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: xkr9 ENSDARG00000026500

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Description

XK, Kell blood group complex subunit-related family, member 9 [Source:NCBI gene (formerly Entrezgene);Acc:678537]

Location

Chromosome 24: 14,202,327-14,212,521 reverse strand.

GRCz11:CM002908.2

About this gene

This gene has 2 transcripts (splice variants), 197 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000130825.3	xkr9-201	1439	378aa	ENSDARP00000107372.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B3DGC8	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,
ENSDART00000180674.1	xkr9-202	1387	378aa	ENSDARP00000145894.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B3DGC8	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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