Homo sapiens SNF2 related chromatin remodeling ATPase with DExD box 1 - Nucleotide

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Genome-wide CRISPR screens identify novel regulators of wild-type and mutant p53 stability. [Mol Syst Biol. 2024]
Genome-wide CRISPR screens identify novel regulators of wild-type and mutant p53 stability.
Lü Y, Cho T, Mukherjee S, Suarez CF, Gonzalez-Foutel NS, Malik A, Martinez S, Dervovic D, Oh RH, Langille E, et al. Mol Syst Biol. 2024 Jun; 20(6):719-740. Epub 2024 Apr 5.
Basan syndrome in a family from South India: a novel SMARCAD1 variant. [Clin Exp Dermatol. 2024]
Basan syndrome in a family from South India: a novel SMARCAD1 variant.
Mathews I, Wagh S, Baby A, Chandrashekar L, Dalal A. Clin Exp Dermatol. 2024 Mar 21; 49(4):437-440.
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability. [Cell. 2023]
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability.
Gall-Duncan T, Luo J, Jurkovic CM, Fischer LA, Fujita K, Deshmukh AL, Harding RJ, Tran S, Mehkary M, Li V, et al. Cell. 2023 Oct 26; 186(22):4898-4919.e25. Epub 2023 Oct 11.

RefSeq alternative splicing
See 13 reference mRNA sequence splice variants for the SMARCAD1 gene.
RefSeq protein product
See the reference protein sequence for SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1 isoform e (NP_001362787.1).

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens SNF2 related chromatin remodeling ATPase with DExD box 1 (SMARCAD1)...
Homo sapiens SNF2 related chromatin remodeling ATPase with DExD box 1 (SMARCAD1), transcript variant 9, mRNA
gi|1772790411|ref|NM_001375858.1|

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Nucleotide