Motile sperm domain containing 3

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Identifiers
Aliases
External IDs	GeneCards: [1]
Orthologs
Species	Human	Mouse
Entrez	n/a	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	n/a	n/a
Wikidata
View/Edit Human

Motile sperm domain containing 3 is a protein that in humans is encoded by the MOSPD3 gene.

Function

This gene encodes a multi-pass membrane protein with a major sperm protein (MSP) domain. The deletion of a similar mouse gene is associated with defective cardiac development and neonatal lethality. Alternate transcriptional splice variants, encoding different isoforms, have been described. [provided by RefSeq, Jul 2008].

Further reading

• Glöckner, G; Scherer, S; Schattevoy, R; Boright, A; Weber, J; Tsui, L. C.; Rosenthal, A (1998). "Large-scale sequencing of two regions in human chromosome 7q22: Analysis of 650 kb of genomic sequence around the EPO and CUTL1 loci reveals 17 genes". Genome Research. 8 (10): 1060–73. doi:10.1101/gr.8.10.1060. PMC 310788. PMID 9799793.
• Pall, G. S.; Wallis, J; Axton, R; Brownstein, D. G.; Gautier, P; Buerger, K; Mulford, C; Mullins, J. J.; Forrester, L. M. (2004). "A novel transmembrane MSP-containing protein that plays a role in right ventricle development". Genomics. 84 (6): 1051–9. doi:10.1016/j.ygeno.2004.08.017. PMID 15533722.

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