ligase protein that in humans is encoded by the CUL7 gene. It is associated with 3-M syndrome. CUL7 has been shown to interact with RBX1. GRCh38: Ensembl...

medical literature in 1972. Mutations in any one of the following three genes: CUL7, OBSL1, and CCDC8 are responsible for the occurrence of this disorder. It...

p53 p63 p73 Other Cdc2 Cdc25 Cdc42 Cellular apoptosis susceptibility protein E2F Maturation promoting factor Wee Cullin (CUL7) Phases and checkpoints...

mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth". Am. J. Hum. Genet. 89 (1): 148–53. doi:10...

HGNC:2554 Q13619 3794 CUL4B HGNC:2555 Q13620 3795 CUL5 HGNC:2556 Q93034 3796 CUL7 HGNC:21024 Q14999 3797 CUL9 HGNC:15982 Q8IWT3 3798 CUTA HGNC:21101 O60888...

(Elongin C - CUL2 - SOCS-box) CUL3, part of CUL3-BTB complex CUL4A CUL4B CUL5 CUL7 CUL9, also known as PARC There is also a more distant member called ANAPC2...

""AKAP11 Gene - A-Kinase Anchoring Protein 11"". GeneCards. December 9, 2024. "CUL7 gene: MedlinePlus Genetics". medlineplus.gov. Retrieved 2024-12-12. ""FBXL17...

monkey kidney cell cultures being used to grow Sabin OPV. The TAg has a CUL7-binding domain, a TP53-binding domain, a Zinc finger, and a Superfamily 3...

turn-over. RBX1 has been shown to interact with: CAND1, CUL1, CUL2, CUL4A, CUL5 CUL7, DCUN1D1, and P70-S6 Kinase 1. GRCh38: Ensembl release 89: ENSG00000100387...

Winter R, Cormier-Daire V (October 2005). "Identification of mutations in CUL7 in 3-M syndrome". Nature Genetics. 37 (10): 1119–24. doi:10.1038/ng1628....