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WormBase Tree Display for Gene: WBGene00003153

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Name Class

WBGene00003153SMapS_parentSequenceY67D8C
IdentityVersion2
NameCGC_namemca-3
Sequence_nameY67D8C.10
Molecular_name (21)
Other_namecup-7Person_evidenceWBPerson170
CELE_Y67D8C.10Accession_evidenceNDBBX284604
Public_namemca-3
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:30WBPerson1971EventAcquires_mergeWBGene00000847
ImportedInitial conversion from geneace
209 Oct 2007 09:36:44WBPerson2970Name_changeOther_namecup-7
Acquires_mergeWBGene00000847
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmca
Allele (491)
Legacy_information[Kraev A] mca for Membrane Calcium ATPase. No mutants known. See mca-1.
StrainWBStrain00032351
WBStrain00008044
WBStrain00008045
WBStrain00007591
RNASeq_FPKM (74)
GO_annotation (30)
Ortholog (55)
Paralog (14)
Structured_descriptionConcise_descriptionmca-3 encodes one of three C. elegans plasma membrane Ca2+ ATPases (PMCAs); by homology, MCA-3 is predicted to function as a molecular pump that couples ATP hydrolysis to extrusion of cytosolic Ca2+; mca-3 activity is required for coelomoycte endocytosis, normal coordinated locomotion, and embryonic and larval development; in regulating endocytosis, MCA-3 is required specifically in the early stages for recruitment of the endocytic machinery to the plasma membrane; an mca-3::gfp reporter is expressed from embryogenesis through adulthood and seen in body wall muscle, the nervous system, intestine, and coelomocytes; in coelomocytes, an MCA-3::GFP fusion protein localizes to the plasma membrane.Paper_evidenceWBPaper00003407
WBPaper00004883
WBPaper00029172
Curator_confirmedWBPerson1843
Date_last_updated30 Apr 2007 00:00:00
Automated_descriptionPredicted to enable P-type calcium transporter activity. Involved in several processes, including negative regulation of cytosolic calcium ion concentration; nematode larval development; and positive regulation of growth rate. Located in plasma membrane. Expressed in body wall musculature; coelomocyte; intestine; nervous system; and touch receptor neurons. Human ortholog(s) of this gene implicated in X-linked spinocerebellar ataxia 1; autosomal dominant intellectual developmental disorder; and nonsyndromic deafness (multiple). Is an ortholog of several human genes including ATP2B1 (ATPase plasma membrane Ca2+ transporting 1); ATP2B2 (ATPase plasma membrane Ca2+ transporting 2); and ATP2B3 (ATPase plasma membrane Ca2+ transporting 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_infoPotential_modelDOID:0060307Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:814)
DOID:0111829Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:816)
DOID:0050564Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:815)
DOID:0110467Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:815)
DOID:11714Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:814,HGNC:815,HGNC:816,HGNC:817)
DOID:10591Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:814,HGNC:815,HGNC:816,HGNC:817)
Molecular_infoCorresponding_CDSY67D8C.10a
Y67D8C.10b
Y67D8C.10c
Y67D8C.10d
Y67D8C.10e
Corresponding_transcript (11)
Other_sequenceJI473155.1
HG08854
HBC14109_1
JI217849.1
FC818452.1
EX913385.1
Acan_isotig22866
MP01944
DA01827
JI164299.1
MH03971
Hbac_isotig00308
BMC08443_1
JI216233.1
CRC01896_1
EX911904.1
Acan_isotig13499
Tcol_isotig25351
JI171148.1
TX01577
HGC04117_1
JI469235.1
MH07094
GR12861
Oden_isotig18568
MH08164
WBC01001_1
BM00603
MA00042
FK801572.1
DAC00006_1
GT571174.1
FG619345.1
MHC10596_1
FC544342.1
MH08942
Hbac_isotig00309
ASC03148_1
GRC01921_1
Oden_isotig21785
CRC04369_1
DI01076
FE907666.1
SR01716
HG05110
GPC02525_1
CBC02831_1
FD515346.1
OF00086
FK804146.1
PSC02290_1
FF678473.1
Dviv_isotig33485
MHC06487_1
AS17732
JI173624.1
MJ00772
CRC04995_1
TM03525
JI483656.1
Dviv_isotig28437
MHC12309_1
JO468808.1
GP02339
MJ03615
GW410509.1
AS16467
ACC25580_1
EX911378.1
CD455739.1
OFC00015_1
FK806146.1
Dviv_isotig33250
SS00976
AS18029
CR05631
SS03313
HBC00464_1
AS09988
GP01842
SRC00540_1
GW411884.1
GP01108
CR06354
GPC01652_1
Acan_isotig08768
BM01518
Dviv_isotig07870
GW915714.1
CV200704.1
MAC00230_1
JO468478.1
FG977858.1
AE02829
SSC04094_1
BMC06835_1
SR01572
GT570804.1
CR00659
EX911134.1
JI474575.1
JI464414.1
SS02107
TMC05117_1
AE01992
DW718478.1
BE238932.1
Acan_isotig17614
BXC01975_1
FC545549.1
JI462209.1
GP03224
EL889437.1
FK804659.1
JI474832.1
AYC01140_1
Dviv_contig17507
FC815351.1
CD455450.1
SSC05731_1
Tcol_isotig17317
CSC02141_1
SRC03646_1
PT04740
DA01826
Associated_feature (33)
Experimental_infoRNAi_resultWBRNAi00103077Inferred_automaticallyRNAi_primary
WBRNAi00009413Inferred_automaticallyRNAi_primary
WBRNAi00110940Inferred_automaticallyRNAi_primary
WBRNAi00057995Inferred_automaticallyRNAi_primary
WBRNAi00026914Inferred_automaticallyRNAi_primary
WBRNAi00103078Inferred_automaticallyRNAi_primary
WBRNAi00103079Inferred_automaticallyRNAi_primary
WBRNAi00066558Inferred_automaticallyRNAi_primary
WBRNAi00021260Inferred_automaticallyRNAi_primary
Expr_pattern (8)
Drives_constructWBCnstr00008391
Construct_productWBCnstr00000243
WBCnstr00000246
WBCnstr00000247
Microarray_results (52)
Expression_cluster (158)
Interaction (38)
Map_infoMapIVPosition-5.83327Error0.101838
PositivePositive_cloneY67D8
Y67D8CInferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point3954
Reference (11)
MethodGene