Contents

SPANXN1

Protein-coding gene in the species Homo sapiens

SPANXN1
Identifiers
Aliases	SPANXN1, CT11.6, SPANX family member N1
External IDs	OMIM: 300664; GeneCards: SPANXN1; OMA:SPANXN1 - orthologs
Gene location (Human) Chr. X chromosome (human)[1] Band Xq27.3 Start 145,247,503 bp[1] End 145,256,208 bp[1]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in testicle gonad right testis left testis n/a More reference expression data BioGPS n/a
Orthologs Species Human Mouse Entrez 494118 n/a Ensembl ENSG00000203923 n/a UniProt Q5VSR9 n/a RefSeq (mRNA) NM_001009614 n/a RefSeq (protein) NP_001009614 n/a Location (UCSC) Chr X: 145.25 – 145.26 Mb n/a PubMed search [2] n/a
Wikidata
View/Edit Human

SPANX family member N1 is a protein that in humans is encoded by the SPANXN1 gene. ^[3]

Function[edit]

This gene represents one of several duplicated family members that are located on chromosome X. This gene family encodes proteins that play a role in spermiogenesis. These proteins represent a specific subgroup of cancer/testis-associated antigens, and they may be candidates for tumor vaccines. This family member belongs to a subgroup of related genes that are present in all primates and rats and mice, and thus, it represents one of the ancestral family members.

References[edit]

Further reading[edit]

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

This article on a gene on the human X chromosome and/or its associated protein is a stub. You can help Wikipedia by expanding it.