Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Xkr8 ENSRNOG00000024312

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Description

XK related 8 [Source:RGD Symbol;Acc:1305649]

Gene Synonyms

LOC313033, MGC124905, RGD1305649, XRG8

Location

Primary_assembly 5: 150,222,061-150,228,564 reverse strand.

GRCr8:CM070395.1

About this gene

This gene has 1 transcript (splice variant), 312 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000017618.8	Xkr8-201	2031	399aa	ENSRNOP00000017619.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5GH55	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,

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Summary

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