Bos taurus Gene: RD3
Summary
InnateDB Gene IDBG-638227.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol RD3
Gene Name Uncharacterized protein
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000024453
Encoded Proteins
retinal degeneration 3
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 ENSG00000198570:
This gene encodes a retinal protein that is associated with promyelocytic leukemia-gene product (PML) bodies in the nucleus. Mutations in this gene cause Leber congenital amaurosis type 12, a disease that results in retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome 16:73866649-73868568
Strand Forward strand
Band
Transcripts
ENSBTAT00000033923 ENSBTAP00000033826
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 1 interaction(s) predicted by orthology.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0060041 retina development in camera-type eye
Cellular Component
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt
TrEMBL E1BP94
UniProt Splice Variant
Entrez Gene 787231
UniGene
RefSeq XM_001254691 XM_002694292
HUGO HGNC:19689
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02043781
GenPept
RNA Seq Atlas 787231