Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
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  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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ID History
- Gene history

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Gene: RMND1 ENSBTAG00000013224

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Description

required for meiotic nuclear division 1 homolog [Source:VGNC Symbol;Acc:VGNC:33995]

Location

Primary_assembly 9: 88,449,225-88,485,099 reverse strand.

ARS-UCD2.0:CM008176.2

About this gene

This gene has 1 transcript (splice variant) and 201 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000017596.6	RMND1-201	3241	453aa	ENSBTAP00000017596.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MS81	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 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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