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: NR2C1 ENSSHAG00000003793

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Description

nuclear receptor subfamily 2 group C member 1 [Source:UniProtKB Gene Name;Acc:A0A7N4PQF1]

Location

Primary_assembly 5: 30,709,667-30,796,775 forward strand.

mSarHar1.11:LR735558.1

About this gene

This gene has 2 transcripts (splice variants), 233 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSHAT00000004351.2	NR2C1-202	2188	656aa	ENSSHAP00000004307.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3VMA2	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,
ENSSHAT00000044501.1	NR2C1-201	2110	584aa	ENSSHAP00000040467.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A7N4PQF1	-

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Summary

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