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
External references
Supporting evidence
ID History
- Gene history

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Gene: NR1D1 ENSPTRG00000009113

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Description

nuclear receptor subfamily 1 group D member 1 [Source:VGNC Symbol;Acc:VGNC:9481]

Location

Chromosome 17: 17,523,085-17,531,019 forward strand.

Pan_tro_3.0:CM000331.3

About this gene

This gene has 1 transcript (splice variant), 377 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000016788.5	NR1D1-201	2765	614aa	ENSPTRP00000015535.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2X348 H2QCV8	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,

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Summary

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