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WormBase Tree Display for Gene: WBGene00016643

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Name Class

WBGene00016643SMapS_parentSequenceC44C1
IdentityVersion2
NameCGC_namevps-45Person_evidenceWBPerson426
Sequence_nameC44C1.4
Molecular_nameC44C1.4
C44C1.4.1
CE04214
Other_nameCELE_C44C1.4Accession_evidenceNDBBX284606
Public_namevps-45
DB_infoDatabaseAceViewgeneXB590
WormQTLgeneWBGene00016643
WormFluxgeneWBGene00016643
NDBlocus_tagCELE_C44C1.4
PanthergeneCAEEL|WormBase=WBGene00016643|UniProtKB=H2KYN0
familyPTHR11679
NCBIgene180449
RefSeqproteinNM_171622.6
TrEMBLUniProtAccH2KYN0
UniProt_GCRPUniProtAccH2KYN0
OMIMgene610035
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:57WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
217 Mar 2006 15:11:54WBPerson2970Name_changeCGC_namevps-45
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classvps
Allele (53)
StrainWBStrain00001664
WBStrain00007582
RNASeq_FPKM (74)
GO_annotation (12)
Ortholog (36)
ParalogWBGene00006757Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00009654Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00015130Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00020298Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00016960Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionInvolved in pinocytosis and receptor-mediated endocytosis. Predicted to be located in Golgi membrane. Expressed in several structures, including coelomocyte; head; hypodermis; intestine; and muscle cell. Human ortholog(s) of this gene implicated in severe congenital neutropenia 5. Is an ortholog of human VPS45 (vacuolar protein sorting 45 homolog).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_infoExperimental_modelDOID:0112132Homo sapiensPaper_evidenceWBPaper00066193
Curator_confirmedWBPerson324
Date_last_updated20 Nov 2023 00:00:00
Potential_modelDOID:0112132Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14579)
Models_disease_assertedWBDOannot00001370
Molecular_infoCorresponding_CDSC44C1.4
Corresponding_CDS_historyC44C1.4b:wp271
Corresponding_transcriptC44C1.4.1
Other_sequence (62)
Associated_featureWBsf653678
WBsf1003908
WBsf1022193
WBsf236984
Experimental_infoRNAi_result (12)
Expr_patternChronogram1749
Expr177
Expr4768
Expr5498
Expr1019066
Expr1037156
Expr1146433
Expr2018031
Expr2036168
Drives_constructWBCnstr00002503
WBCnstr00012230
WBCnstr00027918
Construct_productWBCnstr00004752
WBCnstr00012230
WBCnstr00020072
WBCnstr00022652
WBCnstr00027918
Microarray_results (27)
Expression_cluster (80)
Interaction (346)
Map_infoMapXPosition-18.8773Error0.001578
PositivePositive_cloneC44C1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (13)
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