KEGG   VARIANT: 23137v1
Entry
23137v1                      Variant                               
Name
SMC5 mutation
Type
Loss of function
Gene
SMC5  structural maintenance of chromosomes 5 [KO:K22803]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 609386
Network
nt06506  Double-strand break repair
Disease
H02639  Atelis syndrome
Reference
  Authors
Grange LJ, Reynolds JJ, Ullah F, Isidor B, Shearer RF, Latypova X, Baxley RM, Oliver AW, Ganesh A, Cooke SL, Jhujh SS, McNee GS, Hollingworth R, Higgs MR, Natsume T, Khan T, Martos-Moreno GA, Chupp S, Mathew CG, Parry D, Simpson MA, Nahavandi N, Yuksel Z, Drasdo M, Kron A, Vogt P, Jonasson A, Seth SA, Gonzaga-Jauregui C, Brigatti KW, Stegmann APA, Kanemaki M, Josifova D, Uchiyama Y, Oh Y, Morimoto A, Osaka H, Ammous Z, Argente J, Matsumoto N, Stumpel CTRM, Taylor AMR, Jackson AP, Bielinsky AK, Mailand N, Le Caignec C, Davis EE, Stewart GS
  Title
Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy.
  Journal
Nat Commun 13:6664 (2022)
DOI:10.1038/s41467-022-34349-8
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