Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- 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: Msn ENSRNOG00000030118

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Description

moesin [Source:RGD Symbol;Acc:621260]

Location

Primary_assembly X: 65,005,458-65,075,129 forward strand.

GRCr8:CM070411.1

About this gene

This gene has 3 transcripts (splice variants), 286 orthologues, 6 paralogues and is associated with 8 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000076181.3	Msn-201	3718	549aa	ENSRNOP00000068359.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A096MK30	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,
ENSRNOT00000117318.2	Msn-203	3669	545aa	ENSRNOP00000080802.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZR49	-
ENSRNOT00000093499.3	Msn-202	1068	355aa	ENSRNOP00000076229.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A1W2Q6E9	-

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Summary

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