Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
89832
Gene name Gene Name - the full gene name approved by the HGNC.
CHRNA7 (exons 5-10) and FAM7A (exons A-E) fusion
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CHRFAM7A
Synonyms (NCBI Gene) Gene synonyms aliases
CHRNA7, CHRNA7-DR1, D-10, NACHRA7
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q13.2
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 family member CHRNA7, which is located on chromosome 15 in a region associated with several neu
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017997 hsa-miR-335-5p Microarray 18185580
MIRT025040 hsa-miR-181a-5p Microarray 17612493
MIRT704706 hsa-miR-508-5p HITS-CLIP 23313552
MIRT704705 hsa-miR-6849-3p HITS-CLIP 23313552
MIRT704704 hsa-miR-939-3p HITS-CLIP 23313552
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005230 Function Extracellular ligand-gated ion channel activity IEA
GO:0005515 Function Protein binding IPI 28750690
GO:0005887 Component Integral component of plasma membrane IBA 21873635
GO:0005892 Component Acetylcholine-gated channel complex IBA 21873635
GO:0007165 Process Signal transduction IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
609756 15781 ENSG00000166664
Protein
UniProt ID Q494W8
Protein name CHRNA7-FAM7A fusion protein (CHRNA7-DR1) (D-10)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02931 Neur_chan_LBD 15 140 Neurotransmitter-gated ion-channel ligand binding domain Family
PF02932 Neur_chan_memb 147 397 Neurotransmitter-gated ion-channel transmembrane region Family
Tissue specificity TISSUE SPECIFICITY: Expressed in hippocampus. {ECO:0000269|PubMed:9782083}.
Sequence
Sequence length 412
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 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)
19631623
Associations from Text Mining
Disease Name Relationship Type References
AIDS Associated Nephropathy Associate 26567012
Alzheimer Disease Associate 22486522, 24787912, 27565651, 32818803
Autism Spectrum Disorder Associate 21996756, 27565651
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Associate 23553139
Bipolar Disorder Associate 17192894
Breast Neoplasms Associate 28077796
Colorectal Neoplasms Associate 37828429
COVID 19 Associate 34088975
Cytokine Release Syndrome Associate 34088975
Epilepsy Associate 24024466