KEGG   VARIANT: 1356v1
Entry
1356v1                      Variant                                
Name
CP mutation
Type
Loss of function
Gene
CP  ceruloplasmin [KO:K13624]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 117700
Network
nt06525  Ferroptosis
Disease
H02206  Aceruloplasminemia
Reference
PMID:24209437
  Authors
Kono S
  Title
Aceruloplasminemia: an update.
  Journal
Int Rev Neurobiol 110:125-51 (2013)
DOI:10.1016/B978-0-12-410502-7.00007-7
Reference
PMID:35264864
  Authors
Liu Z, Wang M, Zhang C, Zhou S, Ji G
  Title
Molecular Functions of Ceruloplasmin in Metabolic Disease Pathology.
  Journal
Diabetes Metab Syndr Obes 15:695-711 (2022)
DOI:10.2147/DMSO.S346648
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