Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: NR3C1 ENSBTAG00000019472

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Description

nuclear receptor subfamily 3 group C member 1 [Source:VGNC Symbol;Acc:VGNC:32243]

Location

Primary_assembly 7: 54,344,785-54,463,271 reverse strand.

ARS-UCD2.0:CM008174.2

About this gene

This gene has 2 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
ENSBTAT00000077017.2	NR3C1-202	6719	782aa	ENSBTAP00000069782.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M7I4	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, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSBTAT00000025941.6	NR3C1-201	6264	755aa	ENSBTAP00000025941.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MN19	-

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Summary

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