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

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Gene: TNFSF13B ENSSSCG00000009542

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Description

TNF superfamily member 13b [Source:VGNC Symbol;Acc:VGNC:94269]

Location

Primary_assembly 11: 75,599,598-75,633,041 forward strand.

Sscrofa11.1:CM000822.5

About this gene

This gene has 1 transcript (splice variant), 200 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000010460.3	TNFSF13B-201	2628	233aa	ENSSSCP00000010188.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1U7N3 A0MTC9	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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