Version 5.4
Bos taurus Gene: DFNB31
Summary
InnateDB Gene IDBG-638624.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DFNB31
Gene Name Uncharacterized protein
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000010107
Encoded Proteins
IDBP-690716
deafness, autosomal recessive 31
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000095397:
This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Mar 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 8:105331888-105422354
Strand Reverse strand
Band
Transcripts
ENSBTAT00000013333 ENSBTAP00000013333
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 4 interaction(s) predicted by orthology.
Predicted by orthology
Total 4 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0001895 retina homeostasis
GO:0007605 sensory perception of sound
GO:0050953 sensory perception of light stimulus
GO:0060122 inner ear receptor stereocilium organization
Cellular Component
GO:0002142 stereocilia ankle link complex
GO:0005737 cytoplasm
GO:0005884 actin filament
GO:0005929 cilium
GO:0032420 stereocilium
GO:0032421 stereocilium bundle
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
ENSG00000095397
View Gene Order
ENSMUSG00000039137
View Gene Order
Cross-References
SwissProt
TrEMBL E1B914
UniProt Splice Variant
Entrez Gene 533033
UniGene Bt.111929
RefSeq XM_005210575
HUGO HGNC:16361
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02024584
GenPept
RNA Seq Atlas 533033

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca