Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: Onecut1 ENSRNOG00000008095

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Description

one cut homeobox 1 [Source:RGD Symbol;Acc:2811]

Gene Synonyms

HNF-6, Hnf6

Location

Primary_assembly 8: 75,599,740-75,627,277 forward strand.

mRatBN7.2:CM026981.1

About this gene

This gene has 2 transcripts (splice variants), 203 orthologues, 2 paralogues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000101262.1	Onecut1-202	1546	491aa	ENSRNOP00000096278.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6APA2	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,
ENSRNOT00000032280.5	Onecut1-201	2348	465aa	ENSRNOP00000038480.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3V975	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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