sodium channel modifier 1 isoform 2 [Homo sapiens]

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Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia. [Am J Hum Genet. 2022]
Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia.
Iturrate A, Rivera-Barahona A, Flores CL, Otaify GA, Elhossini R, Perez-Sanz ML, Nevado J, Tenorio-Castano J, Triviño JC, Garcia-Gonzalo FR, et al. Am J Hum Genet. 2022 Oct 6; 109(10):1828-1849. Epub 2022 Sep 8.
SCNM1, a putative RNA splicing factor that modifies disease severity in mice. [Science. 2003]
SCNM1, a putative RNA splicing factor that modifies disease severity in mice.
Buchner DA, Trudeau M, Meisler MH. Science. 2003 Aug 15; 301(5635):967-9.
Evidence for a direct role of the disease modifier SCNM1 in splicing. [Hum Mol Genet. 2007]
Evidence for a direct role of the disease modifier SCNM1 in splicing.
Howell VM, Jones JM, Bergren SK, Li L, Billi AC, Avenarius MR, Meisler MH. Hum Mol Genet. 2007 Oct 15; 16(20):2506-16. Epub 2007 Jul 26.

RefSeq mRNA
See reference mRNA sequence for the SCNM1 gene (NM_001204856.2).
RefSeq protein isoforms
See the other reference sequence protein isoform for the SCNM1 gene (NP_076946.1).

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OncoMX cancer biomarker resource [OncoMX cancer biomarker resou...]
OncoMX cancer biomarker resource
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reagents [ExactAntigen/Labome]
reagents
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