Splet16. avg. 2024 · SHROOM4, which is partially deleted in this patient, is involved in neuronal development and was shown to be associated with X-linked intellectual disability. This is a candidate gene, the loss of ... SpletLegend. Settings. Analysis
The lncRNA Firre anchors the inactive X chromosome to the …
Splet21. mar. 2024 · GeneCards Summary for SHROOM1 Gene. SHROOM1 (Shroom Family Member 1) is a Protein Coding gene. Diseases associated with SHROOM1 include Retroperitoneum Carcinoma and Transient Arthritis . Gene Ontology (GO) annotations related to this gene include actin filament binding . An important paralog of this gene is … Splet01. feb. 2015 · Here we report the clinical and molecular characterization of two Xp11.22 deletions including SHROOM4 and CLCN5 genes. These deletions appeared in the same X chromosome of the same patient. The patient is a six-year-old boy who presented hydrocephalus, severe psychomotor and growth retardation, facial dysmorphism and … rj zug db
(PDF) SHROOM4 Variants Are Associated With X-Linked Epilepsy …
Spletshroom4. sections. tissue brain single cell type tissue cell type pathology disease immune cell blood protein subcellular cell line structure metabolic about. introduction history organization publications antibody submission antibody availability acknowledgments contact news. news articles press room ... Splet28. sep. 2006 · Shroom4 is expressed in a wide range of cell types during mouse development, including vascular endothelium and the polarized epithelium of the neural tube and kidney. In endothelial cells and embryo fibroblasts, endogenous Shroom4 co-distributes with myosin II to a distinct cytoplasmic population of F-actin and ectopic … SpletSHROOM4 (KIAA1202) protein expression summary. Human assay: EFO-21 fixed with PFA, dilution: 1:200 Human assay: HUVEC/TERT2 fixed with PFA, dilution: 1:200 rj11 io box price