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 ENSMICG00000005857

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Description

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

Location

Chromosome 7: 27,052,973-27,101,859 forward strand.

Mmur_3.0:CM007667.1

About this gene

This gene has 2 transcripts (splice variants), 232 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSMICT00000049093.2	NR2C1-201	2598	605aa	ENSMICP00000036912.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C5W9N9	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,
ENSMICT00000005854.3	NR2C1-202	3937	556aa	ENSMICP00000005344.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C5XC52	-

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Summary

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