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WormBase Tree Display for Gene: WBGene00006763

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Name Class

WBGene00006763SMapS_parentSequenceCHROMOSOME_IV
IdentityVersion1
NameCGC_nameunc-26Person_evidenceWBPerson261
Sequence_nameJC8.10
Molecular_name (12)
Other_nameunc-48
CELE_JC8.10Accession_evidenceNDBBX284604
Public_nameunc-26
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:42WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classunc
Reference_alleleWBVar00143035
Allele (250)
Legacy_informatione205 : severe kinker small scrawny flaccid little movement; slow pharyngeal pumping. ES3 ME0 NA9 (e176 e345 (pka unc-48) etc.
See unc-26.
See also ad473, ad701, ad706, e205, e2340, n1307, s1710
[C.elegansII] e205amb : severe kinker, small, scrawny, flaccid little movement; slow pharyngeal pumping; Ric. ES3 ME0 OA>10: e176, e345 (pka unc-48), e314 (strong Exp, weak Unc, Eat), e2340, m2, n1307, s1710mut, ad473, ad701, etc. Some (5/18) alleles have expulsion defect in defecation. Gene is recombinationally large. [Charest et al. 1990; Avery 1993; DA; EG; JT; RM]
Strain (14)
RNASeq_FPKM (74)
GO_annotation00012000
00012001
00012002
00012003
00012004
00012005
00012006
00012007
00012008
00012009
00012010
00012011
00012012
00012013
00012014
00012015
00012016
00012017
00012018
00012019
00012020
00012021
00012022
00012023
00012024
00012025
00012026
00012027
00012028
00012029
00012030
00012031
00012032
00012033
00114769
00114770
Contained_in_operonCEOP4539
Ortholog (43)
ParalogWBGene00012016Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00086546Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00007620Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00007912Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00009264Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00012353Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionunc-26 encodes synaptojanin, a polyphosphoinositide phosphatase orthologous to human synaptojanin 1 (OMIM:604297, 309000, which when mutated leads to Lowe oculocerebrorenal syndrome); UNC-26 is required for normal locomotion, pharyngeal pumping, and defecation, and specifically, appears to function in multiple steps of synaptic vesicle recycling; UNC-26 may also play a role in cytoskeletal organization.Paper_evidenceWBPaper00004275
WBPaper00004637
Curator_confirmedWBPerson1843
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable phosphatidylinositol-3,5-bisphosphate 5-phosphatase activity and phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity. Involved in several processes, including cellular component organization; nitrogen compound transport; and regulation of locomotion. Located in synapse. Expressed in tail and ventral cord neurons. Used to study Down syndrome and early-onset Parkinson's disease. Human ortholog(s) of this gene implicated in Parkinson's disease 20 and developmental and epileptic encephalopathy 53. Is an ortholog of human SYNJ1 (synaptojanin 1).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:14250Homo sapiensPaper_evidenceWBPaper00053600
Curator_confirmedWBPerson324
Date_last_updated05 Mar 2018 00:00:00
DOID:0060894Homo sapiensPaper_evidenceWBPaper00062416
WBPaper00062681
Curator_confirmedWBPerson324
Date_last_updated09 Jun 2022 00:00:00
Potential_modelDOID:0080464Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11503)
DOID:14330Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11503)
DOID:0060898Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11503)
Modifies_diseaseDOID:10652
Models_disease_in_annotationWBDOannot00001244
Modifies_disease_in_annotationWBDOannot00000724
Models_disease_assertedWBDOannot00000491
WBDOannot00001221
Molecular_infoCorresponding_CDSJC8.10a
JC8.10b
JC8.10c
JC8.10d
Corresponding_CDS_historyJC8.10:wp53
Corresponding_transcriptJC8.10a.1
JC8.10b.1
JC8.10c.1
JC8.10d.1
Other_sequence (36)
Associated_feature (11)
Experimental_infoRNAi_result (12)
Expr_pattern (12)
Drives_constructWBCnstr00001637
WBCnstr00002608
WBCnstr00002732
WBCnstr00004403
Construct_product (5)
AntibodyWBAntibody00002627
Microarray_results (35)
Expression_cluster (135)
Interaction (93)
Map_infoMapIVPosition8.51401Error0.001138
Well_ordered
PositiveInside_rearrsDf21
nDp5
Positive_cloneJC8Inferred_automaticallyFrom sequence, transcript, pseudogene data
NegativeOutside_rearrsDf22
Mapping_data2_point21
116
122
142
439
1636
7060
Multi_point (37)
Pos_neg_data976
983
3812
8180
832
4678
4685
4687
798
Landmark_gene
Reference (101)
MethodGene