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: TNFRSF11B ENSSSCG00000027762

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Description

TNF receptor superfamily member 11b [Source:HGNC Symbol;Acc:HGNC:11909]

Location

Primary_assembly 4: 19,850,350-19,879,125 forward strand.

Sscrofa11.1:CM000815.5

About this gene

This gene has 1 transcript (splice variant), 201 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000006589.6	TNFRSF11B-201	2127	399aa	ENSSSCP00000076232.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8W4FAC7	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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