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: NR2C1 ENSOCUG00000004657

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Description

nuclear receptor subfamily 2 group C member 1 [Source:HGNC Symbol;Acc:HGNC:7971]

Location

Chromosome 4: 74,327,627-74,371,580 reverse strand.

OryCun2.0:CM000793.1

About this gene

This gene has 3 transcripts (splice variants), 232 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000051305.1	NR2C1-201	1995	625aa	ENSOCUP00000049363.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSOCUT00000030390.3	NR2C1-203	1518	485aa	ENSOCUP00000021748.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1TXE6	-
ENSOCUT00000062384.1	NR2C1-202	1371	436aa	ENSOCUP00000039958.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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