INHA

Gene Information
 
Gene Symbol
INHA
 
Aliases
-
 
Entrez Gene ID
 
Gene Name
Inhibin subunit alpha
 
Chromosomal Location
2q35
 
HGNC ID
 
Summary
This gene encodes a member of the TGF-beta (transforming growth factor-beta) superfamily of proteins. The encoded preproprotein is proteolytically processed to generate multiple peptide products, including the alpha subunit of the inhibin A and B protein complexes. These complexes negatively regulate follicle stimulating hormone secretion from the pituitary gland. Inhibins have also been implicated in regulating numerous cellular processes including cell proliferation, apoptosis, immune response and hormone secretion. Mutations in this gene may be associated with male infertility and premature ovarian failure in female human patients. [provided by RefSeq, Aug 2016]
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0001501 Biological process Skeletal system development TAS 10865214
GO:0001541 Biological process Ovarian follicle development NAS 9166111
GO:0007050 Biological process Cell cycle arrest TAS 12456957
GO:0007165 Biological process Signal transduction TAS 3267209
GO:0007166 Biological process Cell surface receptor signaling pathway TAS 12456957
Protein Information
 
Protein Name
Inhibin alpha chain, A-inhibin subunit, inhibin alpha subunit
 
Function
Inhibins and activins inhibit and activate, respectively, the secretion of follitropin by the pituitary gland. Inhibins/activins are involved in regulating a number of diverse functions such as hypothalamic and pituitary hormone secretion, gonadal hormone secretion, germ cell development and maturation, erythroid differentiation, insulin secretion, nerve cell survival, embryonic axial development or bone growth, depending on their subunit composition. Inhibins appear to oppose the functions of activins
 
UniProt
 
Pfam
Pfam Accession Pfam ID
PF00019 TGF_beta
Pathways
 
KEGG
 
Reactome
 

Cytokine-cytokine receptor interaction

 

Glycoprotein hormones

Interactions
 
STRING MINT IntAct
ENSP00000269593 P22692 P22692
    View interactions
     

Associated Diseases

Disease groupDisease NameReferences
Endocrine System Diseases
Familial Testotoxicosis
PCOS
Reproductive disorders
Preeclampsia
References
 
 
PubMed ID Associated gene/s Associated condition Genetic Mutation Diagnostic Criteria Association with PCOS Ethnicity Conclusion
 
 
 
 
Direct 
17 women with PCOS, 7 controls 
InhA, P4, and FS increased with follicle volume, and InhB decreased significantly in non-PCOS, but not in PCOS, follicles.  

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