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WormBase Tree Display for Gene: WBGene00022816

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Name Class

WBGene00022816SMapS_parentSequenceCHROMOSOME_III
IdentityVersion3
NameCGC_namefbn-1Person_evidenceWBPerson545
WBPerson3379
WBPerson1983
Sequence_nameZK783.1
Molecular_name (27)
Other_namelet-821
cpg-16Paper_evidenceWBPaper00053350
CELE_ZK783.1Accession_evidenceNDBBX284603
Public_namefbn-1
DB_infoDatabaseAceViewgene3I729
WormQTLgeneWBGene00022816
WormFluxgeneWBGene00022816
OMIMdisease154700
gene134797
612570
NDBlocus_tagCELE_ZK783.1
PanthergeneCAEEL|WormBase=WBGene00022816|UniProtKB=I6Z0I7
familyPTHR24039
NCBIgene176076
RefSeqproteinNM_001276783.3
NM_001276787.4
NM_001276782.4
NM_001276789.4
NM_001276785.3
NM_001276780.3
NM_001276786.3
NM_066269.6
NM_001276788.3
TrEMBLUniProtAccI7J4C9
I7LFE6
I7K4J6
I7LHV9
I7J4C8
Q23587
I6Z0I7
I7K4J2
I7LHV8
UniProt_GCRPUniProtAccI6Z0I7
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:06WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
228 Jul 2005 14:07:57WBPerson2970Name_changeCGC_namefbn-1
320 May 2019 14:10:26WBPerson1983Name_changeCGC_namefbn-1
Other_namelet-821
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classfbn
Allele (207)
StrainWBStrain00054908
RNASeq_FPKM (74)
GO_annotation00023935
00126798
OrthologWBGene00066765Caenorhabditis remaneiFrom_analysisOMA
TreeFam
Inparanoid_8
WormBase-Compara
WBGene00023525Caenorhabditis briggsaeFrom_analysisHillier-set
OrthoMCL
OMA
Inparanoid_8
WormBase-Compara
WBGene00146019Caenorhabditis brenneriFrom_analysisOMA
TreeFam
Inparanoid_8
WormBase-Compara
WBGene00127057Caenorhabditis japonicaFrom_analysisTreeFam
Inparanoid_8
WormBase-Compara
WBGene00114389Pristionchus pacificusFrom_analysisOMA
Inparanoid_8
WBGene00227369Brugia malayiFrom_analysisWormBase-Compara
CBOVI.g4539Caenorhabditis bovisFrom_analysisWormBase-Compara
CSP21.g3972Caenorhabditis parvicaudaFrom_analysisWormBase-Compara
CSP26.g3994Caenorhabditis zanzibariFrom_analysisWormBase-Compara
CSP28.g16326Caenorhabditis panamensisFrom_analysisWormBase-Compara
CSP29.g17144Caenorhabditis beceiFrom_analysisWormBase-Compara
CSP29.g6810Caenorhabditis beceiFrom_analysisWormBase-Compara
CSP31.g630Caenorhabditis uteleiaFrom_analysisWormBase-Compara
CSP32.g17361Caenorhabditis sulstoniFrom_analysisWormBase-Compara
CSP38.g11840Caenorhabditis quiockensisFrom_analysisWormBase-Compara
CSP39.g1993Caenorhabditis waitukubuliFrom_analysisWormBase-Compara
CSP39.g21512Caenorhabditis waitukubuliFrom_analysisWormBase-Compara
CSP39.g27444Caenorhabditis waitukubuliFrom_analysisWormBase-Compara
CSP39.g5805Caenorhabditis waitukubuliFrom_analysisWormBase-Compara
CSP40.g3100Caenorhabditis tribulationisFrom_analysisWormBase-Compara
Cang_2012_03_13_06078.g20042Caenorhabditis angariaFrom_analysisWormBase-Compara
Cni-fbn-1Caenorhabditis nigoniFrom_analysisWormBase-Compara
Cnig_chr_III.g11424Caenorhabditis nigoniFrom_analysisWormBase-Compara
Csp11.Scaffold630.g17205Caenorhabditis tropicalisFrom_analysisWormBase-Compara
Csp5_scaffold_04016.g31838Caenorhabditis sinicaFrom_analysisWormBase-Compara
Csp5_scaffold_07203.g37488Caenorhabditis sinicaFrom_analysisWormBase-Compara
FL83_16656Caenorhabditis latensFrom_analysisWormBase-Compara
FL83_20796Caenorhabditis latensFrom_analysisWormBase-Compara
OTIPU.nOt.2.0.1.g11571Oscheius tipulaeFrom_analysisWormBase-Compara
Sp34_30032600Caenorhabditis inopinataFrom_analysisWormBase-Compara
chrIII_pilon.g8200Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00294114Trichuris murisFrom_analysisWormBase-Compara
ZFIN:ZDB-GENE-090112-3Danio rerioFrom_analysisInparanoid
OMA
HGNC:3603Homo sapiensFrom_analysisInparanoid
OMA
HGNC:3604Homo sapiensFrom_analysisInparanoid
OMA
HGNC:18794Homo sapiensFrom_analysisInparanoid
OMA
MGI:95489Mus musculusFrom_analysisInparanoid
OMA
MGI:95490Mus musculusFrom_analysisInparanoid
OMA
RGD:620908Rattus norvegicusFrom_analysisInparanoid
OMA
ParalogWBGene00003173Caenorhabditis elegansFrom_analysisPanther
WBGene00003482Caenorhabditis elegansFrom_analysisPanther
WBGene00003497Caenorhabditis elegansFrom_analysisPanther
WBGene00007170Caenorhabditis elegansFrom_analysisPanther
WBGene00001106Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00004963Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00009114Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00010134Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00013498Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00013855Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionfbn-1 encodes a protein homologous to the human extracellular matrix protein fibrillin-1 (FBN1); in C. elegans, fbn-1 activity is required for completion of molting, particularly the L3/L4 or L4/Adult molts.Paper_evidenceWBPaper00004103
WBPaper00026763
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated18 Jul 2007 00:00:00
Automated_descriptionPredicted to enable calcium ion binding activity. Predicted to be located in membrane. Expressed in vulval cell. Used to study connective tissue disease. Human ortholog(s) of this gene implicated in several diseases, including CREST syndrome; aortic disease (multiple); and bone disease (multiple). Is an ortholog of human FBN1 (fibrillin 1); FBN2 (fibrillin 2); and FBN3 (fibrillin 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_infoExperimental_modelDOID:65Homo sapiensPaper_evidenceWBPaper00046588
Curator_confirmedWBPerson324
Date_last_updated26 Oct 2018 00:00:00
Potential_model (13)
Disease_relevanceMutations in the human extracellular matrix protein fibrillin-1 (FBN1) lead to Marfan syndrome and several other disorders of connective tissue and skin; Both Marfan and Weill-Marchesani syndromes are characterized by abnormalities in connective tissue leading to heart, eye and skeletal abnormalities; FBN1 gene mutations also cause acromicric dysplasia characterized by severely short stature, short limbs and stiff joints; FBN1 gene mutations also cause MASS syndrome, involving abnormalities of the mitral heart valve, aorta, skeleton and skin; FBN1 gene mutations may also be involved in Shprintzen-Goldberg syndrome in infants which involves premature fusion of certain bones of the skull, and skeletal and skin abnormalities; in elegans mutations in fbn-1/fibrillin1 cause defects in molting.Homo sapiensPaper_evidenceWBPaper00026763
Accession_evidenceOMIM154700
134797
Curator_confirmedWBPerson324
Date_last_updated09 Dec 2013 00:00:00
Models_disease_assertedWBDOannot00000253
Molecular_infoCorresponding_CDSZK783.1a
ZK783.1b
ZK783.1d
ZK783.1e
ZK783.1f
ZK783.1g
ZK783.1h
ZK783.1j
ZK783.1k
Corresponding_CDS_historyZK783.1:wp206
ZK783.1i:wp275
Corresponding_transcriptZK783.1a.1
ZK783.1b.1
ZK783.1d.1
ZK783.1e.1
ZK783.1f.1
ZK783.1g.1
ZK783.1h.1
ZK783.1j.1
ZK783.1k.1
Other_sequence (20)
Associated_feature (22)
Experimental_infoRNAi_result (22)
Expr_patternExpr15951
Expr1025080
Expr1040095
Expr1163127
Expr2011446
Expr2029684
Drives_constructWBCnstr00042617
Construct_productWBCnstr00014819
WBCnstr00042617
Microarray_results (30)
Expression_cluster (280)
Interaction (23)
Map_infoMapIIIPosition-0.655224Error0.002689
PositivePositive_cloneZK783Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5355
4789
Pseudo_map_position
Reference (19)
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