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

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Gene: DAPK2 ENSBTAG00000011820

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Description

death associated protein kinase 2 [Source:VGNC Symbol;Acc:VGNC:55109]

Location

Primary_assembly 10: 45,949,903-46,092,225 forward strand.

ARS-UCD2.0:CM008177.2

About this gene

This gene has 4 transcripts (splice variants), 268 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000015689.7	DAPK2-202	1582	488aa	ENSBTAP00000015689.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MHX3	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,
ENSBTAT00000109877.2	DAPK2-201	4876	373aa	ENSBTAP00000101968.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TUC3	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,
ENSBTAT00000096925.2	DAPK2-203	4860	370aa	ENSBTAP00000083068.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1N4B5 A0AAA9SH90	-
ENSBTAT00000101656.2	DAPK2-204	3666	397aa	ENSBTAP00000079686.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SBS8	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,

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Summary

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