Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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Pathway
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Gene: Tnfsf4 ENSRNOG00000002968

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Description

TNF superfamily member 4 [Source:RGD Symbol;Acc:619816]

Gene Synonyms

Ox40l, Tnlg2b

Location

Primary_assembly 13: 76,256,654-76,280,133 forward strand.

GRCr8:CM070403.1

About this gene

This gene has 1 transcript (splice variant), 95 orthologues and is associated with 15 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000003969.7	Tnfsf4-201	1783	199aa	ENSRNOP00000003969.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0U5JAD2 Q9Z2P3	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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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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