Bos taurus Gene: USH1G
Summary
InnateDB Gene IDBG-643354.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol USH1G
Gene Name Usher syndrome type-1G protein
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000017252
Encoded Proteins
Usher syndrome 1G (autosomal recessive)
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 ENSG00000182040:
This gene encodes a protein that contains three ankyrin domains, a class I PDZ-binding motif and a sterile alpha motif. The encoded protein interacts with harmonin, which is associated with Usher syndrome type 1C. This protein plays a role in the development and maintenance of the auditory and visual systems and functions in the cohesion of hair bundles formed by inner ear sensory cells. Mutations in this gene are associated with Usher syndrome type 1G (USH1G). [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 19:57122385-57126123
Strand Forward strand
Band
Transcripts
ENSBTAT00000022930 ENSBTAP00000022930
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 2 interaction(s) predicted by orthology.
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0030507 spectrin binding
GO:0042803 protein homodimerization activity
Biological Process
GO:0007605 sensory perception of sound
GO:0042472 inner ear morphogenesis
GO:0045494 photoreceptor cell maintenance
GO:0050953 sensory perception of light stimulus
GO:0050957 equilibrioception
GO:0060113 inner ear receptor cell differentiation
Cellular Component
GO:0005737 cytoplasm
GO:0015629 actin cytoskeleton
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt
TrEMBL E1BFU2
UniProt Splice Variant
Entrez Gene 531104
UniGene Bt.63847
RefSeq NM_001192702
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02049536
GenPept
RNA Seq Atlas 531104