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

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Gene: NR1D1 ENSCAFG00845009798

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Description

nuclear receptor subfamily 1 group D member 1 [Source:HGNC Symbol;Acc:HGNC:7962]

Location

Primary_assembly 9: 23,254,822-23,262,435 forward strand.

ROS_Cfam_1.0:CM025108.1

About this gene

This gene has 2 transcripts (splice variants), 377 orthologues and 19 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSCAFT00845017253.1	NR1D1-202	2668	612aa	ENSCAFP00845013445.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C0PLP6 A0A8I3RVG0	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,
ENSCAFT00845017289.1	NR1D1-201	2705	593aa	ENSCAFP00845013474.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I3N8V5	-

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Summary

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