Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Xrcc1 ENSRNOG00000019915

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Description

X-ray repair cross complementing 1 [Source:RGD Symbol;Acc:619823]

Location

Primary_assembly 1: 89,268,644-89,296,613 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 189 orthologues and is associated with 75 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000100887.2	Xrcc1-202	2482	689aa	ENSRNOP00000092376.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AHG8	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,
ENSRNOT00000027057.7	Xrcc1-201	2002	592aa	ENSRNOP00000027057.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9ESZ0	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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Gene tree

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