Gene Gene information from NCBI Gene database.
Entrez ID 91663
Gene name Myeloid associated differentiation marker
Gene symbol MYADM
Synonyms (NCBI Gene)
SB135
Chromosome 19
Chromosome location 19q13.42
miRNA miRNA information provided by mirtarbase database.
917
miRTarBase ID miRNA Experiments Reference
MIRT043210 hsa-miR-324-5p CLASH 23622248
MIRT541174 hsa-miR-329-3p HITS-CLIP 21572407
MIRT541173 hsa-miR-362-3p HITS-CLIP 21572407
MIRT541172 hsa-miR-8485 HITS-CLIP 21572407
MIRT541171 hsa-miR-603 HITS-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
22
GO ID Ontology Definition Evidence Reference
GO:0001726 Component Ruffle IDA 21325632
GO:0005515 Function Protein binding IPI 28514442, 31324722, 32296183, 33961781, 35156780
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IDA 23264465
GO:0005886 Component Plasma membrane IMP 21325632
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609959 7544 ENSG00000179820
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96S97
Protein name Myeloid-associated differentiation marker (Protein SB135)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01284 MARVEL 31 157 Membrane-associating domain Domain
PF01284 MARVEL 168 313 Membrane-associating domain Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed. Not detected in thymus. {ECO:0000269|PubMed:12075932}.
Sequence
Sequence length 322
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
LIVER CIRRHOSIS, EXPERIMENTAL CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PROSTATE CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinoma Hepatocellular Associate 18715028
★☆☆☆☆
Found in Text Mining only
Carcinoma Non Small Cell Lung Associate 36061144
★☆☆☆☆
Found in Text Mining only
Hypertension Associate 28784648
★☆☆☆☆
Found in Text Mining only
Infections Associate 37002207
★☆☆☆☆
Found in Text Mining only
Intracranial Aneurysm Associate 39847889
★☆☆☆☆
Found in Text Mining only
Melanoma Associate 15900300
★☆☆☆☆
Found in Text Mining only