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: hoxa11b ENSDARG00000007009

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Description

homeobox A11b [Source:NCBI gene;Acc:30382]

Gene Synonyms

Hoxa-11, hoxa11, im:7142641

Location

Chromosome 16: 20,904,754-20,907,378 forward strand.

GRCz11:CM002900.2

About this gene

This gene has 1 transcript (splice variant), 188 orthologues and 53 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000006043.6	hoxa11b-201	1878	283aa	ENSDARP00000005174.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1RBM6	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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