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

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Gene: hoxd11a ENSDARG00000059267

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Description

homeobox D11a [Source:NCBI gene;Acc:30405]

Gene Synonyms

fk50b10, hoxd-11, hoxd11, sb:eu641, wu:fk50b10

Location

Chromosome 9: 1,975,818-1,978,090 reverse strand.

GRCz11:CM002893.2

About this gene

This gene has 1 transcript (splice variant), 183 orthologues and 53 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000082344.5	hoxd11a-201	1410	276aa	ENSDARP00000076780.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q90470	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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