Homo sapiens full open reading frame cDNA clone RZPDo834F029D for gene - Nucleotide

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A mutation in CCDC91, Homo sapiens coiled-coil domain containing 91 protein, cause autosomal-dominant acrokeratoelastoidosis. [Eur J Hum Genet. 2024]
A mutation in CCDC91, Homo sapiens coiled-coil domain containing 91 protein, cause autosomal-dominant acrokeratoelastoidosis.
Zhu Y, Bai Y, Yan W, Li M, Wu F, Xu M, Wu N, Ge H, Liu Y. Eur J Hum Genet. 2024 Jun; 32(6):647-655. Epub 2024 Apr 16.
A novel CCDC91 isoform associated with ossification of the posterior longitudinal ligament of the spine works as a non-coding RNA to regulate osteogenic genes. [Am J Hum Genet. 2023]
A novel CCDC91 isoform associated with ossification of the posterior longitudinal ligament of the spine works as a non-coding RNA to regulate osteogenic genes.
Nakajima M, Koido M, Guo L, Terao C, Ikegawa S. Am J Hum Genet. 2023 Apr 6; 110(4):638-647. Epub 2023 Mar 28.
EZH2 depletion potentiates MYC degradation inhibiting neuroblastoma and small cell carcinoma tumor formation. [Nat Commun. 2022]
EZH2 depletion potentiates MYC degradation inhibiting neuroblastoma and small cell carcinoma tumor formation.
Wang L, Chen C, Song Z, Wang H, Ye M, Wang D, Kang W, Liu H, Qing G. Nat Commun. 2022 Jan 10; 13(1):12. Epub 2022 Jan 10.

Homo sapiens full open reading frame cDNA clone RZPDo834F029D for gene FLJ11088,...
Homo sapiens full open reading frame cDNA clone RZPDo834F029D for gene FLJ11088, GGA binding partner; complete cds, incl. stopcodon
gi|48146670|emb|CR457277.1|

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Nucleotide