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WormBase Tree Display for Gene: WBGene00001976

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Name Class

WBGene00001976SMapS_parentSequenceT05A7
IdentityVersion1
NameCGC_namehmg-11
Sequence_nameT05A7.4
Molecular_nameT05A7.4
T05A7.4.1
CE04890
Other_namehmg-I-alphaAccession_evidenceEMBLAF056578
CELE_T05A7.4Accession_evidenceNDBBX284602
Public_namehmg-11
DB_infoDatabaseAceViewgene2E963
WormQTLgeneWBGene00001976
SignaLinkproteinWBGene00001976
WormFluxgeneWBGene00001976
NDBlocus_tagCELE_T05A7.4
NCBIgene173805
RefSeqproteinNM_062424.10
TrEMBLUniProtAccG5EEL9
UniProt_GCRPUniProtAccG5EEL9
OMIMgene600698
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhmg
Allele (11)
StrainWBStrain00001708
WBStrain00031938
RNASeq_FPKM (74)
GO_annotation00109826
OrthologWBGene00108498Pristionchus pacificusFrom_analysisOMA
Inparanoid_8
WBGene00067525Caenorhabditis remaneiFrom_analysisOMA
WBGene00154464Caenorhabditis brenneriFrom_analysisOMA
chrII_pilon.g4289Caenorhabditis elegansFrom_analysisWormBase-Compara
HGNC:5009Homo sapiensFrom_analysisOMA
PhylomeDB
Structured_descriptionAutomated_descriptionPredicted to enable DNA binding activity. Expressed in head. Human ortholog(s) of this gene implicated in several diseases, including Silver-Russell syndrome; leiomyoma; and ovarian cancer. Is an ortholog of human HMGA2 (high mobility group AT-hook 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:127Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5009)
DOID:14681Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5009)
DOID:3315Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5009)
DOID:2394Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5009)
Molecular_infoCorresponding_CDST05A7.4
Corresponding_transcriptT05A7.4.1
Other_sequenceCRC00496_1
CR02174
CRC10991_1
CBC00660_1
Associated_feature (14)
Transcription_factorWBTranscriptionFactor000399
Experimental_infoRNAi_resultWBRNAi00035171Inferred_automaticallyRNAi_primary
WBRNAi00052448Inferred_automaticallyRNAi_primary
WBRNAi00018185Inferred_automaticallyRNAi_primary
WBRNAi00090567Inferred_automaticallyRNAi_primary
WBRNAi00107340Inferred_automaticallyRNAi_primary
Expr_patternChronogram1768
Expr6611
Expr10332
Expr10333
Expr1018682
Expr1031146
Expr1156070
Expr1200182
Expr2012517
Expr2030756
Drives_constructWBCnstr00002532
WBCnstr00015262
WBCnstr00036547
Construct_productWBCnstr00018593
WBCnstr00036547
Microarray_results (21)
Expression_cluster (276)
Interaction (98)
Map_infoMapIIPosition-3.6808Error0.011991
PositivePositive_cloneT05A7Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4996
Pseudo_map_position
ReferenceWBPaper00027309
WBPaper00035567
WBPaper00040135
WBPaper00055090
WBPaper00064064
WBPaper00064315
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