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WormBase Tree Display for Gene: WBGene00004134

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Name Class

WBGene00004134SMapS_parentSequenceCHROMOSOME_II
IdentityVersion2
NameCGC_namemyrf-1Person_evidenceWBPerson7150
Sequence_nameF59B10.1
Molecular_nameF59B10.1
F59B10.1.1
CE36940
Other_namepqn-47Person_evidenceWBPerson625
CELE_F59B10.1Accession_evidenceNDBBX284602
Public_namemyrf-1
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:34WBPerson1971EventImportedInitial conversion from geneace
209 Dec 2014 15:51:18WBPerson2970Name_changeCGC_namemyrf-1
Other_namepqn-47
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmyrf
Allele (84)
Possibly_affected_byWBVar02157207
StrainWBStrain00037532
WBStrain00037768
RNASeq_FPKM (74)
GO_annotation (32)
Ortholog (43)
ParalogWBGene00008999Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
Structured_descriptionConcise_descriptionmyrf-1 encodes a protein with a glutamine/asparagine-rich domain, orthologous to human MYRF (myelin regulatory factor); in C. elegans, MYRF-1 activity is required for regulation of the molting cycle, specifically the completion of larval molts and cessation of molting in reproductively mature adult animals; a MYRF-1::GFP fusion protein is expressed in a wide variety of cells and tissues, including neurons, secretory cells, and hypodermal seam cells, but is not seen in the hyp7 syncytial hypodermis; expression begins in the comma stage of embryogenesis and persists through adulthood; full length C. elegans MYRF-1::GFP localizes to the cytoplasm where it partially overlaps with the endoplasmic reticulum; MYRF-1 contains a well-conserved paralog in the C. elegans genome, MYRF-2, encoded by F21A10.2.Paper_evidenceWBPaper00004651
WBPaper00005487
WBPaper00005654
WBPaper00012811
WBPaper00040293
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated19 Dec 2014 00:00:00
Automated_descriptionPredicted to enable DNA-binding transcription factor activity and sequence-specific DNA binding activity. Involved in ecdysis, collagen and cuticulin-based cuticle and nematode larval development. Located in basal part of cell and endoplasmic reticulum. Expressed in several structures, including ciliated neurons; excretory duct; gonad; pharyngeal cell; and somatic nervous system. Human ortholog(s) of this gene implicated in cerebral infarction; congenital diaphragmatic hernia; and eye disease (multiple). Is an ortholog of human MYRFL (myelin regulatory factor like).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:0080634Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1181)
DOID:3827Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1181)
DOID:9834Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1181)
DOID:1405Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1181)
DOID:3526Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1181)
Molecular_infoCorresponding_CDSF59B10.1
Corresponding_CDS_historyF59B10.1:wp127
Corresponding_transcriptF59B10.1.1
Other_sequenceCR10282
CR10281
CRC03559_1
ACC07624_1
SRC00534_1
EY470006.1
Tcol_isotig21011
SR01712
Name_isotig07910
JI164614.1
Associated_feature (15)
Transcription_factorWBTranscriptionFactor000563
Experimental_infoRNAi_result (46)
Expr_pattern (14)
Drives_constructWBCnstr00004111
WBCnstr00009459
WBCnstr00009460
WBCnstr00014243
WBCnstr00014244
WBCnstr00019909
WBCnstr00037934
Construct_productWBCnstr00009460
WBCnstr00014243
WBCnstr00014244
WBCnstr00037934
Regulate_expr_clusterWBPaper00061377:MYRF-1_interacting
Microarray_results (16)
Expression_cluster (185)
Interaction (679)
Anatomy_functionWBbtf1093
WBbtf1094
WBbtf1095
Map_infoMapIIPosition2.9838Error0.041984
PositivePositive_cloneF59B10Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (14)
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