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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_resultsSMD_F56A11.1
SMD_F56A11.1:2
188154_s_at
A_12_P106014
Aff_F56A11.1
GPL13394_WBGene00001579
GPL13914_F56A11.1
GPL14144_F56A11.1_1500-1559_0.807_94_C
GPL14144_F56A11.1_3287-3346_0.917_12_B
GPL14144_F56A11.1_3570-3629_0.936_5_A
GPL19516_CGZ0024434
GPL21109_F56A11.1
GPL3518_CE31351
GPL8304_CE_WBGene00001579_A
GPL8304_CE_WBGene00001579_B
GPL8673_F56A11_1P02478
GPL8673_F56A11_1P03085
GPL8673_F56A11_1P03317
GPL9450_F56A11.1
cea2.c.29149
Expression_cluster (133)
Interaction (42)
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