Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: TNR ENSPTRG00000001709

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Description

tenascin R [Source:VGNC Symbol;Acc:VGNC:1694]

Location

Chromosome 1: 153,808,171-154,014,312 reverse strand.

Pan_tro_3.0:CM000314.3

About this gene

This gene has 2 transcripts (splice variants), 206 orthologues and 31 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000003092.4	TNR-201	5863	1358aa	ENSPTRP00000002843.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8N700 A0A6D2XL35	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,
ENSPTRT00000080112.1	TNR-202	4023	1340aa	ENSPTRP00000070186.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RZN5	-

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Summary

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