Homo sapiens Gene: CCDC50
Summary
InnateDB Gene IDBG-69803.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CCDC50
Gene Name coiled-coil domain containing 50
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000152492
Encoded Proteins
coiled-coil domain containing 50
coiled-coil domain containing 50
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This 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, Oct 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 3:191329077-191398670
Strand Forward strand
Band q28
Transcripts
ENST00000392456 ENSP00000376250
ENST00000392455 ENSP00000376249
ENST00000460064
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 8 experimentally validated interaction(s) in this database.
Experimentally validated
Total 8 [view]
Protein-Protein 8 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
Cellular Component
GO:0005737 cytoplasm
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
EGFR1 pathway
REACTOME
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.592514 Hs.608697
RefSeq NM_174908 NM_178335
HUGO
OMIM
CCDS CCDS33912 CCDS33913
HPRD 06463
IMGT
EMBL
GenPept
RNA Seq Atlas