beta-myosin heavy chain (1151 AA), partial [Homo sapiens]

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A New Leu714Arg Variant in the Converter Domain of MYH7 is Associated with a Severe Form of Familial Hypertrophic Cardiomyopathy. [Front Biosci (Schol Ed). 2024]
A New Leu714Arg Variant in the Converter Domain of MYH7 is Associated with a Severe Form of Familial Hypertrophic Cardiomyopathy.
Golubenko MV, Pavlyukova EN, Salakhov RR, Makeeva OA, Puzyrev KV, Glotov OS, Puzyrev VP, Nazarenko MS. Front Biosci (Schol Ed). 2024 Feb 23; 16(1):1.
Enhanced myofilament calcium sensitivity aggravates abnormal calcium handling and diastolic dysfunction in patient-specific induced pluripotent stem cell-derived cardiomyocytes with MYH7 mutation. [Cell Calcium. 2024]
Enhanced myofilament calcium sensitivity aggravates abnormal calcium handling and diastolic dysfunction in patient-specific induced pluripotent stem cell-derived cardiomyocytes with MYH7 mutation.
Guo G, Wang L, Li X, Fu W, Cao J, Zhang J, Liu Y, Liu M, Wang M, Zhao G, et al. Cell Calcium. 2024 Jan; 117:102822. Epub 2023 Nov 8.
A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy. [BMC Cardiovasc Disord. 2023]
A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy.
Naderi N, Mohsen-Pour N, Nilipour Y, Pourirahim M, Maleki M, Kalayinia S. BMC Cardiovasc Disord. 2023 Oct 4; 23(1):487. Epub 2023 Oct 4.

RefSeq genomic sequence
See the genomic reference sequence for the MYH7 gene (NG_007884.1).
RefSeq protein isoforms
See 2 reference sequence protein isoforms for the MYH7 gene.

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Transcript/Protein Information [PANTHER Classification System]
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beta-myosin heavy chain (1151 AA), partial [Homo sapiens]
beta-myosin heavy chain (1151 AA), partial [Homo sapiens]
gi|29468|emb|CAA35940.1|

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