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

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Gene: SPO11 ENSBTAG00000044210

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Description

SPO11 initiator of meiotic double strand breaks [Source:VGNC Symbol;Acc:VGNC:35225]

Location

Primary_assembly 13: 58,812,692-58,828,236 reverse strand.

ARS-UCD2.0:CM008180.2

About this gene

This gene has 2 transcripts (splice variants) and 197 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000061470.4	SPO11-202	2058	405aa	ENSBTAP00000053612.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BMM6	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,
ENSBTAT00000132668.1	SPO11-201	2238	357aa	ENSBTAP00000093488.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T3W0	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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Summary

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