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WormBase Tree Display for Gene: WBGene00000050

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Name Class

WBGene00000050SMapS_parentSequenceD2092
IdentityVersion1
NameCGC_nameacr-11Person_evidenceWBPerson1430
Sequence_nameD2092.3
Molecular_nameD2092.3
D2092.3.1
CE09102
Other_nameCELE_D2092.3Accession_evidenceNDBBX284601
Public_nameacr-11
DB_infoDatabaseAceViewgene1H198
WormQTLgeneWBGene00000050
WormFluxgeneWBGene00000050
NDBlocus_tagCELE_D2092.3
PanthergeneCAEEL|WormBase=WBGene00000050|UniProtKB=P91197
familyPTHR18945
NCBIgene191599
RefSeqproteinNM_059505.2
TrEMBLUniProtAccP91197
UniProt_GCRPUniProtAccP91197
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:19WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classacr
Allele (45)
StrainWBStrain00031963
RNASeq_FPKM (74)
GO_annotation (32)
Ortholog (45)
Paralog (100)
Structured_descriptionConcise_descriptionA homolog of an alpha type nicotinic acetylcholine receptor subunit involved in the mediation of fast synaptic transmission at neuromuscular junctions.Paper_evidenceWBPaper00005223
Curator_confirmedWBPerson324
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable acetylcholine receptor activity; excitatory extracellular ligand-gated monoatomic ion channel activity; and transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential. Involved in chemical synaptic transmission. 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_CDSD2092.3
Corresponding_transcriptD2092.3.1
Other_sequenceJI482048.1
JO468908.1
Acan_isotig17242
JI177628.1
JI182272.1
Associated_featureWBsf649250
WBsf219611
Experimental_infoRNAi_resultWBRNAi00043516Inferred_automaticallyRNAi_primary
WBRNAi00102757Inferred_automaticallyRNAi_primary
WBRNAi00113432Inferred_automaticallyRNAi_primary
WBRNAi00003293Inferred_automaticallyRNAi_primary
WBRNAi00066390Inferred_automaticallyRNAi_primary
Expr_patternExpr1023679
Expr1147510
Expr2009179
Expr2027418
Drives_constructWBCnstr00037768
Construct_productWBCnstr00037768
Microarray_results (18)
Expression_cluster (62)
InteractionWBInteraction000163500
WBInteraction000211264
WBInteraction000232397
WBInteraction000387314
WBInteraction000392230
WBInteraction000411228
WBInteraction000441842
WBInteraction000457445
Map_infoMapIPosition1.25616Error0.003426
PositivePositive_cloneD2092Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4955
Pseudo_map_position
Reference (17)
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