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WormBase Tree Display for Gene: WBGene00001579

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Name Class

WBGene00001579SMapS_parentSequenceCHROMOSOME_IV
IdentityVersion1
NameCGC_namegex-2Person_evidenceWBPerson419
Sequence_nameF56A11.1
Molecular_nameF56A11.1
F56A11.1.1
CE31351
Other_nameCELE_F56A11.1Accession_evidenceNDBBX284604
Public_namegex-2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:25WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classgex
Allele (162)
StrainWBStrain00036391
RNASeq_FPKM (74)
GO_annotation (22)
Ortholog (50)
Structured_descriptionConcise_descriptionThe gex-2 gene encodes a homolog of p140/Sra-1, a mammalian protein ligand of the small GTPase Rac1; gex-2 is required for tissue morphogenesis and cell migrations.Paper_evidenceWBPaper00005149
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable RNA 7-methylguanosine cap binding activity. Involved in several processes, including embryonic body morphogenesis; positive regulation of clathrin-dependent endocytosis; and positive regulation of egg-laying behavior. Located in cell junction. Part of SCAR complex. Human ortholog(s) of this gene implicated in several diseases, including Schaaf-Yang syndrome; autism spectrum disorder; and epilepsy (multiple). Is an ortholog of human CYFIP1 (cytoplasmic FMR1 interacting protein 1) and CYFIP2 (cytoplasmic FMR1 interacting protein 2).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:0111715Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:13759)
DOID:0080430Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:13760)
DOID:0060041Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:13759)
DOID:3328Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:13759)
DOID:5419Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:13759)
Molecular_infoCorresponding_CDSF56A11.1
Corresponding_CDS_historyF56A11.1:wp129
Corresponding_transcriptF56A11.1.1
Other_sequence (56)
Associated_featureWBsf645763
WBsf995193
WBsf995194
WBsf1016569
WBsf227856
WBsf227857
WBsf227858
WBsf227859
Experimental_infoRNAi_result (33)
Expr_patternExpr1827
Expr1026712
Expr1030945
Expr1152359
Expr2012023
Expr2030259
Drives_constructWBCnstr00036849
Construct_productWBCnstr00036849
AntibodyWBAntibody00000462
WBAntibody00000463
Microarray_results (20)
Expression_cluster (133)
InteractionWBInteraction000009180
WBInteraction000032873
WBInteraction000033237
WBInteraction000033238
WBInteraction000033239
WBInteraction000033411
WBInteraction000033553
WBInteraction000051768
WBInteraction000135535
WBInteraction000158048
WBInteraction000158053
WBInteraction000158054
WBInteraction000158055
WBInteraction000158056
WBInteraction000158057
WBInteraction000158058
WBInteraction000158059
WBInteraction000158060
WBInteraction000158426
WBInteraction000158434
WBInteraction000158552
WBInteraction000158622
WBInteraction000158641
WBInteraction000162905
WBInteraction000162918
WBInteraction000169398
WBInteraction000173174
WBInteraction000296274
WBInteraction000349811
WBInteraction000351042
WBInteraction000360350
WBInteraction000370249
WBInteraction000402330
WBInteraction000441523
WBInteraction000443564
WBInteraction000503823
WBInteraction000503825
WBInteraction000536176
WBInteraction000541404
WBInteraction000556196
WBInteraction000556413
WBInteraction000556414
Map_infoMapIVPosition-24.7527Error0.274792
PositivePositive_cloneF56A11Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point5641
Pseudo_map_position
Reference (36)
Remarkthe 3' end is on C18H7 (nucleotides 1 to 3,000)
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