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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Mlh1 ENSRNOG00000033809

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Description

mutL homolog 1 [Source:RGD Symbol;Acc:620937]

Location

Primary_assembly 8: 120,065,900-120,112,011 reverse strand.

GRCr8:CM070398.1

About this gene

This gene has 4 transcripts (splice variants), 204 orthologues, 3 paralogues and is associated with 50 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000064581.3	Mlh1-201	2476	786aa	ENSRNOP00000061834.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LSD8	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,
ENSRNOT00000135572.1	Mlh1-204	2757	711aa	ENSRNOP00000102575.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000081718.3	Mlh1-202	2589	765aa	ENSRNOP00000072285.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K2L0 A6I3J1	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,
ENSRNOT00000097589.2	Mlh1-203	2451	735aa	ENSRNOP00000086372.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A8H0	-

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Summary

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