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

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Gene: nr1h5 ENSDARG00000031046

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Description

nuclear receptor subfamily 1, group H, member 5 [Source:NCBI gene (formerly Entrezgene);Acc:557500]

Location

Chromosome 8: 10,903,325-10,932,206 reverse strand.

GRCz11:CM002892.2

About this gene

This gene has 2 transcripts (splice variants), 466 orthologues and 28 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000124313.3	nr1h5-201	1732	486aa	ENSDARP00000105819.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0S5T9	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,
ENSDART00000133770.2	nr1h5-202	810	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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