BRICK1 is a putative micropeptide protein that in humans is encoded by the C3orf10 gene. [5] [6]
BRICK1 is a putative micropeptide protein that in humans is encoded by the C3orf10 gene. [5] [6]
Von Hippel–Lindau disease (VHL), also known as VonHippel–Lindau syndrome, is a rare genetic disorder with multisystem involvement. It is characterized by visceral cysts and benign tumors with potential for subsequent malignant transformation. It is a type of phakomatosis that results from a mutation in the Von Hippel–Lindau tumor suppressor gene on chromosome 3p25.3.
Profilin is an actin-binding protein involved in the dynamic turnover and reconstruction of the actin cytoskeleton. It is found in most eukaryotic organisms. Profilin is important for spatially and temporally controlled growth of actin microfilaments, which is an essential process in cellular locomotion and cell shape changes. This restructuring of the actin cytoskeleton is essential for processes such as organ development, wound healing, and the hunting down of infectious intruders by cells of the immune system.
The Von Hippel–Lindau tumor suppressor also known as pVHL is a protein that, in humans, is encoded by the VHL gene. Mutations of the VHL gene are associated with Von Hippel–Lindau disease, which is characterized by hemangioblastomas of the brain, spinal cord and retina. It is also associated with kidney and pancreatic lesions.
Profilin-1 is a protein that in humans is encoded by the PFN1 gene.
Wiskott-Aldrich syndrome protein family member 2 is a protein that in humans is encoded by the WASF2 gene.
Cytoplasmic protein NCK1 is a protein that in humans is encoded by the NCK1 gene.
Hypoxia-inducible factor 3 alpha is a protein that in humans is encoded by the HIF3A gene.
Dynamin-1 is a protein that in humans is encoded by the DNM1 gene.
Vasodilator-stimulated phosphoprotein is a protein that in humans is encoded by the VASP gene.
Neural Wiskott-Aldrich syndrome protein is a protein that in humans is encoded by the WASL gene.
Wiskott–Aldrich syndrome protein family member 1, also known as WASP-family verprolin homologous protein 1 (WAVE1), is a protein that in humans is encoded by the WASF1 gene.
WAS/WASL-interacting protein (WIP) is a protein that in humans is encoded by the WIPF1 gene.
Cytoplasmic FMR1-interacting protein 2 is a protein that in humans is encoded by the CYFIP2 gene. Cytoplasmic FMR1 interacting protein is a 1253 amino acid long protein and is highly conserved sharing 99% sequence identity to the mouse protein. It is expressed mainly in brain tissues, white blood cells and the kidney.
Profilin-2 is a protein that in humans is encoded by the PFN2 gene.
Nck-associated protein 1 is a protein that in humans is encoded by the NCKAP1 gene.
Cytoplasmic FMR1-interacting protein 1 is a protein that in humans is encoded by the CYFIP1 gene.
JADE1 is a protein that in humans is encoded by the JADE1 gene.
Cdc42 effector protein 2 is a protein that in humans is encoded by the CDC42EP2 gene.
L-2-hydroxyglutarate dehydrogenase, mitochondrial is an enzyme that in humans is encoded by the L2HGDH gene, also known as C14orf160, on chromosome 14.
Myosin-XV is a protein that in humans is encoded by the MYO15A gene.
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