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WormBase Tree Display for Gene: WBGene00004507

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Name Class

WBGene00004507EvidenceCGC_data_submission
SMapS_parentSequenceC18H9
IdentityVersion1
NameCGC_namerpy-1Person_evidenceWBPerson360
Sequence_nameC18H9.7
Molecular_nameC18H9.7
C18H9.7.1
CE51338
C18H9.7.2
Other_namerap-1Person_evidenceWBPerson451
WBPerson360
CELE_C18H9.7Accession_evidenceNDBBX284602
Public_namerpy-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:35WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classrpy
Allele (56)
Legacy_information[Nonet ML] rap for RAPsyn family. Predicted gene C18H9.7
[C.elegansII] NMK. Encodes ras-related protein. [MH]
StrainWBStrain00001487
WBStrain00001386
WBStrain00029059
RNASeq_FPKM (74)
GO_annotation (13)
Ortholog (38)
ParalogWBGene00000092Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00021247Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionrpy-1 is orthologous to the human gene 43KDA ACETYLCHOLINE RECEPTOR-ASSOCIATED PROTEIN (RAPSN; OMIM:601592), which when mutated leads to congenital myasthenic syndrome.Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable acetylcholine receptor binding activity. Predicted to be involved in cholinergic synaptic transmission and positive regulation of neuromuscular synaptic transmission. Predicted to be located in neuromuscular junction and plasma membrane. Expressed in neurons. Human ortholog(s) of this gene implicated in congenital myasthenic syndrome 11 and fetal akinesia deformation sequence syndrome 2. Is an ortholog of human RAPSN (receptor associated protein of the synapse).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:0111378Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9863)
DOID:0110675Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9863)
Molecular_infoCorresponding_CDSC18H9.7
Corresponding_CDS_historyC18H9.7:wp252
Corresponding_transcriptC18H9.7.1
C18H9.7.2
Other_sequenceJI168699.1
OOC01460_1
MJC01218_1
Acan_isotig22916
Oden_isotig20580
MJ00259
MIC05093_1
JI480958.1
Dviv_isotig35264
BUC00303_1
Associated_featureWBsf717691
WBsf988231
WBsf988232
WBsf1012413
WBsf1012414
WBsf223224
Experimental_infoRNAi_resultWBRNAi00113498Inferred_automaticallyRNAi_primary
WBRNAi00094738Inferred_automaticallyRNAi_primary
WBRNAi00011043Inferred_automaticallyRNAi_primary
WBRNAi00040996Inferred_automaticallyRNAi_primary
WBRNAi00084235Inferred_automaticallyRNAi_primary
WBRNAi00029104Inferred_automaticallyRNAi_primary
WBRNAi00076154Inferred_automaticallyRNAi_primary
WBRNAi00023059Inferred_automaticallyRNAi_primary
WBRNAi00117640Inferred_automaticallyRNAi_primary
Expr_pattern (11)
Drives_constructWBCnstr00002277
WBCnstr00004285
WBCnstr00012279
WBCnstr00013178
WBCnstr00017032
WBCnstr00035436
Construct_productWBCnstr00035436
Microarray_results (18)
Expression_cluster (171)
Interaction (93)
Map_infoMapIIPosition-0.027018Error0.008772
PositivePositive_cloneC18H9Person_evidenceWBPerson451
Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4643
Pseudo_map_position
Reference (27)
Remark[Han M] ras-related protein. Very similar to mammalian rap1A (Krev).
This other_name rap-1 is not the same as the CGC main name rap-1 (C27B7.8)CGC_data_submission
Map 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