Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: Mixl1 ENSRNOG00000003176

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Description

Mix paired-like homeobox 1 [Source:RGD Symbol;Acc:1310011]

Gene Synonyms

LOC289311, NEWGENE_1310011

Location

Primary_assembly 13: 94,953,907-94,957,938 reverse strand.

GRCr8:CM070403.1

About this gene

This gene has 1 transcript (splice variant), 152 orthologues and 44 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000004244.5	Mixl1-201	2342	231aa	ENSRNOP00000004244.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JGH3 D4A558	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,

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Summary

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