GJD3 (gap junction protein delta 3) - Rat Genome Database

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Gene: GJD3 (gap junction protein delta 3) Homo sapiens
Analyze
Symbol: GJD3
Name: gap junction protein delta 3
RGD ID: 1319005
HGNC Page HGNC:19147
Description: Predicted to enable gap junction channel activity involved in AV node cell-bundle of His cell electrical coupling. Involved in gap junction assembly. Located in cell surface. Part of connexin complex.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: connexin 31.9; connexin-31.9; Cx30.2; CX31.9; gap junction alpha-11 protein; gap junction chi-1 protein; gap junction delta-3 protein; gap junction protein, chi 1, 31.9kda (connexin 31.9); gap junction protein, delta 3, 31.9kDa; GJA11; GJC1
RGD Orthologs
Mouse
Rat
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
GRCh381740,360,652 - 40,364,737 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1740,360,652 - 40,364,737 (-)EnsemblGRCh38hg38GRCh38
GRCh371738,516,904 - 38,520,989 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361735,770,430 - 35,774,471 (-)NCBINCBI36Build 36hg18NCBI36
Build 341735,770,432 - 35,774,471NCBI
Celera1735,177,047 - 35,181,088 (-)NCBICelera
Cytogenetic Map17q21.2NCBI
HuRef1734,310,022 - 34,314,063 (-)NCBIHuRef
CHM1_11738,752,212 - 38,756,253 (-)NCBICHM1_1
T2T-CHM13v2.01741,224,164 - 41,228,249 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

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

Cellular Component
cell surface  (IDA)
connexin complex  (IBA,IDA,IEA)
gap junction  (IEA)
plasma membrane  (IEA,TAS)

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. High glucose-induced downregulation of connexin 30.2 promotes retinal vascular lesions: implications for diabetic retinopathy. Manasson J, etal., Invest Ophthalmol Vis Sci. 2013 Mar 28;54(3):2361-6. doi: 10.1167/iovs.12-10815.
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12064584   PMID:12154091   PMID:12176752   PMID:12881038   PMID:16772377   PMID:17142249   PMID:18291099   PMID:19168070   PMID:21873635   PMID:33141287   PMID:34079125  


Genomics

Comparative Map Data
GJD3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381740,360,652 - 40,364,737 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1740,360,652 - 40,364,737 (-)EnsemblGRCh38hg38GRCh38
GRCh371738,516,904 - 38,520,989 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361735,770,430 - 35,774,471 (-)NCBINCBI36Build 36hg18NCBI36
Build 341735,770,432 - 35,774,471NCBI
Celera1735,177,047 - 35,181,088 (-)NCBICelera
Cytogenetic Map17q21.2NCBI
HuRef1734,310,022 - 34,314,063 (-)NCBIHuRef
CHM1_11738,752,212 - 38,756,253 (-)NCBICHM1_1
T2T-CHM13v2.01741,224,164 - 41,228,249 (-)NCBIT2T-CHM13v2.0
Gjd3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391198,870,773 - 98,873,846 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1198,873,006 - 98,873,842 (-)EnsemblGRCm39 Ensembl
GRCm381198,979,947 - 98,983,020 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1198,982,180 - 98,983,016 (-)EnsemblGRCm38mm10GRCm38
MGSCv371198,843,494 - 98,844,330 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361198,798,270 - 98,799,106 (-)NCBIMGSCv36mm8
Celera11108,648,034 - 108,648,870 (-)NCBICelera
Cytogenetic Map11DNCBI
cM Map1162.89NCBI
Gjd3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81084,429,923 - 84,432,011 (-)NCBIGRCr8
mRatBN7.21083,933,694 - 83,935,759 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1083,934,135 - 83,934,971 (-)EnsemblmRatBN7.2 Ensembl
Rnor_6.01086,888,982 - 86,891,915 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1086,889,421 - 86,890,257 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01086,674,192 - 86,689,734 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41087,759,290 - 87,760,126 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11087,773,659 - 87,780,168 (-)NCBI
Celera1082,675,110 - 82,678,043 (-)NCBICelera
Cytogenetic Map10q31NCBI
GJD3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21924,589,866 - 24,595,303 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11726,484,724 - 26,491,760 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01716,925,395 - 16,929,683 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11717,149,538 - 17,153,031 (+)NCBIpanpan1.1PanPan1.1panPan2
GJD3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1922,246,891 - 22,248,597 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha921,719,296 - 21,721,036 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0923,039,649 - 23,041,390 (+)NCBIROS_Cfam_1.0
UMICH_Zoey_3.1921,813,709 - 21,815,445 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0922,072,456 - 22,074,183 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0922,197,291 - 22,199,030 (+)NCBIUU_Cfam_GSD_1.0
Gjd3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560221,646,033 - 21,648,437 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493649015,427,263 - 15,428,141 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493649015,426,699 - 15,429,789 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
GJD3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.11222,040,312 - 22,044,238 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21222,348,902 - 22,352,200 (+)NCBISscrofa10.2Sscrofa10.2susScr3
GJD3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11665,811,111 - 65,815,128 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1665,811,981 - 65,812,862 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607736,711,465 - 36,716,211 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Gjd3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247952,930,925 - 2,931,767 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247952,930,425 - 2,933,411 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in GJD3
22 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3 copy number gain See cases [RCV000050957] Chr17:36449220..68170214 [GRCh38]
Chr17:48563237..65936105 [GRCh37]
Chr17:45918236..63677950 [NCBI36]
Chr17:17q21.33-24.2		 pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3		 pathogenic
GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3 copy number gain See cases [RCV000052479] Chr17:39199873..45629579 [GRCh38]
Chr17:37356126..43706945 [GRCh37]
Chr17:34609652..41062728 [NCBI36]
Chr17:17q12-21.31		 pathogenic
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3 copy number gain See cases [RCV000137437] Chr17:36449220..75053130 [GRCh38]
Chr17:57595736..73049225 [GRCh37]
Chr17:54950518..70560820 [NCBI36]
Chr17:17q23.1-25.1		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p11.2-q21.2(chr17:21690653-38772647)x3 copy number gain not provided [RCV000846852] Chr17:21690653..38772647 [GRCh37]
Chr17:17p11.2-q21.2		 pathogenic
NM_152219.4(GJD3):c.266C>G (p.Pro89Arg) single nucleotide variant not specified [RCV004135110] Chr17:40363550 [GRCh38]
Chr17:38519802 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.701C>T (p.Ala234Val) single nucleotide variant not specified [RCV004229003] Chr17:40363115 [GRCh38]
Chr17:38519367 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.230T>C (p.Phe77Ser) single nucleotide variant not specified [RCV004100808] Chr17:40363586 [GRCh38]
Chr17:38519838 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.289A>T (p.Met97Leu) single nucleotide variant not specified [RCV004212631] Chr17:40363527 [GRCh38]
Chr17:38519779 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.391C>T (p.Arg131Cys) single nucleotide variant not specified [RCV004133405] Chr17:40363425 [GRCh38]
Chr17:38519677 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.823G>A (p.Glu275Lys) single nucleotide variant not specified [RCV004095254] Chr17:40362993 [GRCh38]
Chr17:38519245 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.97C>T (p.Arg33Cys) single nucleotide variant not specified [RCV004177274] Chr17:40363719 [GRCh38]
Chr17:38519971 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.161G>C (p.Cys54Ser) single nucleotide variant not specified [RCV004136000] Chr17:40363655 [GRCh38]
Chr17:38519907 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.536G>T (p.Cys179Phe) single nucleotide variant not specified [RCV004130295] Chr17:40363280 [GRCh38]
Chr17:38519532 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.685C>A (p.Arg229Ser) single nucleotide variant not specified [RCV004113210] Chr17:40363131 [GRCh38]
Chr17:38519383 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.439G>A (p.Glu147Lys) single nucleotide variant not specified [RCV004211119] Chr17:40363377 [GRCh38]
Chr17:38519629 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.718C>T (p.Pro240Ser) single nucleotide variant not specified [RCV004287260] Chr17:40363098 [GRCh38]
Chr17:38519350 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.221A>C (p.His74Pro) single nucleotide variant not specified [RCV004268417] Chr17:40363595 [GRCh38]
Chr17:38519847 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.157G>C (p.Val53Leu) single nucleotide variant not specified [RCV004323373] Chr17:40363659 [GRCh38]
Chr17:38519911 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.632A>G (p.His211Arg) single nucleotide variant not specified [RCV004363547] Chr17:40363184 [GRCh38]
Chr17:38519436 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.491C>T (p.Pro164Leu) single nucleotide variant not specified [RCV004337917] Chr17:40363325 [GRCh38]
Chr17:38519577 [GRCh37]
Chr17:17q21.2		 uncertain significance
GRCh37/hg19 17q21.1-21.2(chr17:38390996-38689619)x3 copy number gain not provided [RCV003485157] Chr17:38390996..38689619 [GRCh37]
Chr17:17q21.1-21.2		 uncertain significance
NM_152219.4(GJD3):c.560A>C (p.Lys187Thr) single nucleotide variant not specified [RCV004392903] Chr17:40363256 [GRCh38]
Chr17:38519508 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.581A>G (p.Tyr194Cys) single nucleotide variant not specified [RCV004392904] Chr17:40363235 [GRCh38]
Chr17:38519487 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.635T>C (p.Leu212Pro) single nucleotide variant not specified [RCV004392905] Chr17:40363181 [GRCh38]
Chr17:38519433 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.404G>A (p.Cys135Tyr) single nucleotide variant not specified [RCV004390829] Chr17:40363412 [GRCh38]
Chr17:38519664 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.398G>T (p.Arg133Leu) single nucleotide variant not specified [RCV004627143] Chr17:40363418 [GRCh38]
Chr17:38519670 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_152219.4(GJD3):c.751C>A (p.Pro251Thr) single nucleotide variant not specified [RCV004627144] Chr17:40363065 [GRCh38]
Chr17:38519317 [GRCh37]
Chr17:17q21.2		 uncertain significance
GRCh37/hg19 17q12-22(chr17:41196270-41277589) copy number loss Breast-ovarian cancer, familial, susceptibility to, 1 [RCV004759419] Chr17:41196270..41277589 [GRCh37]
Chr17:17q12-22		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:559
Count of miRNA genes:421
Interacting mature miRNAs:458
Transcripts:ENST00000337376, ENST00000578689
Prediction methods:Microtar, Miranda, Rnahybrid
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
407156436GWAS805412_Hsex hormone-binding globulin measurement QTL GWAS805412 (human)3e-10sex hormone-binding globulin measurement174036329340363294Human
1298406BP16_HBlood pressure QTL 16 (human)0.0004Blood pressurehypertension susceptibility171477864740778647Human
407151203GWAS800179_Hcomplement factor H-related protein 5 measurement QTL GWAS800179 (human)0.000004complement factor H-related protein 5 measurement174036303940363040Human
407413665GWAS1062641_HVaricose veins QTL GWAS1062641 (human)1e-14Varicose veins174036364140363642Human
407179438GWAS828414_Hplatelet component distribution width QTL GWAS828414 (human)2e-11platelet component distribution widthplatelet distribution width (CMO:0001350)174036329340363294Human

Markers in Region
RH44908  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371738,516,985 - 38,517,089UniSTSGRCh37
Build 361735,770,511 - 35,770,615RGDNCBI36
Celera1735,177,128 - 35,177,232RGD
Cytogenetic Map17q21.2UniSTS
HuRef1734,310,103 - 34,310,207UniSTS
GeneMap99-GB4 RH Map17309.33UniSTS
NCBI RH Map17477.5UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
349 828 783 451 1461 772 1267 2 324 537 272 1173 2266 1697 49 573 480 654 882 64

Sequence


Ensembl Acc Id: ENST00000578689   ⟹   ENSP00000463752
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1740,360,652 - 40,364,737 (-)Ensembl
RefSeq Acc Id: NM_152219   ⟹   NP_689343
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381740,360,652 - 40,364,737 (-)NCBI
GRCh371738,516,904 - 38,520,945 (-)ENTREZGENE
Build 361735,770,430 - 35,774,471 (-)NCBI Archive
HuRef1734,310,022 - 34,314,063 (-)ENTREZGENE
CHM1_11738,752,212 - 38,756,253 (-)NCBI
T2T-CHM13v2.01741,224,164 - 41,228,249 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_689343 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAM18801 (Get FASTA)   NCBI Sequence Viewer  
  AAM53649 (Get FASTA)   NCBI Sequence Viewer  
  BAC86102 (Get FASTA)   NCBI Sequence Viewer  
  EAW60660 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000463752
  ENSP00000463752.1
GenBank Protein Q8N144 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_689343   ⟸   NM_152219
- UniProtKB: Q6ZUW6 (UniProtKB/Swiss-Prot),   Q8N144 (UniProtKB/Swiss-Prot),   A0A654IC68 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000463752   ⟸   ENST00000578689
Protein Domains
Connexin N-terminal   Gap junction protein cysteine-rich

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8N144-F1-model_v2 AlphaFold Q8N144 1-294 view protein structure

Promoters
RGD ID:6794175
Promoter ID:HG_KWN:26055
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:ENST00000337376
Position:
Human AssemblyChrPosition (strand)Source
Build 361735,772,971 - 35,773,471 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:19147 AgrOrtholog
COSMIC GJD3 COSMIC
Ensembl Genes ENSG00000183153 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000578689 ENTREZGENE
  ENST00000578689.2 UniProtKB/Swiss-Prot
Gene3D-CATH 1.20.1440.80 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000183153 GTEx
HGNC ID HGNC:19147 ENTREZGENE
Human Proteome Map GJD3 Human Proteome Map
InterPro Connexin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Connexin_CCC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Connexin_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Connexin_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Connexin_N_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:125111 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 125111 ENTREZGENE
OMIM 607425 OMIM
PANTHER GAP JUNCTION DELTA-3 PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR11984 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Connexin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB GJD3 RGD, PharmGKB
PRINTS CONNEXIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE CONNEXINS_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART CNX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Connexin_CCC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A654IC68 ENTREZGENE, UniProtKB/TrEMBL
  CXD3_HUMAN UniProtKB/Swiss-Prot
  Q6ZUW6 ENTREZGENE
  Q8N144 ENTREZGENE
UniProt Secondary Q6ZUW6 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-17 GJD3  gap junction protein delta 3  GJD3  gap junction protein, delta 3, 31.9kDa  Symbol and/or name change 5135510 APPROVED