Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1139
Gene name Gene Name - the full gene name approved by the HGNC.
Cholinergic receptor nicotinic alpha 7 subunit
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CHRNA7
Synonyms (NCBI Gene) Gene synonyms aliases
CHRNA7-2, NACHRA7, nAChR7
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q13.3
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
118511 1960 ENSG00000175344
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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Epilepsy Epilepsy, idiopathic generalized, susceptibility to, 7, epilepsy N/A N/A ClinVar, GenCC
Neurodevelopmental Disorders complex neurodevelopmental disorder N/A N/A GenCC
Associations from Text Mining Disease 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