Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
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Gene: Rdm1 ENSRNOG00000020751

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Description

RAD52 motif containing 1 [Source:RGD Symbol;Acc:1310432]

Gene Synonyms

LOC287726, Rad52b

Location

Primary_assembly 10: 86,539,553-86,573,034 forward strand.

mRatBN7.2:CM026983.1

About this gene

This gene has 4 transcripts (splice variants), 191 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000109969.1	Rdm1-203	1138	297aa	ENSRNOP00000095095.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AMU9	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,
ENSRNOT00000114838.1	Rdm1-204	1453	281aa	ENSRNOP00000077763.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5XWG9	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,
ENSRNOT00000106592.1	Rdm1-202	1124	281aa	ENSRNOP00000084602.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZZZ4	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,
ENSRNOT00000028174.7	Rdm1-201	1076	277aa	ENSRNOP00000028174.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A823	-

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Summary

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