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: NR5A1 ENSPTRG00000021357

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Description

nuclear receptor subfamily 5 group A member 1 [Source:HGNC Symbol;Acc:HGNC:7983]

Location

Chromosome 9: 102,554,276-102,580,563 reverse strand.

Pan_tro_3.0:CM000323.3

About this gene

This gene has 2 transcripts (splice variants), 258 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000039501.4	NR5A1-201	3200	461aa	ENSPTRP00000036496.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XK54 H2QXV6	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,
ENSPTRT00000088382.1	NR5A1-202	1590	421aa	ENSPTRP00000083371.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3T2C6 A0A6D2W627	-

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Summary

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