Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: RUNX1 ENSDARG00000087646

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Description

RUNX family transcription factor 1 [Source:ZFIN;Acc:ZDB-GENE-000605-1]

Location

Chromosome 1: 1,362,932-1,402,303 reverse strand.

GRCz11:CM002885.2

About this gene

This gene has 1 transcript (splice variant), 208 orthologues, 3 paralogues and is associated with 67 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000130697.3	RUNX1-201	2220	451aa	ENSDARP00000112019.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9DGB8	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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