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WormBase Tree Display for Gene: WBGene00010419

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Name Class

WBGene00010419SMapS_parentSequenceH28O16
IdentityVersion3
NameCGC_nameatp-1Person_evidenceWBPerson237
Sequence_nameH28O16.1
Molecular_nameH28O16.1a
H28O16.1a.1
CE18826
Other_namephi-37Person_evidenceWBPerson2582
CELE_H28O16.1Accession_evidenceNDBBX284601
Public_nameatp-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:51WBPerson1971EventImportedInitial conversion from CDS class of WS125
217 Mar 2005 13:54:35WBPerson2970Name_changeOther_namephi-37
301 Aug 2017 12:58:54WBPerson2970Name_changeCGC_nameatp-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classatp
Allele (62)
StrainWBStrain00003396
WBStrain00002785
WBStrain00003081
WBStrain00037556
RNASeq_FPKM (74)
GO_annotation (27)
Ortholog (37)
ParalogWBGene00000229Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00004959Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00006921Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00012040Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00013025Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionH28O16.1 encodes the C. elegans ortholog of the alpha subunit of mitochondrial ATP synthase.Curator_confirmedWBPerson1843
Date_last_updated09 Jul 2014 00:00:00
Automated_descriptionEnables enterobactin binding activity. Involved in iron import into cell. Located in mitochondrion. Expressed in tail. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 22; mitochondrial complex V (ATP synthase) deficiency nuclear type 4 (multiple); and vascular dementia. Is an ortholog of human ATP5F1A (ATP synthase F1 subunit alpha).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:0111498Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:823)
DOID:8725Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:823)
DOID:0070462Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:823)
DOID:0070461Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:823)
Molecular_infoCorresponding_CDSH28O16.1a
Corresponding_CDS_historyH28O16.1b:wp259
H28O16.1c:wp259
H28O16.1d:wp275
Corresponding_transcriptH28O16.1a.1
Other_sequenceBI773018.1
ES411439.1
ES740259.1
FG971493.1
FD516583.1
MIC04471_1
SC00133
FG976492.1
MH01528
FC545317.1
Tcir_isotig11390
FG971811.1
EX912333.1
FG977164.1
FG977916.1
FG976432.1
FG978965.1
CGC00976_1
EX011083.1
OVC00085_1
ACC02553_1
FG977713.1
FG977734.1
SRC00431_1
FG972323.1
FG980509.1
DI01661
CRC02324_1
BUC00178_1
GR18955
AE00673
HBC00080_1
CR11029
BI773190.1
FG971970.1
FK806675.1
ES409743.1
FG972423.1
EX562183.1
JI233521.1
FC809988.1
FC820297.1
MC00179
EX539672.1
TSC00140_1
BI773126.1
HGC02988_1
TSC03086_1
FK800702.1
FG979536.1
Dviv_isotig16050
FK803071.1
HSC01523_1
EX007397.1
AI132821.1
DVC02307_1
FG971963.1
FG974911.1
FD515068.1
FF680992.1
FG585942.1
FG977586.1
FG972206.1
HBC24432_1
FG979904.1
FF678423.1
EX014034.1
FC815355.1
FF680712.1
ES410362.1
SSC06186_1
CBC05203_1
ES744130.1
FG980199.1
FK799867.1
FG619314.1
ES741987.1
FF681326.1
BI772918.1
FF681382.1
EW741550.1
EX910540.1
FK802394.1
FC812171.1
FK805125.1
SSC06329_1
TS00405
FE911737.1
GR977754.1
FG979172.1
EV851142.1
GR979289.1
EX557415.1
FG971645.1
FG976877.1
FG980398.1
EX553168.1
BXC02966_1
GP00339
NBC08639_1
FG978327.1
FG980459.1
PT02913
GPC02829_1
FG976770.1
FG974492.1
FK801265.1
FF678076.1
HS01167
EX911061.1
MCC00383_1
FK801245.1
EX538373.1
EX010065.1
FG978772.1
GW409790.1
FC813965.1
FG971568.1
FG974958.1
FF681127.1
EX534990.1
EX912479.1
CGC01037_1
FE916020.1
ES414230.1
ACC09451_1
GW408584.1
FG976941.1
FC546012.1
BI773164.1
GR979105.1
GW411398.1
FF678755.1
FF681328.1
SRC00431_2
FG972789.1
FG972646.1
AS16590
BI772879.1
ES411786.1
ES739185.1
XI04847
FG970872.1
Tcol_isotig08665
FG981037.1
HC01664
CJC01019_1
MPC01140_1
EX543222.1
FG970688.1
FG979526.1
FG978318.1
FK800206.1
FG978111.1
CRC05787_1
SRC09227_1
OOC01780_1
FG979742.1
MAC00796_1
GPC01508_1
FK805005.1
FG979267.1
ACC01725_1
CBC03180_1
FG976919.1
FG979156.1
FC542343.1
FC820682.1
PPC01181_1
FG978012.1
FG977998.1
FG974315.1
FG980125.1
FK808003.1
FG976117.1
FG976095.1
CR09734
PSC00402_1
EX007490.1
FG977361.1
FC820138.1
FG978633.1
FG978980.1
GR19765
FG978425.1
FK805968.1
JO475376.1
FG976358.1
FE910037.1
FD516630.1
BE721007.1
FK807415.1
GP02368
FK804549.1
FG973001.1
WBC02431_1
EX544143.1
AE03866
FG976187.1
EX014017.1
GO253017.1
XIC03417_1
FF679005.1
FG974997.1
FG973578.1
EX536972.1
MA00436
FG980454.1
FK809946.1
FG971656.1
FG979899.1
EV853448.1
FK804645.1
FG972497.1
ASC19870_1
EX912273.1
EX560575.1
CBC12209_1
FK801552.1
EX551720.1
EL890524.1
ACC18252_1
GO252835.1
EX549050.1
FC548588.1
FF680989.1
ACC25748_1
FG973254.1
GE637990.1
FG975958.1
FG977337.1
GR11148
FF680742.1
JO467814.1
FE917578.1
EX014812.1
WBC01933_1
CR12422
FG972807.1
EX539506.1
HG03306
HBC05475_1
GRC03855_1
HBC03354_1
EX565351.1
FC809714.1
CD455375.1
FE913932.1
FG972736.1
FK806073.1
FG980608.1
CRC06721_1
AYC02400_1
Acan_isotig07646
FC545836.1
MCC03648_1
FD514720.1
GO240292.1
FG970690.1
EX536679.1
FG975535.1
FG972901.1
FK806034.1
FC816928.1
FG976809.1
AS09886
Name_isotig01769
EX008151.1
FC545776.1
FK800244.1
HG02308
FG980252.1
FC819923.1
Tcir_isotig27165
CBC02468_1
FG975853.1
EX547265.1
FG974991.1
OOC01806_1
PTC01868_1
FF680646.1
FG976383.1
ES408808.1
FD516007.1
TS04261
ASC00119_1
EX014002.1
HG11108
EX913757.1
EX551545.1
EX013615.1
FF681251.1
FG975329.1
PT03075
CK725646.1
FD517225.1
FF681205.1
EV851233.1
FG972179.1
FG970686.1
FG974556.1
GRC04161_1
PSC04456_1
HCC01801_1
FK805505.1
FC541716.1
FF678444.1
Tcol_isotig08666
XI02718
GP02946
FG975536.1
HBC00080_2
FF681063.1
FG975023.1
CJC15841_1
FG972474.1
AE03637
AYC02604_1
CK850588.1
FG975293.1
FG975474.1
CRC03092_1
FG978250.1
FG976376.1
ACC12849_1
HS00376
CRC00606_1
FC809993.1
FC814117.1
EX543813.1
FG976801.1
FF680879.1
FG978005.1
DVC01370_1
FF678489.1
FG974362.1
EX536432.1
GO250832.1
FG978443.1
FG976446.1
FC542229.1
FG972603.1
FK800001.1
WBC03050_1
FG979686.1
FG976561.1
FG975217.1
FG976179.1
EX537215.1
FK807155.1
FG975232.1
PVC03564_1
EX556369.1
FG975744.1
FG978375.1
EX545237.1
EX536799.1
FG979620.1
FG981142.1
GR978562.1
AE00187
FF681276.1
BM01226
PP02163
FF680722.1
HC00735
SSC02520_1
HC01887
HBC13729_1
FF680886.1
EX910719.1
FG976673.1
FC815766.1
HBC00140_1
ES411937.1
FG977862.1
FC554648.1
FG975099.1
FG974863.1
Acan_isotig13279
CBC14403_1
FK809770.1
SSC06188_1
JI223515.1
HBC00310_1
FG978172.1
EX007576.1
EX550544.1
HC01562
FG980902.1
FG971024.1
FG973745.1
FG980632.1
SR00416
FC810368.1
ACC06167_1
Hbac_isotig00118
CSC00155_1
FG974929.1
FF681299.1
HBC07136_1
Tcir_isotig06549
FK802044.1
FC554808.1
EV852923.1
AS02747
FG975492.1
GR367874.1
FG977684.1
BMC07869_1
FD516803.1
FG973494.1
FC814606.1
FK809144.1
FG980396.1
FG972176.1
SC00741
FC814253.1
EX910298.1
SR00961
DIC01332_1
MI05182
FG973899.1
OOC02603_1
RSC03518_1
FG971280.1
AS02786
FK809539.1
FG978732.1
FC546294.1
FG974973.1
CBC00814_1
FG971667.1
XI05508
FF681649.1
FD517694.1
HBC10802_1
AYC00128_1
FG978920.1
EX547439.1
CK855183.1
FG977704.1
FG976789.1
BI773182.1
FG974590.1
CJC02101_1
FG981010.1
FE919234.1
FG619692.1
BU086624.1
PT00179
FF681696.1
JI173221.1
FC541600.1
EX541289.1
EX010029.1
FG974167.1
HBC19124_1
RS07814
FG980480.1
FF681101.1
FG976523.1
FC817784.1
FG973616.1
FG978942.1
Acan_isotig09422
FG972296.1
WBC00286_1
EX910918.1
MA02205
FG979929.1
FG977970.1
FC815360.1
PP00884
HCC06882_1
MHC01822_1
FF678787.1
CR02866
FG977102.1
ACC20700_1
FG977051.1
FD516479.1
FK808523.1
FG977982.1
FG979101.1
EX012725.1
MP01250
FG980815.1
HBC17378_1
CD374324.1
Oden_isotig18571
FG977061.1
EX501590.1
HBC07170_1
FK802584.1
FG973807.1
EW742677.1
FG975203.1
NAC01365_1
FG979778.1
FG980119.1
EX915568.1
FK801641.1
FC815038.1
GR14457
FG980927.1
EX010176.1
FG979197.1
FG971853.1
FK800044.1
FG977806.1
FF681035.1
MC03224
CRC07756_1
EX555673.1
FG585947.1
FG972847.1
GU130146.1
FG981086.1
NB11080
Dviv_isotig16051
ES414130.1
FG972083.1
ES743358.1
FC542553.1
XIC05787_1
FF681539.1
FG970881.1
TSC12017_1
FG974500.1
BI772922.1
FG971630.1
EG025695.1
HSC00015_1
Associated_feature (13)
Experimental_infoRNAi_result (29)
Expr_pattern (12)
Drives_constructWBCnstr00003312
WBCnstr00004575
WBCnstr00031428
Construct_productWBCnstr00031428
Microarray_results (47)
Expression_cluster (183)
Interaction (263)
Map_infoMapIPosition13.879
PositivePositive_cloneH28O16Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (17)
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