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WormBase Tree Display for Gene: WBGene00000048

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Name Class

WBGene00000048SMapS_parentSequenceC40C9
IdentityVersion1
NameCGC_nameacr-9Person_evidenceWBPerson1430
Sequence_nameC40C9.2
Molecular_nameC40C9.2
C40C9.2.1
CE37330
Other_nameCELE_C40C9.2Accession_evidenceNDBBX284606
Public_nameacr-9
DB_infoDatabaseAceViewgeneXO262
WormQTLgeneWBGene00000048
WormFluxgeneWBGene00000048
NDBlocus_tagCELE_C40C9.2
PanthergeneCAEEL|WormBase=WBGene00000048|UniProtKB=Q18556
familyPTHR18945
NCBIgene191597
RefSeqproteinNM_077884.5
TrEMBLUniProtAccQ18556
UniProt_GCRPUniProtAccQ18556
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:19WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classacr
Allele (86)
StrainWBStrain00035950
WBStrain00035014
RNASeq_FPKM (74)
GO_annotation (28)
Ortholog (33)
Paralog (100)
Structured_descriptionConcise_descriptionacr-9 encodes a predicted member of the alpha subunit family of nicotinic acetylcholine receptors.Curator_confirmedWBPerson48
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable excitatory extracellular ligand-gated monoatomic ion channel activity and transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential. Predicted to be involved in excitatory postsynaptic potential and monoatomic ion transmembrane transport. Predicted to be located in neuron projection and synapse. Human ortholog(s) of this gene implicated in several diseases, including Alzheimer's disease; Lewy body dementia; carcinoma (multiple); and inflammatory bowel disease (multiple). Is an ortholog of human CHRFAM7A (CHRNA7 (exons 5-10) and FAM7A (exons A-E) fusion) and CHRNA7 (cholinergic receptor nicotinic alpha 7 subunit).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Disease_infoPotential_modelDOID:10652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1960)
DOID:3908Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1960)
DOID:3748Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1960)
DOID:8778Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1960)
DOID:3083Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1960)
DOID:12217Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1960)
DOID:8577Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1960)
DOID:1324Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1960)
DOID:7474Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1960)
DOID:5419Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1960)
Molecular_infoCorresponding_CDSC40C9.2
Corresponding_CDS_historyC40C9.2:wp121
C40C9.2:wp131
Corresponding_transcriptC40C9.2.1
Other_sequence (20)
Associated_featureWBsf654536
WBsf654537
WBsf1007676
WBsf238157
Experimental_infoRNAi_resultWBRNAi00011810Inferred_automaticallyRNAi_primary
WBRNAi00042249Inferred_automaticallyRNAi_primary
WBRNAi00029703Inferred_automaticallyRNAi_primary
WBRNAi00066391Inferred_automaticallyRNAi_primary
WBRNAi00102758Inferred_automaticallyRNAi_primary
Expr_patternExpr1010409
Expr1146240
Expr1200297
Expr2009198
Expr2027436
Drives_constructWBCnstr00037769
Construct_productWBCnstr00037769
Microarray_results (19)
Expression_cluster (112)
InteractionWBInteraction000149612
WBInteraction000239096
WBInteraction000304002
WBInteraction000518503
Map_infoMapXPosition14.0194Error0.038412
PositivePositive_cloneC40C9Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5297
Pseudo_map_position
Reference (15)
RemarkMap position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.CGC_data_submission
MethodGene