Gene Gene information from NCBI Gene database.
Entrez ID 23585
Gene name Transmembrane protein 50A
Gene symbol TMEM50A
Synonyms (NCBI Gene)
IFNRCSMP1
Chromosome 1
Chromosome location 1p36.11
Summary This gene is located in the RH gene locus, between the RHD and RHCE genes. The function of its protein product is unknown; however, its sequence has potential transmembrane domains suggesting that it may be an integral membrane protein. Its position betwe
miRNA miRNA information provided by mirtarbase database.
401
miRTarBase ID miRNA Experiments Reference
MIRT030331 hsa-miR-26b-5p Microarray 19088304
MIRT045670 hsa-miR-149-5p CLASH 23622248
MIRT041778 hsa-miR-484 CLASH 23622248
MIRT637184 hsa-miR-374c-3p HITS-CLIP 23824327
MIRT637183 hsa-miR-6838-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005737 Component Cytoplasm IEA
GO:0005783 Component Endoplasmic reticulum IDA
GO:0016020 Component Membrane IEA
GO:0032511 Process Late endosome to vacuole transport via multivesicular body sorting pathway IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605348 30590 ENSG00000183726
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O95807
Protein name Transmembrane protein 50A (Small membrane protein 1)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05255 UPF0220 5 156 Uncharacterised protein family (UPF0220) Family
Sequence
Sequence length 157
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Familial cancer of breast Uncertain significance rs146519311 RCV005928834