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

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Gene: Klra22 ENSRNOG00000053772

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Description

killer cell lectin-like receptor subfamily A, member 22 [Source:RGD Symbol;Acc:3023]

Gene Synonyms

Klra1, Ly49, Ly49s2

Location

Primary_assembly 4: 165,721,602-165,751,546 reverse strand.

GRCr8:CM070394.1

About this gene

This gene has 3 transcripts (splice variants), 398 orthologues and 58 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000079429.3	Klra22-201	1144	354aa	ENSRNOP00000071751.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K195	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,
ENSRNOT00000090110.3	Klra22-203	1265	329aa	ENSRNOP00000070244.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5MPW6	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,
ENSRNOT00000080017.3	Klra22-202	1042	290aa	ENSRNOP00000071779.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K1B9	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,

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Summary

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