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WormBase Tree Display for Gene: WBGene00007053

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Name Class

WBGene00007053SMapS_parentSequenceCHROMOSOME_I
IdentityVersion3
NameCGC_namechd-7Person_evidenceWBPerson232
Sequence_nameT04D1.4
Molecular_nameT04D1.4
T04D1.4.1
CE41928
Other_nametag-192Person_evidenceWBPerson201
scd-3
CELE_T04D1.4Accession_evidenceNDBBX284601
Public_namechd-7
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 13:09:06WBPerson1845EventCreated
205 Oct 2005 17:16:53WBPerson2970EventAcquires_mergeWBGene00020213
Name_changeSequence_nameT04D1.4
331 Mar 2011 08:58:20WBPerson2970Name_changeCGC_namechd-7
Acquires_mergeWBGene00020213
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classchd
Allele (148)
StrainWBStrain00035914
WBStrain00035970
RNASeq_FPKM (74)
GO_annotation (16)
Ortholog (48)
Paralog (19)
Structured_descriptionAutomated_descriptionPredicted to enable several functions, including ATP hydrolysis activity; ATP-dependent chromatin remodeler activity; and chromatin binding activity. Predicted to be involved in chromatin remodeling and regulation of gene expression. Predicted to be located in nucleus. Predicted to be part of chromatin. Used to study CHARGE syndrome. Human ortholog(s) of this gene implicated in CHARGE syndrome and hypogonadotropic hypogonadism 5 with or without anosmia. Is an ortholog of human CHD6 (chromodomain helicase DNA binding protein 6).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_infoExperimental_modelDOID:0050834Homo sapiensPaper_evidenceWBPaper00061343
WBPaper00063926
Curator_confirmedWBPerson324
Date_last_updated08 Jun 2022 00:00:00
Potential_modelEFO:0003756Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20153)
DOID:0050834Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20626)
DOID:0090084Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20626)
Models_disease_assertedWBDOannot00001073
WBDOannot00001074
WBDOannot00001075
WBDOannot00001076
WBDOannot00001241
Molecular_infoCorresponding_CDST04D1.4
Corresponding_CDS_historyT04D1.4:wp185
Corresponding_transcriptT04D1.4.1
Other_sequence (13)
Associated_feature (19)
Transcription_factorWBTranscriptionFactor000910
Experimental_infoRNAi_resultWBRNAi00116566Inferred_automaticallyRNAi_primary
WBRNAi00052387Inferred_automaticallyRNAi_primary
WBRNAi00117695Inferred_automaticallyRNAi_primary
WBRNAi00075563Inferred_automaticallyRNAi_primary
WBRNAi00113481Inferred_automaticallyRNAi_primary
Expr_patternExpr1022989
Expr1033028
Expr1156012
Expr2009957
Expr2028197
Drives_constructWBCnstr00037874
Construct_productWBCnstr00016541
WBCnstr00016546
WBCnstr00021818
WBCnstr00037874
Regulate_expr_clusterWBPaper00063926:chd-7(gk290)_downregulated
WBPaper00063926:chd-7(gk290)_upregulated
Microarray_results (20)
Expression_cluster (170)
Interaction (118)
Map_infoMapIPosition-0.928876Error0.028449
PositivePositive_cloneT04D1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5620
4936
Pseudo_map_position
Reference (12)
Remarktag-192 is parsed from CGC strain VC606
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