Identity
HGNC
LOCATION
20q11.22
LOCUSID
ALIAS
MHC14,MYH14
FUSION GENES
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: 57644
MIM: 609928
HGNC: 15906
Ensembl: ENSG00000078814
Variants:
dbSNP: 57644
ClinVar: 57644
TCGA: ENSG00000078814
COSMIC: MYH7B
RNA/Proteins
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36334627 | 2023 | Functional divergence of the sarcomeric myosin, MYH7b, supports species-specific biological roles. | 10 |
| 36963494 | 2023 | Distinct effects of two hearing loss-associated mutations in the sarcomeric myosin MYH7b. | 1 |
| 36334627 | 2023 | Functional divergence of the sarcomeric myosin, MYH7b, supports species-specific biological roles. | 10 |
| 36963494 | 2023 | Distinct effects of two hearing loss-associated mutations in the sarcomeric myosin MYH7b. | 1 |
| 33895132 | 2021 | Myosin 7b is a regulatory long noncoding RNA (lncMYH7b) in the human heart. | 10 |
| 33895132 | 2021 | Myosin 7b is a regulatory long noncoding RNA (lncMYH7b) in the human heart. | 10 |
| 27666969 | 2016 | Myosin-7b Promotes Distal Tip Localization of the Intermicrovillar Adhesion Complex. | 31 |
| 27666969 | 2016 | Myosin-7b Promotes Distal Tip Localization of the Intermicrovillar Adhesion Complex. | 31 |
| 23800289 | 2013 | Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. | 20 |
| 23800289 | 2013 | Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. | 20 |
| 19948655 | 2010 | Two novel/ancient myosins in mammalian skeletal muscles: MYH14/7b and MYH15 are expressed in extraocular muscles and muscle spindles. | 67 |
| 20154144 | 2010 | Uncoupling of expression of an intronic microRNA and its myosin host gene by exon skipping. | 72 |
| 20224305 | 2010 | Modest association of malignant melanoma with the rs910873 and rs1885120 markers on chromosome 20: a population-based study. | 1 |
| 20520619 | 2010 | Common genetic variants in pre-microRNAs and risk of gallbladder cancer in North Indian population. | 44 |
| 20628086 | 2010 | Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study. | 15 |
Citation
Dessen P
MYH7B (myosin heavy chain 7B)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/70610/myh7b-(myosin-heavy-chain-7b)
