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WormBase Tree Display for Gene: WBGene00003020

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Name Class

WBGene00003020SMapS_parentSequenceC32F10
IdentityVersion1
NameCGC_namelin-35Person_evidenceWBPerson261
Sequence_nameC32F10.2
Molecular_nameC32F10.2
C32F10.2.1
CE24823
Other_nameCELE_C32F10.2Accession_evidenceNDBBX284601
Public_namelin-35
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:30WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classlin
Allele (104)
Legacy_informationn745 : wildtype alone Muv in homozygotes with lin-8 lin-38 or lin-15(n767). ES2. NA2 (n373 (similar phenotype)).
See also n373, n745
[C.elegansII] n745 : almost WT alone (reduced fertility); Muv (extra vulval differentiation) in homozygotes with lin-8, lin-38 or lin-15(n767). ES2. OA1: n373 (similar). [Ferguson and Horvitz 1989; MT; PS]
Strain (17)
Component_of_genotypeWBGenotype00000009
RNASeq_FPKM (74)
GO_annotation (50)
Ortholog (43)
Structured_description (2)
Disease_infoExperimental_modelDOID:1059Homo sapiensPaper_evidenceWBPaper00024322
Accession_evidenceOMIM309580
Curator_confirmedWBPerson324
Date_last_updated18 Apr 2013 00:00:00
Potential_model (16)
Disease_relevanceHuman ATRX encodes a protein with a ATPase/helicase domain involved in chromatin remodeling, mutations in which, have been associated with alpha-thalassemia and X-linked mental retardation; the elegans ortholog, xnp-1 is required for gonadal development and acts in association with lin-35/Retinoblastoma (RB), components of the NuRD complex and hpl-2/HP1 genes; the requirement of xnp-1 with lin-35/ Rb in larval development in C. elegans can be compared with the observation that in humans, XNP/ATR-X mutation is also associated, with short stature and skeletal abnormalities during development.Homo sapiensPaper_evidenceWBPaper00024322
WBPaper00024692
WBPaper00003646
Curator_confirmedWBPerson324
Date_last_updated23 Apr 2013 00:00:00
Models_disease_assertedWBDOannot00000614
WBDOannot00001021
Molecular_infoCorresponding_CDSC32F10.2
Corresponding_transcriptC32F10.2.1
Associated_featureWBsf643315
WBsf643316
WBsf656335
WBsf656336
WBsf656337
WBsf656338
WBsf983774
WBsf217712
Gene_product_binds (376)
Transcription_factorWBTranscriptionFactor000270
Experimental_infoRNAi_result (78)
Expr_patternChronogram622
Expr1291
Expr3128
Expr1015789
Expr1031411
Expr1145718
Expr2013177
Expr2031409
Drives_constructWBCnstr00004066
WBCnstr00006281
WBCnstr00011156
WBCnstr00017294
WBCnstr00036281
Construct_productWBCnstr00006281
WBCnstr00011156
WBCnstr00017287
WBCnstr00017294
WBCnstr00017295
WBCnstr00017296
WBCnstr00021077
WBCnstr00021078
WBCnstr00021079
WBCnstr00036281
Regulate_expr_cluster (16)
AntibodyWBAntibody00000200
WBAntibody00001176
WBAntibody00003008
WBAntibody00003009
Microarray_results (20)
Expression_cluster (156)
Interaction (322)
Product_binds_matrixWBPmat00005534
WBPmat00005535
WBPmat00005536
WBPmat00005540
WBPmat00005541
WBPmat00005542
WBPmat00005543
WBPmat00005544
WBPmat00005545
Map_infoMapIPosition0.461719Error0.000997
Well_ordered
PositivePositive_cloneC32F10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point283
308
309
4517
Reference (253)
PictureWBPicture0000013091
MethodGene