Webb16 jan. 2024 · PHIP (pleckstrin homology domain interacting protein; OMIM *612870) was originally identified as a candidate gene for intellectual disability (ID) in one individual … WebbPHIP-related disorder, also known as Chung-Jansen syndrome, is a rare condition caused by a change in the pleckstrin homology domain-interacting protein (PHIP) gene. The most common signs and symptoms, include mild to severe learning problems, behavior …

PHIP as a therapeutic target for driver-negative subtypes of

WebbGenetic disorders occur when a mutation (a harmful change to a gene, also known as a pathogenic variant) affects your genes or when you have the wrong amount of genetic material. Genes are made of DNA (deoxyribonucleic acid), which contain instructions for cell functioning and the characteristics that make you unique. WebbDescription MYH9 -related disorder is a condition that can have many signs and symptoms, including bleeding problems, hearing loss, kidney (renal) disease, and clouding of the lens of the eyes ( cataracts ). The bleeding problems in people with MYH9 -related disorder are due to thrombocytopenia. cytogen whey protein

The phenotypic spectrum of proximal 6q deletions based on a …

Webb1 nov. 2024 · Interestingly, PHIP encodes two protein-isoforms, PHIP/DCAF14 and NDRP, each involved in neurodevelopmental processes, including E3 ubiquitination and … Webb13 nov. 2024 · Variants in the pleckstrin homology domain-interacting protein (PHIP) gene are implicated in the clinical phenotype of Chung–Jansen syndrome, which includes dysmorphic features, cognitive dysfunction, aberrant behavior, and childhood onset obesity.Following a systematic literature review, 35 patients are reported to have unique … WebbThe first 5 individuals with loss-of-function point mutations in the PHIP gene were ascertained from a cohort of 3,275 patients with intellectual disability collected through … cytoglobin function