Mus musculus Gene: Rd3
Summary
InnateDB Gene IDBG-208912.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Rd3
Gene Name retinal degeneration 3
Synonyms 3322402L07Rik; rd-3; rd3
Species Mus musculus
Ensembl Gene ENSMUSG00000049353
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 1:191977373-191988282
Strand Forward strand
Band H6
Transcripts
ENSMUST00000053463 ENSMUSP00000050188
ENSMUST00000175680 ENSMUSP00000135650
ENSMUST00000181512 ENSMUSP00000137756
ENSMUST00000180463 ENSMUSP00000138049
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:0007601 visual perception
GO:0050896 response to stimulus
GO:0060041 retina development in camera-type eye
Cellular Component
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL K3W4N1
UniProt Splice Variant
Entrez Gene 74023
UniGene Mm.274393 Mm.475401
RefSeq NM_001177900 NM_023727
OMIM
CCDS CCDS15626
HPRD
IMGT
MGI ID MGI:1921273
MGI Symbol Rd3
EMBL AB030195 AC182412 AK014383 AK045045 BC103778 BC116935 BC116937
GenPept AAI03779 AAI16936 AAI16938 BAA92758 BAB29312 BAC32196
RNA Seq Atlas 74023