KEGG   VARIANT: 23594v1
Entry
23594v1                      Variant                               
Name
ORC6 mutation
Type
Loss of function
Gene
ORC6  origin recognition complex subunit 6 [KO:K02608]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 607213
Network
nt06509  DNA replication
Disease
H01889  Meier-Gorlin syndrome
Reference
PMID:25691413
  Authors
Shalev SA, Khayat M, Etty DS, Elpeleg O
  Title
Further insight into the phenotype associated with a mutation in the ORC6 gene, causing Meier-Gorlin syndrome 3.
  Journal
Am J Med Genet A 167A:607-11 (2015)
DOI:10.1002/ajmg.a.36906
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