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

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Gene: KAT6B ENSDARG00000055429

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Description

lysine acetyltransferase 6B [Source:HGNC Symbol;Acc:HGNC:17582]

Location

Chromosome 13: 24,871,050-24,906,307 reverse strand.

GRCz11:CM002897.2

About this gene

This gene has 5 transcripts (splice variants), 222 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSDART00000136624.2	KAT6B-202	4107	1368aa	ENSDARP00000114005.1	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, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000077775.5	KAT6B-203	3114	1037aa	ENSDARP00000072241.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-
ENSDART00000148191.2	KAT6B-201	1938	646aa	ENSDARP00000122224.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSDART00000189810.1	KAT6B-204	978	325aa	ENSDARP00000153761.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-
ENSDART00000182705.1	KAT6B-205	453	150aa	ENSDARP00000147569.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	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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