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: CXCR1 ENSBTAG00000026753

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Description

chemokine (C-X-C motif) receptor 1 [Source:NCBI gene (formerly Entrezgene);Acc:281863]

Gene Synonyms

CXCR2, IL8RA, IL8RB

Location

Primary_assembly 2: 106,212,222-106,219,154 reverse strand.

ARS-UCD2.0:CM008169.2

About this gene

This gene has 3 transcripts (splice variants), 225 orthologues and 25 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000038197.6	CXCR1-203	2239	379aa	ENSBTAP00000056463.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G5E6Q0	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,
ENSBTAT00000127310.1	CXCR1-201	4631	360aa	ENSBTAP00000081052.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	J3QY08	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,
ENSBTAT00000133564.1	CXCR1-202	2736	360aa	ENSBTAP00000098246.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	J3QY08	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,

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Summary

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