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WormBase Tree Display for Gene: WBGene00001823

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Name Class

WBGene00001823EvidenceAccession_evidenceEMBLAY052772
CGC_data_submission
SMapS_parentSequenceZC395
IdentityVersion1
NameCGC_namehap-1Person_evidenceWBPerson247
Sequence_nameZC395.7
Molecular_nameZC395.7
ZC395.7.1
CE25662
Other_nameCELE_ZC395.7Accession_evidenceNDBBX284603
Public_namehap-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:25WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhap
Allele (15)
RNASeq_FPKM (74)
GO_annotation (20)
Contained_in_operonCEOP3272
Ortholog (33)
Structured_descriptionAutomated_descriptionPredicted to enable nucleoside triphosphate diphosphatase activity. Predicted to be involved in nucleoside triphosphate catabolic process. Predicted to be located in cytoplasm. Human ortholog(s) of this gene implicated in several diseases, including developmental and epileptic encephalopathy 35; hepatitis C; and rheumatoid arthritis. Is an ortholog of human ITPA (inosine triphosphatase).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:7148Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6176)
DOID:1588Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6176)
DOID:9952Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6176)
DOID:1883Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6176)
DOID:0080458Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6176)
DOID:2355Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6176)
DOID:583Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6176)
Molecular_infoCorresponding_CDSZC395.7
Corresponding_transcriptZC395.7.1
Other_sequence (57)
Associated_featureWBsf224897
WBsf224898
Experimental_infoRNAi_resultWBRNAi00041881Inferred_automaticallyRNAi_primary
WBRNAi00006650Inferred_automaticallyRNAi_primary
WBRNAi00041883Inferred_automaticallyRNAi_primary
WBRNAi00058878Inferred_automaticallyRNAi_primary
WBRNAi00005819Inferred_automaticallyRNAi_primary
WBRNAi00041880Inferred_automaticallyRNAi_primary
WBRNAi00005774Inferred_automaticallyRNAi_primary
WBRNAi00038036Inferred_automaticallyRNAi_primary
Expr_patternExpr1019344
Expr1031070
Expr1162313
Expr2012367
Expr2030603
Drives_constructWBCnstr00036666
Construct_productWBCnstr00036666
Microarray_results (19)
Expression_cluster (63)
Interaction (44)
Map_infoMapIIIPosition-1.85254Error0.000658
PositivePositive_cloneZC395Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
Remarkham-1 was once wrongly associated with hap-1 [030311 ck1]
Map 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