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

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Gene: TK2 ENSBTAG00000005152

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Description

thymidine kinase 2 [Source:VGNC Symbol;Acc:VGNC:103723]

Location

Primary_assembly 18: 34,248,312-34,275,680 reverse strand.

ARS-UCD2.0:CM008185.2

About this gene

This gene has 7 transcripts (splice variants), 205 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000098920.1	TK2-204	2328	375aa	ENSBTAP00000078433.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S0E6	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,
ENSBTAT00000069872.3	TK2-201	1974	257aa	ENSBTAP00000063371.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M097	-
ENSBTAT00000085212.3	TK2-202	1953	250aa	ENSBTAP00000061766.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M164	-
ENSBTAT00000079179.2	TK2-203	1707	168aa	ENSBTAP00000069558.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MES5	-
ENSBTAT00000104492.2	TK2-205	1689	162aa	ENSBTAP00000099260.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TLE6	-
ENSBTAT00000080732.2	TK2-206	1283	304aa	ENSBTAP00000063251.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1N233	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSBTAT00000006795.6	TK2-207	995	264aa	ENSBTAP00000006795.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MNI9	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Summary

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