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WormBase Tree Display for Gene: WBGene00004754

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Name Class

WBGene00004754SMapS_parentSequenceY113G7A
IdentityVersion1
NameCGC_namesec-23Person_evidenceWBPerson297
Sequence_nameY113G7A.3
Molecular_nameY113G7A.3
Y113G7A.3.1
CE27230
Other_nameY113G7A.nCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
CELE_Y113G7A.3Accession_evidenceNDBBX284605
Public_namesec-23
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsec
Allele (341)
StrainWBStrain00008607
RNASeq_FPKM (74)
GO_annotation (19)
Ortholog (44)
Structured_descriptionConcise_descriptionsec-23 encodes a component of COPII (coat protein complex II)-coated vesicles orthologous to Saccharomyces cerevisiae Sec23p; by homology, SEC-23 is predicted to be involved in endoplasmic reticulum (ER)-to-Golgi transport; loss of sec-23 activity results in defects in oogenesis, morphogenesis, and extracellular matrix secretion; a SEC-23::GFP fusion protein localizes to the apical region of the endoplasmic reticulum of hypodermal cells, consistent with localization to endoplasmic reticulum exit sites.Paper_evidenceWBPaper00006236
Curator_confirmedWBPerson1843
Date_last_updated02 May 2014 00:00:00
Automated_descriptionPredicted to enable GTPase activator activity. Predicted to be involved in COPII-coated vesicle cargo loading. Located in endoplasmic reticulum exit site. Expressed in hypodermis. Human ortholog(s) of this gene implicated in Cowden syndrome 7; congenital dyserythropoietic anemia type II; and craniolenticulosutural dysplasia. Is an ortholog of human SEC23B (SEC23 homolog B, COPII coat complex component).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:0081003Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10702)
DOID:0070307Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10701)
DOID:0111401Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10702)
Molecular_infoCorresponding_CDSY113G7A.3
Corresponding_CDS_historyY113G7A.3:wp47
Corresponding_transcriptY113G7A.3.1
Other_sequence (54)
Associated_feature (17)
Experimental_infoRNAi_result (29)
Expr_patternExpr2790
Expr1022212
Expr1032351
Expr1158901
Expr2015713
Expr2033945
Drives_constructWBCnstr00004952
WBCnstr00010950
Construct_productWBCnstr00010950
Microarray_results (23)
Expression_cluster (122)
Interaction (129)
Anatomy_functionWBbtf0239
Map_infoMapVPosition24.7157Error0.024791
PositivePositive_cloneY113G7AInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4325
4800
5484
Pseudo_map_position
Reference (17)
RemarkSequence connection from [Johnstone IL], [020809 krb]
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