Gene Gene information from NCBI Gene database.
Entrez ID 51338
Gene name Membrane spanning 4-domains A4A
Gene symbol MS4A4A
Synonyms (NCBI Gene)
4SPAN1CD20-L1CD20L1HDCME31PMS4A4MS4A7
Chromosome 11
Chromosome location 11q12.2
Summary This gene encodes a member of the membrane-spanning 4A gene family. Members of this nascent protein family are characterized by common structural features, similar intron/exon splice boundaries, and display unique expression patterns in hematopoietic cell
miRNA miRNA information provided by mirtarbase database.
52
miRTarBase ID miRNA Experiments Reference
MIRT025653 hsa-miR-7-5p Microarray 17612493
MIRT509336 hsa-miR-4700-3p PAR-CLIP 23446348
MIRT509335 hsa-miR-4433b-3p PAR-CLIP 23446348
MIRT509334 hsa-miR-6504-3p PAR-CLIP 23446348
MIRT509333 hsa-miR-4433a-3p PAR-CLIP 23446348
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
8
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 30833792, 32296183
GO:0005783 Component Endoplasmic reticulum IDA 31413141
GO:0005794 Component Golgi apparatus IBA
GO:0005794 Component Golgi apparatus IDA 31413141
GO:0005886 Component Plasma membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
606547 13371 ENSG00000110079
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96JQ5
Protein name Membrane-spanning 4-domains subfamily A member 4A (CD20 antigen-like 1) (Four-span transmembrane protein 1)
Protein function May be involved in signal transduction as a component of a multimeric receptor complex.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04103 CD20 65 207 CD20-like family Family
Tissue specificity TISSUE SPECIFICITY: Variable expression in multiple hemopoietic cell lines.
Sequence
MHQTYSRHCRPEESTFSAAMTTMQGMEQAMPGAGPGVPQLGNMAVIHSHLWKGLQEKFLK
GEPKVLGVVQILTALMSLSMGITMMCMASNTYGSNPISVYIGYTIWGSVMFIISGSLSIA
AGIRTTKGLVRGSLGMNITSSVLAASGILINTFSLAFYSFHHPYCNYYGNSNNCHGTMSI
LMGLDGMVLLLSVLEFCIAVSLSAFGC
KVLCCTPGGVVLILPSHSHMAETASPTPLNEV
Sequence length 239
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Familial cancer of breast Uncertain significance rs377643559 RCV005929271
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 25778476, 28199971, 30859738, 31144443, 33712570, 38172904
Arthritis Rheumatoid Associate 32483203, 34346525
Cerebral Infarction Associate 30859738
COVID 19 Associate 34346525
Diabetic Nephropathies Associate 37622120
Esophageal Neoplasms Associate 36569220
Immune System Diseases Associate 25717186
Inflammation Associate 36569220
Lymphoma Follicular Associate 37373066
Mast Cell Activation Disorders Associate 25717186