The CLTC gene homepage

General information
Gene symbol CLTC
Gene name clathrin, heavy chain (Hc)
Chromosome 17
Chromosomal band q11-qter
Imprinted Unknown
Genomic reference NC_000017.10
Transcript reference NM_004859.3
Exon/intron information NM_004859.3 exon/intron table
Associated with diseases MR, MRD56
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 62
Unique public DNA variants reported 56
Individuals with public variants 16
Hidden variants 3
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created May 03, 2013
Date last updated April 19, 2024
Version CLTC:240419

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_004859.3.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/CLTC
HGNC 2092
Entrez Gene 1213
PubMed articles CLTC
OMIM - Gene 118955
OMIM - Diseases MRD56 (intellectual developmental disorder, autosomal dominant, type 56)
HGMD CLTC
GeneCards CLTC
GeneTests CLTC
Orphanet CLTC


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00005342 17 clathrin, heavy chain (Hc) NM_004859.3 NP_004850.1 62


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