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

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Gene: ELOVL6 ENSPTRG00000016368

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Description

ELOVL fatty acid elongase 6 [Source:VGNC Symbol;Acc:VGNC:596]

Location

Chromosome 4: 113,027,574-113,184,772 reverse strand.

Pan_tro_3.0:CM000318.3

About this gene

This gene has 1 transcript (splice variant), 233 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000030447.3	ELOVL6-201	3009	265aa	ENSPTRP00000028113.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2Y3G2 H2QQ14	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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