IGHG1 (immunoglobulin heavy constant gamma 1 (G1m marker)) - Rat Genome Database

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Gene: IGHG1 (immunoglobulin heavy constant gamma 1 (G1m marker)) Homo sapiens
Analyze
Symbol: IGHG1
Name: immunoglobulin heavy constant gamma 1 (G1m marker)
RGD ID: 1344505
HGNC Page HGNC:5525
Description: Enables Fc-gamma receptor I complex binding activity. Involved in antibody-dependent cellular cytotoxicity and complement-dependent cytotoxicity. Located in IgG immunoglobulin complex and extracellular space.
Type: gene (Ensembl: IG_C_gene)
RefSeq Status: VALIDATED
RGD Orthologs
Mouse
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
GRCh3814105,741,473 - 105,743,070 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl14105,736,343 - 105,743,071 (-)EnsemblGRCh38hg38GRCh38
GRCh3714106,207,810 - 106,209,407 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3614105,278,749 - 105,280,452 (-)NCBINCBI36Build 36hg18NCBI36
Celera1486,146,753 - 86,148,456 (-)NCBICelera
Cytogenetic Map14q32.33NCBI
HuRef1486,340,115 - 86,341,712 (-)NCBIHuRef
CHM1_114106,106,771 - 106,107,520 (-)NCBICHM1_1
T2T-CHM13v2.014100,012,671 - 100,014,268 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
4. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
5. Transcriptomic characteristics of bronchoalveolar lavage fluid and peripheral blood mononuclear cells in COVID-19 patients. Xiong Y, etal., Emerg Microbes Infect. 2020 Dec;9(1):761-770. doi: 10.1080/22221751.2020.1747363.
Additional References at PubMed
PMID:826475   PMID:955567   PMID:992566   PMID:1002129   PMID:1522589   PMID:4138920   PMID:4923144   PMID:5489771   PMID:5530842   PMID:6287432   PMID:6811139   PMID:6884994  
PMID:7236608   PMID:9530559   PMID:9661813   PMID:10681448   PMID:10917521   PMID:11183784   PMID:11257305   PMID:11297532   PMID:11498595   PMID:11525169   PMID:11567028   PMID:11711607  
PMID:12039524   PMID:12477932   PMID:12527303   PMID:12552112   PMID:14702039   PMID:15037082   PMID:15174051   PMID:15517630   PMID:16502470   PMID:16646632   PMID:16944158   PMID:17044868  
PMID:17177686   PMID:17400754   PMID:17933503   PMID:17960657   PMID:18821675   PMID:19317746   PMID:19319024   PMID:19380743   PMID:19542624   PMID:19608861   PMID:19725029   PMID:19738201  
PMID:20176268   PMID:20214683   PMID:21565611   PMID:21654544   PMID:21800051   PMID:21873635   PMID:22516433   PMID:22839360   PMID:23117283   PMID:23225573   PMID:23376485   PMID:23533145  
PMID:23580065   PMID:23956138   PMID:24244333   PMID:24304136   PMID:24453475   PMID:24457600   PMID:24662005   PMID:24711643   PMID:25358868   PMID:25416956   PMID:25437307   PMID:25645918  
PMID:25925696   PMID:25940394   PMID:25963833   PMID:26186194   PMID:26485645   PMID:26949251   PMID:27393575   PMID:27591049   PMID:27705803   PMID:28514442   PMID:28515276   PMID:28685749  
PMID:28902428   PMID:29117863   PMID:29449217   PMID:29467282   PMID:29507755   PMID:29802200   PMID:29945307   PMID:30021884   PMID:30198883   PMID:30319994   PMID:30413534   PMID:30561431  
PMID:30796180   PMID:31010829   PMID:31180492   PMID:31355278   PMID:31409639   PMID:31594818   PMID:31862882   PMID:31992359   PMID:32120844   PMID:32905556   PMID:32989256   PMID:33545068  
PMID:33567341   PMID:33644029   PMID:33742100   PMID:33961781   PMID:34205175   PMID:34591612   PMID:34825085   PMID:34943047   PMID:35013218   PMID:35133976   PMID:35256949   PMID:35271311  
PMID:35337019   PMID:35384245   PMID:35583604   PMID:35831895   PMID:36147463   PMID:36199071   PMID:36215168   PMID:36243803   PMID:36339263   PMID:36404682   PMID:36574265   PMID:36736099  
PMID:36964488   PMID:38113892  


Genomics

Comparative Map Data
IGHG1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3814105,741,473 - 105,743,070 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl14105,736,343 - 105,743,071 (-)EnsemblGRCh38hg38GRCh38
GRCh3714106,207,810 - 106,209,407 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3614105,278,749 - 105,280,452 (-)NCBINCBI36Build 36hg18NCBI36
Celera1486,146,753 - 86,148,456 (-)NCBICelera
Cytogenetic Map14q32.33NCBI
HuRef1486,340,115 - 86,341,712 (-)NCBIHuRef
CHM1_114106,106,771 - 106,107,520 (-)NCBICHM1_1
T2T-CHM13v2.014100,012,671 - 100,014,268 (-)NCBIT2T-CHM13v2.0
Ighg1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3912113,290,161 - 113,294,143 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl12113,288,860 - 113,294,143 (-)EnsemblGRCm39 Ensembl
GRCm3812113,326,541 - 113,330,523 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl12113,325,240 - 113,330,523 (-)EnsemblGRCm38mm10GRCm38
MGSCv3712114,564,755 - 114,568,734 (-)NCBIGRCm37MGSCv37mm9NCBIm37
Celera12114,512,547 - 114,780,893 (-)NCBICelera
Cytogenetic Map12F1NCBI
cM Map1262.1NCBI
Ighg1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2 Ensembl6132,389,370 - 132,393,397 (-)EnsemblmRatBN7.2 Ensembl
Rnor_6.06139,140,572 - 139,784,388 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl6139,140,679 - 139,142,218 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.06147,106,967 - 147,241,786 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Rnor_5.06148,128,786 - 148,134,027 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.46138,310,041 - 138,311,688 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera6129,920,648 - 129,922,321 (-)NCBICelera
Cytogenetic Map6q32NCBI

Variants

.
Variants in IGHG1
1 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 14q32.2-32.33(chr14:100309382-106855263)x1 copy number loss See cases [RCV000050938] Chr14:100309382..106855263 [GRCh38]
Chr14:100775719..107263478 [GRCh37]
Chr14:99845472..106334523 [NCBI36]
Chr14:14q32.2-32.33		 pathogenic
GRCh38/hg38 14q32.2-32.33(chr14:97938637-106855263)x1 copy number loss See cases [RCV000050696] Chr14:97938637..106855263 [GRCh38]
Chr14:98404974..107263478 [GRCh37]
Chr14:97474727..106334523 [NCBI36]
Chr14:14q32.2-32.33		 pathogenic
GRCh38/hg38 14q32.31-32.33(chr14:101994084-106855405)x1 copy number loss See cases [RCV000051578] Chr14:101994084..106855405 [GRCh38]
Chr14:102460421..107263620 [GRCh37]
Chr14:101530174..106334665 [NCBI36]
Chr14:14q32.31-32.33		 pathogenic
GRCh38/hg38 14q32.33(chr14:103784758-106870558)x1 copy number loss See cases [RCV000051581] Chr14:103784758..106870558 [GRCh38]
Chr14:104251095..107278770 [GRCh37]
Chr14:103320848..106349815 [NCBI36]
Chr14:14q32.33		 pathogenic
GRCh38/hg38 14q32.2-32.33(chr14:100590353-106855264)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051553]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051553]|See cases [RCV000051553] Chr14:100590353..106855264 [GRCh38]
Chr14:101056690..107263479 [GRCh37]
Chr14:100126443..106334524 [NCBI36]
Chr14:14q32.2-32.33		 pathogenic
GRCh38/hg38 14q32.33(chr14:105141364-106855263)x1 copy number loss See cases [RCV000051204] Chr14:105141364..106855263 [GRCh38]
Chr14:105607701..107263478 [GRCh37]
Chr14:104678746..106334523 [NCBI36]
Chr14:14q32.33		 uncertain significance
GRCh38/hg38 14q32.2-32.33(chr14:100808300-106855263)x1 copy number loss See cases [RCV000051113] Chr14:100808300..106855263 [GRCh38]
Chr14:101274637..107263478 [GRCh37]
Chr14:100344390..106334523 [NCBI36]
Chr14:14q32.2-32.33		 pathogenic
GRCh38/hg38 14q31.3-32.33(chr14:86094030-106832642)x3 copy number gain See cases [RCV000052295] Chr14:86094030..106832642 [GRCh38]
Chr14:86560374..107240869 [GRCh37]
Chr14:85630127..106311914 [NCBI36]
Chr14:14q31.3-32.33		 pathogenic
GRCh38/hg38 14q32.13-32.33(chr14:94628219-106451054)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052298]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052298]|See cases [RCV000052298] Chr14:94628219..106451054 [GRCh38]
Chr14:95094556..106906960 [GRCh37]
Chr14:94164309..105978005 [NCBI36]
Chr14:14q32.13-32.33		 pathogenic
GRCh38/hg38 14q32.33(chr14:105141364-105987610)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052102]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052102]|See cases [RCV000052102] Chr14:105141364..105987610 [GRCh38]
Chr14:105607701..106453697 [GRCh37]
Chr14:104678746..105524742 [NCBI36]
Chr14:14q32.33		 uncertain significance
GRCh38/hg38 14q31.2-32.33(chr14:83912345-106855405)x3 copy number gain See cases [RCV000052294] Chr14:83912345..106855405 [GRCh38]
Chr14:84378689..107263620 [GRCh37]
Chr14:83448442..106334665 [NCBI36]
Chr14:14q31.2-32.33		 pathogenic
GRCh38/hg38 14q32.12-32.33(chr14:91455861-106832642)x3 copy number gain See cases [RCV000052296] Chr14:91455861..106832642 [GRCh38]
Chr14:91922205..107240869 [GRCh37]
Chr14:90991958..106311914 [NCBI36]
Chr14:14q32.12-32.33		 pathogenic
GRCh38/hg38 14q32.2-32.33(chr14:99831655-106855263)x1 copy number loss See cases [RCV000133831] Chr14:99831655..106855263 [GRCh38]
Chr14:100297992..107263478 [GRCh37]
Chr14:99367745..106334523 [NCBI36]
Chr14:14q32.2-32.33		 pathogenic
GRCh38/hg38 14q24.3-32.33(chr14:73655772-106879298)x3 copy number gain See cases [RCV000134000] Chr14:73655772..106879298 [GRCh38]
Chr14:74122475..107287505 [GRCh37]
Chr14:73192228..106358550 [NCBI36]
Chr14:14q24.3-32.33		 pathogenic
GRCh38/hg38 14q32.33(chr14:104953508-106873666)x1 copy number loss See cases [RCV000135387] Chr14:104953508..106873666 [GRCh38]
Chr14:105419845..107281875 [GRCh37]
Chr14:104490890..106352920 [NCBI36]
Chr14:14q32.33		 uncertain significance
GRCh38/hg38 14q32.2-32.33(chr14:100309382-105987610)x3 copy number gain See cases [RCV000135410] Chr14:100309382..105987610 [GRCh38]
Chr14:100775719..106453697 [GRCh37]
Chr14:99845472..105524742 [NCBI36]
Chr14:14q32.2-32.33		 pathogenic
GRCh38/hg38 14q32.2-32.33(chr14:97638520-106855263)x3 copy number gain See cases [RCV000135400] Chr14:97638520..106855263 [GRCh38]
Chr14:98104857..107263478 [GRCh37]
Chr14:97174610..106334523 [NCBI36]
Chr14:14q32.2-32.33		 pathogenic
GRCh38/hg38 14q32.2-32.33(chr14:99448012-106850609)x3 copy number gain See cases [RCV000135875] Chr14:99448012..106850609 [GRCh38]
Chr14:99914349..107258824 [GRCh37]
Chr14:98984102..106329869 [NCBI36]
Chr14:14q32.2-32.33		 pathogenic
GRCh38/hg38 14q32.33(chr14:104622881-106678844)x1 copy number loss See cases [RCV000135781] Chr14:104622881..106678844 [GRCh38]
Chr14:105017236..107134861 [GRCh37]
Chr14:104088281..106205906 [NCBI36]
Chr14:14q32.33		 uncertain significance
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3 copy number gain See cases [RCV000135543] Chr14:20151149..106855263 [GRCh38]
Chr14:20619308..107263478 [GRCh37]
Chr14:19689148..106334523 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh38/hg38 14q32.33(chr14:105023396-106850750)x1 copy number loss See cases [RCV000135897] Chr14:105023396..106850750 [GRCh38]
Chr14:105489733..107258965 [GRCh37]
Chr14:104560778..106330010 [NCBI36]
Chr14:14q32.33		 pathogenic
GRCh38/hg38 14q32.13-32.33(chr14:95524407-106879501)x1 copy number loss See cases [RCV000136032] Chr14:95524407..106879501 [GRCh38]
Chr14:95990744..107287708 [GRCh37]
Chr14:95060497..106358753 [NCBI36]
Chr14:14q32.13-32.33		 pathogenic
NCBI36/hg18 14q32.33(chr14:105143707-105280567)x1 copy number loss See cases [RCV000136963] Chr14:105143707..105280567 [NCBI36]
Chr14:14q32.33		 benign
GRCh38/hg38 14q32.33(chr14:105573256-106855263)x3 copy number gain See cases [RCV000137104] Chr14:105573256..106855263 [GRCh38]
Chr14:106252705..107263478 [GRCh37]
Chr14:105080340..106334523 [NCBI36]
Chr14:14q32.33		 pathogenic
GRCh38/hg38 14q32.33(chr14:105105705-106879501)x1 copy number loss See cases [RCV000138844] Chr14:105105705..106879501 [GRCh38]
Chr14:105572042..107287708 [GRCh37]
Chr14:104643087..106358753 [NCBI36]
Chr14:14q32.33		 uncertain significance
GRCh38/hg38 14q24.3-32.33(chr14:77222795-106879298)x3 copy number gain See cases [RCV000138230] Chr14:77222795..106879298 [GRCh38]
Chr14:77689138..107287505 [GRCh37]
Chr14:76758891..106358550 [NCBI36]
Chr14:14q24.3-32.33		 pathogenic
GRCh38/hg38 14q32.31-32.33(chr14:101925670-106876323)x1 copy number loss See cases [RCV000139633] Chr14:101925670..106876323 [GRCh38]
Chr14:102392007..107284531 [GRCh37]
Chr14:101461760..106355576 [NCBI36]
Chr14:14q32.31-32.33		 pathogenic
GRCh38/hg38 14q32.31-32.33(chr14:102239422-106877229)x1 copy number loss See cases [RCV000141932] Chr14:102239422..106877229 [GRCh38]
Chr14:102705759..107285437 [GRCh37]
Chr14:101775512..106356482 [NCBI36]
Chr14:14q32.31-32.33		 pathogenic
GRCh38/hg38 14q32.31-32.33(chr14:101665602-106855263)x1 copy number loss See cases [RCV000142453] Chr14:101665602..106855263 [GRCh38]
Chr14:102131939..107263478 [GRCh37]
Chr14:101201692..106334523 [NCBI36]
Chr14:14q32.31-32.33		 pathogenic
GRCh38/hg38 14q32.33(chr14:104051258-106877229)x1 copy number loss See cases [RCV000142333] Chr14:104051258..106877229 [GRCh38]
Chr14:104517595..107285437 [GRCh37]
Chr14:103587348..106356482 [NCBI36]
Chr14:14q32.33		 pathogenic
GRCh38/hg38 14q32.33(chr14:105224887-106877229)x6 copy number gain See cases [RCV000142058] Chr14:105224887..106877229 [GRCh38]
Chr14:105691224..107285437 [GRCh37]
Chr14:104762269..106356482 [NCBI36]
Chr14:14q32.33		 uncertain significance
GRCh38/hg38 14q32.33(chr14:105138612-106877229)x1 copy number loss See cases [RCV000142111] Chr14:105138612..106877229 [GRCh38]
Chr14:105604949..107285437 [GRCh37]
Chr14:104675994..106356482 [NCBI36]
Chr14:14q32.33		 uncertain significance
GRCh38/hg38 14q32.33(chr14:105453295-106879298)x1 copy number loss See cases [RCV000142956] Chr14:105453295..106879298 [GRCh38]
Chr14:106252705..107287505 [GRCh37]
Chr14:104990677..106358550 [NCBI36]
Chr14:14q32.33		 pathogenic|uncertain significance
GRCh38/hg38 14q32.33(chr14:103823600-106879298)x1 copy number loss See cases [RCV000142803] Chr14:103823600..106879298 [GRCh38]
Chr14:104289937..107287505 [GRCh37]
Chr14:103359690..106358550 [NCBI36]
Chr14:14q32.33		 pathogenic
GRCh38/hg38 14q32.32-32.33(chr14:103322414-106855263)x3 copy number gain See cases [RCV000142593] Chr14:103322414..106855263 [GRCh38]
Chr14:103788751..107263478 [GRCh37]
Chr14:102858504..106334523 [NCBI36]
Chr14:14q32.32-32.33		 pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3 copy number gain See cases [RCV000143373] Chr14:20043514..106877229 [GRCh38]
Chr14:20511673..107285437 [GRCh37]
Chr14:19581513..106356482 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh38/hg38 14q32.31-32.33(chr14:102605096-106879298)x1 copy number loss See cases [RCV000143154] Chr14:102605096..106879298 [GRCh38]
Chr14:103071433..107287505 [GRCh37]
Chr14:102141186..106358550 [NCBI36]
Chr14:14q32.31-32.33		 pathogenic
GRCh38/hg38 14q32.2-32.33(chr14:100582059-106877229)x1 copy number loss See cases [RCV000143662] Chr14:100582059..106877229 [GRCh38]
Chr14:101048396..107285437 [GRCh37]
Chr14:100118149..106356482 [NCBI36]
Chr14:14q32.2-32.33		 pathogenic
Single allele duplication Gestational diabetes mellitus uncontrolled [RCV000161750] Chr14:105951611..107287663 [GRCh37]
Chr14:14q32.33		 not provided
Single allele duplication Normal pregnancy [RCV000161751] Chr14:105998544..107287663 [GRCh37]
Chr14:14q32.33		 not provided
GRCh37/hg19 14q32.3(chr14:106252705-106538480)x1 copy number loss See cases [RCV000051222] Chr14:106252705..106538480 [GRCh37]
Chr14:105143707..105609525 [NCBI36]
Chr14:14q32.3		 benign
GRCh37/hg19 14q32.33(chr14:106124720-106949307)x3 copy number gain Premature ovarian failure [RCV000225198] Chr14:106124720..106949307 [GRCh37]
Chr14:14q32.33		 benign
GRCh37/hg19 14q32.2-32.33(chr14:100575917-107281934) copy number gain not provided [RCV000767752] Chr14:100575917..107281934 [GRCh37]
Chr14:14q32.2-32.33		 pathogenic
GRCh37/hg19 14q32.32-32.33(chr14:103711336-107285437)x1 copy number loss See cases [RCV000446081] Chr14:103711336..107285437 [GRCh37]
Chr14:14q32.32-32.33		 pathogenic
GRCh37/hg19 14q32.2-32.33(chr14:98051841-107285437)x3 copy number gain See cases [RCV000446497] Chr14:98051841..107285437 [GRCh37]
Chr14:14q32.2-32.33		 likely pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3 copy number gain See cases [RCV000446256] Chr14:19794561..107234280 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q23.2-32.33(chr14:62493932-107285437)x3 copy number gain See cases [RCV000448557] Chr14:62493932..107285437 [GRCh37]
Chr14:14q23.2-32.33		 pathogenic
GRCh37/hg19 14q32.31-32.33(chr14:103153637-107285437)x1 copy number loss See cases [RCV000510629] Chr14:103153637..107285437 [GRCh37]
Chr14:14q32.31-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437) copy number gain See cases [RCV000512041] Chr14:20511673..107285437 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q32.33(chr14:105814886-107285437)x1 copy number loss See cases [RCV000511369] Chr14:105814886..107285437 [GRCh37]
Chr14:14q32.33		 uncertain significance
GRCh37/hg19 14q32.32-32.33(chr14:103965059-107285437)x1 copy number loss See cases [RCV000511801] Chr14:103965059..107285437 [GRCh37]
Chr14:14q32.32-32.33		 pathogenic
GRCh37/hg19 14q32.33(chr14:104915608-107285437)x1 copy number loss See cases [RCV000511076] Chr14:104915608..107285437 [GRCh37]
Chr14:14q32.33		 pathogenic
GRCh37/hg19 14q32.2-32.33(chr14:100661319-107285437)x1 copy number loss See cases [RCV000511171] Chr14:100661319..107285437 [GRCh37]
Chr14:14q32.2-32.33		 pathogenic
GRCh37/hg19 14q32.31-32.33(chr14:102670706-107285437)x1 copy number loss See cases [RCV000511173] Chr14:102670706..107285437 [GRCh37]
Chr14:14q32.31-32.33		 pathogenic
GRCh37/hg19 14q32.33(chr14:105587643-106560949)x3 copy number gain See cases [RCV000512193] Chr14:105587643..106560949 [GRCh37]
Chr14:14q32.33		 likely benign
GRCh37/hg19 14q24.2-32.33(chr14:73750741-107285437)x3 copy number gain See cases [RCV000512497] Chr14:73750741..107285437 [GRCh37]
Chr14:14q24.2-32.33		 pathogenic
GRCh37/hg19 14q32.33(chr14:106020225-107285437)x1 copy number loss not provided [RCV000683620] Chr14:106020225..107285437 [GRCh37]
Chr14:14q32.33		 likely benign
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3 copy number gain not provided [RCV000738412] Chr14:19000422..107289053 [GRCh37]
Chr14:14q11.1-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3 copy number gain not provided [RCV000738413] Chr14:19280733..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3 copy number gain not provided [RCV000738414] Chr14:19327823..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q32.33(chr14:105436222-107287663)x3 copy number gain not provided [RCV000751145] Chr14:105436222..107287663 [GRCh37]
Chr14:14q32.33		 benign
GRCh37/hg19 14q32.33(chr14:105871769-106327640)x3 copy number gain not provided [RCV000751148] Chr14:105871769..106327640 [GRCh37]
Chr14:14q32.33		 benign
GRCh37/hg19 14q32.2-32.33(chr14:99794230-107285437)x3 copy number gain not provided [RCV000849272] Chr14:99794230..107285437 [GRCh37]
Chr14:14q32.2-32.33		 pathogenic
GRCh37/hg19 14q32.31-32.33(chr14:102931119-107285437)x1 copy number loss not provided [RCV000847188] Chr14:102931119..107285437 [GRCh37]
Chr14:14q32.31-32.33		 pathogenic
GRCh37/hg19 14q32.33(chr14:105067651-107285437)x1 copy number loss not provided [RCV000848291] Chr14:105067651..107285437 [GRCh37]
Chr14:14q32.33		 uncertain significance
GRCh37/hg19 14q32.31-32.33(chr14:101627916-107147698)x1 copy number loss not provided [RCV000848417] Chr14:101627916..107147698 [GRCh37]
Chr14:14q32.31-32.33		 pathogenic
GRCh37/hg19 14q32.33(chr14:104764078-107285437)x1 copy number loss not provided [RCV001006659] Chr14:104764078..107285437 [GRCh37]
Chr14:14q32.33		 pathogenic
GRCh37/hg19 14q32.33(chr14:105303584-107285437)x1 copy number loss not provided [RCV001006660] Chr14:105303584..107285437 [GRCh37]
Chr14:14q32.33		 pathogenic
GRCh37/hg19 14q32.12-32.33(chr14:91969028-107285437)x3 copy number gain not provided [RCV000848687] Chr14:91969028..107285437 [GRCh37]
Chr14:14q32.12-32.33		 pathogenic
GRCh37/hg19 14q31.2-32.33(chr14:84537502-107285437)x3 copy number gain not provided [RCV002472581] Chr14:84537502..107285437 [GRCh37]
Chr14:14q31.2-32.33		 pathogenic
GRCh37/hg19 14q32.31-32.33(chr14:103153637-107285437)x1 copy number loss not provided [RCV001006656] Chr14:103153637..107285437 [GRCh37]
Chr14:14q32.31-32.33		 pathogenic
GRCh37/hg19 14q32.2-32.33(chr14:96829290-107287663)x1 copy number loss See cases [RCV001195078] Chr14:96829290..107287663 [GRCh37]
Chr14:14q32.2-32.33		 pathogenic
GRCh37/hg19 14q32.31-32.33(chr14:102615953-107285437)x1 copy number loss not provided [RCV001259801] Chr14:102615953..107285437 [GRCh37]
Chr14:14q32.31-32.33		 pathogenic
GRCh37/hg19 14q32.31-32.33(chr14:101732158-107285437) copy number loss not specified [RCV002052456] Chr14:101732158..107285437 [GRCh37]
Chr14:14q32.31-32.33		 pathogenic
GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2 copy number gain See cases [RCV002286356] Chr14:37671058..106985955 [GRCh37]
Chr14:14q13.3-32.33		 pathogenic
GRCh37/hg19 14q32.32-32.33(chr14:103636647-107285437)x1 copy number loss not provided [RCV003323337] Chr14:103636647..107285437 [GRCh37]
Chr14:14q32.32-32.33		 pathogenic
GRCh38/hg38 14q32.31-32.33(chr14:102263440-106874929)x1 copy number loss Neurodevelopmental disorder [RCV003327606] Chr14:102263440..106874929 [GRCh38]
Chr14:14q32.31-32.33		 pathogenic
GRCh37/hg19 14q32.2-32.33(chr14:101024609-107285437)x1 copy number loss not provided [RCV003483217] Chr14:101024609..107285437 [GRCh37]
Chr14:14q32.2-32.33		 pathogenic
GRCh37/hg19 14q31.3-32.33(chr14:88580184-107285437)x3 copy number gain not provided [RCV003485051] Chr14:88580184..107285437 [GRCh37]
Chr14:14q31.3-32.33		 pathogenic
GRCh37/hg19 14q32.33(chr14:105122914-107285437)x3 copy number gain not provided [RCV003485055] Chr14:105122914..107285437 [GRCh37]
Chr14:14q32.33		 uncertain significance
GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3 copy number gain not provided [RCV003485036] Chr14:58894502..107227240 [GRCh37]
Chr14:14q23.1-32.33		 pathogenic
GRCh37/hg19 14q32.31-32.33(chr14:102098959-107285437)x1 copy number loss not specified [RCV003987056] Chr14:102098959..107285437 [GRCh37]
Chr14:14q32.31-32.33		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1478
Count of miRNA genes:690
Interacting mature miRNAs:794
Transcripts:ENST00000390542, ENST00000390548, ENST00000390549
Prediction methods: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.

Markers in Region
PMC151015P1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3714106,207,831 - 106,208,447UniSTSGRCh37
GRCh3714106,134,604 - 106,135,217UniSTSGRCh37
Build 3614105,205,649 - 105,206,262RGDNCBI36
Celera1486,146,880 - 86,147,496RGD
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map14q32.33UniSTS
HuRef1486,340,136 - 86,340,752UniSTS
RH71306  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map14q32.33UniSTS
GeneMap99-GB4 RH Map14283.81UniSTS
RH44825  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map14q32.33UniSTS
GeneMap99-GB4 RH Map14279.78UniSTS
NCBI RH Map141118.3UniSTS
D14S1342  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map14q32.33UniSTS
GeneMap99-G3 RH Map144372.0UniSTS
A010A33  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map14q32.33UniSTS
GeneMap99-GB4 RH Map14279.78UniSTS
NCBI RH Map141118.3UniSTS
RH66790  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map15q11.2UniSTS


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
High 74 58 142 43 535 39 22 1 4 17 66 238 4 23 8
Medium 1022 1277 841 464 1078 322 1002 184 455 231 664 878 142 781 532
Low 1123 1396 677 80 251 66 2510 1581 1818 97 586 288 15 382 1789 2
Below cutoff 112 231 23 4 21 2 556 388 1336 14 28 31 3 18 453

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_001019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AJ294730 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK057754 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK057775 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK093636 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097010 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097354 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097356 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097357 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097359 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097360 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097361 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097363 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097364 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097365 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097366 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097367 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK098516 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK123070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK123800 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK125632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK125633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK126281 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK127409 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK128301 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK128313 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK128394 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK129508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK129510 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK129512 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK129514 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK129517 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK129776 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK129787 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK129809 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK130434 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK130585 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK130586 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK130611 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK130642 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK130813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK130817 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL122127 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC006402 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC014258 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC014667 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC018747 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC019046 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC019337 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC025314 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC026038 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC037361 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC051328 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC062336 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC064496 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC066642 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC067091 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC069016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC069020 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC072419 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC073782 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC073789 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC075840 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC075842 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC075846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC078670 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC078671 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC080557 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC089417 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC090938 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC090939 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC090940 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC092518 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX538118 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX640619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX640621 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX640622 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX640627 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Y14735 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Y17957 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000390542   ⟹   ENSP00000374984
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl14105,741,339 - 105,743,071 (-)Ensembl
RefSeq Acc Id: ENST00000390548   ⟹   ENSP00000374990
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl14105,736,343 - 105,743,071 (-)Ensembl
RefSeq Acc Id: ENST00000390549   ⟹   ENSP00000374991
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl14105,741,338 - 105,743,071 (-)Ensembl
Protein Sequences
GenBank Protein BAB71560 (Get FASTA)   NCBI Sequence Viewer  
  BAC04208 (Get FASTA)   NCBI Sequence Viewer  
  BAC04926 (Get FASTA)   NCBI Sequence Viewer  
  BAC05012 (Get FASTA)   NCBI Sequence Viewer  
  BAC05013 (Get FASTA)   NCBI Sequence Viewer  
  BAC05014 (Get FASTA)   NCBI Sequence Viewer  
  BAC05016 (Get FASTA)   NCBI Sequence Viewer  
  BAC05017 (Get FASTA)   NCBI Sequence Viewer  
  BAC05018 (Get FASTA)   NCBI Sequence Viewer  
  BAC05019 (Get FASTA)   NCBI Sequence Viewer  
  BAC05020 (Get FASTA)   NCBI Sequence Viewer  
  BAC05021 (Get FASTA)   NCBI Sequence Viewer  
  BAC05022 (Get FASTA)   NCBI Sequence Viewer  
  BAC05023 (Get FASTA)   NCBI Sequence Viewer  
  BAC85171 (Get FASTA)   NCBI Sequence Viewer  
  BAC85172 (Get FASTA)   NCBI Sequence Viewer  
  BAC85173 (Get FASTA)   NCBI Sequence Viewer  
  BAC85174 (Get FASTA)   NCBI Sequence Viewer  
  BAC85175 (Get FASTA)   NCBI Sequence Viewer  
  BAC85232 (Get FASTA)   NCBI Sequence Viewer  
  BAC85235 (Get FASTA)   NCBI Sequence Viewer  
  BAC85237 (Get FASTA)   NCBI Sequence Viewer  
  BAC85350 (Get FASTA)   NCBI Sequence Viewer  
  BAC85387 (Get FASTA)   NCBI Sequence Viewer  
  BAC85388 (Get FASTA)   NCBI Sequence Viewer  
  BAC85394 (Get FASTA)   NCBI Sequence Viewer  
  BAC85401 (Get FASTA)   NCBI Sequence Viewer  
  BAC85434 (Get FASTA)   NCBI Sequence Viewer  
  BAC85436 (Get FASTA)   NCBI Sequence Viewer  
  BAC85529 (Get FASTA)   NCBI Sequence Viewer  
  BAC85697 (Get FASTA)   NCBI Sequence Viewer  
  BAC86225 (Get FASTA)   NCBI Sequence Viewer  
  BAC86226 (Get FASTA)   NCBI Sequence Viewer  
  BAC86514 (Get FASTA)   NCBI Sequence Viewer  
  BAC86964 (Get FASTA)   NCBI Sequence Viewer  
  BAC87374 (Get FASTA)   NCBI Sequence Viewer  
  BAC87380 (Get FASTA)   NCBI Sequence Viewer  
  BAC87418 (Get FASTA)   NCBI Sequence Viewer  
  CAA75030 (Get FASTA)   NCBI Sequence Viewer  
  CAC20454 (Get FASTA)   NCBI Sequence Viewer  
  CAD98026 (Get FASTA)   NCBI Sequence Viewer  
  CAE45773 (Get FASTA)   NCBI Sequence Viewer  
  CAE45775 (Get FASTA)   NCBI Sequence Viewer  
  CAE45776 (Get FASTA)   NCBI Sequence Viewer  
  CAE45781 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000374984.2
  ENSP00000374990.2
  ENSP00000374991.2
  ENSP00000487867.1
  ENSP00000488387.1
  ENSP00000488811.1
GenBank Protein P01857 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: ENSP00000374990   ⟸   ENST00000390548
RefSeq Acc Id: ENSP00000374991   ⟸   ENST00000390549
RefSeq Acc Id: ENSP00000374984   ⟸   ENST00000390542
Protein Domains
Ig-like

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P01857-F1-model_v2 AlphaFold P01857 1-330 view protein structure

Promoters
RGD ID:6791647
Promoter ID:HG_KWN:20459
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000326461,   OTTHUMT00000326504,   OTTHUMT00000326505
Position:
Human AssemblyChrPosition (strand)Source
Build 3614105,280,046 - 105,280,547 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:5525 AgrOrtholog
COSMIC IGHG1 COSMIC
Ensembl Genes ENSG00000211896 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000277633 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000390542.6 UniProtKB/TrEMBL
  ENST00000390548.6 UniProtKB/Swiss-Prot
  ENST00000390549.6 UniProtKB/Swiss-Prot
  ENST00000631402.1 UniProtKB/TrEMBL
  ENST00000631466.1 UniProtKB/Swiss-Prot
  ENST00000631539.1 UniProtKB/Swiss-Prot
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000211896 GTEx
  ENSG00000277633 GTEx
HGNC ID HGNC:5525 ENTREZGENE
Human Proteome Map IGHG1 Human Proteome Map
InterPro Ig-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig/MHC_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_C1-set UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene IGHG1 ENTREZGENE
OMIM 147100 OMIM
PANTHER IMMUNOGLOBULIN HEAVY CONSTANT GAMMA 1-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TAPASIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam C1-set UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA29716 PharmGKB
PROSITE IG_LIKE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  IG_MHC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART IGc1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48726 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0A0MS07_HUMAN UniProtKB/TrEMBL
  IGHG1_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary A0A0A0MS08 UniProtKB/Swiss-Prot