000014)203554979135549792Human
597431906GWAS1527980_Hprotein measurement QTL GWAS1527980 (human)7e-19protein measurement203555448635554487Human
597338693GWAS1434767_Hsexual dimorphism measurement QTL GWAS1434767 (human)4e-10sexual dimorphism measurement203554979135549792Human

Markers in Region
STS-R93394  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,141,083 - 34,141,203UniSTSGRCh37
Build 362033,604,497 - 33,604,617RGDNCBI36
Celera2030,889,396 - 30,889,516RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,918,585 - 30,918,705UniSTS
GeneMap99-GB4 RH Map20200.06UniSTS
NCBI RH Map20299.8UniSTS
RH93363  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,145,281 - 34,145,381UniSTSGRCh37
Build 362033,608,695 - 33,608,795RGDNCBI36
Celera2030,893,594 - 30,893,694RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,922,787 - 30,922,887UniSTS
GeneMap99-GB4 RH Map20200.06UniSTS
SHGC-58582  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,141,178 - 34,141,309UniSTSGRCh37
Build 362033,604,592 - 33,604,723RGDNCBI36
Celera2030,889,491 - 30,889,622RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,918,680 - 30,918,811UniSTS
TNG Radiation Hybrid Map2016120.0UniSTS
ECD01883  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,144,295 - 34,145,144UniSTSGRCh37
Build 362033,607,709 - 33,608,558RGDNCBI36
Celera2030,892,608 - 30,893,457RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,921,801 - 30,922,650UniSTS
ECD10263  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,130,171 - 34,130,777UniSTSGRCh37
Build 362033,593,585 - 33,594,191RGDNCBI36
Celera2030,878,495 - 30,879,101RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,907,706 - 30,908,312UniSTS
ECD10524  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,136,096 - 34,136,695UniSTSGRCh37
Build 362033,599,510 - 33,600,109RGDNCBI36
Celera2030,884,416 - 30,885,015RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,913,598 - 30,914,197UniSTS
ECD11124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,129,518 - 34,130,099UniSTSGRCh37
Build 362033,592,932 - 33,593,513RGDNCBI36
Celera2030,877,842 - 30,878,423RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,907,053 - 30,907,634UniSTS
ECD13482  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,141,928 - 34,142,444UniSTSGRCh37
Build 362033,605,342 - 33,605,858RGDNCBI36
Celera2030,890,241 - 30,890,757RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,919,431 - 30,919,947UniSTS
ECD14540  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,142,504 - 34,142,995UniSTSGRCh37
Build 362033,605,918 - 33,606,409RGDNCBI36
Celera2030,890,817 - 30,891,308RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,920,007 - 30,920,498UniSTS
ECD14799  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,143,629 - 34,144,114UniSTSGRCh37
Build 362033,607,043 - 33,607,528RGDNCBI36
Celera2030,891,942 - 30,892,427RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,921,132 - 30,921,620UniSTS
ECD17093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,135,073 - 34,135,486UniSTSGRCh37
Build 362033,598,487 - 33,598,900RGDNCBI36
Celera2030,883,393 - 30,883,806RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,912,575 - 30,912,988UniSTS
ECD17650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,128,785 - 34,129,174UniSTSGRCh37
Build 362033,592,199 - 33,592,588RGDNCBI36
Celera2030,877,109 - 30,877,498RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,906,320 - 30,906,709UniSTS
ECD18140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,132,148 - 34,132,519UniSTSGRCh37
Build 362033,595,562 - 33,595,933RGDNCBI36
Celera2030,880,468 - 30,880,839RGD
Cytogenetic Map20q11.2UniSTS
Cytogenetic Map20pter-q12UniSTS
HuRef2030,909,679 - 30,910,050UniSTS
ECD19387  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,141,503 - 34,141,826UniSTSGRCh37
Build 362033,604,917 - 33,605,240RGDNCBI36
Celera2030,889,816 - 30,890,139RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,919,005 - 30,919,329UniSTS
ECD22997  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,130,888 - 34,131,089UniSTSGRCh37
Build 362033,594,302 - 33,594,503RGDNCBI36
Celera2030,879,212 - 30,879,413RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,908,423 - 30,908,624UniSTS
REN58145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,128,009 - 34,128,238UniSTSGRCh37
Build 362033,591,423 - 33,591,652RGDNCBI36
Celera2030,876,333 - 30,876,562RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,905,544 - 30,905,773UniSTS
REN58146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,128,219 - 34,128,449UniSTSGRCh37
Build 362033,591,633 - 33,591,863RGDNCBI36
Celera2030,876,543 - 30,876,773RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,905,754 - 30,905,984UniSTS
REN58147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,128,440 - 34,128,691UniSTSGRCh37
Build 362033,591,854 - 33,592,105RGDNCBI36
Celera2030,876,764 - 30,877,015RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,905,975 - 30,906,226UniSTS
REN58148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,128,685 - 34,128,929UniSTSGRCh37
Build 362033,592,099 - 33,592,343RGDNCBI36
Celera2030,877,009 - 30,877,253RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,906,220 - 30,906,464UniSTS
REN58149  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,128,928 - 34,129,179UniSTSGRCh37
Build 362033,592,342 - 33,592,593RGDNCBI36
Celera2030,877,252 - 30,877,503RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,906,463 - 30,906,714UniSTS
REN58150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,129,174 - 34,129,427UniSTSGRCh37
Build 362033,592,588 - 33,592,841RGDNCBI36
Celera2030,877,498 - 30,877,751RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,906,709 - 30,906,962UniSTS
REN58151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,129,396 - 34,129,663UniSTSGRCh37
Build 362033,592,810 - 33,593,077RGDNCBI36
Celera2030,877,720 - 30,877,987RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,906,931 - 30,907,198UniSTS
REN58152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,129,639 - 34,129,904UniSTSGRCh37
Build 362033,593,053 - 33,593,318RGDNCBI36
Celera2030,877,963 - 30,878,228RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,907,174 - 30,907,439UniSTS
REN58153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,129,885 - 34,130,145UniSTSGRCh37
Build 362033,593,299 - 33,593,559RGDNCBI36
Celera2030,878,209 - 30,878,469RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,907,420 - 30,907,680UniSTS
REN58154  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,130,143 - 34,130,392UniSTSGRCh37
Build 362033,593,557 - 33,593,806RGDNCBI36
Celera2030,878,467 - 30,878,716RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,907,678 - 30,907,927UniSTS
REN58155  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,130,364 - 34,130,594UniSTSGRCh37
Build 362033,593,778 - 33,594,008RGDNCBI36
Celera2030,878,688 - 30,878,918RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,907,899 - 30,908,129UniSTS
REN58156  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,130,572 - 34,130,816UniSTSGRCh37
Build 362033,593,986 - 33,594,230RGDNCBI36
Celera2030,878,896 - 30,879,140RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,908,107 - 30,908,351UniSTS
REN58157  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,130,787 - 34,131,029UniSTSGRCh37
Build 362033,594,201 - 33,594,443RGDNCBI36
Celera2030,879,111 - 30,879,353RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,908,322 - 30,908,564UniSTS
REN58158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,131,005 - 34,131,257UniSTSGRCh37
Build 362033,594,419 - 33,594,671RGDNCBI36
Celera2030,879,329 - 30,879,581RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,908,540 - 30,908,792UniSTS
REN58159  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,131,252 - 34,131,496UniSTSGRCh37
Build 362033,594,666 - 33,594,910RGDNCBI36
Celera2030,879,576 - 30,879,820RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,908,787 - 30,909,031UniSTS
REN58160  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,131,473 - 34,131,725UniSTSGRCh37
Build 362033,594,887 - 33,595,139RGDNCBI36
Celera2030,879,797 - 30,880,049RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,909,008 - 30,909,260UniSTS
REN58161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,131,522 - 34,131,765UniSTSGRCh37
Build 362033,594,936 - 33,595,179RGDNCBI36
Celera2030,879,846 - 30,880,089RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,909,057 - 30,909,300UniSTS
REN58162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,132,091 - 34,132,316UniSTSGRCh37
Build 362033,595,505 - 33,595,730RGDNCBI36
Celera2030,880,411 - 30,880,636RGD
Cytogenetic Map20q11.2UniSTS
Cytogenetic Map20pter-q12UniSTS
HuRef2030,909,622 - 30,909,847UniSTS
REN58163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,132,294 - 34,132,526UniSTSGRCh37
Build 362033,595,708 - 33,595,940RGDNCBI36
Celera2030,880,614 - 30,880,846RGD
Cytogenetic Map20q11.2UniSTS
Cytogenetic Map20pter-q12UniSTS
HuRef2030,909,825 - 30,910,057UniSTS
REN58164  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,132,365 - 34,132,595UniSTSGRCh37
Build 362033,595,779 - 33,596,009RGDNCBI36
Celera2030,880,685 - 30,880,915RGD
Cytogenetic Map20q11.2UniSTS
Cytogenetic Map20pter-q12UniSTS
HuRef2030,909,896 - 30,910,126UniSTS
REN58165  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,133,352 - 34,133,584UniSTSGRCh37
Build 362033,596,766 - 33,596,998RGDNCBI36
Celera2030,881,672 - 30,881,904RGD
Cytogenetic Map20q11.2UniSTS
Cytogenetic Map20pter-q12UniSTS
HuRef2030,910,854 - 30,911,086UniSTS
REN58166  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,133,582 - 34,133,831UniSTSGRCh37
Build 362033,596,996 - 33,597,245RGDNCBI36
Celera2030,881,902 - 30,882,151RGD
Cytogenetic Map20q11.2UniSTS
Cytogenetic Map20pter-q12UniSTS
HuRef2030,911,084 - 30,911,333UniSTS
REN58167  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,133,827 - 34,134,082UniSTSGRCh37
Build 362033,597,241 - 33,597,496RGDNCBI36
Celera2030,882,147 - 30,882,402RGD
Cytogenetic Map20q11.2UniSTS
Cytogenetic Map20pter-q12UniSTS
HuRef2030,911,329 - 30,911,584UniSTS
REN58168  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,134,062 - 34,134,307UniSTSGRCh37
Build 362033,597,476 - 33,597,721RGDNCBI36
Celera2030,882,382 - 30,882,627RGD
Cytogenetic Map20q11.2UniSTS
Cytogenetic Map20pter-q12UniSTS
HuRef2030,911,564 - 30,911,809UniSTS
REN58169  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,134,306 - 34,134,565UniSTSGRCh37
Build 362033,597,720 - 33,597,979RGDNCBI36
Celera2030,882,626 - 30,882,885RGD
Cytogenetic Map20q11.2UniSTS
Cytogenetic Map20pter-q12UniSTS
HuRef2030,911,808 - 30,912,067UniSTS
REN58170  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,134,552 - 34,134,800UniSTSGRCh37
Build 362033,597,966 - 33,598,214RGDNCBI36
Celera2030,882,872 - 30,883,120RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,912,054 - 30,912,302UniSTS
REN58171  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,134,768 - 34,135,029UniSTSGRCh37
Build 362033,598,182 - 33,598,443RGDNCBI36
Celera2030,883,088 - 30,883,349RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,912,270 - 30,912,531UniSTS
REN58172  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,135,016 - 34,135,262UniSTSGRCh37
Build 362033,598,430 - 33,598,676RGDNCBI36
Celera2030,883,336 - 30,883,582RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,912,518 - 30,912,764UniSTS
REN58173  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,135,239 - 34,135,488UniSTSGRCh37
Build 362033,598,653 - 33,598,902RGDNCBI36
Celera2030,883,559 - 30,883,808RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,912,741 - 30,912,990UniSTS
REN58174  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,135,487 - 34,135,737UniSTSGRCh37
Build 362033,598,901 - 33,599,151RGDNCBI36
Celera2030,883,807 - 30,884,057RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,912,989 - 30,913,239UniSTS
REN58175  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,135,712 - 34,135,960UniSTSGRCh37
Build 362033,599,126 - 33,599,374RGDNCBI36
Celera2030,884,032 - 30,884,280RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,913,214 - 30,913,462UniSTS
REN58176  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,135,937 - 34,136,180UniSTSGRCh37
Build 362033,599,351 - 33,599,594RGDNCBI36
Celera2030,884,257 - 30,884,500RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,913,439 - 30,913,682UniSTS
REN58177  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,136,158 - 34,136,420UniSTSGRCh37
Build 362033,599,572 - 33,599,834RGDNCBI36
Celera2030,884,478 - 30,884,740RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,913,660 - 30,913,922UniSTS
REN58178  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,136,406 - 34,136,653UniSTSGRCh37
Build 362033,599,820 - 33,600,067RGDNCBI36
Celera2030,884,726 - 30,884,973RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,913,908 - 30,914,155UniSTS
REN58179  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,136,626 - 34,136,862UniSTSGRCh37
Build 362033,600,040 - 33,600,276RGDNCBI36
Celera2030,884,946 - 30,885,182RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,914,128 - 30,914,364UniSTS
REN58180  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,136,831 - 34,137,081UniSTSGRCh37
Build 362033,600,245 - 33,600,495RGDNCBI36
Celera2030,885,151 - 30,885,401RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,914,333 - 30,914,583UniSTS
REN58181  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,137,057 - 34,137,282UniSTSGRCh37
Build 362033,600,471 - 33,600,696RGDNCBI36
Celera2030,885,377 - 30,885,602RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,914,559 - 30,914,784UniSTS
REN58182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,137,146 - 34,137,374UniSTSGRCh37
Build 362033,600,560 - 33,600,788RGDNCBI36
Celera2030,885,466 - 30,885,694RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,914,648 - 30,914,876UniSTS
REN58183  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,137,681 - 34,137,929UniSTSGRCh37
Build 362033,601,095 - 33,601,343RGDNCBI36
Celera2030,886,001 - 30,886,249RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,915,183 - 30,915,431UniSTS
REN58184  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,137,859 - 34,138,092UniSTSGRCh37
Build 362033,601,273 - 33,601,506RGDNCBI36
Celera2030,886,179 - 30,886,412RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,915,361 - 30,915,594UniSTS
REN58185  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,138,389 - 34,138,617UniSTSGRCh37
Build 362033,601,803 - 33,602,031RGDNCBI36
Celera2030,886,709 - 30,886,937RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,915,891 - 30,916,119UniSTS
REN58186  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,138,568 - 34,138,804UniSTSGRCh37
Build 362033,601,982 - 33,602,218RGDNCBI36
Celera2030,886,888 - 30,887,124RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,916,070 - 30,916,306UniSTS
REN58187  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,139,077 - 34,139,308UniSTSGRCh37
Build 362033,602,491 - 33,602,722RGDNCBI36
Celera2030,887,397 - 30,887,628RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,916,579 - 30,916,810UniSTS
REN58188  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,139,286 - 34,139,555UniSTSGRCh37
Build 362033,602,700 - 33,602,969RGDNCBI36
Celera2030,887,606 - 30,887,875RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,916,788 - 30,917,057UniSTS
REN58189  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,139,532 - 34,139,772UniSTSGRCh37
Build 362033,602,946 - 33,603,186RGDNCBI36
Celera2030,887,852 - 30,888,092RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,917,034 - 30,917,274UniSTS
REN58190  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,139,749 - 34,139,993UniSTSGRCh37
Build 362033,603,163 - 33,603,407RGDNCBI36
Celera2030,888,069 - 30,888,313RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,917,251 - 30,917,495UniSTS
REN58191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,139,982 - 34,140,221UniSTSGRCh37
Build 362033,603,396 - 33,603,635RGDNCBI36
Celera2030,888,302 - 30,888,541RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,917,484 - 30,917,723UniSTS
REN58192  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,140,216 - 34,140,465UniSTSGRCh37
Build 362033,603,630 - 33,603,879RGDNCBI36
Celera2030,888,536 - 30,888,785RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,917,718 - 30,917,967UniSTS
REN58193  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,140,452 - 34,140,702UniSTSGRCh37
Build 362033,603,866 - 33,604,116RGDNCBI36
Celera2030,888,772 - 30,889,022RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,917,954 - 30,918,204UniSTS
REN58194  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,140,641 - 34,140,879UniSTSGRCh37
Build 362033,604,055 - 33,604,293RGDNCBI36
Celera2030,888,961 - 30,889,192RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,918,143 - 30,918,381UniSTS
REN58195  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,141,040 - 34,141,277UniSTSGRCh37
Build 362033,604,454 - 33,604,691RGDNCBI36
Celera2030,889,353 - 30,889,590RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,918,542 - 30,918,779UniSTS
REN58196  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,141,268 - 34,141,518UniSTSGRCh37
Build 362033,604,682 - 33,604,932RGDNCBI36
Celera2030,889,581 - 30,889,831RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,918,770 - 30,919,020UniSTS
REN58197  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,141,497 - 34,141,736UniSTSGRCh37
Build 362033,604,911 - 33,605,150RGDNCBI36
Celera2030,889,810 - 30,890,049RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,918,999 - 30,919,238UniSTS
REN58198  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,141,722 - 34,141,966UniSTSGRCh37
Build 362033,605,136 - 33,605,380RGDNCBI36
Celera2030,890,035 - 30,890,279RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,919,224 - 30,919,469UniSTS
REN58199  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,141,965 - 34,142,196UniSTSGRCh37
Build 362033,605,379 - 33,605,610RGDNCBI36
Celera2030,890,278 - 30,890,509RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,919,468 - 30,919,699UniSTS
REN58200  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,142,179 - 34,142,413UniSTSGRCh37
Build 362033,605,593 - 33,605,827RGDNCBI36
Celera2030,890,492 - 30,890,726RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,919,682 - 30,919,916UniSTS
REN58201  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,142,395 - 34,142,648UniSTSGRCh37
Build 362033,605,809 - 33,606,062RGDNCBI36
Celera2030,890,708 - 30,890,961RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,919,898 - 30,920,151UniSTS
REN58202  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,142,628 - 34,142,864UniSTSGRCh37
Build 362033,606,042 - 33,606,278RGDNCBI36
Celera2030,890,941 - 30,891,177RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,920,131 - 30,920,367UniSTS
REN58203  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,142,841 - 34,143,080UniSTSGRCh37
Build 362033,606,255 - 33,606,494RGDNCBI36
Celera2030,891,154 - 30,891,393RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,920,344 - 30,920,583UniSTS
REN58204  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,143,058 - 34,143,307UniSTSGRCh37
Build 362033,606,472 - 33,606,721RGDNCBI36
Celera2030,891,371 - 30,891,620RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,920,561 - 30,920,810UniSTS
REN58205  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,143,284 - 34,143,519UniSTSGRCh37
Build 362033,606,698 - 33,606,933RGDNCBI36
Celera2030,891,597 - 30,891,832RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,920,787 - 30,921,022UniSTS
REN58206  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,143,415 - 34,143,663UniSTSGRCh37
Build 362033,606,829 - 33,607,077RGDNCBI36
Celera2030,891,728 - 30,891,976RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,920,918 - 30,921,166UniSTS
REN58207  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,143,641 - 34,143,891UniSTSGRCh37
Build 362033,607,055 - 33,607,305RGDNCBI36
Celera2030,891,954 - 30,892,204RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,921,144 - 30,921,395UniSTS
REN58208  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,143,845 - 34,144,110UniSTSGRCh37
Build 362033,607,259 - 33,607,524RGDNCBI36
Celera2030,892,158 - 30,892,423RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,921,349 - 30,921,616UniSTS
REN58209  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,144,089 - 34,144,356UniSTSGRCh37
Build 362033,607,503 - 33,607,770RGDNCBI36
Celera2030,892,402 - 30,892,669RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,921,595 - 30,921,862UniSTS
REN58210  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,144,332 - 34,144,575UniSTSGRCh37
Build 362033,607,746 - 33,607,989RGDNCBI36
Celera2030,892,645 - 30,892,888RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,921,838 - 30,922,081UniSTS
REN58211  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,144,524 - 34,144,787UniSTSGRCh37
Build 362033,607,938 - 33,608,201RGDNCBI36
Celera2030,892,837 - 30,893,100RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,922,030 - 30,922,293UniSTS
REN58212  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,144,765 - 34,145,033UniSTSGRCh37
Build 362033,608,179 - 33,608,447RGDNCBI36
Celera2030,893,078 - 30,893,346RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,922,271 - 30,922,539UniSTS
REN58213  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,145,031 - 34,145,280UniSTSGRCh37
Build 362033,608,445 - 33,608,694RGDNCBI36
Celera2030,893,344 - 30,893,593RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,922,537 - 30,922,786UniSTS
REN58214  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,145,239 - 34,145,486UniSTSGRCh37
Build 362033,608,653 - 33,608,900RGDNCBI36
Celera2030,893,552 - 30,893,799RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,922,745 - 30,922,992UniSTS
REN58215  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,145,456 - 34,145,713UniSTSGRCh37
Build 362033,608,870 - 33,609,127RGDNCBI36
Celera2030,893,769 - 30,894,026RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,922,962 - 30,923,219UniSTS
D20S1029  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,138,526 - 34,138,625UniSTSGRCh37
Build 362033,601,940 - 33,602,039RGDNCBI36
Celera2030,886,846 - 30,886,945RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,916,028 - 30,916,127UniSTS
Whitehead-RH Map20206.8UniSTS
Whitehead-YAC Contig Map20 UniSTS
NCBI RH Map20301.1UniSTS
MARC_26120-26121:1030366872:1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,135,215 - 34,136,393UniSTSGRCh37
Build 362033,598,629 - 33,599,807RGDNCBI36
Celera2030,883,535 - 30,884,713RGD
HuRef2030,912,717 - 30,913,895UniSTS
stSG636694  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,128,785 - 34,129,886UniSTSGRCh37
Build 362033,592,199 - 33,593,300RGDNCBI36
Celera2030,877,109 - 30,878,210RGD
HuRef2030,906,320 - 30,907,421UniSTS
stSG636695  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,129,867 - 34,130,099UniSTSGRCh37
Build 362033,593,281 - 33,593,513RGDNCBI36
Celera2030,878,191 - 30,878,423RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,907,402 - 30,907,634UniSTS
stSG636696  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,130,100 - 34,131,334UniSTSGRCh37
Build 362033,593,514 - 33,594,748RGDNCBI36
Celera2030,878,424 - 30,879,658RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,907,635 - 30,908,869UniSTS
stSG636697  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,131,316 - 34,132,370UniSTSGRCh37
Build 362033,594,730 - 33,595,784RGDNCBI36
Celera2030,879,640 - 30,880,690RGD
Cytogenetic Map20pter-q12UniSTS
HuRef2030,908,851 - 30,909,901UniSTS
stSG636698  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,134,718 - 34,135,724UniSTSGRCh37
Build 362033,598,132 - 33,599,138RGDNCBI36
Celera2030,883,038 - 30,884,044RGD
HuRef2030,912,220 - 30,913,226UniSTS
stSG636699  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,135,705 - 34,137,010UniSTSGRCh37
Build 362033,599,119 - 33,600,424RGDNCBI36
Celera2030,884,025 - 30,885,330RGD
HuRef2030,913,207 - 30,914,512UniSTS
stSG636700  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,141,504 - 34,142,579UniSTSGRCh37
Build 362033,604,918 - 33,605,993RGDNCBI36
Celera2030,889,817 - 30,890,892RGD
HuRef2030,919,006 - 30,920,082UniSTS
stSG636701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,142,560 - 34,143,892UniSTSGRCh37
Build 362033,605,974 - 33,607,306RGDNCBI36
Celera2030,890,873 - 30,892,205RGD
HuRef2030,920,063 - 30,921,396UniSTS
stSG636702  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372034,143,873 - 34,145,199UniSTSGRCh37
Build 362033,607,287 - 33,608,613RGDNCBI36
Celera2030,892,186 - 30,893,512RGD
HuRef2030,921,377 - 30,922,705UniSTS
D11S3114  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map10q11.1-q24UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic MapXq13.1-q21.1UniSTS
Cytogenetic Map20pter-q12UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map9p23UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map6p12UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map22q12.3-q13.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map19q11UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map1p32.2-p32.1UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map4q13.2UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map14q24.2UniSTS
L17877  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map4p15.31UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map18q21.31UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map20pter-q12UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map9q21.3UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map8q13.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map17q25.3UniSTS


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_015966 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_198398 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AF077030 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF091085 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF116614 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF151812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF308298 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074550 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK096484 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK300916 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL121586 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL161963 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC009765 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC014014 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU528333 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA489637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471077 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068258 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF206690 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FO393401 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000279052
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,542,082 - 35,545,404 (+)Ensembl
Ensembl Acc Id: ENST00000348547   ⟹   ENSP00000341358
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,542,078 - 35,557,634 (+)Ensembl
Ensembl Acc Id: ENST00000357394   ⟹   ENSP00000349970
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,542,038 - 35,557,634 (+)Ensembl
Ensembl Acc Id: ENST00000411577   ⟹   ENSP00000414490
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,542,116 - 35,543,909 (+)Ensembl
Ensembl Acc Id: ENST00000413587   ⟹   ENSP00000402480
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,542,130 - 35,557,066 (+)Ensembl
Ensembl Acc Id: ENST00000416206   ⟹   ENSP00000399124
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,542,102 - 35,557,546 (+)Ensembl
Ensembl Acc Id: ENST00000438317   ⟹   ENSP00000389398
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,542,079 - 35,547,471 (+)Ensembl
Ensembl Acc Id: ENST00000442139   ⟹   ENSP00000408840
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,556,043 - 35,557,455 (+)Ensembl
Ensembl Acc Id: ENST00000447986
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,542,069 - 35,549,783 (+)Ensembl
Ensembl Acc Id: ENST00000451605   ⟹   ENSP00000416402
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,556,095 - 35,557,633 (+)Ensembl
Ensembl Acc Id: ENST00000461043
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,542,192 - 35,548,865 (+)Ensembl
Ensembl Acc Id: ENST00000465298
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,554,857 - 35,557,096 (+)Ensembl
Ensembl Acc Id: ENST00000475211
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,554,916 - 35,556,560 (+)Ensembl
Ensembl Acc Id: ENST00000482338
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,547,487 - 35,556,432 (+)Ensembl
Ensembl Acc Id: ENST00000486268
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,542,079 - 35,543,139 (+)Ensembl
Ensembl Acc Id: ENST00000488384
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,556,610 - 35,557,634 (+)Ensembl
Ensembl Acc Id: ENST00000488935
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,556,579 - 35,557,450 (+)Ensembl
Ensembl Acc Id: ENST00000489071
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,547,262 - 35,548,979 (+)Ensembl
Ensembl Acc Id: ENST00000496172
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,542,443 - 35,556,262 (+)Ensembl
Ensembl Acc Id: ENST00000640748   ⟹   ENSP00000491710
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2035,542,105 - 35,557,633 (+)Ensembl
RefSeq Acc Id: NM_015966   ⟹   NP_057050
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382035,542,078 - 35,557,634 (+)NCBI
GRCh372034,129,778 - 34,145,405 (+)RGD
Build 362033,593,192 - 33,608,819 (+)NCBI Archive
Celera2030,878,102 - 30,893,718 (+)RGD
HuRef2030,907,313 - 30,922,911 (+)ENTREZGENE
CHM1_12034,031,121 - 34,046,732 (+)NCBI
T2T-CHM13v2.02037,262,891 - 37,278,470 (+)NCBI
Sequence:
RefSeq Acc Id: NM_198398   ⟹   NP_938408
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382035,542,078 - 35,557,634 (+)NCBI
GRCh372034,129,778 - 34,145,405 (+)RGD
Build 362033,593,192 - 33,608,819 (+)NCBI Archive
Celera2030,878,102 - 30,893,718 (+)RGD
HuRef2030,907,313 - 30,922,911 (+)ENTREZGENE
CHM1_12034,031,121 - 34,046,732 (+)NCBI
T2T-CHM13v2.02037,262,891 - 37,278,470 (+)NCBI
Sequence:
RefSeq Acc Id: NP_057050   ⟸   NM_015966
- Peptide Label: isoform b
- UniProtKB: Q9H276 (UniProtKB/Swiss-Prot),   Q6ZWP7 (UniProtKB/Swiss-Prot),   Q5JWS3 (UniProtKB/Swiss-Prot),   Q9P1L3 (UniProtKB/Swiss-Prot),   Q9Y282 (UniProtKB/Swiss-Prot),   A2TJK5 (UniProtKB/TrEMBL),   Q5JWS0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_938408   ⟸   NM_198398
- Peptide Label: isoform a
- UniProtKB: Q5JWS0 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000389398   ⟸   ENST00000438317
Ensembl Acc Id: ENSP00000414490   ⟸   ENST00000411577
Ensembl Acc Id: ENSP00000416402   ⟸   ENST00000451605
Ensembl Acc Id: ENSP00000341358   ⟸   ENST00000348547
Ensembl Acc Id: ENSP00000402480   ⟸   ENST00000413587
Ensembl Acc Id: ENSP00000399124   ⟸   ENST00000416206
Ensembl Acc Id: ENSP00000408840   ⟸   ENST00000442139
Ensembl Acc Id: ENSP00000491710   ⟸   ENST00000640748
Ensembl Acc Id: ENSP00000349970   ⟸   ENST00000357394
Protein Domains
Endoplasmic reticulum vesicle transporter C-   Endoplasmic reticulum vesicle transporter N-

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9Y282-F1-model_v2 AlphaFold Q9Y282 1-383 view protein structure

Promoters
RGD ID:6798766
Promoter ID:HG_KWN:39206
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000355563,   ENST00000357394,   NM_198398,   OTTHUMT00000078880,   OTTHUMT00000126225,   OTTHUMT00000126226,   OTTHUMT00000126227,   OTTHUMT00000126228,   OTTHUMT00000315986,   UC002XCQ.1,   UC002XCR.1,   UC002XCU.1,   UC002XCV.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362033,593,046 - 33,593,546 (+)MPROMDB
RGD ID:6852088
Promoter ID:EP73850
Type:initiation region
Name:HS_SDBCAG84
Description:Serologically defined breast cancer antigen 84.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:NEDO full length human cDNA sequencing project.; Oligo-capping
Position:
Human AssemblyChrPosition (strand)Source
Build 362033,593,244 - 33,593,304EPD
RGD ID:6812032
Promoter ID:HG_ACW:49072
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:ERGIC3.KAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 362033,599,526 - 33,600,026 (+)MPROMDB
RGD ID:13206787
Promoter ID:EPDNEW_H26974
Type:initiation region
Name:ERGIC3_1
Description:ERGIC and golgi 3
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
GRCh382035,542,079 - 35,542,139EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:15927 AgrOrtholog
COSMIC ERGIC3 COSMIC
Ensembl Genes ENSG00000125991 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000348547 ENTREZGENE
  ENST00000348547.7 UniProtKB/Swiss-Prot
  ENST00000357394 ENTREZGENE
  ENST00000357394.8 UniProtKB/Swiss-Prot
  ENST00000411577.5 UniProtKB/TrEMBL
  ENST00000413587.5 UniProtKB/TrEMBL
  ENST00000416206.5 UniProtKB/TrEMBL
  ENST00000438317.5 UniProtKB/TrEMBL
  ENST00000442139.5 UniProtKB/TrEMBL
  ENST00000451605.1 UniProtKB/TrEMBL
GTEx ENSG00000125991 GTEx
HGNC ID HGNC:15927 ENTREZGENE
Human Proteome Map ERGIC3 Human Proteome Map
InterPro Erv UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Erv_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Erv_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:51614 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 51614 ENTREZGENE
OMIM 616971 OMIM
PANTHER ENDOPLASMIC RETICULUM-GOLGI INTERMEDIATE COMPARTMENT PROTEIN 3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR10984 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam COPIIcoated_ERV UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ERGIC_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA38050 PharmGKB
UniProt A0A0C4DH46_HUMAN UniProtKB/TrEMBL
  A2TJK5 ENTREZGENE, UniProtKB/TrEMBL
  A6PVJ2_HUMAN UniProtKB/TrEMBL
  A6PVJ3_HUMAN UniProtKB/TrEMBL
  ERGI3_HUMAN UniProtKB/Swiss-Prot
  H0Y5K5_HUMAN UniProtKB/TrEMBL
  H0Y621_HUMAN UniProtKB/TrEMBL
  H0Y6Z0_HUMAN UniProtKB/TrEMBL
  H0Y802_HUMAN UniProtKB/TrEMBL
  Q5JWS0 ENTREZGENE, UniProtKB/TrEMBL
  Q5JWS1_HUMAN UniProtKB/TrEMBL
  Q5JWS2_HUMAN UniProtKB/TrEMBL
  Q5JWS3 ENTREZGENE
  Q6ZWP7 ENTREZGENE
  Q9H276 ENTREZGENE
  Q9P1L3 ENTREZGENE
  Q9Y282 ENTREZGENE
UniProt Secondary Q5JWS3 UniProtKB/Swiss-Prot
  Q6ZWP7 UniProtKB/Swiss-Prot
  Q9H276 UniProtKB/Swiss-Prot
  Q9P1L3 UniProtKB/Swiss-Prot