Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Gene: WBGene00002258

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00002258SMapS_parentSequenceW02D3
IdentityVersion1
NameCGC_namelbp-6Person_evidenceWBPerson492
Sequence_nameW02D3.5
Molecular_nameW02D3.5
W02D3.5.1
CE14426
Other_nameCELE_W02D3.5Accession_evidenceNDBBX284601
Public_namelbp-6
DB_infoDatabaseAceViewgene1H304
WormQTLgeneWBGene00002258
WormFluxgeneWBGene00002258
NDBlocus_tagCELE_W02D3.5
PanthergeneCAEEL|WormBase=WBGene00002258|UniProtKB=O01812
familyPTHR11955
NCBIgene172390
RefSeqproteinNM_059525.7
SwissProtUniProtAccO01812
UniProt_GCRPUniProtAccO01812
OMIMgene170715
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:27WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classlbp
Allele (17)
StrainWBStrain00037907
RNASeq_FPKM (74)
GO_annotation00025784
00025785
00025786
00025787
00025788
00025789
00110323
Ortholog (56)
ParalogWBGene00002255Caenorhabditis elegansFrom_analysisTreeFam
WBGene00002257Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00002259Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00002260Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00021486Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable fatty acid binding activity. Predicted to be involved in fatty acid transport. Predicted to be located in cytosol and nucleus. Human ortholog(s) of this gene implicated in several diseases, including Alzheimer's disease; Charcot-Marie-Tooth disease type 1G; Down syndrome; and artery disease (multiple). Is an ortholog of several human genes including FABP3 (fatty acid binding protein 3); FABP4 (fatty acid binding protein 4); and FABP7 (fatty acid binding protein 7).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:10652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3557)
DOID:9352Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3557)
DOID:14250Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3557)
DOID:5844Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3557)
DOID:10591Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3559)
DOID:10763Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3557)
DOID:3068Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3562)
DOID:0111560Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9117)
DOID:9970Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3557)
Molecular_infoCorresponding_CDSW02D3.5
Corresponding_transcriptW02D3.5.1
Other_sequencePT03837
MP02031
EX913109.1
MI08761
MP01487
EX011441.1
ES410454.1
EX013456.1
CJC09261_1
MI07724
MI08067
HC04756
CR04687
MI01946
MI07749
MH10453
ES742125.1
EX009705.1
ES412658.1
ES744047.1
EX012348.1
ES744603.1
ES742228.1
EX008598.1
EX009627.1
ES410012.1
HCC06137_1
EX008775.1
ES411835.1
AYC00210_1
EX010413.1
ES411214.1
ES411861.1
ES741129.1
BUC01588_1
EX911548.1
EX910192.1
ES409929.1
ES739355.1
Name_isotig03427
MI08073
ES743182.1
Tcol_isotig01348
ES412761.1
MJ00020
EX013824.1
EX009593.1
EX012469.1
EX912995.1
PT01129
EX913863.1
CN477943.1
MH10433
Acan_isotig15008
MI08466
ES743604.1
EX914571.1
EX012523.1
ES739310.1
CBC03569_1
MI08064
ES743874.1
HBC13210_1
ES740682.1
ES741440.1
ES410380.1
EX012464.1
ES743799.1
ES409610.1
EX910003.1
MI09111
ES742090.1
ES410276.1
CN477953.1
BXC02872_1
Tcol_isotig01344
PTC00456_1
ES412520.1
MP02038
HBC00254_1
EX913481.1
EX911560.1
MH10659
ES409460.1
MPC01585_1
ES411465.1
EX916383.1
BUC00448_1
EX013144.1
ES409186.1
EX916040.1
MJ00018
ES411168.1
EX910098.1
MP02205
EX911766.1
MIC08203_1
EX008301.1
EX910348.1
EX008908.1
MH10627
Hbac_isotig07114
CBC09798_1
EX914965.1
MH10647
AE01634
EX011164.1
MI07961
EX013545.1
EX008187.1
ES410247.1
MPC00564_1
EX013138.1
EX010639.1
EX915916.1
EX009597.1
EX911363.1
EX914339.1
EX012136.1
EX913188.1
EX914011.1
ES413639.1
EX009957.1
EX910099.1
EX007639.1
EX910172.1
MJC00377_1
EX914799.1
MIC07318_1
MP02153
EX006991.1
EX007388.1
MH10672
EX010697.1
MI08389
EX914978.1
ES741326.1
DVC01444_1
EX911181.1
EX013371.1
CRC04256_1
EX914426.1
ES740255.1
ES744150.1
MP02048
MIC06994_1
EX914441.1
EX914886.1
EX013321.1
ES413303.1
ES411469.1
HC07837
MI07907
EX911486.1
EX009777.1
EX910244.1
ES740315.1
MH10434
MH10658
MH10646
ES743397.1
ES411876.1
MP01875
HC09585
EX915391.1
MH10628
MH10673
Tcol_isotig01346
EX912304.1
MI08396
MI07865
EX910059.1
HBC17387_1
MI08735
ES409357.1
Dviv_isotig12196
ES740720.1
MI08759
MIC05335_1
EX011452.1
ES740181.1
EX013597.1
AM743667.1
EX915229.1
MIC06811_1
Oden_isotig17772
ES410018.1
EX912679.1
CN478206.1
EX012298.1
EX010772.1
EX912776.1
MJ01203
EX911330.1
AE01527
ES412353.1
ES743100.1
MPC00411_1
MI08790
Dviv_isotig12195
MP00671
HBC05176_1
MP01489
Tcol_isotig01351
CN477980.1
EV852197.1
EX915439.1
ES739182.1
MP01462
EX012870.1
EX913381.1
EX009853.1
MI07723
ES409757.1
EX009197.1
MI01923
MI08677
Hbac_isotig06132
ES741377.1
ACC02606_1
EX916103.1
ES412647.1
ES743607.1
ES740964.1
Oden_isotig18060
EX010391.1
EX007718.1
CJC01267_1
EX914369.1
EX013479.1
EX015098.1
ES741183.1
MH10644
FK802022.1
EX012077.1
EX011749.1
EX914035.1
EX012107.1
EX008077.1
EX911477.1
ES742564.1
Dviv_isotig12197
Tcol_isotig01343
ES409981.1
MP01410
EX914782.1
ES744494.1
MI08451
MH10454
EX913552.1
ES741907.1
MP01553
EX012816.1
ES413160.1
EX012057.1
CN477668.1
ES740440.1
ES739762.1
EX915440.1
HBC02765_1
EX008453.1
CN478178.1
CN478328.1
EX011929.1
HBC00018_1
HC01927
EX012596.1
ES741098.1
MP01418
Oden_isotig18061
MH10645
PTC03424_1
EX911132.1
ES743300.1
EX010218.1
MI08736
EX911488.1
Associated_featureWBsf649253
WBsf981032
WBsf219624
WBsf219625
Experimental_infoRNAi_result (20)
Expr_patternExpr1015324
Expr1031330
Expr1158134
Expr2013023
Expr2031255
Drives_constructWBCnstr00036353
Construct_productWBCnstr00036353
Microarray_results (18)
Expression_cluster (233)
Interaction (75)
Map_infoMapIPosition1.3Error0.00019
PositivePositive_cloneW02D3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (15)
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