CD3G (CD3g molecule) - Rat Genome Database
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Gene: CD3G (CD3g molecule) Homo sapiens
Analyze
Symbol: CD3G
Name: CD3g molecule
RGD ID: 1317072
HGNC Page HGNC
Description: Exhibits identical protein binding activity; protein heterodimerization activity; and transmembrane signaling receptor activity. Involved in several processes, including establishment or maintenance of cell polarity; protein transport; and regulation of lymphocyte apoptotic process. Localizes to cytosol and plasma membrane. Implicated in immunodeficiency 17.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: CD3-GAMMA; CD3g antigen, gamma polypeptide (TiT3 complex); CD3g molecule, epsilon (CD3-TCR complex); CD3g molecule, gamma (CD3-TCR complex); FLJ17620; FLJ17664; FLJ79544; FLJ94613; IMD17; MGC138597; T-cell antigen receptor complex, gamma subunit of T3; T-cell receptor T3 gamma chain; T-cell surface glycoprotein CD3 gamma chain; T3G
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl11118,344,344 - 118,355,161 (+)EnsemblGRCh38hg38GRCh38
GRCh3811118,344,344 - 118,355,161 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh3711118,215,059 - 118,225,876 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3611117,720,311 - 117,729,261 (+)NCBINCBI36hg18NCBI36
Build 3411117,720,310 - 117,729,261NCBI
Celera11115,372,928 - 115,382,366 (+)NCBI
Cytogenetic Map11q23.3NCBI
HuRef11114,148,956 - 114,158,393 (+)NCBIHuRef
CHM1_111118,101,492 - 118,110,943 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Molecular Pathway Annotations     Click to see Annotation Detail View
References

Additional References at PubMed
PMID:1385321   PMID:1387664   PMID:1535555   PMID:1635567   PMID:1709425   PMID:1826255   PMID:1832084   PMID:1979339   PMID:2111780   PMID:2138083   PMID:2139676   PMID:2540970  
PMID:2547833   PMID:2826124   PMID:2944745   PMID:3112151   PMID:3478717   PMID:7506554   PMID:7517794   PMID:7533164   PMID:7539755   PMID:7774645   PMID:8125298   PMID:8125527  
PMID:8145026   PMID:8636209   PMID:8647168   PMID:8809126   PMID:9045614   PMID:9263011   PMID:9485181   PMID:9510190   PMID:9582308   PMID:9743208   PMID:10722370   PMID:11048639  
PMID:11186279   PMID:11298321   PMID:11827988   PMID:12374807   PMID:12407027   PMID:12410792   PMID:12477932   PMID:12794121   PMID:14967045   PMID:15459203   PMID:15489334   PMID:15489916  
PMID:15638726   PMID:15778375   PMID:15879122   PMID:16094384   PMID:16344560   PMID:16777597   PMID:16888097   PMID:16888650   PMID:16916653   PMID:17001685   PMID:17023417   PMID:17176095  
PMID:17632570   PMID:17652306   PMID:17822534   PMID:17923503   PMID:17928336   PMID:18051367   PMID:18473783   PMID:18541215   PMID:18808677   PMID:18815285   PMID:19056690   PMID:19536290  
PMID:19724882   PMID:19726522   PMID:19759518   PMID:19860678   PMID:19898481   PMID:20012528   PMID:20179761   PMID:20237496   PMID:20478055   PMID:20511557   PMID:20594957   PMID:20660709  
PMID:20824090   PMID:21669053   PMID:21669059   PMID:21670311   PMID:21764047   PMID:21873635   PMID:21984702   PMID:22401598   PMID:22482414   PMID:22731821   PMID:22911005   PMID:23224761  
PMID:23336327   PMID:23348211   PMID:23590417   PMID:24187576   PMID:24495362   PMID:24794251   PMID:24910257   PMID:24966976   PMID:25113399   PMID:25467409   PMID:25505066   PMID:25760691  
PMID:25920998   PMID:25957593   PMID:26109064   PMID:29653965   PMID:30863395   PMID:32296183  


Genomics

Comparative Map Data
CD3G
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl11118,344,344 - 118,355,161 (+)EnsemblGRCh38hg38GRCh38
GRCh3811118,344,344 - 118,355,161 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh3711118,215,059 - 118,225,876 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3611117,720,311 - 117,729,261 (+)NCBINCBI36hg18NCBI36
Build 3411117,720,310 - 117,729,261NCBI
Celera11115,372,928 - 115,382,366 (+)NCBI
Cytogenetic Map11q23.3NCBI
HuRef11114,148,956 - 114,158,393 (+)NCBIHuRef
CHM1_111118,101,492 - 118,110,943 (+)NCBICHM1_1
Cd3g
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39944,880,870 - 44,891,729 (-)NCBIGRCm39mm39
GRCm39 Ensembl944,880,870 - 44,891,729 (-)Ensembl
GRCm38944,969,572 - 44,980,431 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl944,969,572 - 44,980,431 (-)EnsemblGRCm38mm10GRCm38
MGSCv37944,777,655 - 44,788,514 (-)NCBIGRCm37mm9NCBIm37
MGSCv36944,720,683 - 44,731,419 (-)NCBImm8
Celera942,234,684 - 42,245,549 (-)NCBICelera
Cytogenetic Map9A5.2NCBI
cM Map924.84NCBI
Cd3g
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2845,280,797 - 45,287,271 (-)NCBI
Rnor_6.0 Ensembl849,274,960 - 49,280,901 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0849,274,553 - 49,280,943 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0847,892,428 - 47,898,819 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4847,924,369 - 47,930,550 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1847,932,753 - 47,939,309 (-)NCBI
Celera844,865,997 - 44,871,910 (-)NCBICelera
Cytogenetic Map8q22NCBI
Cd3g
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541219,486,284 - 19,494,922 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495541219,486,066 - 19,496,474 (+)NCBIChiLan1.0ChiLan1.0
CD3G
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.111117,111,132 - 117,120,566 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl11117,111,132 - 117,120,566 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v011113,179,270 - 113,190,104 (+)NCBIMhudiblu_PPA_v0panPan3
CD3G
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1515,379,788 - 15,391,271 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl515,380,633 - 15,391,214 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha515,429,235 - 15,442,031 (-)NCBI
ROS_Cfam_1.0515,320,796 - 15,333,597 (-)NCBI
UMICH_Zoey_3.1515,459,062 - 15,471,859 (-)NCBI
UNSW_CanFamBas_1.0515,362,517 - 15,375,316 (-)NCBI
UU_Cfam_GSD_1.0515,403,667 - 15,416,467 (-)NCBI
Cd3g
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404947100,482,219 - 100,490,660 (+)NCBI
SpeTri2.0NW_0049365423,405,084 - 3,412,104 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CD3G
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl945,645,364 - 45,704,745 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1945,645,243 - 45,656,779 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2950,686,376 - 50,697,901 (+)NCBISscrofa10.2Sscrofa10.2susScr3
CD3G
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11109,721,150 - 109,730,267 (+)NCBI
ChlSab1.1 Ensembl1109,720,789 - 109,732,014 (+)Ensembl
Cd3g
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462478413,738,424 - 13,748,311 (+)NCBI

Position Markers
GDB:197879  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711118,219,739 - 118,220,484UniSTSGRCh37
Build 3611117,724,949 - 117,725,694RGDNCBI36
Celera11115,377,608 - 115,378,353RGD
Cytogenetic Map11q23UniSTS
HuRef11114,153,635 - 114,154,380UniSTS
RH80031  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8q21.3UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map1p36.12-p35.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map18q21.31UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic MapXq21.2UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map11q23UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
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Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
D11S4362  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map11q23UniSTS
TNG Radiation Hybrid Map1154594.0UniSTS
GeneMap99-GB4 RH Map11380.67UniSTS
Whitehead-RH Map11524.9UniSTS
Whitehead-YAC Contig Map11 UniSTS
GeneMap99-G3 RH Map115211.0UniSTS
D1S1425  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map2p23-p22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic Map2p11.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map2p12-p11.2UniSTS
Cytogenetic Map3q11.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map15q11-q12UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map4q31.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map10p15-p14UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map15q24-q25UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map6q16UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map16q24.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic MapXq21.1UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2296
Count of miRNA genes:901
Interacting mature miRNAs:1063
Transcripts:ENST00000292144, ENST00000392883, ENST00000527777, ENST00000528540, ENST00000532903, ENST00000532917, ENST00000533462
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.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 54 182 17 3 379 3 4 6 7 21
Low 887 875 691 250 1011 156 672 88 193 189 582 1217 95 585 225 2 2
Below cutoff 1436 1698 985 356 201 291 3295 1739 2884 192 820 362 77 617 2204 3

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_007566 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_000073 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005271724 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006718941 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB583162 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK223314 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299997 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK310578 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK310622 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313966 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315895 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP001582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC069685 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC113830 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB116263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC378393 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF444965 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X04145 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X06026 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X06027 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X06028 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X06029 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X06030 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X06031 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X06032 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X60492 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000292144   ⟹   ENSP00000292144
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl11118,344,365 - 118,353,837 (+)Ensembl
RefSeq Acc Id: ENST00000392883   ⟹   ENSP00000376621
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl11118,344,344 - 118,353,782 (+)Ensembl
RefSeq Acc Id: ENST00000527777
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl11118,344,344 - 118,350,909 (+)Ensembl
RefSeq Acc Id: ENST00000528540   ⟹   ENSP00000498162
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl11118,344,386 - 118,349,876 (+)Ensembl
RefSeq Acc Id: ENST00000532903
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl11118,344,407 - 118,353,247 (+)Ensembl
RefSeq Acc Id: ENST00000532917   ⟹   ENSP00000431445
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl11118,344,344 - 118,355,161 (+)Ensembl
RefSeq Acc Id: ENST00000533462
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl11118,344,344 - 118,350,198 (+)Ensembl
RefSeq Acc Id: NM_000073   ⟹   NP_000064
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811118,344,344 - 118,355,161 (+)NCBI
GRCh3711118,215,032 - 118,224,497 (+)NCBI
Build 3611117,720,311 - 117,729,261 (+)NCBI Archive
HuRef11114,148,956 - 114,158,393 (+)ENTREZGENE
CHM1_111118,101,492 - 118,110,943 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005271724   ⟹   XP_005271781
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811118,344,353 - 118,350,903 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006718941   ⟹   XP_006719004
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811118,344,353 - 118,353,550 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_000064   ⟸   NM_000073
- Peptide Label: precursor
- UniProtKB: P09693 (UniProtKB/Swiss-Prot),   B0YIY5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005271781   ⟸   XM_005271724
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_006719004   ⟸   XM_006718941
- Peptide Label: isoform X2
- UniProtKB: P09693 (UniProtKB/Swiss-Prot),   B0YIY5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000292144   ⟸   ENST00000292144
RefSeq Acc Id: ENSP00000431445   ⟸   ENST00000532917
RefSeq Acc Id: ENSP00000376621   ⟸   ENST00000392883
RefSeq Acc Id: ENSP00000498162   ⟸   ENST00000528540
Protein Domains
Ig-like   Ig_4   IGc2   ITAM

Promoters
RGD ID:6788595
Promoter ID:HG_KWN:14315
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   Jurkat
Transcripts:ENST00000292144,   ENST00000392883
Position:
Human AssemblyChrPosition (strand)Source
Build 3611117,719,994 - 117,720,494 (+)MPROMDB
RGD ID:6850392
Promoter ID:EP17096
Type:multiple initiation site
Name:HS_CD3G
Description:T-cell differentiation antigen CD3 (T3) gamma.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Nuclease protection with homologous sequence ladder
Regulation:T (repressed by or weakly expressed in) cells
Position:
Human AssemblyChrPosition (strand)Source
Build 3611117,720,274 - 117,720,334EPD
RGD ID:7222299
Promoter ID:EPDNEW_H16895
Type:initiation region
Name:CD3G_1
Description:CD3g molecule
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811118,344,344 - 118,344,404EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_000073.2(CD3G):c.1A>G (p.Met1Val) single nucleotide variant Immunodeficiency 17 [RCV000087021] Chr11:118344424 [GRCh38]
Chr11:118215139 [GRCh37]
Chr11:11q23.3
pathogenic
GRCh38/hg38 11q23.3-25(chr11:116851395-134998513)x3 copy number gain See cases [RCV000050331] Chr11:116851395..134998513 [GRCh38]
Chr11:116722111..134868407 [GRCh37]
Chr11:116227321..134373617 [NCBI36]
Chr11:11q23.3-25
pathogenic
GRCh38/hg38 11q23.2-23.3(chr11:113444446-120648921)x3 copy number gain See cases [RCV000050627] Chr11:113444446..120648921 [GRCh38]
Chr11:113315168..120519630 [GRCh37]
Chr11:112820378..120024840 [NCBI36]
Chr11:11q23.2-23.3
pathogenic
GRCh38/hg38 11q22.1-25(chr11:100348599-135040246)x3 copy number gain See cases [RCV000053638] Chr11:100348599..135040246 [GRCh38]
Chr11:100219331..134910140 [GRCh37]
Chr11:99724541..134415350 [NCBI36]
Chr11:11q22.1-25
pathogenic
NM_000073.2(CD3G):c.80_96del deletion Immunodeficiency 17 [RCV000087022] Chr11:118349741..118349757 [GRCh38]
Chr11:118220456..118220472 [GRCh37]
Chr11:11q23.3
pathogenic
NM_000073.2(CD3G):c.205A>T (p.Lys69Ter) single nucleotide variant Immunodeficiency 17 [RCV000087023] Chr11:118349868 [GRCh38]
Chr11:118220583 [GRCh37]
Chr11:11q23.3
pathogenic
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3
pathogenic
GRCh38/hg38 11q23.3-25(chr11:116851372-134998526)x3 copy number gain See cases [RCV000134064] Chr11:116851372..134998526 [GRCh38]
Chr11:116722088..134868420 [GRCh37]
Chr11:116227298..134373630 [NCBI36]
Chr11:11q23.3-25
pathogenic
GRCh38/hg38 11q23.3-25(chr11:116868935-135075271)x3 copy number gain See cases [RCV000137453] Chr11:116868935..135075271 [GRCh38]
Chr11:116739651..134945165 [GRCh37]
Chr11:116244861..134450377 [NCBI36]
Chr11:11q23.3-25
pathogenic|conflicting data from submitters
GRCh38/hg38 11q23.2-25(chr11:112864326-131189315)x3 copy number gain See cases [RCV000137582] Chr11:112864326..131189315 [GRCh38]
Chr11:112832130..131059210 [GRCh37]
Chr11:112240259..130564420 [NCBI36]
Chr11:11q23.2-25
pathogenic
GRCh38/hg38 11q23.3-25(chr11:116806268-135075271)x3 copy number gain See cases [RCV000138307] Chr11:116806268..135075271 [GRCh38]
Chr11:116676984..134945165 [GRCh37]
Chr11:116182194..134450377 [NCBI36]
Chr11:11q23.3-25
pathogenic
GRCh38/hg38 11q23.3-24.2(chr11:117333952-127709156)x3 copy number gain See cases [RCV000139362] Chr11:117333952..127709156 [GRCh38]
Chr11:117204668..127579051 [GRCh37]
Chr11:116709878..127084261 [NCBI36]
Chr11:11q23.3-24.2
pathogenic
GRCh38/hg38 11q23.3-25(chr11:116851395-134998513)x3 copy number gain See cases [RCV000148276] Chr11:116851395..134998513 [GRCh38]
Chr11:116722111..134868407 [GRCh37]
Chr11:116227321..134373617 [NCBI36]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:116691675-134889485) copy number gain not provided [RCV000767667] Chr11:116691675..134889485 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q23.3(chr11:115215434-120559928)x3 copy number gain See cases [RCV000240308] Chr11:115215434..120559928 [GRCh37]
Chr11:11q23.3
pathogenic
NM_000073.2(CD3G):c.307+13C>T single nucleotide variant Immunodeficiency due to defect in CD3-gamma [RCV000345972] Chr11:118349983 [GRCh38]
Chr11:118220698 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.*453G>T single nucleotide variant Immunodeficiency 17 [RCV000305705] Chr11:118353553 [GRCh38]
Chr11:118224268 [GRCh37]
Chr11:11q23.3
benign|likely benign
NM_000073.3(CD3G):c.390T>C (p.Ala130=) single nucleotide variant Immunodeficiency 17 [RCV000288417]|not specified [RCV000454974] Chr11:118350634 [GRCh38]
Chr11:118221349 [GRCh37]
Chr11:11q23.3
benign|likely benign
NM_000073.2(CD3G):c.*244A>G single nucleotide variant Immunodeficiency 17 [RCV000349036] Chr11:118353344 [GRCh38]
Chr11:118224059 [GRCh37]
Chr11:11q23.3
benign|likely benign
NM_000073.2(CD3G):c.32T>C (p.Ile11Thr) single nucleotide variant Immunodeficiency 17 [RCV000376087] Chr11:118344455 [GRCh38]
Chr11:118215170 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.158T>C (p.Ile53Thr) single nucleotide variant Immunodeficiency 17 [RCV000651965]|not provided [RCV001091037] Chr11:118349821 [GRCh38]
Chr11:118220536 [GRCh37]
Chr11:11q23.3
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_000073.2(CD3G):c.*450T>G single nucleotide variant Immunodeficiency 17 [RCV000354876] Chr11:118353550 [GRCh38]
Chr11:118224265 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.*451del deletion Immunodeficiency due to defect in CD3-gamma [RCV000259817] Chr11:118353551 [GRCh38]
Chr11:118224266 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.-17G>T single nucleotide variant Immunodeficiency 17 [RCV000322487] Chr11:118344407 [GRCh38]
Chr11:118215122 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.391G>T (p.Val131Phe) single nucleotide variant Immunodeficiency 17 [RCV000352643]|not specified [RCV000455537] Chr11:118350635 [GRCh38]
Chr11:118221350 [GRCh37]
Chr11:11q23.3
benign|likely benign
NM_000073.2(CD3G):c.*308G>A single nucleotide variant Immunodeficiency 17 [RCV000404601] Chr11:118353408 [GRCh38]
Chr11:118224123 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.511T>C (p.Tyr171His) single nucleotide variant Immunodeficiency 17 [RCV000921146] Chr11:118352431 [GRCh38]
Chr11:118223146 [GRCh37]
Chr11:11q23.3
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_000073.2(CD3G):c.308-4A>G single nucleotide variant Immunodeficiency 17 [RCV000381948] Chr11:118350548 [GRCh38]
Chr11:118221263 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.*112C>T single nucleotide variant Immunodeficiency 17 [RCV000313018] Chr11:118353212 [GRCh38]
Chr11:118223927 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.-46_-43delGCTG microsatellite Immunodeficiency due to defect in CD3-gamma [RCV000267460]|Severe Combined Immune Deficiency [RCV000342221] Chr11:118344361..118344364 [GRCh38]
Chr11:118215076..118215079 [GRCh37]
Chr11:11q23.3
benign|likely benign
NM_000073.2(CD3G):c.*450dup duplication Immunodeficiency due to defect in CD3-gamma [RCV000300036] Chr11:118353524..118353525 [GRCh38]
Chr11:118224239..118224240 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.*500G>A single nucleotide variant Immunodeficiency 17 [RCV000360486] Chr11:118353600 [GRCh38]
Chr11:118224315 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.64G>A (p.Ala22Thr) single nucleotide variant Immunodeficiency 17 [RCV000534288] Chr11:118349035 [GRCh38]
Chr11:118219750 [GRCh37]
Chr11:11q23.3
benign
GRCh37/hg19 11q23.3-25(chr11:116700253-134904063) copy number gain not provided [RCV000767816] Chr11:116700253..134904063 [GRCh37]
Chr11:11q23.3-25
pathogenic
NM_000073.2(CD3G):c.390_391delinsCT (p.Val131Phe) indel Immunodeficiency 17 [RCV000558113] Chr11:118350634..118350635 [GRCh38]
Chr11:118221349..118221350 [GRCh37]
Chr11:11q23.3
benign
GRCh37/hg19 11q23.3-25(chr11:116681007-134938470)x3 copy number gain See cases [RCV000449449] Chr11:116681007..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:116684163-134938470)x3 copy number gain See cases [RCV000447848] Chr11:116684163..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
NM_000073.2(CD3G):c.170A>C (p.Lys57Thr) single nucleotide variant Immunodeficiency 17 [RCV000651961] Chr11:118349833 [GRCh38]
Chr11:118220548 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.213del (p.Lys71fs) deletion Immunodeficiency 17 [RCV000651962] Chr11:118349868 [GRCh38]
Chr11:118220583 [GRCh37]
Chr11:11q23.3
pathogenic|conflicting interpretations of pathogenicity
NM_000073.2(CD3G):c.496C>A (p.Arg166=) single nucleotide variant Immunodeficiency 17 [RCV000651963] Chr11:118352416 [GRCh38]
Chr11:118223131 [GRCh37]
Chr11:11q23.3
benign|conflicting interpretations of pathogenicity
NM_000073.2(CD3G):c.56G>A (p.Gly19Asp) single nucleotide variant Immunodeficiency 17 [RCV000651964]|not provided [RCV001091036] Chr11:118349027 [GRCh38]
Chr11:118219742 [GRCh37]
Chr11:11q23.3
likely benign|conflicting interpretations of pathogenicity|uncertain significance
GRCh37/hg19 11q23.3-25(chr11:116681007-134938470)x3 copy number gain See cases [RCV000512291] Chr11:116681007..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
NM_000073.2(CD3G):c.79+10A>G single nucleotide variant Immunodeficiency 17 [RCV000551445] Chr11:118349060 [GRCh38]
Chr11:118219775 [GRCh37]
Chr11:11q23.3
benign|conflicting interpretations of pathogenicity
NM_000073.2(CD3G):c.439+12C>T single nucleotide variant not provided [RCV000513970] Chr11:118350695 [GRCh38]
Chr11:118221410 [GRCh37]
Chr11:11q23.3
uncertain significance
GRCh37/hg19 11q23.3-25(chr11:116681007-134938470)x3 copy number gain not provided [RCV000683373] Chr11:116681007..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
GRCh37/hg19 11q23.3(chr11:116669751-120979377)x3 copy number gain not provided [RCV000683365] Chr11:116669751..120979377 [GRCh37]
Chr11:11q23.3
likely pathogenic
NM_000073.2(CD3G):c.33C>G (p.Ile11Met) single nucleotide variant Immunodeficiency 17 [RCV000704598] Chr11:118344456 [GRCh38]
Chr11:118215171 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.213dup (p.Trp72fs) duplication Immunodeficiency 17 [RCV000704172] Chr11:118349867..118349868 [GRCh38]
Chr11:118220582..118220583 [GRCh37]
Chr11:11q23.3
pathogenic
NM_000073.2(CD3G):c.187G>A (p.Gly63Ser) single nucleotide variant Immunodeficiency 17 [RCV000694313] Chr11:118349850 [GRCh38]
Chr11:118220565 [GRCh37]
Chr11:11q23.3
uncertain significance
Single allele deletion Short stature [RCV001003892] Chr11:114433313..131230466 [GRCh37]
Chr11:11q23.2-25
likely pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11q23.3-25(chr11:116697066-134934063)x3 copy number gain not provided [RCV000737686] Chr11:116697066..134934063 [GRCh37]
Chr11:11q23.3-25
pathogenic
NC_000011.9:g.(?_117856768)_(118972385_?)del deletion Immunodeficiency 19 [RCV001031688] Chr11:117856768..118972385 [GRCh37]
Chr11:11q23.3
pathogenic
NM_000073.3(CD3G):c.353T>C (p.Phe118Ser) single nucleotide variant Immunodeficiency 17 [RCV001053373] Chr11:118350597 [GRCh38]
Chr11:118221312 [GRCh37]
Chr11:11q23.3
uncertain significance
NC_000011.9:g.(?_117856768)_(118972385_?)dup duplication Glucose-6-phosphate transport defect [RCV001031254]|Immunodeficiency 18 [RCV001338286] Chr11:117856768..118972385 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.219T>C (p.Asn73=) single nucleotide variant not provided [RCV000979418] Chr11:118349882 [GRCh38]
Chr11:118220597 [GRCh37]
Chr11:11q23.3
likely benign
NM_000073.3(CD3G):c.56-5T>C single nucleotide variant Immunodeficiency 17 [RCV000977933] Chr11:118349022 [GRCh38]
Chr11:118219737 [GRCh37]
Chr11:11q23.3
likely benign
NM_000073.2(CD3G):c.389_391delinsTCT (p.Ala130_Val131delinsValPhe) indel Immunodeficiency 17 [RCV000818977] Chr11:118350633..118350635 [GRCh38]
Chr11:118221348..118221350 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.122C>T (p.Ser41Leu) single nucleotide variant Immunodeficiency 17 [RCV000819383] Chr11:118349785 [GRCh38]
Chr11:118220500 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.128T>C (p.Leu43Pro) single nucleotide variant Immunodeficiency 17 [RCV000803506] Chr11:118349791 [GRCh38]
Chr11:118220506 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.40A>G (p.Ile14Val) single nucleotide variant Immunodeficiency 17 [RCV000796961] Chr11:118344463 [GRCh38]
Chr11:118215178 [GRCh37]
Chr11:11q23.3
uncertain significance
NC_000011.9:g.(?_118007722)_(119170511_?)del deletion Long QT syndrome 10 [RCV000816632] Chr11:118007722..119170511 [GRCh37]
Chr11:11q23.3
uncertain significance
GRCh37/hg19 11q23.3-25(chr11:117830263-134938470)x3 copy number gain not provided [RCV000848151] Chr11:117830263..134938470 [GRCh37]
Chr11:11q23.3-25
pathogenic
NM_000073.2(CD3G):c.326A>G (p.Glu109Gly) single nucleotide variant Immunodeficiency 17 [RCV000798059] Chr11:118350570 [GRCh38]
Chr11:118221285 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.273G>C (p.Gln91His) single nucleotide variant Immunodeficiency 17 [RCV000793727] Chr11:118349936 [GRCh38]
Chr11:118220651 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.2(CD3G):c.36G>A (p.Leu12=) single nucleotide variant Immunodeficiency 17 [RCV000804936] Chr11:118344459 [GRCh38]
Chr11:118215174 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.13A>T (p.Lys5Ter) single nucleotide variant Immunodeficiency 17 [RCV001239548] Chr11:118344436 [GRCh38]
Chr11:118215151 [GRCh37]
Chr11:11q23.3
pathogenic
NM_000073.3(CD3G):c.11G>T (p.Gly4Val) single nucleotide variant Immunodeficiency 17 [RCV001222825] Chr11:118344434 [GRCh38]
Chr11:118215149 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.308-13_308-6del deletion Immunodeficiency 17 [RCV001221250] Chr11:118350538..118350545 [GRCh38]
Chr11:118221253..118221260 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.467A>G (p.Asn156Ser) single nucleotide variant Immunodeficiency 17 [RCV001107087] Chr11:118351655 [GRCh38]
Chr11:118222370 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.*141G>A single nucleotide variant Immunodeficiency 17 [RCV001107088] Chr11:118353241 [GRCh38]
Chr11:118223956 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.*617G>T single nucleotide variant Immunodeficiency 17 [RCV001104109] Chr11:118353717 [GRCh38]
Chr11:118224432 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.*426T>G single nucleotide variant Immunodeficiency 17 [RCV001107757] Chr11:118353526 [GRCh38]
Chr11:118224241 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.417G>A (p.Gln139=) single nucleotide variant not provided [RCV000933520] Chr11:118350661 [GRCh38]
Chr11:118221376 [GRCh37]
Chr11:11q23.3
likely benign
NM_000073.3(CD3G):c.*253G>A single nucleotide variant Immunodeficiency 17 [RCV001107755] Chr11:118353353 [GRCh38]
Chr11:118224068 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.223G>A (p.Gly75Arg) single nucleotide variant Immunodeficiency 17 [RCV001205989] Chr11:118349886 [GRCh38]
Chr11:118220601 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.*650C>T single nucleotide variant Immunodeficiency 17 [RCV001104110] Chr11:118353750 [GRCh38]
Chr11:118224465 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.*363C>T single nucleotide variant Immunodeficiency 17 [RCV001107756] Chr11:118353463 [GRCh38]
Chr11:118224178 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.*551C>T single nucleotide variant Immunodeficiency 17 [RCV001107758] Chr11:118353651 [GRCh38]
Chr11:118224366 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.243T>C (p.Pro81=) single nucleotide variant Immunodeficiency 17 [RCV001104327] Chr11:118349906 [GRCh38]
Chr11:118220621 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.*216C>A single nucleotide variant Immunodeficiency 17 [RCV001107089] Chr11:118353316 [GRCh38]
Chr11:118224031 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.37G>A (p.Ala13Thr) single nucleotide variant Immunodeficiency 17 [RCV001048213] Chr11:118344460 [GRCh38]
Chr11:118215175 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.79+4G>A single nucleotide variant Immunodeficiency 17 [RCV001070205] Chr11:118349054 [GRCh38]
Chr11:118219769 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.79+3A>G single nucleotide variant Immunodeficiency 17 [RCV001320273] Chr11:118349053 [GRCh38]
Chr11:118219768 [GRCh37]
Chr11:11q23.3
uncertain significance
NC_000011.9:g.(?_117856768)_(118972385_?)dup duplication Immunodeficiency 17 [RCV001313154]|Immunodeficiency 19 [RCV001322413] Chr11:117856768..118972385 [GRCh37]
Chr11:11q23.3
uncertain significance
NC_000011.9:g.(?_118007722)_(119170511_?)del deletion Long QT syndrome 10 [RCV001309948] Chr11:118007722..119170511 [GRCh37]
Chr11:11q23.3
uncertain significance
NM_000073.3(CD3G):c.437G>C (p.Arg146Thr) single nucleotide variant Immunodeficiency 17 [RCV001307571] Chr11:118350681 [GRCh38]
Chr11:118221396 [GRCh37]
Chr11:11q23.3
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:1675 AgrOrtholog
COSMIC CD3G COSMIC
Ensembl Genes ENSG00000160654 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000292144 UniProtKB/TrEMBL
  ENSP00000376621 UniProtKB/TrEMBL
  ENSP00000431445 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000498162 UniProtKB/TrEMBL
Ensembl Transcript ENST00000292144 UniProtKB/TrEMBL
  ENST00000392883 UniProtKB/TrEMBL
  ENST00000527777 ENTREZGENE
  ENST00000528540 UniProtKB/TrEMBL
  ENST00000532917 ENTREZGENE, UniProtKB/Swiss-Prot
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000160654 GTEx
HGNC ID HGNC:1675 ENTREZGENE
Human Proteome Map CD3G Human Proteome Map
InterPro CD3_esu/gsu/dsu UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_sub2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Phos_immunorcpt_sig_ITAM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:917 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 917 ENTREZGENE
OMIM 186740 OMIM
  615607 OMIM
PANTHER PTHR10570 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Ig_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ITAM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA26217 PharmGKB
PROSITE ITAM_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART IGc2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ITAM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48726 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A3B3IUD8_HUMAN UniProtKB/TrEMBL
  A2N8H4_HUMAN UniProtKB/TrEMBL
  A2N8H5_HUMAN UniProtKB/TrEMBL
  A8MUH3_HUMAN UniProtKB/TrEMBL
  B0YIY5 ENTREZGENE, UniProtKB/TrEMBL
  CD3G_HUMAN UniProtKB/Swiss-Prot
  J3KNA5_HUMAN UniProtKB/TrEMBL
  P09693 ENTREZGENE
UniProt Secondary Q2HIZ6 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-01-12 CD3G  CD3g molecule    CD3g molecule, gamma (CD3-TCR complex)  Symbol and/or name change 5135510 APPROVED
2011-08-16 CD3G  CD3g molecule, gamma (CD3-TCR complex)  CD3G  CD3g molecule, gamma (CD3-TCR complex)  Symbol and/or name change 5135510 APPROVED