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WormBase Tree Display for Gene: WBGene00020375

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Name Class

WBGene00020375SMapS_parentSequenceCHROMOSOME_I
IdentityVersion2
NameCGC_namepigv-1Person_evidenceWBPerson7529
Sequence_nameT09B4.1
Molecular_nameT09B4.1
T09B4.1.1
CE13457
Other_namemal-3Person_evidenceWBPerson247
CELE_T09B4.1Accession_evidenceNDBBX284601
Public_namepigv-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:03WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
211 Nov 2013 09:38:46WBPerson2970EventAcquires_mergeWBGene00003127
Name_changeCGC_namepigv-1
Other_namemal-3
Acquires_mergeWBGene00003127
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpigv
Allele (34)
Legacy_information[Hekimi S] Maternal-effect morphologically abnormal. head frequently deformed because buccal opening displaced ventrally, dorsally or laterally; some embryonic lethality, very high larval lethality; full zygotic and maternal rescue. NA1. [MQ]
[C.elegansII] qm34 : head frequently deformed because buccal opening displaced ventrally, dorsally or laterally; some embryonic lethality, very high larval lethality; full zygotic and maternal rescue. NA1. [MQ]
StrainWBStrain00026656
WBStrain00049378
RNASeq_FPKM (74)
GO_annotation (14)
Contained_in_operonCEOP1308
Ortholog (35)
Structured_descriptionAutomated_descriptionPredicted to enable mannosyltransferase activity. Predicted to be involved in GPI anchor biosynthetic process. Predicted to be located in endoplasmic reticulum membrane. Predicted to be part of mannosyltransferase complex. Expressed in excretory cell; hypodermis; intestine; pharynx; and rectal epithelium. Human ortholog(s) of this gene implicated in hyperphosphatasia with impaired intellectual development syndrome 1. Is an ortholog of human PIGV (phosphatidylinositol glycan anchor biosynthesis class V).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:0070433Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:26031)
Molecular_infoCorresponding_CDST09B4.1
Corresponding_transcriptT09B4.1.1
Other_sequenceCR01703
Oden_isotig20668
CRC00418_1
Associated_featureWBsf643341
WBsf976718
WBsf976719
WBsf976720
WBsf983859
WBsf217765
WBsf217766
Experimental_infoRNAi_result (17)
Expr_patternExpr12350
Expr1022823
Expr1038878
Expr1156530
Expr2014925
Expr2033160
Drives_constructWBCnstr00020800
WBCnstr00025182
Construct_productWBCnstr00020800
WBCnstr00025182
Microarray_results (22)
Expression_cluster (153)
Interaction (268)
Map_infoPositivePositive_cloneT09B4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point7064
Multi_point3410
3411
Interpolated_map_positionI0.876894
ReferenceWBPaper00002340
WBPaper00021822
WBPaper00038491
WBPaper00045573
WBPaper00046712
WBPaper00055090
WBPaper00064339
MethodGene