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

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Gene: POLG2 ENSPTRG00000009541

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Description

DNA polymerase gamma 2, accessory subunit [Source:VGNC Symbol;Acc:VGNC:9533]

Location

Chromosome 17: 63,974,214-63,996,322 reverse strand.

Pan_tro_3.0:CM000331.3

About this gene

This gene has 1 transcript (splice variant), 191 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000017496.5	POLG2-201	3417	485aa	ENSPTRP00000016205.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2W1Q8 H2QDP3	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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