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CGB3 (chorionic gonadotropin subunit beta 3)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1082
Gene nameGene Name - the full gene name approved by the HGNC.
Chorionic gonadotropin subunit beta 3
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
CGB3
SynonymsGene synonyms aliases
CGB, CGB5, CGB7, CGB8, LHB, hCGB
ChromosomeChromosome number
19
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.33
SummarySummary of gene provided in NCBI Entrez Gene.
This gene is a member of the glycoprotein hormone beta chain family and encodes the beta 3 subunit of chorionic gonadotropin (CG). Glycoprotein hormones are heterodimers consisting of a common alpha subunit and an unique beta subunit which confers biologi
Transcription factors
Transcription factor Regulation Reference
TFAP2A Unknown 10648798
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005179 Function Hormone activity IBA 21873635
GO:0005515 Function Protein binding IPI 7922031, 31467278, 32296183
GO:0005576 Component Extracellular region TAS
GO:0005615 Component Extracellular space IBA 21873635
GO:0005737 Component Cytoplasm IBA 21873635
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
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.
 
Reactome
    Glycoprotein hormones
TFAP2 (AP-2) family regulates transcription of growth factors and their receptors
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Hypogonadotropic hypogonadism Hypogonadotropic hypogonadism rs104894702, rs104893836, rs104893837, rs104893842, rs121909628, rs138249161, rs1601946139 9334596, 8263139
Unknown
Disease name Disease term dbSNP ID References
Fetal resorption Fetal Resorption 3816235
Hypogonadism Hypogonadism, Primary hypogonadism, Hypogonadism, Isolated Hypogonadotropic 8263139, 9334596, 9334596, 8263139

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