Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: RELT ENSBTAG00000016494

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Description

RELT TNF receptor [Source:VGNC Symbol;Acc:VGNC:33862]

Location

Primary_assembly 15: 52,862,934-52,880,874 forward strand.

ARS-UCD2.0:CM008182.2

About this gene

This gene has 1 transcript (splice variant), 197 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000021927.7	RELT-201	2598	430aa	ENSBTAP00000021927.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N3F7	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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