KEGG   VARIANT: 9423v1
Entry
9423v1                      Variant                                
Name
NTN1 mutation
Type
Loss of function
Gene
NTN1  netrin 1 [KO:K06843]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 601614
Network
nt06541  Cytoskeleton in neurons
Disease
H01287  Congenital mirror movements
Reference
  Authors
Meneret A, Franz EA, Trouillard O, Oliver TC, Zagar Y, Robertson SP, Welniarz Q, Gardner RJM, Gallea C, Srour M, Depienne C, Jasoni CL, Dubacq C, Riant F, Lamy JC, Morel MP, Guerois R, Andreani J, Fouquet C, Doulazmi M, Vidailhet M, Rouleau GA, Brice A, Chedotal A, Dusart I, Roze E, Markie D
  Title
Mutations in the netrin-1 gene cause congenital mirror movements.
  Journal
J Clin Invest 127:3923-3936 (2017)
DOI:10.1172/JCI95442
Reference
  Authors
Lai Wing Sun K, Correia JP, Kennedy TE
  Title
Netrins: versatile extracellular cues with diverse functions.
  Journal
Development 138:2153-69 (2011)
DOI:10.1242/dev.044529
Reference
  Authors
Ahmed G, Shinmyo Y
  Title
Multiple Functions of Draxin/Netrin-1 Signaling in the Development of Neural Circuits in the Spinal Cord and the Brain.
  Journal
Front Neuroanat 15:766911 (2021)
DOI:10.3389/fnana.2021.766911
LinkDB

DBGET integrated database retrieval system