MS4A3
Sign in to saveAlso known as CD20L, HTM4, membrane spanning 4-domains A3
Membrane-spanning 4-domains subfamily A member 3 is a protein that in humans is encoded by the MS4A3 gene.
Gene data
MS4A3- Name
- membrane spanning 4-domains A3
- Type
- protein-coding
- Aliases
- CD20L, HTM4
This gene encodes a member of the membrane-spanning 4A gene family. Members of this protein family are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. This family member likely plays a role in signal transduction and may function as a subunit associated with receptor complexes. The gene encoding this protein is localized to 11q12, among a cluster of related family members. Alternative splicing may result in multiple transcript variants; however, not all variants have been fully described. [provided by RefSeq, Jul 2008].
via MyGene.info
Gene · Ensembl
membrane spanning 4-domains A3
- Symbol
- MS4A3
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 11:60,056,587-60,071,115
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 4472
- exact match
- identifiers.org/ncbigene/932
- genomic end
- 60071115
- genomic start
- 59824060
- cytogenetic location
- 11q12.1
via Wikidata · CC0
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Article
3 sectionsContents
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Membrane-spanning 4-domains subfamily A member 3 is a protein that in humans is encoded by the MS4A3 gene.
This gene encodes a member of the membrane-spanning 4A gene family. Members of this protein family are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. This family member likely plays a role in signal transduction and may function as a subunit associated with receptor complexes. The gene encoding this protein is localized to 11q12, among a cluster of related family members. Alternative splicing may result in multiple transcript variants; however, not all variants have been fully described.