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WormBase Tree Display for Gene: WBGene00000565

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Name Class

WBGene00000565EvidenceAccession_evidenceEMBLAJ132698
AJ132699
SMapS_parentSequenceY17G7B
IdentityVersion2
NameCGC_namecnt-1
Sequence_nameY17G7B.15
Molecular_name (12)
Other_namecnt-1AAccession_evidenceEMBLAJ132698
cnt-1BAccession_evidenceEMBLAJ132699
cps-2Paper_evidenceWBPaper00045987
CELE_Y17G7B.15Accession_evidenceNDBBX284602
Public_namecnt-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:21WBPerson1971EventImportedInitial conversion from geneace
210 Dec 2014 10:20:36WBPerson2970Name_changeOther_namecps-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcnt
Allele (598)
RNASeq_FPKM (74)
GO_annotation (33)
Ortholog (48)
ParalogWBGene00000566Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00008805Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00010500Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00012359Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00017217Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00017760Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptioncnt-1 encodes a homolog of centaurin beta, an Arf GTPase activating protein (Arf GAP) that also contains a pleckstrin homology domain and C-terminal ankyrin repeats; by homology, CNT-1 is predicted to function as an Arf GAP that stimulates Arf GTPase activity and links cell signaling with cytoskeletal rearrangements and membrane trafficking; however, as loss of cnt-1 activity via large-scale RNAi screens does not result in any obvious abnormalities, the precise role of cnt-1 in C. elegans development and/or behavior is not yet known; cnt-1 is broadly expressed, being detected in the pharynx, excretory cell, spermatheca, distal tip cells of the gonad, neurons of the head and nerve ring, and anal epithelial cells; CNT-1 is able to bind the phosphoinositides PIP2 and PIP3 and upon production of PIP3, can translocate from the cytoplasm to the membrane.Paper_evidenceWBPaper00005654
WBPaper00005655
WBPaper00011327
WBPaper00011676
WBPaper00023203
Curator_confirmedWBPerson1843
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionEnables phosphatidylinositol phosphate binding activity and small GTPase binding activity. Involved in apoptotic process; negative regulation of 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate biosynthetic process; and positive regulation of endosome to plasma membrane protein transport. Located in basolateral plasma membrane; cytoplasmic side of apical plasma membrane; and endosome membrane. Used to study cancer. Is an ortholog of human ACAP1 (ArfGAP with coiled-coil, ankyrin repeat and PH domains 1); ACAP2 (ArfGAP with coiled-coil, ankyrin repeat and PH domains 2); and ACAP3 (ArfGAP with coiled-coil, ankyrin repeat and PH domains 3).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:162Homo sapiensPaper_evidenceWBPaper00046697
Curator_confirmedWBPerson324
Date_last_updated15 Jul 2015 00:00:00
Models_disease_in_annotationWBDOannot00000354
Molecular_infoCorresponding_CDSY17G7B.15a
Y17G7B.15b
Y17G7B.15c
Y17G7B.15d
Corresponding_transcriptY17G7B.15a.1
Y17G7B.15b.1
Y17G7B.15c.1
Y17G7B.15d.1
Other_sequence (38)
Associated_featureWBsf666223
WBsf666224
WBsf666225
WBsf990002
WBsf990003
WBsf990004
WBsf1013383
WBsf224030
Experimental_infoRNAi_result (17)
Expr_patternExpr10541
Expr12067
Expr1023574
Expr1030341
Expr1159079
Expr2010284
Expr2028526
Drives_constructWBCnstr00015750
Construct_productWBCnstr00014846
WBCnstr00014847
WBCnstr00015750
AntibodyWBAntibody00002574
Microarray_results (30)
Expression_cluster (87)
Interaction (28)
Map_infoMapIIPosition6.45814Error0.096169
PositivePositive_cloneY17G7BInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (16)
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