Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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Molecular interactions
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Gene: Rad52 ENSRNOG00000009742

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Description

RAD52 homolog, DNA repair protein [Source:RGD Symbol;Acc:1304975]

Gene Synonyms

LOC297561

Location

Primary_assembly 4: 154,778,320-154,800,021 forward strand.

GRCr8:CM070394.1

About this gene

This gene has 2 transcripts (splice variants), 199 orthologues and is associated with 16 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000013070.10	Rad52-201	2489	434aa	ENSRNOP00000013070.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZZL1	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 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,
ENSRNOT00000084520.3	Rad52-202	2408	407aa	ENSRNOP00000073295.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K552	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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