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

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Gene: Hoxb7 ENSRNOG00000007611

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Description

homeo box B7 [Source:RGD Symbol;Acc:1559918]

Gene Synonyms

Hox2r1b, R1b

Location

Primary_assembly 10: 81,749,097-81,752,550 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 1 transcript (splice variant), 163 orthologues, 40 paralogues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000031035.6	Hoxb7-201	1248	219aa	ENSRNOP00000033609.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HIE3 P18864	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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