Entity Details

Primary name INSL3
Entity type gene
Source Source Link

Details

PrimaryID3640
RefseqGeneNG_012092
SymbolINSL3
Nameinsulin like 3
Chromosome19
Location19p13.11
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1994-04-18
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsINSL3_HUMAN

GO terms

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GOName
GO:0001664 G protein-coupled receptor binding
GO:0002020 protease binding
GO:0002862 negative regulation of inflammatory response to antigenic stimulus
GO:0005102 signaling receptor binding
GO:0005158 insulin receptor binding
GO:0005179 hormone activity
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0007186 G protein-coupled receptor signaling pathway
GO:0007193 adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway
GO:0007267 cell-cell signaling
GO:0007283 spermatogenesis
GO:0010634 positive regulation of epithelial cell migration
GO:0090303 positive regulation of wound healing

Diseases

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Disease IDSourceNameDescription
219050 OMIMCryptorchidism (CRYPTO)One of the most frequent congenital abnormalities in humans, involving 2-5% of male births. Cryptorchidism is associated with increased risk of infertility and testicular cancer. The disease may be caused by variants affecting the gene represented in this entry.

Interactions

10 interactions