Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: Hcrt ENSRNOG00000018892

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Description

hypocretin neuropeptide precursor [Source:RGD Symbol;Acc:2786]

Location

Primary_assembly 10: 85,689,465-85,691,210 reverse strand.

mRatBN7.2:CM026983.1

About this gene

This gene has 2 transcripts (splice variants), 173 orthologues and is associated with 15 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000025547.4	Hcrt-201	568	130aa	ENSRNOP00000025547.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	O55232	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,
ENSRNOT00000095773.1	Hcrt-202	411	106aa	ENSRNOP00000081572.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZSA6	-

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Summary

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