Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3061
Gene name Gene Name - the full gene name approved by the HGNC.
Hypocretin receptor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HCRTR1
Synonyms (NCBI Gene) Gene synonyms aliases
ORXR1, OX1R, OXR1
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p35.2
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a G-protein coupled receptor involved in the regulation of feeding behavior. The encoded protein selectively binds the hypothalamic neuropeptide orexin A. A related gene (HCRTR2) encodes a G-protein coupled receptor tha
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018468 hsa-miR-335-5p Microarray 18185580
MIRT1042241 hsa-miR-3124-3p CLIP-seq
MIRT1042242 hsa-miR-3125 CLIP-seq
MIRT1042243 hsa-miR-3164 CLIP-seq
MIRT1042244 hsa-miR-3184 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IBA 21873635
GO:0005515 Function Protein binding IPI 28717967
GO:0005886 Component Plasma membrane TAS
GO:0005887 Component Integral component of plasma membrane IBA 21873635
GO:0005887 Component Integral component of plasma membrane IDA 26950369
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602392 4848 ENSG00000121764
Protein
UniProt ID O43613
Protein name Orexin/Hypocretin receptor type 1 (Hypocretin receptor type 1) (Orexin receptor type 1) (Ox-1-R) (Ox1-R) (Ox1R)
Protein function Moderately selective excitatory receptor for orexin-A and, with a lower affinity, for orexin-B neuropeptide (PubMed:26950369, PubMed:9491897). Triggers an increase in cytoplasmic Ca(2+) levels in response to orexin-A binding (PubMed:26950369, Pu
PDB 4ZJ8 , 4ZJC , 6TO7 , 6TOD , 6TOS , 6TOT , 6TP3 , 6TP4 , 6TP6 , 6TQ4 , 6TQ6 , 6TQ7 , 6TQ9 , 6V9S
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 63 358 7 transmembrane receptor (rhodopsin family) Family
Sequence
Sequence length 425
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Neuroactive ligand-receptor interaction
Hormone signaling
  Orexin and neuropeptides FF and QRFP bind to their respective receptors
G alpha (q) signalling events
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
15978554, 17999203
Unknown
Disease term Disease name Evidence References Source
Mental depression Mental Depression, Depressive disorder 21377495, 22617356 ClinVar
Hypoalbuminemia Hypoalbuminemia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Agoraphobia Associate 30718541
Anxiety Associate 30718541
Hepatitis B Inhibit 31106596
Migraine Disorders Associate 21344296
Migraine without Aura Associate 21344296
Myalgia Associate 30718541
Neurologic Manifestations Associate 38191899
Obesity Associate 27421018
Panic Disorder Associate 30718541
Sleep Wake Disorders Associate 33568662