Gene: CLTC ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies. 29100083 2017
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Prevalence and architecture of de novo mutations in developmental disorders. 28135719 2017
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR CLTC as a clinically novel gene associated with multiple malformations and developmental delay. 26822784 2016
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR ClinVar: public archive of relationships among sequence variation and human phenotype. 24234437 2014
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Activities at the Universal Protein Resource (UniProt). 24253303 2014
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR A draft map of the human proteome. 24870542 2014
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network. 23911319 2013
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Diversity of clathrin function: new tricks for an old protein. 22831640 2012
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. 22511880 2012
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR The NCBI BioSystems database. 19854944 2010
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Identification of a recurrent microdeletion at 17q23.1q23.2 flanked by segmental duplications associated with heart defects and limb abnormalities. 20206336 2010
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR The Human Gene Mutation Database: 2008 update. 19348700 2009
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Inactivation of clathrin heavy chain inhibits synaptic recycling but allows bulk membrane uptake. 18762582 2008
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Requirement of clathrin heavy chain for p53-mediated transcription. 16618797 2006
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Clathrin-mediated endocytosis is the dominant mechanism of vesicle retrieval at hippocampal synapses. 16982422 2006
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Clathrin is required for the function of the mitotic spindle. 15858577 2005
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR The synaptic vesicle cycle. 15217342 2004
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Nonsense-mediated decay approaches the clinic. 15284851 2004
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Endophilin mutations block clathrin-mediated endocytosis but not neurotransmitter release. 11955450 2002
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Visualizing secretion and synaptic transmission with pH-sensitive green fluorescent proteins. 9671304 1998
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Disruption of the clathrin heavy chain-like gene (CLTCL) associated with features of DGS/VCFS: a balanced (21;22)(p12;q11) translocation. 9147638 1997
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR The Drosophila clathrin heavy chain gene: clathrin function is essential in a multicellular organism. 8375651 1993
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.100 CausalMutation group CLINVAR Clathrin: a unique protein associated with intracellular transfer of membrane by coated vesicles. 1063406 1976