MS4A3 (Gene)

Organism:

Homo sapiens

Synonyms:CD20L, ENTREZ:932, HGNC:7317, HTM4, MIM:606498, MS4A3, NM_001031666, NM_001031809, NM_006138, NP_001026836, NP_001026979, NP_006129, XM_011545363, XP_011543665, membrane spanning 4-domains A3

Id:ENSG00000284903

Description:membrane spanning 4-domains A3 [Source:HGNC Symbol;Acc:HGNC:7317]

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]

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CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View MS4A3's neighborhood in the knowledge graph.

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Playbook Workflow Builder: Gene-Centric Workflow

View Gene-Centric information about the gene from a pre-built PWB workflow. View the workflow with MS4A3.

CFDE Gene-Centric Appyter

The CFDE Gene Centric Appyter Resolves and Displays Gene-Centric information from CFDE APIs. Execute the Appyter using MS4A3.

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GDLPA Landing Pages Links

The Gene and Drug Landing Page Aggregator (GDLPA) finds links to primary and secondary source information from CFDE and other resources. Discover landing pages for MS4A3.

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Playbook Workflow Builder

The Playbook Workflow Builder helps you interactively construct workflows leveraging CFDE APIs without code. Start a new workflow with MS4A3.

Results found

Linked to

	Label	Description
	Hypospadias Phenotype (Entity type)	Abnormal position of urethral meatus on the ventral penile shaft (underside) characterized by displa...
	Myopathy Phenotype (Entity type)	A disorder of muscle unrelated to impairment of innervation or neuromuscular junction.
	Autoimmunity Phenotype (Entity type)	The occurrence of an immune reaction against the organism's own cells or tissues.
	Arthralgia Phenotype (Entity type)	Joint pain.
	Arthritis Phenotype (Entity type)	Inflammation of a joint.

Hypospadias

Phenotype (Entity type)

Abnormal position of urethral meatus on the ventral penile shaft (underside) characterized by displa...

Myopathy

Phenotype (Entity type)

A disorder of muscle unrelated to impairment of innervation or neuromuscular junction.

Autoimmunity

Phenotype (Entity type)

The occurrence of an immune reaction against the organism's own cells or tissues.

Arthralgia

Phenotype (Entity type)

Joint pain.

Arthritis

Phenotype (Entity type)

Inflammation of a joint.

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The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

Consortium

Community

Resources

CFDE Workbench

The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

@CFDE Workbench 2026

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