Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Msh3 ENSRNOG00000064838

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Description

mutS homolog 3 [Source:NCBI gene (formerly Entrezgene);Acc:499505]

Location

Primary_assembly 2: 25,179,400-25,321,102 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 204 orthologues, 4 paralogues and is associated with 17 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000172709.1	Msh3-202	3979	1105aa	ENSRNOP00000109273.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000100720.2	Msh3-201	697	165aa	ENSRNOP00000077811.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5YC19	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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