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WormBase Tree Display for Gene: WBGene00016735

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Name Class

WBGene00016735SMapS_parentSequenceC46H11
IdentityVersion2
NameCGC_namefhod-1Person_evidenceWBPerson399
WBPerson3066
Sequence_nameC46H11.11
Molecular_name (24)
Other_nameC46H11.aCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
CELE_C46H11.11Accession_evidenceNDBBX284601
Public_namefhod-1
DB_infoDatabaseWormQTLgeneWBGene00016735
WormFluxgeneWBGene00016735
NDBlocus_tagCELE_C46H11.11
PanthergeneCAEEL|WormBase=C46H11.11e|UniProtKB=A0A0K3AU72
familyPTHR45920
NCBIgene172133
RefSeqproteinNM_059112.4
NM_001313490.3
NM_001313489.3
NM_001313486.4
NM_001313484.2
NM_001313488.4
NM_001313487.3
NM_001313485.3
TrEMBLUniProtAccG5EFZ9
A0A0K3AR77
A0A0K3AQN9
A0A0K3AWK6
A0A0K3AR72
A0A0K3ATM4
A0A0K3ATM7
A0A0K3AU72
UniProt_GCRPUniProtAccA0A0K3AU72
OMIMgene609691
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:57WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
204 Mar 2005 10:23:45WBPerson2970Name_changeCGC_namefhod-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classfhod
Allele (125)
StrainWBStrain00003122
RNASeq_FPKM (74)
GO_annotation00000582
00000583
00000584
00000585
00001214
00001215
00001216
00001217
Contained_in_operonCEOP1899
Ortholog (44)
ParalogWBGene00000872Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00008848Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00018976Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00019030Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00021473Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00021698Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable actin filament binding activity. Involved in actin filament organization and embryonic body morphogenesis. Located in actin cytoskeleton. Expressed in muscle cell; pharyngeal muscle cell; and seam cell. Human ortholog(s) of this gene implicated in familial hypertrophic cardiomyopathy. Is an ortholog of human FHOD1 (formin homology 2 domain containing 1) and FHOD3 (formin homology 2 domain containing 3).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:0080326Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:26178)
Molecular_infoCorresponding_CDSC46H11.11a
C46H11.11b
C46H11.11c
C46H11.11d
C46H11.11e
C46H11.11f
C46H11.11g
C46H11.11h
Corresponding_CDS_historyC46H11.11a:wp178
C46H11.11b:wp178
Corresponding_transcriptC46H11.11a.1
C46H11.11b.1
C46H11.11c.1
C46H11.11d.1
C46H11.11e.1
C46H11.11f.1
C46H11.11g.1
C46H11.11h.1
Other_sequence (53)
Associated_feature (28)
Experimental_infoRNAi_resultWBRNAi00117058Inferred_automaticallyRNAi_primary
WBRNAi00111040Inferred_automaticallyRNAi_primary
WBRNAi00022306Inferred_automaticallyRNAi_primary
WBRNAi00111039Inferred_automaticallyRNAi_primary
WBRNAi00029884Inferred_automaticallyRNAi_primary
WBRNAi00042624Inferred_automaticallyRNAi_primary
Expr_pattern (12)
Drives_constructWBCnstr00003605
WBCnstr00014784
WBCnstr00027843
Construct_productWBCnstr00014784
WBCnstr00027843
Regulate_expr_clusterWBPaper00060634:fhod-1(tm2363)_downregulated
WBPaper00060634:fhod-1(tm2363)_upregulated
AntibodyWBAntibody00002372
WBAntibody00002509
WBAntibody00002510
Microarray_results (25)
Expression_cluster (191)
Interaction (48)
Map_infoMapIPosition-0.421363Error0.000374
PositivePositive_cloneC46H11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (23)
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