Gene Gene information from NCBI Gene database.
Entrez ID 25829
Gene name Transmembrane protein 184B
Gene symbol TMEM184B
Synonyms (NCBI Gene)
C22orf5FM08HS5O6AHSPC256SLC51C2
Chromosome 22
Chromosome location 22q13.1
miRNA miRNA information provided by mirtarbase database.
498
miRTarBase ID miRNA Experiments Reference
MIRT003891 hsa-miR-15a-5p Luciferase reporter assay 15131085
MIRT022780 hsa-miR-124-3p Microarray 18668037
MIRT003891 hsa-miR-15a-5p Reporter assay 15131085
MIRT051816 hsa-let-7c-5p CLASH 23622248
MIRT049428 hsa-miR-92a-3p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0016020 Component Membrane IBA
GO:0016020 Component Membrane IEA
GO:0022857 Function Transmembrane transporter activity IBA
GO:0055085 Process Transmembrane transport 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.
Q9Y519
Protein name Transmembrane protein 184B (Putative MAPK-activating protein FM08)
Protein function May activate the MAP kinase signaling pathway.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03619 Solute_trans_a 46 319 Organic solute transporter Ostalpha Family
Sequence
Sequence length 407
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BREAST CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
LIVER CIRRHOSIS, EXPERIMENTAL CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
NEUROMUSCULAR DISEASES Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Breast Neoplasms Stimulate 25342443
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 25668004
★☆☆☆☆
Found in Text Mining only
Squamous Cell Carcinoma of Head and Neck Associate 25668004, 36254814
★☆☆☆☆
Found in Text Mining only