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WormBase Tree Display for Gene: WBGene00001491

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Name Class

WBGene00001491SMapS_parentSequenceC24A11
IdentityVersion1
NameCGC_namefrm-4Person_evidenceWBPerson204
Sequence_nameC24A11.8
Molecular_name (11)
Other_nameCELE_C24A11.8Accession_evidenceNDBBX284601
Public_namefrm-4
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:24WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classfrm
Allele (98)
StrainWBStrain00001366
RNASeq_FPKM (74)
GO_annotation00022001
00022002
00022003
Ortholog (40)
ParalogWBGene00001488Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00001489Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00001333Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionfrm-4 encodes a predicted transmembrane protein that contains an N-terminal FERM (Band 4.1-ezrin-radixin-moesin) domain; by homology, FRM-4 is predicted to function as a membrane-cytoskeleton linker protein that plays a role in cell adhesion, migration, or organization of cell surface structures; however, as loss of frm-4 activity via large-scale RNAi screens does not result in any obvious abnormalities, the precise role of FRM-4 in C. elegans development and/or behavior is not yet known.Paper_evidenceWBPaper00004402
WBPaper00004651
Curator_confirmedWBPerson1843
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to be involved in actomyosin structure organization. Predicted to be located in cytoskeleton. Expressed in PVDL; PVDR; head; and tail. Human ortholog(s) of this gene implicated in neurodevelopmental disorder with eye movement abnormalities and ataxia. Is an ortholog of human FRMD3 (FERM domain containing 3) and FRMD5 (FERM domain containing 5).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:0081275Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:28214)
Molecular_infoCorresponding_CDSC24A11.8a
C24A11.8b
C24A11.8c
Corresponding_transcriptC24A11.8a.1
C24A11.8a.2
C24A11.8b.1
C24A11.8b.2
C24A11.8c.1
Other_sequence (31)
Associated_featureWBsf716920
WBsf983685
WBsf983686
WBsf1009820
WBsf1009821
WBsf1009822
WBsf219419
WBsf219420
WBsf219421
Experimental_infoRNAi_resultWBRNAi00002993Inferred_automaticallyRNAi_primary
WBRNAi00114829Inferred_automaticallyRNAi_primary
WBRNAi00029127Inferred_automaticallyRNAi_primary
WBRNAi00002992Inferred_automaticallyRNAi_primary
WBRNAi00116825Inferred_automaticallyRNAi_primary
WBRNAi00041048Inferred_automaticallyRNAi_primary
WBRNAi00001501Inferred_automaticallyRNAi_primary
WBRNAi00090549Inferred_automaticallyRNAi_primary
WBRNAi00117464Inferred_automaticallyRNAi_primary
WBRNAi00002996Inferred_automaticallyRNAi_primary
Expr_patternChronogram1052
Expr5320
Expr5321
Expr11988
Expr1018021
Expr1030892
Expr1145087
Expr2011886
Expr2030124
Drives_constructWBCnstr00002256
WBCnstr00004273
WBCnstr00036912
Construct_productWBCnstr00036912
Microarray_results (33)
Expression_cluster (142)
Interaction (26)
Map_infoMapIPosition-0.025651Error0.00187
PositivePositive_cloneC24A11Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00024261
WBPaper00031913
WBPaper00038491
WBPaper00055090
WBPaper00064339
Remarkdata submitted by [Gobel V]
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