Splet146. Nr 4–6. Zawał serca. WIADOMOŚCI LEKARSKIE 2008, LXI, 4–6. Małgorzata Z. Lisik, Aleksander L. Sieroń. NIEPEŁNOSPRAWNOŚĆ INTELEKTUALNA Splet03. dec. 2024 · SHROOM4 shroom family member 4 [ (human)] Gene ID: 57477, updated on 3-Dec-2024. Summary. This gene encodes a member of the APX/Shroom family, which contain an N-terminal PDZ domain and a C-terminal ASD2 motif. The encoded protein may play a role in cytoskeletal architecture. Mutations in this gene have been linked to the X …
SHROOM4 protein expression summary - The Human Protein Atlas
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 ... 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 … black academy game
Tissue expression of SHROOM4 - Summary - Protein Atlas
SpletPROTEIN SUMMARY SECTION OVERVIEW RNA DATA ANTIBODY DATA. SHROOM4 INFORMATION. Proteini. Full gene name according to HGNC. Shroom family member 4. … SpletSHROOM4 and members of this protein family have been shown to localize at the cytoskeleton, and play a role in neurulation, cellular architecture, actin remodeling, ion … SpletDefects in SHROOM4 are the cause of mental retardation syndromic X-linked Stocco dos Santos type (SDSX) [MIM:300434]. A syndrome characterized by severe mental retardation with hyperactivity, aggressive behavior, delayed or no speech, and seizures. Additional features include congenital bilateral hip luxation, short stature, and kyphosis. black academy badge mercier padded jacket