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WormBase Tree Display for Gene: WBGene00019608

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Name Class

WBGene00019608SMapS_parentSequenceK10B2
IdentityVersion2
NameCGC_nameani-2Person_evidenceWBPerson1816
WBPerson1836
Sequence_nameK10B2.5
Molecular_nameK10B2.5
K10B2.5.1
CE02012
Other_nametag-221Curator_confirmedWBPerson2970
CELE_K10B2.5Accession_evidenceNDBBX284602
Public_nameani-2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:01WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
215 Nov 2004 11:05:03WBPerson2970Name_changeCGC_nameani-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classani
Allele (51)
StrainWBStrain00035994
RNASeq_FPKM (74)
GO_annotation (13)
Contained_in_operonCEOP2244
Ortholog (35)
ParalogWBGene00007409Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00012835Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00013038Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionani-2 encodes one of three C. elegans anillins; ANI-2 activity is required in the syncytial gonad for proper gonad structure and oocyte formation; specifically, ANI-2 appears to be required for maintaining the structure of the rachis, the syncytial compartment of germline cytoplasm that connects developing ooctyes; in the adult gonad, ANI-2 localizes to the surface of the rachis.Paper_evidenceWBPaper00025229
Curator_confirmedWBPerson1843
Date_last_updated15 Nov 2007 00:00:00
Automated_descriptionInvolved in several processes, including female gamete generation; gonad development; and syncytium formation. Located in cytoplasm. Expressed in germ line. Human ortholog(s) of this gene implicated in focal segmental glomerulosclerosis 8. Is an ortholog of human ANLN (anillin, actin binding protein).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:0111133Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14082)
Molecular_infoCorresponding_CDSK10B2.5
Corresponding_transcriptK10B2.5.1
Other_sequenceCR04952
CBC17633_1
CBC01419_1
CRC03165_1
CBC08095_1
CGC00761_1
CBC00636_1
CBC04982_1
CJC06779_1
CGC01113_1
Associated_featureWBsf650141
WBsf665604
WBsf223168
WBsf223169
Experimental_infoRNAi_result (21)
Expr_patternExpr3281
Expr1012967
Expr1038467
Expr1154185
Expr2009336
Expr2027572
Drives_constructWBCnstr00025732
Construct_productWBCnstr00019412
WBCnstr00025732
AntibodyWBAntibody00000928
WBAntibody00002425
Microarray_results (19)
Expression_cluster (157)
Interaction (148)
Map_infoMapIIPosition-0.380478Error0.000395
PositivePositive_cloneK10B2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5272
Pseudo_map_position
Reference (21)
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