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WormBase Tree Display for Gene: WBGene00004231

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Name Class

WBGene00004231EvidenceCGC_data_submission
SMapS_parentSequenceY18D10A
IdentityVersion1
NameCGC_nameptr-17Person_evidenceWBPerson349
Sequence_nameY18D10A.7
Molecular_nameY18D10A.7
Y18D10A.7.1
CE53875
Other_nameCELE_Y18D10A.7Accession_evidenceNDBBX284601
Public_nameptr-17
DB_infoDatabaseAceViewgene1N433
WormQTLgeneWBGene00004231
WormFluxgeneWBGene00004231
NDBlocus_tagCELE_Y18D10A.7
PanthergeneCAEEL|WormBase=WBGene00004231|UniProtKB=Q5DTE5
familyPTHR10796
NCBIgene173150
RefSeqproteinNM_001377664.2
TrEMBLUniProtAccA0A5S9MNL4
UniProt_GCRPUniProtAccA0A5S9MNL4
OMIMgene300828
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:34WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classptr
Allele (156)
RNASeq_FPKM (74)
GO_annotation00004192
00004193
00004194
00004195
00004196
00112523
Ortholog (51)
Paralog (30)
Structured_descriptionConcise_descriptionptr-17 encodes a divergent ortholog of Drosophila and human PTCHD3,which defines one of seven paralogous families of sterol sensing domain(SSD) proteins; PTR-17 is required for normal adult alae formation.Paper_evidenceWBPaper00026841
WBPaper00027263
Curator_confirmedWBPerson567
Date_last_updated08 Nov 2006 00:00:00
Automated_descriptionPredicted to be involved in endocytosis and molting cycle. Predicted to be located in cytoplasmic vesicle membrane and plasma membrane. Human ortholog(s) of this gene implicated in autistic disorder. Is an ortholog of human PTCHD1 (patched domain containing 1).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:12849Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:26392)
Molecular_infoCorresponding_CDSY18D10A.7
Corresponding_CDS_historyY18D10A.7:wp104
Y18D10A.7:wp139
Y18D10A.7a:wp274
Y18D10A.7b:wp274
Y18D10A.7c:wp274
Corresponding_transcriptY18D10A.7.1
Other_sequenceAS15382
ASC17683_1
JI168139.1
Dviv_isotig30522
JI219817.1
ACC08186_1
FE909914.1
BMC06021_1
EX548935.1
Associated_featureWBsf985698
WBsf985699
WBsf985700
WBsf985701
WBsf985702
WBsf985703
WBsf1010972
WBsf1010973
WBsf1010974
WBsf1010975
Experimental_infoRNAi_resultWBRNAi00076925Inferred_automaticallyRNAi_primary
WBRNAi00076957Inferred_automaticallyRNAi_primary
WBRNAi00076968Inferred_automaticallyRNAi_primary
WBRNAi00055621Inferred_automaticallyRNAi_primary
WBRNAi00036699Inferred_automaticallyRNAi_primary
WBRNAi00004547Inferred_automaticallyRNAi_primary
Expr_patternExpr1017885
Expr1159131
Expr2015160
Expr2033398
Microarray_results (32)
Expression_cluster (152)
Interaction (23)
Map_infoMapIPosition14.1442Error0.002279
PositivePositive_cloneY18D10AInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00004265
WBPaper00026841
WBPaper00038491
WBPaper00055090
WBPaper00064105
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