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: WBGene00022394

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00022394SMapS_parentSequenceY97E10AL
IdentityVersion2
NameCGC_namenatb-1Paper_evidenceWBPaper00050461
Person_evidenceWBPerson113
Sequence_nameY97E10AL.3
Molecular_nameY97E10AL.3
Y97E10AL.3.1
CE25639
Other_nameY97E10AL.aCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
CELE_Y97E10AL.3Accession_evidenceNDBBX284605
Public_namenatb-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:05WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
216 Feb 2017 15:37:28WBPerson2970Name_changeCGC_namenatb-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnatb
Allele (12)
StrainWBStrain00051114
RNASeq_FPKM (74)
GO_annotation00093946
00093947
00093948
00093949
00093950
00130420
Ortholog (36)
ParalogWBGene00000923Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00015074Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00018238Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00018831Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable peptide alpha-N-acetyltransferase activity. Predicted to be involved in regulation of actin cytoskeleton organization. Predicted to be part of NatB complex. Human ortholog(s) of this gene implicated in autosomal recessive intellectual developmental disorder 73. Is an ortholog of human NAA20 (N-alpha-acetyltransferase 20, NatB catalytic subunit).Paper_evidenceWBPaper00065943
WBPaper00067038
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS296 version of WormBase
Date_last_updated20 Mar 2025 00:00:00
Disease_infoPotential_modelDOID:0081233Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15908)
Molecular_infoCorresponding_CDSY97E10AL.3
Corresponding_transcriptY97E10AL.3.1
Other_sequence (46)
Associated_featureWBsf1000557
WBsf1019969
WBsf234012
Experimental_infoRNAi_resultWBRNAi00037927Inferred_automaticallyRNAi_primary
WBRNAi00058676Inferred_automaticallyRNAi_primary
WBRNAi00061951Inferred_automaticallyRNAi_primary
WBRNAi00013928Inferred_automaticallyRNAi_primary
Expr_patternExpr1012760
Expr1039887
Expr1162096
Expr2013895
Expr2032135
Drives_constructWBCnstr00024258
Construct_productWBCnstr00024258
Microarray_results (17)
Expression_cluster (128)
Interaction (44)
Map_infoMapVPosition0.999335
PositivePositive_cloneY97E10ALInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
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