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WormBase Tree Display for Gene: WBGene00004219

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Name Class

WBGene00004219EvidenceCGC_data_submission
SMapS_parentSequenceC45B2
IdentityVersion1
NameCGC_nameptr-4Person_evidenceWBPerson349
Sequence_nameC45B2.7
Molecular_nameC45B2.7
C45B2.7.1
CE30905
Other_nameCELE_C45B2.7Accession_evidenceNDBBX284606
Public_nameptr-4
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:34WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classptr
Allele (74)
StrainWBStrain00036331
RNASeq_FPKM (74)
GO_annotation00089867
00089868
00089869
00089870
00089871
00089872
00089873
00089874
00112509
Ortholog (31)
Paralog (30)
Structured_descriptionConcise_descriptionptr-4 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-4 isstrongly required for normal molting from L4 to adult stages male taildevelopment (a role conserved in C. briggsae); PTR-4 is also requiredfor normal endocytosis of yolk by oocytes, adult alae formation, growthto full size, locomotion, and viability.Paper_evidenceWBPaper00026763
WBPaper00026841
WBPaper00027263
WBPaper00027756
Curator_confirmedWBPerson567
Date_last_updated08 Nov 2006 00:00:00
Automated_descriptionInvolved in endocytosis and molting cycle. Acts upstream of or within nematode male tail mating organ morphogenesis. Predicted to be located in cytoplasmic vesicle membrane and plasma membrane. Expressed in cuticular ala; epithelial cell; hyp7 syncytium; rectum; and vulva. Human ortholog(s) of this gene implicated in autistic disorder. Is an ortholog of human PTCHD1 (patched domain containing 1) 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_CDSC45B2.7
Corresponding_transcriptC45B2.7.1
Other_sequence (19)
Associated_feature (17)
Experimental_infoRNAi_result (21)
Expr_patternExpr16290
Expr16291
Expr1025279
Expr1032075
Expr1146509
Expr2015171
Expr2033409
Drives_constructWBCnstr00035629
WBCnstr00042884
Construct_productWBCnstr00035629
Microarray_results (24)
Expression_cluster (296)
Interaction (148)
Map_infoMapXPosition-3.78247Error0.008974
PositivePositive_cloneC45B2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5639
4344
4562
Pseudo_map_position
Reference (16)
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