Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
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Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: TNFRSF12A ENSSSCG00000027130

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Description

TNF receptor superfamily member 12A [Source:NCBI gene (formerly Entrezgene);Acc:100217390]

Gene Synonyms

Fn14, TWEAKR

Location

Primary_assembly 3: 39,166,298-39,168,302 reverse strand.

Sscrofa11.1:CM000814.5

About this gene

This gene has 1 transcript (splice variant) and 86 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000026802.4	TNFRSF12A-201	864	94aa	ENSSSCP00000020074.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0PY28 I3L7R8	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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