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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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MYO16
myosin XVI
Chromosome 13 · 13q33.3
NCBI Gene: 23026Ensembl: ENSG00000041515.16HGNC: HGNC:29822UniProt: F8W883
27PubMed Papers
20Diseases
0Drugs
1Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
nucleoplasmperinuclear region of cytoplasmprotein bindingactin filament bindingopen-angle glaucomaglaucomaadolescent idiopathic scoliosisprostate carcinoma
✦AI Summary

MYO16 (myosin XVI) is a vertebrate-specific, actin-based motor protein predominantly expressed in neural tissues during critical developmental periods 1. The protein exists as two principal isoforms: Myo16a (tailless, cytoplasmic) and Myo16b (full-length, with cytoplasmic and nuclear localization) 1. Both isoforms contain an N-terminal ankyrin repeat domain that binds protein phosphatase catalytic subunits 1. Functionally, MYO16 serves as a signal transduction element integrating cell signaling to actin cytoskeleton reorganization 2. In the cytoplasm, Myo16b activates the PI3K pathway and recruits the WAVE complex to regulate neuronal morphogenesis and actin cytoskeleton reorganization 1. Nuclear Myo16b may regulate cell cycle progression 1. MYO16 interacts with neuronal proteins including MAP1B and KIRREL3, contributing to neurodevelopment 3. Dysregulation of MYO16 expression is implicated in multiple neuropsychiatric disorders including autism, schizophrenia, and bipolar disorder 1, and variants in MYO16 associate with structural brain connectivity measures 4. Beyond neurodevelopment, MYO16-related long non-coding RNAs regulate glucose metabolism and invasion in lung and bladder cancers 5, 6.

Sources cited
1
MYO16 is a vertebrate-specific motor protein expressed in neural tissues; describes both Myo16a and Myo16b isoforms, their localization, ankyrin repeat domain binding to PP1 catalytic subunit, and roles in PI3K activation and WAVE complex recruitment
PMID: 32451869
2
MYO16 functions as a signal transduction element integrating cell signaling pathways to actin cytoskeleton reorganization; emphasizes neural tissue expression and neurological disorder associations
PMID: 32824179
3
MYO16 interacts with neuronal proteins MAP1B and KIRREL3; demonstrates MYO16 deletions in patients with intellectual disability, autism, and microcephaly; describes MYO16's role in actin cytoskeleton through WAVE1 complex interaction
PMID: 25902260
4
MYO16 variants associate with structural connectivity measures in large-scale GWAS of brain white-matter organization; implicates MYO16 in cytoskeletal organization affecting myelinated axon connections
PMID: 38438384
5
MYO16-AS1 (lncRNA) regulates glucose metabolism and LUAD cell invasion through IGF2BP3-HK2 mRNA interactions
PMID: 38041756
6
MYO16-AS1 functions as an oncogenic lncRNA in bladder cancer, enhancing cell migration and invasion
PMID: 33270518
Disease Associationsⓘ20
open-angle glaucomaOpen Targets
0.45Moderate
glaucomaOpen Targets
0.43Moderate
adolescent idiopathic scoliosisOpen Targets
0.34Weak
prostate carcinomaOpen Targets
0.34Weak
StutteringOpen Targets
0.33Weak
systemic lupus erythematosusOpen Targets
0.33Weak
response to steroidOpen Targets
0.33Weak
idiopathic osteonecrosis of the femoral headOpen Targets
0.33Weak
ulcerative colitisOpen Targets
0.31Weak
abscessOpen Targets
0.31Weak
cellulitisOpen Targets
0.31Weak
injuryOpen Targets
0.30Weak
diabetes mellitusOpen Targets
0.29Weak
diabetic ketoacidosisOpen Targets
0.29Weak
type 2 diabetes mellitusOpen Targets
0.29Weak
neurodegenerative diseaseOpen Targets
0.28Weak
nervous system diseaseOpen Targets
0.28Weak
complex regional pain syndromeOpen Targets
0.28Weak
alcohol dependenceOpen Targets
0.28Weak
Chest painOpen Targets
0.26Weak
Pathogenic Variants1
NM_001198950.3(MYO16):c.1477C>T (p.Pro493Ser)Likely pathogenic
MYO16-associated developmental delay
★☆☆☆2018→ Residue 493
View on ClinVar ↗
Related Genes
NYAP1Shared pathway40%NYAP2Shared pathway40%ZBTB7CShared pathway20%ZNF655Shared pathway20%PPP1R12CShared pathway20%TESShared pathway20%
Tissue Expression6 tissues
Brain
100%
Heart
64%
Liver
47%
Lung
9%
Bone Marrow
8%
Ovary
4%
Gene Interaction Network
Click a node to explore
MYO16NYAP1NYAP2ZBTB7CZNF655PPP1R12CTES
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt Q9Y6X6
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
0.58Moderately Constrained
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.47 [0.39–0.58]
RankingsWhere MYO16 stands among ~20K protein-coding genes
  • #12,609of 20,598
    Most Researched27
  • #5,288of 5,498
    Most Pathogenic Variants1
  • #3,836of 17,882
    Most Constrained (LOEUF)0.58 · top quartile
Genes detectedMYO16
Sources retrieved10 papers
Response time—
📄 Sources
10â–¼
1
Myosin XVI.
PMID: 32451869
Adv Exp Med Biol · 2020
1.00
2
Myosin XVI in the Nervous System.
PMID: 32824179
Cells · 2020
0.90
3
Genetic architecture of the structural connectome.
PMID: 38438384
Nat Commun · 2024
0.80
4
Autism and Intellectual Disability-Associated KIRREL3 Interacts with Neuronal Proteins MAP1B and MYO16 with Potential Roles in Neurodevelopment.
PMID: 25902260
PLoS One · 2015
0.70
5
Genomically Complex Human Angiosarcoma and Canine Hemangiosarcoma Establish Convergent Angiogenic Transcriptional Programs Driven by Novel Gene Fusions.
PMID: 33649193
Mol Cancer Res · 2021
0.60