Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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- Structural variants
Gene expression
Pathway
Molecular interactions
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External references
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Gene: Hhex ENSRNOG00000016595

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Description

hematopoietically expressed homeobox [Source:RGD Symbol;Acc:619932]

Gene Synonyms

Hex

Location

Primary_assembly 1: 244,602,825-244,608,604 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 1 transcript (splice variant), 34 orthologues and is associated with 5 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000022384.7	Hhex-201	1794	271aa	ENSRNOP00000022384.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A9K3Y8F2 Q9WV22	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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