MYH3 Chromosome 17

Myosin heavy chain 3
186 variants 186 Health Risk

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What This Gene Does
Myosin is a major contractile protein which converts chemical energy into mechanical energy through the hydrolysis of ATP. Myosin is a hexameric protein composed of a pair of myosin heavy chains (MYH) and two pairs of nonidentical light chains. This gene is a member of the MYH family and encodes a protein with an IQ domain and a myosin head-like domain. Mutations in this gene have been associated with two congenital contracture (arthrogryposis) syndromes, Freeman-Sheldon syndrome and Sheldon-Hall syndrome. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Myosin heavy chains, class II
Locus Type
gene with protein product
Location
17p13.1
Ensembl
ENSG00000109063
Associated Conditions (26)
Contractures
pterygia
and spondylocarpotarsal fusion syndrome 1A
Distal arthrogryposis type 2B1
Freeman-Sheldon syndrome
MYH3-related disorder
Arthrogryposis
distal
type 2B3
Inborn genetic diseases
Rhabdomyolysis
Meniere disease
and variable skeletal fusions syndrome 1B
Gastric cancer
Hepatocellular carcinoma
Clear cell carcinoma of kidney
Thyroid cancer
nonmedullary
1
Melanoma
+6 more conditions
Key Variants
RS1031781302
Conflicting classifications of pathogenicity
Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
Health Risk
RS1057518008
Conflicting classifications of pathogenicity
Health Risk
RS115742228
Conflicting classifications of pathogenicity
Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, MYH3-related disorder
Health Risk
RS121913621
Conflicting classifications of pathogenicity
Arthrogryposis, distal, type 2B3
Health Risk
RS121913623
Conflicting classifications of pathogenicity
Arthrogryposis, distal, type 2B3
Health Risk
RS1377740859
Conflicting classifications of pathogenicity
Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
Health Risk
RS137974114
Conflicting classifications of pathogenicity
Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
Health Risk
RS138194008
Conflicting classifications of pathogenicity
Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Inborn genetic diseases
Health Risk
RS139480342
Conflicting classifications of pathogenicity
Rhabdomyolysis, Distal arthrogryposis type 2B1, MYH3-related disorder
Health Risk
RS139544273
Conflicting classifications of pathogenicity
Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1
Health Risk
RS139978727
Conflicting classifications of pathogenicity
Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
Health Risk
RS140074626
Conflicting classifications of pathogenicity
Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
Health Risk
All Variants (186)
RSID Category Clinical Significance Conditions
RS1031781302 Health Risk Conflicting classifications of pathogenicity Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
RS1057518008 Health Risk Conflicting classifications of pathogenicity
RS115742228 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, MYH3-related disorder
RS121913621 Health Risk Conflicting classifications of pathogenicity Arthrogryposis, distal, type 2B3
RS121913623 Health Risk Conflicting classifications of pathogenicity Arthrogryposis, distal, type 2B3
RS1377740859 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
RS137974114 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
RS138194008 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Inborn genetic diseases
RS139480342 Health Risk Conflicting classifications of pathogenicity Rhabdomyolysis, Distal arthrogryposis type 2B1, MYH3-related disorder
RS139544273 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1
RS139978727 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
RS140074626 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
RS140144159 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1
RS140180067 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Inborn genetic diseases
RS140218185 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, MYH3-related disorder
RS142002449 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Inborn genetic diseases
RS144312976 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1
RS145080512 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Arthrogryposis
RS147024680 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Meniere disease
RS147304568 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Gastric cancer
RS149260479 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
RS151028057 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, MYH3-related disorder
RS1567560718 Health Risk Conflicting classifications of pathogenicity
RS180886846 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS185355384 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1
RS189005323 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
RS191571748 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1
RS193224181 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, MYH3-related disorder
RS199513213 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, MYH3-related disorder
RS199834077 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Contractures
RS200031876 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1
RS200111154 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
RS200191762 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1
RS200780612 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1
RS200964415 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Inborn genetic diseases
RS201488879 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
RS201532275 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1
RS201602783 Health Risk Conflicting classifications of pathogenicity
RS201674457 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
RS201787435 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS201955505 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
RS202129717 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1
RS2142395389 Health Risk Conflicting classifications of pathogenicity
RS34165480 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, MYH3-related disorder
RS368171012 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Inborn genetic diseases
RS368299686 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1
RS370685666 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1
RS371043485 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
RS372079063 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome, MYH3-related disorder
RS372305218 Health Risk Conflicting classifications of pathogenicity Freeman-Sheldon syndrome, Distal arthrogryposis type 2B1, Freeman-Sheldon syndrome
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