Homo sapiens ATP binding cassette subfamily C member 9 (ABCC9), transc - Nucleotide

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Novel loss-of-function variants expand ABCC9-related intellectual disability and myopathy syndrome. [Brain. 2024]
Novel loss-of-function variants expand ABCC9-related intellectual disability and myopathy syndrome.
Efthymiou S, Scala M, Nagaraj V, Ochenkowska K, Komdeur FL, Liang RA, Abdel-Hamid MS, Sultan T, Barøy T, Van Ghelue M, et al. Brain. 2024 May 3; 147(5):1822-1836.
Vascular K(ATP) channel structural dynamics reveal regulatory mechanism by Mg-nucleotides. [Proc Natl Acad Sci U S A. 2021]
Vascular K(ATP) channel structural dynamics reveal regulatory mechanism by Mg-nucleotides.
Sung MW, Yang Z, Driggers CM, Patton BL, Mostofian B, Russo JD, Zuckerman DM, Shyng SL. Proc Natl Acad Sci U S A. 2021 Nov 2; 118(44).
Consequences of SUR2[A478V] Mutation in Skeletal Muscle of Murine Model of Cantu Syndrome. [Cells. 2021]
Consequences of SUR2[A478V] Mutation in Skeletal Muscle of Murine Model of Cantu Syndrome.
Scala R, Maqoud F, Zizzo N, Passantino G, Mele A, Camerino GM, McClenaghan C, Harter TM, Nichols CG, Tricarico D. Cells. 2021 Jul 15; 10(7). Epub 2021 Jul 15.

RefSeq protein product
See the reference protein sequence for ATP-binding cassette sub-family C member 9 isoform 5 (NP_001364203.1).

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens myocyte enhancer factor 2C (MEF2C), transcript variant 4, mRNA
Homo sapiens myocyte enhancer factor 2C (MEF2C), transcript variant 4, mRNA
gi|301069381|ref|NM_001193348.1|

Nucleotide
PPP1R3C [Microcebus murinus]
PPP1R3C [Microcebus murinus]
Gene ID:105872005

Gene

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Nucleotide