Anosmin 1 is a protein that in humans is encoded by the ANOS1 gene. [3]

ANOS1
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
AliasesANOS1, ADMLX, HH1, HHA, KAL, KALIG-1, KMS, WFDC19, KAL1, anosmin 1
External IDsOMIM: 300836; HomoloGene: 55445; GeneCards: ANOS1; OMA:ANOS1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000216

n/a

RefSeq (protein)

NP_000207

n/a

Location (UCSC)Chr X: 8.53 – 8.73 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

Function

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Mutations in this gene cause the X-linked Kallmann Syndrome. The encoded protein is similar in sequence to proteins known to function in neural cell adhesion and axonal migration. In addition, this cell surface protein is N-glycosylated, and may have antiprotease activity. [provided by RefSeq, Jul 2008].

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000011201Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^ "Entrez Gene: Anosmin 1". Retrieved 2018-08-18.

Further reading

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This article incorporates text from the United States National Library of Medicine, which is in the public domain.