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WormBase Tree Display for Gene: WBGene00004755

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Name Class

WBGene00004755SMapS_parentSequenceF12F6
IdentityVersion1
NameCGC_namesec-24.1Person_evidenceWBPerson297
Sequence_nameF12F6.6
Molecular_nameF12F6.6
F12F6.6.1
CE05594
Other_nameCELE_F12F6.6Accession_evidenceNDBBX284604
Public_namesec-24.1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsec
Allele (47)
RNASeq_FPKM (74)
GO_annotation (14)
Contained_in_operonCEOP4452
Ortholog (60)
ParalogWBGene00004756Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionsec-24.1 encodes one of two C. elegans Sec24 homologs; in Saccharomyces cerevisiae, Sec24 is a member of the Sec24-Sec23 subunit of the COPII coat complex, assembly of which is essential for the first step of secretory protein transport from the endoplasmic reticulum (ER) to the Golgi; by homology with Sec24, SEC-24.1 is predicted to facilitate vesicle cargo selection, and likely contains multiple, independent sites for binding to secreted proteins; loss of sec-24.1 activity via RNAi indicates that SEC-24.1 is required for cuticle secretion and oogenesis.Paper_evidenceWBPaper00011684
WBPaper00013299
Curator_confirmedWBPerson1843
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable SNARE binding activity and zinc ion binding activity. Predicted to be involved in COPII-coated vesicle cargo loading. Predicted to be located in endoplasmic reticulum exit site. Predicted to be part of COPII vesicle coat. Expressed widely. Human ortholog(s) of this gene implicated in Cole-Carpenter syndrome. Is an ortholog of human SEC24D (SEC24 homolog D, 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:0060438Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10706)
Molecular_infoCorresponding_CDSF12F6.6
Corresponding_transcriptF12F6.6.1
Other_sequence (65)
Associated_featureWBsf668347
WBsf981824
WBsf997872
WBsf997873
WBsf997874
WBsf1018224
WBsf230894
WBsf230895
Experimental_infoRNAi_result (12)
Expr_patternExpr5746
Expr13312
Expr1017366
Expr1032352
Expr1148399
Expr2015714
Expr2033946
Drives_constructWBCnstr00002791
WBCnstr00035408
Construct_productWBCnstr00018415
WBCnstr00018416
WBCnstr00035408
Microarray_results (23)
Expression_cluster (136)
Interaction (52)
Map_infoMapIVPosition5.00291Error0.000895
PositivePositive_cloneF12F6Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00028945
WBPaper00038491
WBPaper00049330
WBPaper00050029
WBPaper00055090
WBPaper00058870
WBPaper00060970
WBPaper00062332
WBPaper00064057
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