DISEASES

Disease-gene associations mined from literature

Literature associating NIPA1 and autosomal recessive congenital ichthyosis

NIPA1 [ENSP00000337452]

Non-imprinted in Prader-Willi/Angelman syndrome region protein 1; Acts as a Mg(2+) transporter. Can also transport other divalent cations such as Fe(2+), Sr(2+), Ba(2+), Mn(2+) and Co(2+) but to a much less extent than Mg(2+) (By similarity); Belongs to the NIPA family.

Synonyms:  NIPA1,  NIPA1p,  hNIPA1,  A0A024R344,  H0YLJ9 ...

Linkouts:  STRING  Pharos  UniProt  OMIM