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WormBase Tree Display for Gene: WBGene00004230

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Name Class

WBGene00004230EvidenceCGC_data_submission
SMapS_parentSequenceT21H3
IdentityVersion1
NameCGC_nameptr-16Person_evidenceWBPerson349
Sequence_nameT21H3.2
Molecular_nameT21H3.2a
T21H3.2a.1
CE50972
T21H3.2b
CE50961
T21H3.2b.1
Other_nameCELE_T21H3.2Accession_evidenceNDBBX284605
Public_nameptr-16
DB_infoDatabaseAceViewgene5B651
WormQTLgeneWBGene00004230
WormFluxgeneWBGene00004230
NDBlocus_tagCELE_T21H3.2
PanthergeneCAEEL|WormBase=WBGene00004230|UniProtKB=A0A0K3ASC2
familyPTHR10796
NCBIgene191750
RefSeqproteinNM_001313273.5
NM_001313272.3
TrEMBLUniProtAccA0A0K3AV55
A0A0K3ASC2
UniProt_GCRPUniProtAccA0A0K3ASC2
OMIMgene300828
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:34WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classptr
Allele (190)
StrainWBStrain00037812
RNASeq_FPKM (74)
GO_annotation00000969
00000970
00000971
00000972
00000973
00112522
Ortholog (40)
Paralog (30)
Structured_descriptionConcise_descriptionptr-16 encodes a nematode-specific member of the sterol sensing domain(SSD) proteins, distantly paralogous to Drosophila PATCHED (PTC) andhuman PTCH (OMIM:601309, mutated in basal cell nevus syndrome); PTR-16is partially required for normal molting from L2 to L3 larval stages;however, PTR-16 and PTR-1 together are strongly required for bothmolting and viability, with double ptr-1/-16 RNAi animals showingpronounced molting defects and lethality; PTR-16 is also required fornormal growth to full size and locomotion.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); PTCHD3 (patched domain containing 3 (gene/pseudogene)); and PTCHD4 (patched domain containing 4).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_CDST21H3.2a
T21H3.2b
Corresponding_CDS_historyT21H3.2:wp231
T21H3.2:wp249
Corresponding_transcriptT21H3.2a.1
T21H3.2b.1
Other_sequence (13)
Associated_featureWBsf661120
WBsf999266
WBsf231394
WBsf231395
WBsf231396
Experimental_infoRNAi_resultWBRNAi00018989Inferred_automaticallyRNAi_primary
WBRNAi00076924Inferred_automaticallyRNAi_primary
WBRNAi00053762Inferred_automaticallyRNAi_primary
WBRNAi00076956Inferred_automaticallyRNAi_primary
WBRNAi00077029Inferred_automaticallyRNAi_primary
Expr_patternExpr1014389
Expr1032082
Expr1157312
Expr2015159
Expr2033397
Microarray_results (14)
Expression_cluster (192)
Interaction (219)
Map_infoMapVPosition-19.8499Error0.000282
PositivePositive_cloneT21H3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00004265
WBPaper00024393
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