Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
51338
Gene name Gene Name - the full gene name approved by the HGNC.
Membrane spanning 4-domains A4A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MS4A4A
Synonyms (NCBI Gene) Gene synonyms aliases
4SPAN1, CD20-L1, CD20L1, HDCME31P, MS4A4, MS4A7
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q12.2
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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 IDA 31413141
GO:0005886 Component Plasma membrane IDA 23874341
GO:0016021 Component Integral component of membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606547 13371 ENSG00000110079
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Alzheimer disease Familial Alzheimer Disease (FAD), Alzheimer Disease, Late Onset, Alzheimer Disease, Early Onset, Alzheimer`s Disease, Alzheimer`s Disease, Focal Onset rs63750215, rs28936379, rs63749851, rs63749884, rs28936380, rs63750048, rs63750579, rs63750264, rs63749964, rs63750671, rs281865161, rs63750066, rs63750399, rs63750734, rs63751039
View all (65 more)
21460841, 21627779, 25778476, 29777097, 30617256
Arthritis Juvenile arthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 19565504
Unknown
Disease term Disease name Evidence References Source
Hypertrophic cardiomyopathy Hypertrophic cardiomyopathy GWAS
Associations from Text Mining
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