Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 283446
MIM: 614636
HGNC: 13879
Ensembl: ENSG00000174527
Variants:
dbSNP: 283446
ClinVar: 283446
TCGA: ENSG00000174527
COSMIC: MYO1H
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000174527 | ENST00000310903 | A0A140TA25 |
| ENSG00000174527 | ENST00000431443 | Q8N1T3 |
| ENSG00000174527 | ENST00000543960 | S4R387 |
Expression (GTEx)
Protein levels (Protein atlas)
PharmGKB
| Entity ID | Name | Type | Evidence | Association | PK | PD | PMIDs |
|---|---|---|---|---|---|---|---|
| PA447199 | Bipolar Disorder | Disease | ClinicalAnnotation | associated | PD | 29121268 | |
| PA450243 | lithium | Chemical | ClinicalAnnotation | associated | PD | 29121268 |
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35704118 | 2022 | MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia. | 1 |
| 35704118 | 2022 | MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia. | 1 |
| 33448167 | 2020 | Relationship of the rs10850110 and rs11611277 polymorphisms of the MYO1H gene with non-syndromic mandibular prognathism in the Iranian population. | 4 |
| 33448167 | 2020 | Relationship of the rs10850110 and rs11611277 polymorphisms of the MYO1H gene with non-syndromic mandibular prognathism in the Iranian population. | 4 |
| 30366217 | 2019 | Genetic variants in ACTN3 and MYO1H are associated with sagittal and vertical craniofacial skeletal patterns. | 18 |
| 30366217 | 2019 | Genetic variants in ACTN3 and MYO1H are associated with sagittal and vertical craniofacial skeletal patterns. | 18 |
| 29986156 | 2018 | Identification and Functional Studies of MYO1H for Mandibular Prognathism. | 11 |
| 29986156 | 2018 | Identification and Functional Studies of MYO1H for Mandibular Prognathism. | 11 |
| 28779001 | 2017 | Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction. | 10 |
| 28779001 | 2017 | Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction. | 10 |
| 27131252 | 2016 | Role of myosin 1H gene polymorphisms in mandibular retrognathism. | 8 |
| 27131252 | 2016 | Role of myosin 1H gene polymorphisms in mandibular retrognathism. | 8 |
| 22196185 | 2012 | Genetic variation in myosin 1H contributes to mandibular prognathism. | 39 |
| 22196185 | 2012 | Genetic variation in myosin 1H contributes to mandibular prognathism. | 39 |
Citation
Dessen P
MYO1H (myosin IH)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/70632/myo1h-(myosin-ih)
