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WormBase Tree Display for Gene: WBGene00000879

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Name Class

WBGene00000879SMapS_parentSequenceY75B12B
IdentityVersion2
NameCGC_namecyn-3Person_evidenceWBPerson466
Sequence_nameY75B12B.5
Molecular_nameY75B12B.5
Y75B12B.5.1
CE20374
Other_namecyp-3Person_evidenceWBPerson466
CELE_Y75B12B.5Accession_evidenceNDBBX284605
Public_namecyn-3
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:21WBPerson1971EventImportedInitial conversion from geneace
220 Sep 2004 16:20:03WBPerson1971Name_changeCGC_namecyp-3 -> cyn-3
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcyn
Allele (28)
Legacy_information[C.elegansII] NMK. Cyclophilin family, transspliced to SL1. YAC Y15F7. [TP]
RNASeq_FPKM (74)
GO_annotation (15)
Contained_in_operonCEOP5521
Ortholog (54)
Paralog (18)
Structured_descriptionConcise_descriptioncyn-3 encodes an abundantly expressed cyclophilin A isoform with peptidyl-prolyl isomerase activity in vitro, which closely resembles the prototypical CypA and is thus likely to be a member of the cytosolic CsA-binding cyclophilin subfamily; cyn-3 is exclusively expressed in the single anterior excretory cell, and is dispensable for viability and gross morphology in mass RNAi screens.Paper_evidenceWBPaper00002472
WBPaper00003820
WBPaper00005654
WBPaper00026884
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated20 Mar 2007 00:00:00
Automated_descriptionEnables peptidyl-prolyl cis-trans isomerase activity. Predicted to be involved in protein folding. Located in obsolete cell. Expressed in excretory system. Human ortholog(s) of this gene implicated in several diseases, including Bell's palsy; aggressive periodontitis; and gastrointestinal system cancer (multiple). Is an ortholog of human PPIA (peptidylprolyl isomerase A); PPIAL4C (peptidylprolyl isomerase A like 4C); and PPIF (peptidylprolyl isomerase F).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:4947Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9253)
DOID:9261Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9253)
DOID:1474Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9253)
DOID:526Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9253)
DOID:12506Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9253)
Molecular_infoCorresponding_CDSY75B12B.5
Corresponding_transcriptY75B12B.5.1
Other_sequenceU31077
HSC01591_1
MC04529
MJC03416_1
ES410560.1
AM743421.1
RS07649
GRC00341_1
NB07599
GO252597.1
RSC02810_1
BF599212.1
BXC00733_1
MJ00021
AS03056
SS00170
Dviv_isotig16822
JI625639.1
EX014303.1
AS02793
AYC00194_2
JI463044.1
HCC00822_3
MJC00401_1
EG025472.1
MA01922
EH005629.1
PT02146
PE00078
ES412014.1
JI239671.1
CBC14468_1
HBC04166_1
AW600038.1
HC00013
HS00290
AI363650.1
FG581023.1
SRC05997_1
ACC28445_1
FE910012.1
GR11923
AI130079.1
BMC02578_1
Name_isotig06234
Dviv_isotig16823
EX911673.1
MCC02593_1
EX561321.1
OVC01099_1
PEC00274_1
HG03434
TS01412
MIC09181_1
BU086576.1
JI257349.1
AAC00250_1
Tcir_isotig13512
JI219938.1
HC00039
HCC00822_2
BQ804066.1
TS03678
CBC05026_1
MH02853
MJC03416_2
ES410604.1
HBC16162_1
TDC02902_1
BF064305.1
EX007830.1
GR367571.1
BG310637.1
ASC04448_1
JI212713.1
MH06323
JI221507.1
GT737483.1
MC04676
JI475500.1
HG03202
GR17216
FE910742.1
AIC00120_1
FE918756.1
HGC06301_1
CRC06479_1
BI773129.1
DN557765.1
EX013978.1
MHC00281_1
ES741831.1
EX010379.1
EX910926.1
ASC17437_1
GR17581
U47812.1
Tcir_isotig07131
BMC04073_1
EX008115.1
JI483999.1
BI772921.1
FE915542.1
JK315350.1
CBC00147_1
JI225260.1
EX556301.1
Hbac_isotig00273
JI466355.1
GW408822.1
PPC03295_1
GPC00018_1
HG11884
MJ00669
PPC03363_1
MHC11560_1
JK315949.1
DAC00185_1
JI211694.1
JI257347.1
PP01013
Hbac_isotig02984
HCC00822_1
NB06582
GR17215
PT01563
GW413506.1
EH005161.1
MI01736
FE912735.1
AS01408
CR08988
MIC01281_2
MC04727
OF00831
BI773560.1
GR18152
BF599155.1
OOC03051_1
ES411893.1
U47813.1
EX912229.1
MP01502
NBC03598_1
MH11001
CR00411
EH005296.1
NB07160
PVC02246_1
CBC04860_1
HGC00913_1
DA00260
FC817860.1
JI217581.1
GRC00236_1
MC01137
MJ00094
EL888729.1
AE01335
EL888086.1
NBC00066_1
HG02046
PPC12528_1
GO251056.1
GW411427.1
JK314763.1
JI213541.1
LSC00823_1
HBC20577_1
Hbac_isotig00272
MIC01281_1
PSC02695_2
MI02417
HGC01931_1
EV852614.1
Tcol_isotig06027
OVC07850_1
FE910242.1
BE720997.1
FE919815.1
MI02067
GO253156.1
GR11873
HC02233
BMC00215_1
MHC07362_1
MCC04717_1
GP01773
EX563076.1
Acan_isotig16664
MI04337
DN191151.1
NAC01344_1
JO472858.1
DVC03169_1
FC812482.1
ACC14614_1
MAC01248_1
Name_isotig02508
ES412760.1
ASC00145_1
JI166556.1
Associated_feature (7)
Experimental_infoRNAi_resultWBRNAi00076847Inferred_automaticallyRNAi_primary
WBRNAi00021430Inferred_automaticallyRNAi_primary
WBRNAi00058423Inferred_automaticallyRNAi_primary
WBRNAi00027819Inferred_automaticallyRNAi_primary
Expr_patternExpr984
Expr985
Expr1018223
Expr1030544
Expr1161844
Expr2010671
Expr2028911
Drives_constructWBCnstr00013833
WBCnstr00037227
Construct_productWBCnstr00013833
WBCnstr00037227
Microarray_results (23)
Expression_cluster (127)
Interaction (105)
Map_infoMapVPosition7.54862Error0.006411
PositivePositive_cloneY15F7Author_evidencePage AM
Y75B12BInferred_automaticallyFrom sequence, transcript, pseudogene data
ZK526
Pseudo_map_position
ReferenceWBPaper00002472
WBPaper00003820
WBPaper00018604
WBPaper00026884
WBPaper00032230
WBPaper00038491
WBPaper00041771
WBPaper00049828
WBPaper00055090
Remark[Page AM] Is transpliced by SL-1. Isolated from mixed stage cDNA by A. P. Page using SL1, and known 3' seq from CEESH95F. (not mapped); Genbank U31077.
[JAH]Partial sequence identity 64% to human CYP gene, 66% to yeast CSBY.
CEESH95F,CEMSB85F,CEMSB85FB,CEMSB85R removed from sequence list and replaced by genomic_canonical Y75B12B.5. sdm 11/00
PPIase or cyclophilin, EC 5.2.1.8
This gene has been renamed with approval of the CGC (cyp-3->cyn-3)Person_evidenceWBPerson466
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