ⓘ MEGF10

                                     

ⓘ MEGF10

Multiple EGF-like-domains 10 is a protein that in humans is encoded by the MEGF10 gene.

MEGF10 is a regulator of satellite cell myogenesis and interacts with Notch1 in myoblasts. Been shown to be the cause of the early appearance of myopathy, areflexia, respiratory distress and dysphagia.

MEGF10 and MEGF11, play a crucial role in the formation of mosaics by two retinal interneurons subtypes, starburst amacrine cells and horizontal cells in mice. These cells are less likely to be near neighbours of the same subtype than would occur by chance, resulting in zones that separate them. Mosaic arrangements provide a mechanism of distribution of each cell type evenly across the retina, ensuring that all parts of the visual field have access to the full set of processing elements.

                                     
  • Sci. 200 1141 441 61. doi: 10 1098 rspb.1978.0026. PMID 26058. Kay, JN Chu, MW Sanes, JR 2012 MEGF10 and MEGF 11 mediate homotypic interactions
  • the visual field have access to a full set of processing elements. MEGF10 and MEGF 11 transmembrane proteins have critical roles in the formation of the
  • Megf 8 also known as Multiple Epidermal Growth Factor - like Domains 8, is a protein coding gene that encodes a single pass membrane protein, known to participate
  • Polyneuropathy Achilles and plantar reflexes Hyperreflexia, exaggerated reflexes. MEGF10 Hyporeflexia - an overview ScienceDirect Topics www.sciencedirect.com
  • common recessive mutations causing this condition include those in the TTN, MEGF10 and CACNA1S genes. Automsomal dominant mutations associated with this disease
  • LAMA4 LAMA5 LAMB1 LAMB2 LAMB3 LAMB4 LAMC1 LAMC2 LAMC3 MEGF10 MEGF 12 MEGF 6 MEGF 8 MEGF 9 NSR1 NTN1 NTN2L NTN4 NTNG1 NTNG2 RESDA1 SCARF1 SCARF2
  • LRP - 4 also known as multiple epidermal growth factor - like domains 7 MEGF 7 is a protein that in humans is encoded by the LRP4 gene. LRP - 4 is a member
  • is located on chromosome 6 in humans. Additionally, three key SNPs in the MEGF 8 gene, located on chromosome 19 at 19q13.2, have been identified as primary
  • Greek dys meaning bad or disordered, and the root phag - meaning eat MEGF10 Pseudodysphagia, an irrational fear of swallowing or choking Aphagia Smithard
  • known as multiple epidermal growth factor EGF repeat - containing protein MEGF 7 LDLR - related protein 1 LDLR - related protein 1b Megalin. Listed below are
  • KLHL32 KLHL34 KLHL4 KLHL40 KLHL5 KLHL6 KLHL7 KLHL8 KLHL9 LZTR1 MEGF 8 MKLN1 RABEPK SARCOSIN UNDERSTANDING THE FUNCTION OF ACTIN - BINDING PROTEINS