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
External references
Supporting evidence
ID History
- Gene history

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Gene: NR3C2 ENSGGOG00000001102

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Description

nuclear receptor subfamily 3 group C member 2 [Source:HGNC Symbol;Acc:HGNC:7979]

Location

Chromosome 4: 160,442,369-160,795,379 reverse strand.

gorGor4:FR853097.2

About this gene

This gene has 2 transcripts (splice variants), 211 orthologues and 9 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGGOT00000001110.4	NR3C2-201	2967	988aa	ENSGGOP00000001086.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3QFL0	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,
ENSGGOT00000061897.1	NR3C2-202	2604	867aa	ENSGGOP00000033341.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I2YEL8	-

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Summary

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