CCR4-NOT transcription complex subunit 9 isoform X2 [Homo sapiens]

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Identify Conserved Domains
View conserved domains detected in this protein sequence using CD-search.

De novo variants in CNOT9 cause a neurodevelopmental disorder with or without epilepsy. [Genet Med. 2023]
De novo variants in CNOT9 cause a neurodevelopmental disorder with or without epilepsy.
von Wintzingerode L, Ben-Zeev B, Cesario C, Chan KM, Depienne C, Elpeleg O, Iascone M, Kelley WV, Nassogne MC, Niceta M, et al. Genet Med. 2023 Jul; 25(7):100859. Epub 2023 Apr 20.
Whole exome sequencing identifies a recurrent RQCD1 P131L mutation in cutaneous melanoma. [Oncotarget. 2015]
Whole exome sequencing identifies a recurrent RQCD1 P131L mutation in cutaneous melanoma.
Wong SQ, Behren A, Mar VJ, Woods K, Li J, Martin C, Sheppard KE, Wolfe R, Kelly J, Cebon J, et al. Oncotarget. 2015 Jan 20; 6(2):1115-27.
Involvement of RQCD1 overexpression, a novel cancer-testis antigen, in the Akt pathway in breast cancer cells. [Int J Oncol. 2009]
Involvement of RQCD1 overexpression, a novel cancer-testis antigen, in the Akt pathway in breast cancer cells.
Ajiro M, Katagiri T, Ueda K, Nakagawa H, Fukukawa C, Lin ML, Park JH, Nishidate T, Daigo Y, Nakamura Y. Int J Oncol. 2009 Oct; 35(4):673-81.

RefSeq mRNA
See reference mRNA sequence for the CNOT9 gene (XM_047446272.1).
RefSeq protein isoforms
See 7 reference sequence protein isoforms for the CNOT9 gene.

Your browsing activity is empty.

Activity recording is turned off.

Protein