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
- Variant table
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- Structural variants
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ID History
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Gene: Hmx FBgn0264005

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Description

H6-like-homeobox

Gene Synonyms

Hmx

Location

Primary_assembly 3R: 17,558,930-17,569,097 forward strand.

BDGP6.54:AE014297.3

About this gene

This gene has 3 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0330386	Hmx-RD	2691	718aa	FBpp0303412	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0B4KHN8	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,
FBtr0346339	Hmx-RE	3384	592aa	FBpp0312056	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0B4LHJ7 Q9VEI9	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,
FBtr0330385	Hmx-RC	2691	592aa	FBpp0303411	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0B4LHJ7 Q9VEI9	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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