Homo sapiens Gene: OTOR
Summary
InnateDB Gene IDBG-55796.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol OTOR
Gene Name otoraplin
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000125879
Encoded Proteins
otoraplin
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene is secreted via the Golgi apparatus and may function in cartilage development and maintenance. A frequent polymorphism in the translation start codon of this gene can abolish translation and may be associated with forms of deafness. This gene is a member of the melanoma-inhibiting activity gene family. In addition, alternate polyA sites exist for this gene. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 20:16748358-16770062
Strand Forward strand
Band p12.1
Transcripts
ENST00000246081 ENSP00000246081
ENST00000486129
ENST00000490148
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0001502 cartilage condensation
GO:0007605 sensory perception of sound
Cellular Component
GO:0005576 extracellular region
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q9NRC9
TrEMBL
UniProt Splice Variant
Entrez Gene 56914
UniGene Hs.41119
RefSeq NM_020157 XM_005260762
HUGO HGNC:8517
OMIM 606067
CCDS CCDS13124
HPRD
IMGT
EMBL AF233261 AF243505 AJ242552 AJ252324 AJ252325 AJ252326 AJ252327 AL034428 AY359082 BC101688 BC101690 CH471133
GenPept AAF82078 AAG42356 AAI01689 AAI01691 AAQ89441 CAC16848 CAC27443 CAC28085 EAX10282 EAX10283
RNA Seq Atlas 56914