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

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Gene: STK26 ENSBTAG00000019652

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Description

serine/threonine kinase 26 [Source:VGNC Symbol;Acc:VGNC:35392]

Location

Primary_assembly X: 15,912,813-15,979,088 forward strand.

ARS-UCD1.3:CM008197.2

About this gene

This gene has 5 transcripts (splice variants), 214 orthologues and 37 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000128975.1	STK26-201	3364	467aa	ENSBTAP00000090744.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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 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,
ENSBTAT00000026189.7	STK26-203	3139	392aa	ENSBTAP00000026189.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N5W5	-
ENSBTAT00000117260.1	STK26-202	3025	354aa	ENSBTAP00000092802.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000077830.2	STK26-204	2765	339aa	ENSBTAP00000064125.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1N3K3	-
ENSBTAT00000085775.2	STK26-205	1233	410aa	ENSBTAP00000070987.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MJL8	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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