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WormBase Tree Display for Gene: WBGene00001972

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Name Class

WBGene00001972SMapS_parentSequenceF47D12
IdentityVersion1
NameCGC_namehmg-1.2
Sequence_nameF47D12.4
Molecular_name (9)
Other_nameson-1CGC_data_submission
CELE_F47D12.4Accession_evidenceNDBBX284603
Public_namehmg-1.2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhmg
Allele (28)
StrainWBStrain00001623
WBStrain00030872
WBStrain00030873
WBStrain00030879
WBStrain00036586
RNASeq_FPKM (74)
GO_annotation (14)
Ortholog (61)
ParalogWBGene00001973Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001974Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00008081Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00012209Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00022182Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionEnables transcription cis-regulatory region binding activity. Involved in several processes, including gonad development; positive regulation of transcription by RNA polymerase II; and vulval development. Located in nucleus. Expressed in several structures, including tail. Human ortholog(s) of this gene implicated in several diseases, including Kawasaki disease; cerebral infarction; and syndromic microphthalmia 13. Is an ortholog of human HMGB3 (high mobility group box 3).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:6000Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4983)
DOID:332Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4983)
DOID:0111811Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5004)
DOID:3526Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4983)
DOID:13378Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4983)
DOID:418Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4983)
Molecular_infoCorresponding_CDSF47D12.4a
F47D12.4b
F47D12.4c
Corresponding_transcriptF47D12.4a.1
F47D12.4b.1
F47D12.4c.1
Other_sequence (117)
Associated_feature (13)
Transcription_factorWBTranscriptionFactor000385
Experimental_infoRNAi_result (45)
Expr_pattern (12)
Drives_constructWBCnstr00002462
WBCnstr00002481
WBCnstr00003263
WBCnstr00012419
WBCnstr00015261
WBCnstr00017071
WBCnstr00019876
WBCnstr00036551
Construct_productWBCnstr00012419
WBCnstr00019997
WBCnstr00019999
WBCnstr00036551
Microarray_results (34)
Expression_cluster (166)
Interaction (312)
WBProcessWBbiopr:00000071
WBbiopr:00000072
Map_infoMapIIIPosition-1.40577Error0.000741
PositivePositive_cloneF47D12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4334
4407
Pseudo_map_position
ReferenceWBPaper00003453
WBPaper00027309
WBPaper00030511
WBPaper00032575
WBPaper00032967
WBPaper00033954
WBPaper00034515
WBPaper00036514
WBPaper00038491
WBPaper00041799
WBPaper00045125
WBPaper00055090
WBPaper00061708
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