Entity Details

Primary name KISS1
Entity type gene
Source Source Link

Details

PrimaryID3814
RefseqGeneNG_032151
SymbolKISS1
NameKiSS-1 metastasis suppressor
Chromosome1
Location1q32.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-11-20
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsKISS1_HUMAN

GO terms

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GOName
GO:0005576 extracellular region
GO:0007010 cytoskeleton organization
GO:0007186 G protein-coupled receptor signaling pathway
GO:0007204 positive regulation of cytosolic calcium ion concentration
GO:0031773 kisspeptin receptor binding
GO:0043005 neuron projection

Diseases

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Disease IDSourceNameDescription
614842 OMIMHypogonadotropic hypogonadism 13 with or without anosmia (HH13)A disorder characterized by absent or incomplete sexual maturation by the age of 18 years, in conjunction with low levels of circulating gonadotropins and testosterone and no other abnormalities of the hypothalamic-pituitary axis. In some cases, it is associated with non-reproductive phenotypes, such as anosmia, cleft palate, and sensorineural hearing loss. Anosmia or hyposmia is related to the absence or hypoplasia of the olfactory bulbs and tracts. Hypogonadism is due to deficiency in gonadotropin-releasing hormone and probably results from a failure of embryonic migration of gonadotropin-releasing hormone-synthesizing neurons. In the presence of anosmia, idiopathic hypogonadotropic hypogonadism is referred to as Kallmann syndrome, whereas in the presence of a normal sense of smell, it has been termed normosmic idiopathic hypogonadotropic hypogonadism (nIHH). The disease is caused by variants affecting the gene represented in this entry.

Interactions

9 interactions