Overview

Variant ID 17806
Entrez Gene ID 23026
Gene MYO16 (GeneCards)
Location hg19 13:109277640-109277640
hg38 13:108625292-108625292
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000013.10:g.109277640 C>T (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 115169878

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.0531
CADD Raw score (version 1.3) 0.117174 (Deleterious)
FATHMM raw prediction score 0.15254 (Tolerated)
Deleterious probability by DeFine 0.4613 (Neutral)
Entrez Gene ID 23026 (NCBI Gene)
Official Gene Symbol MYO16 (GeneCards)
Number of variants in MYO16 in this database 16 (view all the variants)
Full name myosin XVI
Band 13q33.3
Other IDs OMIM: 615479
HGNC: HGNC:29822
Ensembl: ENSG00000041515
Other names MYR8, MYAP3, NYAP3, Myo16b, PPP1R107
Summary This gene encodes an unconventional myosin protein. The encoded protein has been proposed to act as a serine/threonine phosphatase-1 targeting or regulatory subunit. Studies in a rat cell line suggest that this protein may regulate cell cycle progression. A variant within this gene may be associated with susceptibility to schizophrenia and elevated expression of this gene has been observed in the frontal cortex of human schizophrenia patients. [provided by RefSeq, Mar 2017]

Individual #1

Individual ID 29217584.15 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;