Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Rrh ENSRNOG00000053349

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Description

retinal pigment epithelium derived rhodopsin homolog [Source:RGD Symbol;Acc:1308948]

Gene Synonyms

LOC310869

Location

Primary_assembly 2: 221,036,436-221,048,627 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 198 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000093631.3	Rrh-202	1439	337aa	ENSRNOP00000076275.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A1W2Q6H2	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSRNOT00000085096.3	Rrh-201	1148	240aa	ENSRNOP00000072493.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HVP7 D3ZY73	-

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Summary

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