Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Gene: WBGene00004993

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00004993EvidenceAuthor_evidencePatthy L
Hodgkin JA
SMapS_parentSequenceC28C12
IdentityVersion1
NameCGC_namespp-8
Sequence_nameC28C12.5
Molecular_nameC28C12.5
C28C12.5.1
CE04112
Other_nameCELE_C28C12.5Accession_evidenceNDBBX284604
Public_namespp-8
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:37WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classspp
Allele (26)
Possibly_affected_byWBVar02153248
StrainWBStrain00037700
RNASeq_FPKM (74)
Ortholog (33)
ParalogWBGene00004992Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00004998Caenorhabditis elegansFrom_analysisPanther
WBGene00005000Caenorhabditis elegansFrom_analysisPanther
WBGene00004995Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionEnriched in OLL; PVD; hermaphrodite distal tip cell; intestine; and male distal tip cell based on SAGE; microarray; tiling array; RNA-seq; and single-cell RNA-seq studies. Is affected by several genes including daf-16; daf-2; and skn-1 based on microarray and RNA-seq studies. Is affected by twenty-two chemicals including 1-methylnicotinamide; mianserin; and D-glucose based on RNA-seq and microarray studies. Human ortholog(s) of this gene implicated in atypical Gaucher's disease due to saposin c deficiency; combined saposin deficiency; and late onset Parkinson's disease. Human PSAP enables several functions, including ganglioside binding activity; protein homodimerization activity; and scaffold protein binding activity. Is predicted to encode a protein with the following domains: Saposin B type, region 2; Saposin B type domain; Saposin-like type B, region 2; and Saposin-like. Is an ortholog of human PSAP (prosaposin).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:0110961Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9498)
DOID:0060892Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9498)
DOID:0111330Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9498)
Molecular_infoCorresponding_CDSC28C12.5
Corresponding_transcriptC28C12.5.1
Other_sequenceCBC05108_1
CJC00917_1
CRC05139_1
CJC05336_1
CR01091
FD515225.1
CBC04916_1
CSC01755_1
Associated_featureWBsf997227
WBsf997228
WBsf997229
WBsf1017851
WBsf228685
WBsf228686
Experimental_infoRNAi_resultWBRNAi00011294Inferred_automaticallyRNAi_primary
WBRNAi00029296Inferred_automaticallyRNAi_primary
WBRNAi00041402Inferred_automaticallyRNAi_primary
WBRNAi00075912Inferred_automaticallyRNAi_primary
Expr_patternExpr15193
Expr1014155
Expr1032484
Expr1145433
Expr2016086
Expr2034322
Microarray_results (17)
Expression_cluster (253)
Interaction (53)
Map_info (3)
ReferenceWBPaper00024209
WBPaper00038491
WBPaper00041771
WBPaper00055090
WBPaper00060006
WBPaper00065331
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