Homo sapiens immunoglobulin superfamily, member 1, mRNA (cDNA clone MG - Nucleotide

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[Clinical characteristics and genetic analysis of four patients with central hypothyroidism due to IGSF1 gene variants]. [Zhonghua Yi Xue Yi Chuan Xue Z...]
[Clinical characteristics and genetic analysis of four patients with central hypothyroidism due to IGSF1 gene variants].
Zhang C, Chen L, Chen X, Xie R, Wang F, Chen T, Wang X, Sun H, Zhang D, Wu H. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Mar 10; 40(3):322-327.
IGSF1 mutation as a cause of isolated central hypothyroidism. [Endocrinol Diabetes Nutr (Engl...]
IGSF1 mutation as a cause of isolated central hypothyroidism.
Costas Eimil J, Sánchez-Sobrino P. Endocrinol Diabetes Nutr (Engl Ed). 2022 Dec; 69(10):913-914. Epub 2022 Dec 1.
IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency. [Eur J Endocrinol. 2022]
IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency.
Fourneaux R, Reynaud R, Mougel G, Castets S, Bretones P, Dauriat B, Edouard T, Raverot G, Barlier A, Brue T, et al. Eur J Endocrinol. 2022 Dec 1; 187(6):787-795. Epub 2022 Nov 3.

RefSeq alternative splicing
See 19 reference mRNA sequence splice variants for the IGSF1 gene.

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UI-E-EJ0-ahf-m-23-0-UI.r1 UI-E-EJ0 Homo sapiens cDNA clone UI-E-EJ0-ahf-m-23-0-U...
UI-E-EJ0-ahf-m-23-0-UI.r1 UI-E-EJ0 Homo sapiens cDNA clone UI-E-EJ0-ahf-m-23-0-UI 5', mRNA sequence
gi|19025257|gnl|dbEST|11292932|gb|B 99.1|

Nucleotide
Homo sapiens ribosomal protein S24 (RPS24), RefSeqGene (LRG_1145) on chromosome ...
Homo sapiens ribosomal protein S24 (RPS24), RefSeqGene (LRG_1145) on chromosome 10
gi|255522845|ref|NG_012633.1||gnl|L G_1145

Nucleotide

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Nucleotide