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

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Gene: kansl1l ENSDARG00000075284

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Description

KAT8 regulatory NSL complex subunit 1-like [Source:ZFIN;Acc:ZDB-GENE-081104-473]

Gene Synonyms

si:dkeyp-73b1.2

Location

Chromosome 9: 38,712,474-38,774,403 forward strand.

GRCz11:CM002893.2

About this gene

This gene has 3 transcripts (splice variants), 182 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000182874.1	kansl1l-203	5460	809aa	ENSDARP00000152422.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2R8QF34	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,
ENSDART00000147652.2	kansl1l-201	2109	615aa	ENSDARP00000122921.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A9C3V7	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000148262.3	kansl1l-202	851	206aa	ENSDARP00000115380.1	Nonsense mediated decay	F1Q784	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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