Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
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: Cyp2c66 ENSRNOG00000056733

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Description

cytochrome P450, family 2, subfamily c, polypeptide 66 [Source:RGD Symbol;Acc:6488119]

Gene Synonyms

AABR07004539.1, LOC100912265

Location

Primary_assembly 1: 248,272,336-248,309,323 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 1 transcript (splice variant), 166 orthologues and 46 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000092928.3	Cyp2c66-201	1456	480aa	ENSRNOP00000076032.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A1B0GWV3	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,

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Summary

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