The KRT16 gene homepage

General information
Gene symbol KRT16
Gene name keratin 16
Chromosome 17
Chromosomal band q21.2
Imprinted Unknown
Genomic reference NG_008301.1
Transcript reference NM_005557.3
Exon/intron information NM_005557.3 exon/intron table
Associated with diseases FNEPPK1, PC1
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 88
Unique public DNA variants reported 35
Individuals with public variants 95
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 July 07, 2023
Version KRT16:230707

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_005557.3.
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
HGNC 6423
Entrez Gene 3868
PubMed articles KRT16
OMIM - Gene 148067
OMIM - Diseases FNEPPK1 (keratoderma, palmoplantar, nonepidermolytic, focal, type 1 (FNEPPK-1))
PC1 (pachyonychia congenita, type 1)
GeneCards KRT16
GeneTests KRT16
Orphanet KRT16

Active transcripts




NCBI ID     

NCBI Protein ID     

00001488 17 keratin 16 NM_005557.3 NP_005548.2 88

Copyright & disclaimer
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