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WormBase Tree Display for Gene: WBGene00011867

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Name Class

WBGene00011867SMapS_parentSequenceT20G5
IdentityVersion3
NameCGC_namechc-1Person_evidenceWBPerson217
Sequence_nameT20G5.1
Molecular_nameT20G5.1
T20G5.1.1
CE00480
Other_nameclhc-1Paper_evidenceWBPaper00031805
CELE_T20G5.1Accession_evidenceNDBBX284603
Public_namechc-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:53WBPerson1971EventImportedInitial conversion from CDS class of WS125
204 Nov 2004 16:11:20WBPerson2970Name_changeCGC_namechc-1
330 Apr 2008 14:28:36WBPerson2970Name_changeOther_nameclhc-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classchc
Allele (82)
Possibly_affected_byWBVar02153072
WBVar00000423
StrainWBStrain00037310
WBStrain00005825
RNASeq_FPKM (74)
GO_annotation (34)
Contained_in_operonCEOP3858
Ortholog (47)
Structured_descriptionConcise_descriptionchc-1 encodes the C. elegans clathrin heavy chain ortholog; loss of chc-1 activity via RNAi results in defects in receptor-mediated yolk endocytosis and thus, embryonic lethality.Paper_evidenceWBPaper00003831
Curator_confirmedWBPerson1843
Date_last_updated21 Mar 2008 00:00:00
Automated_descriptionPredicted to enable clathrin light chain binding activity. Involved in several processes, including apical protein localization; determination of adult lifespan; and positive regulation of clathrin-dependent endocytosis. Located in cell periphery; clathrin-coated endocytic vesicle; and mitotic spindle. Expressed in coelomocyte; germ line; hyp7 syncytium; hypodermal cell; and pharyngeal cell. Human ortholog(s) of this gene implicated in autosomal dominant intellectual developmental disorder 56. Is an ortholog of human CLTC (clathrin heavy chain) and CLTCL1 (clathrin heavy chain like 1).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:0080226Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2092)
Molecular_infoCorresponding_CDST20G5.1
Corresponding_transcriptT20G5.1.1
Other_sequence (98)
Associated_featureWBsf659485
WBsf659486
WBsf993933
WBsf993934
WBsf1015749
WBsf225683
Experimental_infoRNAi_result (68)
Expr_pattern (13)
Drives_constructWBCnstr00000149
WBCnstr00017705
WBCnstr00030323
Construct_product (16)
AntibodyWBAntibody00000734
WBAntibody00001390
Microarray_results (19)
Expression_cluster (145)
Interaction (243)
Map_infoMapIIIPosition2.01234Error0.001699
PositivePositive_cloneT20G5Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (42)
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