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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: NR1D2 ENSOCUG00000009329

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Description

nuclear receptor subfamily 1 group D member 2 [Source:HGNC Symbol;Acc:HGNC:7963]

Location

Chromosome 14: 10,293,402-10,326,792 forward strand.

OryCun2.0:CM000803.1

About this gene

This gene has 2 transcripts (splice variants), 468 orthologues and 20 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000046582.1	NR1D2-202	2735	612aa	ENSOCUP00000042306.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSOCUT00000009330.4	NR1D2-201	2630	577aa	ENSOCUP00000017956.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1TLV2	-

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Summary

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