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: NR3C1 ENSMMUG00000000421

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Description

nuclear receptor subfamily 3 group C member 1 [Source:VGNC Symbol;Acc:VGNC:75515]

Location

Primary_assembly 6: 140,690,415-140,844,024 reverse strand.

Mmul_10:CM014341.1

About this gene

This gene has 3 transcripts (splice variants), 279 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSMMUT00000000616.4	NR3C1-201	6342	777aa	ENSMMUP00000000567.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H9FTF1	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,
ENSMMUT00000040911.3	NR3C1-202	6126	777aa	ENSMMUP00000033941.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H9FTF1	-
ENSMMUT00000000618.4	NR3C1-203	5934	777aa	ENSMMUP00000000569.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H9FTF1	-

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Summary

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