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HLA-G (major histocompatibility complex, class I, G)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3135
Gene nameGene Name - the full gene name approved by the HGNC.
Major histocompatibility complex, class I, G
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
HLA-G
SynonymsGene synonyms aliases
MHC-G
ChromosomeChromosome number
6
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p22.1
SummarySummary of gene provided in NCBI Entrez Gene.
HLA-G belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-G is expressed on fetal derived placenta
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT000297 hsa-miR-148a-3p Luciferase reporter assay 17847008
MIRT000295 hsa-miR-148b-3p Luciferase reporter assay 17847008
MIRT000293 hsa-miR-152-3p Luciferase reporter assay 17847008
MIRT731747 hsa-miR-152-5p ELISA, Luciferase reporter assay, qRT-PCR 26187665
MIRT731747 hsa-miR-152-5p ELISA, Luciferase reporter assay, qRT-PCR 26187665
Transcription factors
Transcription factor Regulation Reference
CIITA Unknown 11137218
GLI3 Repression 23592762
HIVEP2 Unknown 1409593
HSF1 Unknown 11005379
IRF1 Unknown 11087747
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane TAS
GO:0001915 Process Negative regulation of T cell mediated cytotoxicity IDA 11290782
GO:0001916 Process Positive regulation of T cell mediated cytotoxicity IBA 21873635
GO:0002451 Process Peripheral B cell tolerance induction IDA 24453251
GO:0002474 Process Antigen processing and presentation of peptide antigen via MHC class I TAS
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID P17693
Protein name HLA class I histocompatibility antigen, alpha chain G (HLA G antigen) (MHC class I antigen G) [Cleaved into: Soluble HLA class I histocompatibility antigen, alpha chain G (sHLA-G)]
Protein function [Isoform 1]: Non-classical major histocompatibility class Ib molecule involved in immune regulatory processes at the maternal-fetal interface (PubMed:19304799, PubMed:23184984, PubMed:29262349). In complex with B2M/beta-2 microglobulin binds a l
PDB 1YDP , 2D31 , 2DYP , 3BZE , 3CDG , 3CII , 3KYN , 3KYO , 6AEE , 6K60
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00129 MHC_I
25 203
Class I Histocompatibility antigen, domains alpha 1 and 2
Domain
PF07654 C1-set
211 290
Immunoglobulin C1-set domain
Domain
Sequence
Sequence length 338
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Endocytosis
Phagosome
Cellular senescence
Cell adhesion molecules
Antigen processing and presentation
Natural killer cell mediated cytotoxicity
Type I diabetes mellitus
Human cytomegalovirus infection
Human papillomavirus infection
Human T-cell leukemia virus 1 infection
Kaposi sarcoma-associated herpesvirus infection
Herpes simplex virus 1 infection
Epstein-Barr virus infection
Human immunodeficiency virus 1 infection
Viral carcinogenesis
Autoimmune thyroid disease
Allograft rejection
Graft-versus-host disease
Viral myocarditis
  ER-Phagosome pathway
Endosomal/Vacuolar pathway
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
Interferon gamma signaling
Interferon alpha/beta signaling
Antigen Presentation: Folding, assembly and peptide loading of class I MHC
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Asthma Asthma rs324981, rs121912630, rs150116809, rs4950928, rs708494, rs1581842283
Unknown
Disease name Disease term dbSNP ID References
Bipolar disorder Bipolar Disorder 23246584

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