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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_sequenceDA00020
EY471718.1
CBC10533_1
FC549313.1
CRC00764_1
EW741455.1
OOC00566_1
EX563823.1
ACC11829_1
SSC02710_1
SR04818
PPC19728_1
CRC05110_1
Oden_isotig25640
CR02277
MJ02223
PP01795
CJC14495_1
SRC06373_1
CRC04833_1
FC552130.1
ES565688.1
FK806121.1
HGC11719_1
CGC00412_1
HBC13889_1
Oden_isotig12181
PT02300
RS07434
SS02172
XI05137
CRC10255_1
FC549112.1
EX912117.1
XIC04217_1
Dviv_isotig13764
GW411561.1
OFC00596_1
XI04526
PPC00778_1
HG00225
RSC02974_1
ACC07040_1
CJC03059_1
EV853107.1
HG03580
EY468924.1
Hbac_isotig02521
Oden_isotig22825
MJC01238_1
PSC04871_1
ACC07040_2
Acan_isotig02702
FC553155.1
EX544672.1
CR08647
DAC00071_1
HCC06850_1
Dviv_isotig13763
Dviv_isotig33062
Dviv_isotig13765
Dviv_isotig13766
CR02285
EY458328.1
EX550299.1
SSC05976_1
JI472373.1
HC05346
PTC01712_1
EE724184.1
JI164067.1
CR08648
CBC17784_1
DVC02338_1
FC542839.1
FC551994.1
HGC10409_1
FC549887.1
SRC01903_1
FC820012.1
Acan_isotig10121
FC816046.1
FC814040.1
Oden_isotig12180
Tcir_isotig06674
EY471749.1
OF00074
SR02783
HG04765
Acan_isotig02701
TSC11240_1
HGC10560_1
ACC10168_1
FC810615.1
SS01134
ACC11532_1
EX539438.1
SRC07597_1
Associated_featureWBsf659485
WBsf659486
WBsf993933
WBsf993934
WBsf1015749
WBsf225683
Experimental_infoRNAi_result (68)
Expr_pattern (13)
Drives_constructWBCnstr00000149
WBCnstr00017705
WBCnstr00030323
Construct_product (16)
Antibody (2)
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