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

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Gene: NR0B1 ENSGGOG00000002391

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Description

nuclear receptor subfamily 0 group B member 1 [Source:HGNC Symbol;Acc:HGNC:7960]

Location

Chromosome X: 30,583,838-30,589,003 reverse strand.

gorGor4:FR853103.2

About this gene

This gene has 2 transcripts (splice variants), 230 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGGOT00000002406.3	NR0B1-201	1762	470aa	ENSGGOP00000002355.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3QIY2	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,
ENSGGOT00000049533.1	NR0B1-202	318	105aa	ENSGGOP00000030038.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I2Y562	-

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Summary

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