mothers against decapentaplegic homolog 1 [Homo sapiens]

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SMAD1 Loss-of-Function Variant Responsible for Congenital Heart Disease. [Biomed Res Int. 2022]
SMAD1 Loss-of-Function Variant Responsible for Congenital Heart Disease.
Wang Z, Qiao XH, Xu YJ, Liu XY, Huang RT, Xue S, Qiu HY, Yang YQ. Biomed Res Int. 2022; 2022:9916325. Epub 2022 Mar 3.
Variants of SMAD1 gene increase the risk of colorectal cancer in the Bangladeshi population. [Tumour Biol. 2020]
Variants of SMAD1 gene increase the risk of colorectal cancer in the Bangladeshi population.
Karmokar PF, Shabnaz S, Aziz MA, Asaduzzaman M, Shahriar M, Bhuiyan MA, Mosaddek ASM, Islam MS. Tumour Biol. 2020 Sep; 42(9):1010428320958955.
SMAD1 promoter hypermethylation and lack of SMAD1 expression in Hodgkin lymphoma: a potential target for hypomethylating drug therapy. [Haematologica. 2021]
SMAD1 promoter hypermethylation and lack of SMAD1 expression in Hodgkin lymphoma: a potential target for hypomethylating drug therapy.
Gerlach MM, Stelling-Germani A, Ting Wu C, Newrzela S, Döring C, Vela V, Müller A, Hartmann S, Tzankov A. Haematologica. 2021 Feb 1; 106(2):619-621. Epub 2021 Feb 1.

RefSeq genomic sequence
See the genomic reference sequence for the SMAD1 gene (NG_042284.1).
RefSeq mRNA
See reference mRNA sequence for the SMAD1 gene (NM_001354811.1).
RefSeq protein isoforms
See 21 reference sequence protein isoforms for the SMAD1 gene.

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Protein