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: KLHL22 ENSBTAG00000020161

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Description

kelch like family member 22 [Source:VGNC Symbol;Acc:VGNC:30651]

Location

Primary_assembly 17: 72,484,080-72,505,905 forward strand.

ARS-UCD2.0:CM008184.2

About this gene

This gene has 5 transcripts (splice variants), 192 orthologues and 54 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000129150.1	KLHL22-205	2716	685aa	ENSBTAP00000078208.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RXH3	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,
ENSBTAT00000089108.2	KLHL22-202	3039	661aa	ENSBTAP00000096627.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9THR2	-
ENSBTAT00000143467.1	KLHL22-201	2819	634aa	ENSBTAP00000106020.1	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,
ENSBTAT00000085830.2	KLHL22-204	2619	652aa	ENSBTAP00000073854.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MPJ6	-
ENSBTAT00000026853.6	KLHL22-203	2551	653aa	ENSBTAP00000026853.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N1V7	-

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Summary

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