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WormBase Tree Display for Gene: WBGene00003963

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Name Class

WBGene00003963SMapS_parentSequenceC07A12
IdentityVersion1
NameCGC_namepdi-2Person_evidenceWBPerson466
Sequence_nameC07A12.4
Molecular_nameC07A12.4
C07A12.4.1
CE03972
C07A12.4.2
Other_nameCELE_C07A12.4Accession_evidenceNDBBX284606
Public_namepdi-2
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:33WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpdi
Allele (51)
StrainWBStrain00002794
WBStrain00034929
WBStrain00034930
WBStrain00036011
WBStrain00036126
RNASeq_FPKM (74)
GO_annotation (24)
Ortholog (40)
Paralog (13)
Structured_descriptionConcise_descriptionpdi-2 encodes a protein disulfide isomerase beta subunit; by homology, PDI-2 is predicted to function in oxidative protein folding in the endoplasmic reticulum (ER); PDI-2 activity is required for several organismal processes including body morphology, locomotion, fertility, molting, and collagen deposition; pdi-2 transcript levels are increased in response to ER stress; pdi-2 is expressed in the hypodermis which secretes the collagen-based cuticle.Paper_evidenceWBPaper00005422
WBPaper00005432
WBPaper00030802
Curator_confirmedWBPerson1843
Date_last_updated07 Apr 2011 00:00:00
Automated_descriptionEnables protein disulfide isomerase activity and protein-glutamine gamma-glutamyltransferase activity. Contributes to peptidyl-proline 4-dioxygenase activity. Involved in macromolecule modification and obsolete oxidation-reduction process. Located in endoplasmic reticulum. Part of procollagen-proline 4-dioxygenase complex. Expressed in several structures, including germ line and hypodermis. Human ortholog(s) of this gene implicated in Cole-Carpenter syndrome. Is an ortholog of human P4HB (prolyl 4-hydroxylase subunit beta).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:0060438Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8548)
Molecular_infoCorresponding_CDSC07A12.4
Corresponding_CDS_historyC07A12.4b:wp172
C07A12.4b:wp271
C07A12.4c:wp271
Corresponding_transcriptC07A12.4.1
C07A12.4.2
Other_sequence (458)
Associated_feature (19)
Experimental_infoRNAi_result (22)
Expr_patternChronogram1612
Expr1930
Expr1933
Expr4051
Expr1022503
Expr1031887
Expr1144042
Expr2014806
Expr2033040
Drives_constructWBCnstr00001638
WBCnstr00003321
WBCnstr00006664
WBCnstr00010526
WBCnstr00014417
WBCnstr00035770
Construct_productWBCnstr00035770
AntibodyWBAntibody00000540
Microarray_results (38)
Expression_cluster (292)
Interaction (251)
WBProcessWBbiopr:00000124
Map_infoMapXPosition-7.35044Error0.00847
PositivePositive_cloneC07A12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4692
Pseudo_map_position
Reference (40)
RemarkSequence connections from Darin St. Louis [020930 ck1]
Map 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