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WormBase Tree Display for Gene: WBGene00005013

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Name Class

WBGene00005013SMapS_parentSequenceF43G6
IdentityVersion2
NameCGC_namejmjd-1.1Person_evidenceWBPerson260
Sequence_nameF43G6.6
Molecular_nameF43G6.6
F43G6.6.1
CE20788
Other_nameCELE_F43G6.6Accession_evidenceNDBBX284602
Public_namejmjd-1.1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:37WBPerson1971EventImportedInitial conversion from geneace
230 Sep 2011 16:40:15WBPerson2970Name_changeCGC_namejmjd-1.1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classjmjd
Allele (87)
StrainWBStrain00000428
RNASeq_FPKM (74)
GO_annotation00067953
00067954
00067955
00067956
00067957
00067958
00067959
00067960
Contained_in_operonCEOP2758
Ortholog (43)
ParalogWBGene00017920Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00020821Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionjmjd-1.1 encodes a PHD and JmjC domain-containing protein that is a member of a family of proteins containing members, such as jmjd-1.2 and human PHF8, with histone demethylase activity.Paper_evidenceWBPaper00036110
Curator_confirmedWBPerson1843
Date_last_updated08 Apr 2010 00:00:00
Automated_descriptionPredicted to enable histone demethylase activity and transcription coregulator activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. Human ortholog(s) of this gene implicated in melanoma; prostate cancer; and syndromic X-linked intellectual disability Siderius type. Is an ortholog of human KDM7A (lysine demethylase 7A).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:10283Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20672)
DOID:1909Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:22224)
DOID:0060812Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20672)
Molecular_infoCorresponding_CDSF43G6.6
Corresponding_transcriptF43G6.6.1
Associated_featureWBsf989910
WBsf222201
Experimental_infoRNAi_resultWBRNAi00014891Inferred_automaticallyRNAi_primary
WBRNAi00112536Inferred_automaticallyRNAi_primary
WBRNAi00047212Inferred_automaticallyRNAi_primary
WBRNAi00091483Inferred_automaticallyRNAi_primary
WBRNAi00113489Inferred_automaticallyRNAi_primary
Expr_patternExpr1027915
Expr1151071
Microarray_results (18)
Expression_cluster (125)
InteractionWBInteraction000240534
WBInteraction000391002
WBInteraction000410988
WBInteraction000419752
WBInteraction000455929
WBInteraction000521427
WBInteraction000521429
WBInteraction000527426
Map_infoMapIIPosition4.05094Error0.002474
PositivePositive_cloneF43G6Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (11)
RemarkThis gene was previously incorrectly identified as spt-1 based on an unintended error in the CGC strain data filesCurator_confirmedWBPerson1971
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