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: Sebox ENSRNOG00000009979

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Description

SEBOX homeobox [Source:RGD Symbol;Acc:62077]

Gene Synonyms

Og9x

Location

Primary_assembly 10: 63,897,217-63,898,719 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 1 transcript (splice variant), 163 orthologues and 44 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000013296.4	Sebox-201	1198	188aa	ENSRNOP00000013296.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HH55 G3V797	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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