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 ENSMMUG00000018898

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Description

nuclear receptor subfamily 2 group C member 1 [Source:VGNC Symbol;Acc:VGNC:75508]

Location

Primary_assembly 11: 94,832,056-94,883,112 reverse strand.

Mmul_10:CM014346.1

About this gene

This gene has 2 transcripts (splice variants), 233 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSMMUT00000060329.2	NR2C1-202	2692	604aa	ENSMMUP00000050972.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H9FZ60	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,
ENSMMUT00000026568.4	NR2C1-201	2330	604aa	ENSMMUP00000024865.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H9FZ60	-

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Summary

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