Homo sapiens cDNA FLJ16764 fis, clone BRAWH2010980, highly similar to - Nucleotide

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IMPDH1-associated autosomal dominant retinitis pigmentosa: natural history of novel variant Lys314Gln and a comprehensive literature search. [Ophthalmic Genet. 2023]
IMPDH1-associated autosomal dominant retinitis pigmentosa: natural history of novel variant Lys314Gln and a comprehensive literature search.
Sakti DH, Cornish EE, Nash BM, Jamieson RV, Grigg JR. Ophthalmic Genet. 2023 Oct; 44(5):437-455. Epub 2023 May 31.
The E3 ligase RBCK1 reduces the sensitivity of ccRCC to sunitinib through the ANKRD35-MITD1-ANXA1 axis. [Oncogene. 2023]
The E3 ligase RBCK1 reduces the sensitivity of ccRCC to sunitinib through the ANKRD35-MITD1-ANXA1 axis.
Wang Y, Peng M, Zhong Y, Xiong W, Zhu L, Jin X. Oncogene. 2023 Mar; 42(13):952-966. Epub 2023 Feb 2.
c-Myc-IMPDH1/2 axis promotes tumourigenesis by regulating GTP metabolic reprogramming. [Clin Transl Med. 2023]
c-Myc-IMPDH1/2 axis promotes tumourigenesis by regulating GTP metabolic reprogramming.
Zhang Q, Cui K, Yang X, He Q, Yu J, Yang L, Yao G, Guo W, Luo Z, Liu Y, et al. Clin Transl Med. 2023 Jan; 13(1):e1164.

RefSeq alternative splicing
See 25 reference mRNA sequence splice variants for the IMPDH1 gene.

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Nucleotide