myosin-binding protein C, slow-type isoform X13 [Homo sapiens]

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Congenital tremor and myopathy secondary to novel MYBPC1 variant. [J Neurol Sci. 2024]
Congenital tremor and myopathy secondary to novel MYBPC1 variant.
Leduc-Pessah H, Smith IC, Kernohan KD, Sampaio M, Melkus G, Strasser L, Chisholm C, Huang L, Hanes I, Tran MA, et al. J Neurol Sci. 2024 Feb 15; 457:122864. Epub 2024 Jan 4.
A Case Series of Patients With MYBPC1 Gene Variants Featuring Undulating Tongue Movements as Myogenic Tremor. [Pediatr Neurol. 2023]
A Case Series of Patients With MYBPC1 Gene Variants Featuring Undulating Tongue Movements as Myogenic Tremor.
Uneoka S, Kobayashi T, Numata-Uematsu Y, Oikawa Y, Katata Y, Okubo Y, Abe Y, Kikuchi A, Takayama J, Tamiya G, et al. Pediatr Neurol. 2023 Sep; 146:16-20. Epub 2023 Jun 12.
MYBPC1 is a key regulator for laryngeal carcinoma formation. [Anticancer Drugs. 2023]
MYBPC1 is a key regulator for laryngeal carcinoma formation.
Liu J, Song J, Li C. Anticancer Drugs. 2023 Jan 1; 34(1):1-8. Epub 2022 Oct 22.

RefSeq genomic sequence
See the genomic reference sequence for the MYBPC1 gene (NG_031912.2).
RefSeq mRNA
See reference mRNA sequence for the MYBPC1 gene (XM_017019320.2).

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SNP
Related SNPs

myosin-binding protein C, slow-type isoform X13 [Homo sapiens]
myosin-binding protein C, slow-type isoform X13 [Homo sapiens]
gi|1034579625|ref|XP_016874809.1|

Protein
Homo sapiens myosin binding protein C1 (MYBPC1), transcript variant 9, mRNA
Homo sapiens myosin binding protein C1 (MYBPC1), transcript variant 9, mRNA
gi|2222724830|ref|NM_001254722.3|

Nucleotide
Homo sapiens potassium calcium-activated channel subfamily N member 1 (KCNN1), t...
Homo sapiens potassium calcium-activated channel subfamily N member 1 (KCNN1), transcript variant 3, mRNA
gi|1905437360|ref|NM_001386975.1|

Nucleotide

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Protein