The MYO18B gene homepage

General information
Gene symbol MYO18B
Gene name myosin XVIIIB
Chromosome 22
Chromosomal band q12.1
Imprinted Unknown
Genomic reference NC_000022.10
Transcript reference NM_032608.5
Associated with diseases KFS4
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 48
Unique public DNA variants reported 43
Individuals with public variants 19
Hidden variants 7
Date created September 13, 2012
Date last updated February 26, 2024
Version MYO18B:240226

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
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
HGNC 18150
Entrez Gene 84700
PubMed articles MYO18B
OMIM - Gene 607295
OMIM - Diseases KFS4 (Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism)
HGMD MYO18B
GeneCards MYO18B
GeneTests MYO18B
Orphanet MYO18B


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001621 22 myosin XVIIIB NM_032608.5 NP_115997.5 48


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