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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for CCDC50 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID152137
Official gene symbolCCDC50
Full namecoiled-coil domain containing 50
Aliases,C3orf6,DFNA44,YMER,
Gene summaryThis gene encodes a soluble, cytoplasmic, tyrosine-phosphorylated protein with multiple ubiquitin-interacting domains. Mutations in this gene cause nonsyndromic, postlingual, progressive sensorineural DFNA44 hearing loss. In mouse, the protein is expressed in the inner ear during development and postnatal maturation and associates with microtubule-based structures. This protein may also function as a negative regulator of NF-kB signaling and as an effector of epidermal growth factor (EGF)-mediated cell signaling. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq]
LocationChromosome: 3   Locus: 3q28
Gene position191046874 - 191116459  Map Viewer
Gene orientationplus
Gene size69586 bp
Gene sequence
OMIM ID611051