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: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Men1 ENSRNOG00000021054

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Description

menin 1 [Source:RGD Symbol;Acc:3078]

Gene Synonyms

MGC114329

Location

Primary_assembly 1: 213,068,166-213,074,120 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 176 orthologues and is associated with 43 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000028592.8	Men1-201	2727	616aa	ENSRNOP00000028592.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QI00 A6HZG1	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,
ENSRNOT00000099846.2	Men1-202	1793	555aa	ENSRNOP00000076697.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9WVR8-2	-

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Summary

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