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

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Gene: Tex13c ENSRNOG00000045953

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Description

TEX13 family member C [Source:RGD Symbol;Acc:1563975]

Gene Synonyms

LOC298164, RGD1563975

Location

Primary_assembly X: 127,342,268-127,345,416 forward strand.

GRCr8:CM070411.1

About this gene

This gene has 1 transcript (splice variant), 68 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000074996.3	Tex13c-201	2844	608aa	ENSRNOP00000065777.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A1A5Q8	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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