Gene Gene information from NCBI Gene database.
Entrez ID 139422
Gene name MAGE family member B10
Gene symbol MAGEB10
Synonyms (NCBI Gene)
-
Chromosome X
Chromosome location Xp21.3
Summary This gene encodes a member of the B subfamily of the melanoma associated antigen protein family. The encoded protein is specifically expressed in testis and tumor cells. [provided by RefSeq, Apr 2010]
miRNA miRNA information provided by mirtarbase database.
199
miRTarBase ID miRNA Experiments Reference
MIRT441956 hsa-miR-1470 PAR-CLIP 22291592
MIRT441955 hsa-miR-4667-3p PAR-CLIP 22291592
MIRT441954 hsa-miR-4780 PAR-CLIP 22291592
MIRT441953 hsa-miR-6780b-3p PAR-CLIP 22291592
MIRT441952 hsa-miR-4287 PAR-CLIP 22291592
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:0000122 Process Negative regulation of transcription by RNA polymerase II IBA
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
300761 25377 ENSG00000177689
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96LZ2
Protein name Melanoma-associated antigen B10 (MAGE-B10 antigen)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12440 MAGE_N 5 95 Melanoma associated antigen family N terminal Family
PF01454 MAGE 118 286 MAGE family Family
Sequence
Sequence length 347
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 Evidence Score
ATYPICAL FEMORAL FRACTURE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Sarcoma Sarcoma Pubtator 34307667 Stimulate
★☆☆☆☆
Found in Text Mining only