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WormBase Tree Display for Gene: WBGene00009192

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Name Class

WBGene00009192SMapS_parentSequenceF27E5
IdentityVersion2
NameCGC_nameasah-2Person_evidenceWBPerson237
Sequence_nameF27E5.1
Molecular_nameF27E5.1
F27E5.1.1
CE01562
Other_nameCELE_F27E5.1Accession_evidenceNDBBX284602
Public_nameasah-2
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:49WBPerson1971EventImportedInitial conversion from CDS class of WS125
225 Oct 2016 11:59:12WBPerson2970Name_changeCGC_nameasah-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classasah
AlleleWBVar00091850Inferred_automaticallyFrom strain object: RB782
WBVar00228210
WBVar00228211
WBVar01499702
WBVar00760639
WBVar00760640
WBVar00760641
WBVar00760642
WBVar00760643
WBVar00760644
WBVar00760645
WBVar01498435
WBVar00760646
WBVar00760647
WBVar00760648
WBVar00760649
WBVar00760650
WBVar00760651
WBVar01310654
WBVar00760652
WBVar00375521
WBVar00375522
WBVar00375523
WBVar00375524
WBVar00375525
WBVar00261531
WBVar00552413
WBVar01394028
WBVar00249644
WBVar01498940
StrainWBStrain00031495
RNASeq_FPKM (74)
GO_annotation00051990
00051991
00051992
00051993
00051994
00051995
00111734
00111735
00111736
Ortholog (35)
ParalogWBGene00010769Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00021917Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable N-acylsphingosine amidohydrolase activity. Predicted to be involved in fatty acid metabolic process and sphingolipid metabolic process. Predicted to be located in lysosome. Human ortholog(s) of this gene implicated in Farber lipogranulomatosis; sphingolipidosis; and spinal muscular atrophy with progressive myoclonic epilepsy. Is an ortholog of human ASAH1 (N-acylsphingosine amidohydrolase 1).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS292 version of WormBase
Date_last_updated24 Apr 2024 00:00:00
Disease_infoPotential_modelDOID:0111527Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:735)
DOID:1927Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:735)
DOID:0050464Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:735)
Molecular_infoCorresponding_CDSF27E5.1
Corresponding_transcriptF27E5.1.1
Other_sequence (13)
Associated_featureWBsf221969
WBsf221970
WBsf221971
Experimental_infoRNAi_resultWBRNAi00045755Inferred_automaticallyRNAi_primary
WBRNAi00031502Inferred_automaticallyRNAi_primary
Expr_patternExpr1875
Expr1876
Expr1010559
Expr1149664
Expr2009442
Expr2027679
Drives_constructWBCnstr00032384
Construct_productWBCnstr00032384
AntibodyWBAntibody00000505
Microarray_results (19)
Expression_cluster (248)
Interaction (164)
Map_infoMapIIPosition1.97775
PositivePositive_cloneF27E5Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00032243
WBPaper00038491
WBPaper00042257
WBPaper00055090
WBPaper00062863
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