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
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: TRIM13 ENSPTRG00000031189

.

Description

tripartite motif containing 13 [Source:VGNC Symbol;Acc:VGNC:5127]

Location

Chromosome 13: 35,027,424-35,043,711 forward strand.

Pan_tro_3.0:CM000327.3

About this gene

This gene has 1 transcript (splice variant), 209 orthologues and 87 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000010806.6	TRIM13-201	1623	410aa	ENSPTRP00000010004.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XT51 H2Q7K8	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,

.

Summary

.

.