KEGG   VARIANT: 148738v1
Entry
148738v1                      Variant                              
Name
HJV mutation
Type
Loss of function
Gene
HJV  hemojuvelin BMP co-receptor [KO:K23100]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 608374
Network
nt06507  TGFB signaling
Disease
H00211  Hemochromatosis
Reference
PMID:30420953
  Authors
Pantopoulos K
  Title
Inherited Disorders of Iron Overload.
  Journal
Front Nutr 5:103 (2018)
DOI:10.3389/fnut.2018.00103
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