Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: RAD51B ENSSSCG00000028877

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Description

RAD51 paralog B [Source:VGNC Symbol;Acc:VGNC:92058]

Location

Primary_assembly 7: 91,592,424-92,345,294 forward strand.

Sscrofa11.1:CM000818.5

About this gene

This gene has 3 transcripts (splice variants), 151 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000087100.1	RAD51B-202	1191	365aa	ENSSSCP00000073155.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1U1T8 A0A5G2R7V0	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,
ENSSSCT00000077443.1	RAD51B-201	5674	279aa	ENSSSCP00000070304.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2RGG8 A0A8D1QJZ2	-
ENSSSCT00000023246.4	RAD51B-203	2147	350aa	ENSSSCP00000021921.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1U1U7 I3LCZ3	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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