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: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Mnd1 ENSRNOG00000024733

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Description

meiotic nuclear divisions 1 [Source:RGD Symbol;Acc:1309007]

Gene Synonyms

LOC295160, RGD1309007

Location

Primary_assembly 2: 171,731,523-171,794,095 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants) and 214 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000031179.7	Mnd1-201	887	205aa	ENSRNOP00000034074.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LWN6	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,
ENSRNOT00000095075.2	Mnd1-202	842	190aa	ENSRNOP00000080190.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZQ57	-

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Summary

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