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Gene Gene information from NCBI Gene database.
Entrez ID 219995
Gene name Membrane spanning 4-domains A15
Gene symbol MS4A15
Synonyms (NCBI Gene)
-
Chromosome 11
Chromosome location 11q12.2
miRNA miRNA information provided by mirtarbase database.
61 Show/Hide all (61)
miRTarBase ID miRNA Experiments Reference
MIRT1160947 hsa-miR-1321 CLIP-seq
MIRT1160948 hsa-miR-2861 CLIP-seq
MIRT1160949 hsa-miR-3126-5p CLIP-seq
MIRT1160950 hsa-miR-3150a-3p CLIP-seq
MIRT1160951 hsa-miR-3175 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0005886 Component Plasma membrane IBA
GO:0007166 Process Cell surface receptor signaling pathway IBA
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N5U1
Protein name Membrane-spanning 4-domains subfamily A member 15
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 73 → 165 CD20-like family Family
Sequence
MSAAPASNGVFVVIPPNNASGLCPPPAILPTSMCQPPGIMQFEEPPLGAQTPRATQPPDL
RPVETFLTGEPKVLGTVQILIGLIHLGFGSVLLMVRRGHVGIFFIEGGVPFWGGACFIIS
GSLSVAAEKNHTSCLVRSSLGTNILSVMAAFAGTAILLMDFGVTN
RDVDRGYLAVLTIFT
VLEFFTAVIAMHFGCQAIHAQASAPVIFLPNAFSADFNIPSPAASAPPAYDNVAYAQGVV
Sequence length 240
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Reference Evidence Score
EBV-positive nodal T- and NK-cell lymphoma Likely benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations