The GLDN gene homepage

General information
Gene symbol GLDN
Gene name gliomedin
Chromosome 15
Chromosomal band q15.3
Imprinted Unknown
Genomic reference NG_054933.1
Transcript reference NM_181789.2
Exon/intron information NM_181789.2 exon/intron table
Associated with diseases LCCS11
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 29
Unique public DNA variants reported 21
Individuals with public variants 17
Hidden variants 1
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created September 13, 2012
Date last updated November 01, 2022
Version GLDN:221101

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_181789.2.
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/GLDN
HGNC 29514
Entrez Gene 342035
PubMed articles GLDN
OMIM - Gene 608603
OMIM - Diseases LCCS11 (contraction, lethal, congenital syndrome, type 11 (LCCS-11))
HGMD GLDN
GeneCards GLDN
GeneTests GLDN
Orphanet GLDN


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001060 15 gliomedin NM_181789.2 NP_861454.2 29


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