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WormBase Tree Display for Gene: WBGene00017269

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Name Class

WBGene00017269SMapS_parentSequenceF08F8
IdentityVersion2
NameCGC_nameeco-1Person_evidenceWBPerson136
Sequence_nameF08F8.4
Molecular_nameF08F8.4
F08F8.4.1
CE27932
Other_nameCELE_F08F8.4Accession_evidenceNDBBX284603
Public_nameeco-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:58WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
229 Sep 2022 20:06:24WBPerson21950Name_changeCGC_nameeco-1
Other_nameCA
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classeco
Allele (14)
RNASeq_FPKM (74)
GO_annotation00063927
00063928
00063929
00063930
00063931
00063932
00063933
00063934
00063935
00063936
Contained_in_operonCEOP3428
Ortholog (38)
ParalogWBGene00014066Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00017696Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00018721Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable peptide-lysine-N-acetyltransferase activity. Predicted to be involved in mitotic sister chromatid cohesion. Predicted to be located in nucleus. Predicted to be part of chromatin. Human ortholog(s) of this gene implicated in Roberts syndrome; lung adenocarcinoma; and rheumatoid arthritis. Is an ortholog of human ESCO2 (establishment of sister chromatid cohesion N-acetyltransferase 2).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:27230)
DOID:5325Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:27230)
DOID:3910Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:27230)
DOID:1324Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:27230)
Molecular_infoCorresponding_CDSF08F8.4
Corresponding_transcriptF08F8.4.1
Other_sequenceCBC00674_1
Associated_featureWBsf651202
WBsf667069
WBsf667070
WBsf667071
WBsf981507
WBsf992995
WBsf1015227
WBsf226966
WBsf226967
Experimental_infoRNAi_resultWBRNAi00110492Inferred_automaticallyRNAi_primary
WBRNAi00044029Inferred_automaticallyRNAi_primary
WBRNAi00110511Inferred_automaticallyRNAi_primary
WBRNAi00110524Inferred_automaticallyRNAi_primary
Expr_patternExpr1027926
Expr1037419
Expr1147995
Expr2002300
Expr2020519
Drives_constructWBCnstr00027439
Construct_productWBCnstr00027439
Microarray_results (16)
Expression_cluster (123)
Interaction (35)
Map_infoMapIIIPosition-0.74893
PositivePositive_cloneF08F8Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
WBPaper00065070
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