Gene Gene information from NCBI Gene database.
Entrez ID 1139
Gene name Cholinergic receptor nicotinic alpha 7 subunit
Gene symbol CHRNA7
Synonyms (NCBI Gene)
CHRNA7-2NACHRA7nAChR7
Chromosome 15
Chromosome location 15q13.3
Summary The nicotinic acetylcholine receptors (nAChRs) are members of a superfamily of ligand-gated ion channels that mediate fast signal transmission at synapses. The nAChRs are thought to be hetero-pentamers composed of homologous subunits. The proposed structu
miRNA miRNA information provided by mirtarbase database.
96
miRTarBase ID miRNA Experiments Reference
MIRT016843 hsa-miR-335-5p Microarray 18185580
MIRT891887 hsa-miR-1827 CLIP-seq
MIRT891888 hsa-miR-186 CLIP-seq
MIRT891889 hsa-miR-3133 CLIP-seq
MIRT891890 hsa-miR-3160-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
99
GO ID Ontology Definition Evidence Reference
GO:0001540 Function Amyloid-beta binding IPI 10681545
GO:0001666 Process Response to hypoxia IDA 12189247
GO:0004888 Function Transmembrane signaling receptor activity IDA 16968406
GO:0004888 Function Transmembrane signaling receptor activity IEA
GO:0005216 Function Monoatomic ion channel activity IDA 17898229
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
118511 1960 ENSG00000175344
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Calcium signaling pathway
Neuroactive ligand-receptor interaction
Cholinergic synapse
Alzheimer disease
Pathways of neurodegeneration - multiple diseases
Nicotine addiction
Chemical carcinogenesis - receptor activation
  Highly calcium permeable postsynaptic nicotinic acetylcholine receptors
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
10
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
CHRNA7-related disorder Likely benign; Benign rs771965146, rs140842241, rs200390587, rs201727782 RCV003902309
RCV003943093
RCV003920577
RCV003970385
Chromosome 15q13.3 microdeletion syndrome Uncertain significance rs1412812395 RCV003455887
Clear cell carcinoma of kidney Benign rs34476605 RCV005868201
Epilepsy, idiopathic generalized, susceptibility to, 7 no classifications from unflagged records rs1566846736 RCV000679952
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Acute cholinergic dysautonomia Associate 33679766
Adenocarcinoma of Lung Associate 27228072, 31096457
AIDS Associated Nephropathy Associate 26567012
Alzheimer Disease Associate 19433665, 20061627, 24391883, 24787912, 24951635, 27249957, 31707211, 32582986, 32803965
Anxiety Disorders Associate 30029151
Arthritis Rheumatoid Associate 19404936
Attention Deficit Disorder with Hyperactivity Associate 22420046, 22420048, 26651393, 27853923
Autism Spectrum Disorder Associate 27565651, 27853923, 34356041, 36750796
Autistic Disorder Associate 21840925, 26651393, 34320968, 34356041
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Associate 23553139