Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
11255
Gene name Gene Name - the full gene name approved by the HGNC.
Histamine receptor H3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HRH3
Synonyms (NCBI Gene) Gene synonyms aliases
GPCR97, HH3R
Chromosome Chromosome number
20
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
20q13.33
Summary Summary of gene provided in NCBI Entrez Gene.
Histamine is a ubiquitous messenger molecule released from mast cells, enterochromaffin-like cells, and neurons. Its various actions are mediated by histamine receptors H1, H2, H3 and H4. This gene encodes one of the histamine receptors (H3) which belongs
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT756048 hsa-miR-4696 Microarray, qRT-PCR 35899934
MIRT756049 hsa-miR-1275 Microarray, qRT-PCR 35899934
MIRT1054689 hsa-miR-1207-5p CLIP-seq
MIRT1054690 hsa-miR-2682 CLIP-seq
MIRT1054691 hsa-miR-3151 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004969 Function Histamine receptor activity IEA
GO:0004993 Function G protein-coupled serotonin receptor activity IBA 21873635
GO:0005886 Component Plasma membrane TAS
GO:0005887 Component Integral component of plasma membrane IBA 21873635
GO:0007186 Process G protein-coupled receptor signaling pathway TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604525 5184 ENSG00000101180
Protein
UniProt ID Q9Y5N1
Protein name Histamine H3 receptor (H3R) (HH3R) (G-protein coupled receptor 97)
Protein function The H3 subclass of histamine receptors could mediate the histamine signals in CNS and peripheral nervous system. Signals through the inhibition of adenylate cyclase and displays high constitutive activity (spontaneous activity in the absence of
PDB 7F61 , 8YN5 , 8YN6 , 8YN7 , 8YN8 , 8YUU , 8YUV
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 51 412 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Expressed predominantly in the CNS, with the greatest expression in the thalamus and caudate nucleus. The various isoforms are mainly coexpressed in brain, but their relative expression level varies in a region-specific manner. Isoform
Sequence
Sequence length 445
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Neuroactive ligand-receptor interaction   Histamine receptors
G alpha (i) signalling events
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Hypertension Hypertensive disease rs13306026 9050021
Unknown
Disease term Disease name Evidence References Source
Oligodendroglioma Oligodendroglioma GWAS
Restless Legs Syndrome Restless Legs Syndrome GWAS
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 29701013
Anaphylaxis Associate 28465562
Anxiety Associate 28969474
Autism Spectrum Disorder Associate 35877665
Carcinoma Non Small Cell Lung Stimulate 33159174
Cognition Disorders Associate 37329185
Colorectal Neoplasms Associate 36902343
Cystitis Interstitial Associate 31718622
Diarrhea Associate 28465562
Heart Failure Associate 26989676