Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Cyp4f39 ENSRNOG00000029478

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Description

cytochrome P450, family 4, subfamily f, polypeptide 39 [Source:RGD Symbol;Acc:1308796]

Gene Synonyms

LOC299566, RGD1308796

Location

Primary_assembly 7: 12,169,922-12,187,540 forward strand.

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants), 204 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000075589.4	Cyp4f39-202	2050	543aa	ENSRNOP00000067362.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8J8Y394	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,
ENSRNOT00000060284.6	Cyp4f39-201	3190	524aa	ENSRNOP00000057034.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4AB65	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as the principal variant. 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 P4,

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Paralogues

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