Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: Tagln ENSRNOG00000017628

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Description

transgelin [Source:RGD Symbol;Acc:3723]

Gene Synonyms

Sm22

Location

Primary_assembly 8: 46,222,472-46,230,668 reverse strand.

mRatBN7.2:CM026981.1

About this gene

This gene has 2 transcripts (splice variants), 294 orthologues, 7 paralogues and is associated with 17 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000024030.7	Tagln-201	1077	231aa	ENSRNOP00000024030.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QCF4	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,
ENSRNOT00000081737.2	Tagln-202	1169	199aa	ENSRNOP00000069919.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JWK7	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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