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WormBase Tree Display for Gene: WBGene00006768

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Name Class

WBGene00006768SMapS_parentSequenceZK637
IdentityVersion1
NameCGC_nameunc-32Person_evidenceWBPerson261
Sequence_nameZK637.8
Molecular_name (18)
Other_nameCELE_ZK637.8Accession_evidenceNDBBX284603
Public_nameunc-32
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:42WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classunc
Reference_alleleWBVar00143023
AlleleWBVar00145310Inferred_automaticallyFrom strain object: FF275
WBVar01629165
WBVar01629166
WBVar01629167
WBVar01500260
WBVar01645735
WBVar01266750
WBVar01266752
WBVar01499774
WBVar00067090
WBVar00067095
WBVar00067100
WBVar00564479
WBVar00847436
WBVar00847437
WBVar00847438
WBVar00847439
WBVar00847440
WBVar00847441
WBVar00847442
WBVar00847443
WBVar00143023
WBVar00847444
WBVar00604032
WBVar00069683
WBVar00847445
WBVar00847446
WBVar00404284
WBVar00847447
WBVar00404285
WBVar00847448
WBVar00069688
WBVar00847449
WBVar00404286
WBVar00847450
WBVar00404287
WBVar00847451
WBVar00404288
WBVar00404289
WBVar00847452
WBVar00069693
WBVar00404290
WBVar00847453
WBVar00847454
WBVar00404291
WBVar00404292
WBVar00847455
WBVar00404293
WBVar00847456
WBVar00847457
WBVar00404294
WBVar00847458
WBVar00404295
WBVar00404296
WBVar00847459
WBVar00847460
WBVar00278278
WBVar00847461
WBVar01474203
WBVar00145307
WBVar00145308
WBVar00145313
WBVar01447307
WBVar01723064
WBVar01723065
WBVar01723067
WBVar01962931
WBVar01409065
WBVar01409066
WBVar01567090
WBVar01567091
Possibly_affected_byWBVar02157789
WBVar02157790
Legacy_informatione189 : severe coiler little movement in adult; moves well in L1 but coils in response to touch in L2 and later stages; rather small and thin; weakly Egl-c. ES3 ME0 NA1 (rare mutation).
[Thierry-Mieg]
See also eIs16, f120, f121, f123
[C.elegansII] e189 : severe coiler, little movement in adult; moves well in L1 but coils in response to touch in L2 and later stages; rather small and thin; weakly Egl-c; Ric. ES3 ME0. OA>5: f123 (lethal, f123/e189 coiler),f121 (lethal, f121/e189 almost WT), ut61, ut111(embryonic lethals, irregular shape). Most alleles lethal. Cloned: probably encodes protein with homology to glutathione reductase (ZK637.10); downstream gene in operon. [Brenner 1974; Nguyen et al. 1995; FF; JC]
Strain (305)
RNASeq_FPKM (74)
GO_annotation (28)
Contained_in_operonCEOP3556
Ortholog (59)
ParalogWBGene00043993Caenorhabditis elegansFrom_analysismodENCODE_Pseudogenes
WBGene00006916Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00006915Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006914Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionunc-32 encodes, by alternative splicing, six isoforms of an ortholog of subunit a of the membrane-bound (V0) domain of vacuolar proton-translocating ATPase (V-ATPase); UNC-32 is orthologous to human ATP6N1A (OMIM:192130), ATP6V0A2, ATP6V0A4 (OMIM:605239, mutated in distal renal tubular acidosis), and TCIRG1 (OMIM:604592, mutated in osteopetrosis); one UNC-32 isoform is essential for locomotion and normal synaptic vesicle morphology in motoneurons, is expressed solely in the nervous system, and is specifically mutated by unc-32(e189) or unc-32(f120); other UNC-32 isoforms are essential for embryonic and larval development; UNC-32 is expressed throughout the life cycle, strongly in the nervous system, but also in vulvae, spermathecal-uterine valves, intestine, and pharynx; UNC-32 is required for necrosis, since mutations of unc-32 suppress necrotic neurodegeneration and thapsigargin-induced cell death; in S. cerevisiae, different V0 a-subunits (Stv1p and Vph1p) direct the assembly of V-ATPases to different membranes and organelles, suggesting that the profusion of such subunits in C. elegans (co-orthologous VHA-5, VHA-6, VHA-7, and six UNC-32 isoforms) may have a similar function; alternative splicing of the unc-32 pre-mRNA is dependent on ASD-1 and FOX-1, and in neurons, is also dependent on UNC-75, which binds unc-32 intron 7a in vitro.Paper_evidenceWBPaper00004601
WBPaper00004842
WBPaper00025183
WBPaper00028773
WBPaper00028774
WBPaper00028775
WBPaper00042088
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated26 Mar 2013 00:00:00
Automated_descriptionPredicted to enable ATPase binding activity. Involved in several processes, including cholinergic synaptic transmission; defense response to Gram-positive bacterium; and positive regulation of neurotransmitter secretion. Part of vacuolar proton-transporting V-type ATPase complex. Expressed in several structures, including alimentary muscle; hermaphrodite gonad; neurons; somatic nervous system; and vulva. Human ortholog(s) of this gene implicated in several diseases, including autosomal recessive cutis laxa type IIA; autosomal recessive osteopetrosis 1; and developmental and epileptic encephalopathy 104. Is an ortholog of human ATP6V0A1 (ATPase H+ transporting V0 subunit a1).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:0070390Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:865)
DOID:0110942Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11647)
DOID:14219Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:866)
DOID:0112171Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18481)
EFO:MONDO:0015827Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:866)
DOID:0070134Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18481)
Molecular_infoCorresponding_CDSZK637.8a
ZK637.8b
ZK637.8c
ZK637.8d
ZK637.8e
ZK637.8f
Corresponding_CDS_historyZK637.8a:wp77
ZK637.8b:wp77
Corresponding_transcriptZK637.8a.1
ZK637.8b.1
ZK637.8c.1
ZK637.8d.1
ZK637.8e.1
ZK637.8f.1
Other_sequence (98)
Associated_feature (12)
Experimental_infoRNAi_result (28)
Expr_patternExpr21
Expr848
Expr849
Expr2405
Expr1026854
Expr1032841
Expr1163008
Expr2017865
Expr2036001
Drives_constructWBCnstr00000434
WBCnstr00006396
WBCnstr00010008
WBCnstr00010009
WBCnstr00010814
WBCnstr00013318
WBCnstr00017554
Construct_productWBCnstr00000434
WBCnstr00006396
WBCnstr00014414
WBCnstr00015831
WBCnstr00017091
WBCnstr00017553
WBCnstr00041445
Microarray_results (39)
Expression_cluster (124)
Interaction (84)
Map_infoMapIIIPosition0
Well_ordered
PositiveInside_rearrmnDp37
Positive_cloneA1D10
A1F1
T05B2
ZK637Inferred_automaticallyFrom sequence, transcript, pseudogene data
NegativeOutside_rearrtnDf2
Mapping_data2_point (34)
Multi_point (263)
Pos_neg_data806
3726
8637
8642
9451
Landmark_gene
Reference (150)
MethodGene