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

Configure this page

Share this page

Bookmark this page

.

Gene: TNFRSF11B ENSPTRG00000020528

.

Description

TNF receptor superfamily member 11b [Source:VGNC Symbol;Acc:VGNC:2999]

Location

Chromosome 8: 121,159,817-121,188,475 reverse strand.

Pan_tro_3.0:CM000322.4

About this gene

This gene has 2 transcripts (splice variants), 200 orthologues and 22 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000037984.5	TNFRSF11B-201	2397	428aa	ENSPTRP00000035110.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2QWM3	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,
ENSPTRT00000094643.1	TNFRSF11B-202	1182	393aa	ENSPTRP00000081487.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SY25	-

.

Summary

.

.