Browse All / Genes / NIPA1

NIPA1

NIPA magnesium transporter 1
2 disorders 1 causative 1 no genetic record 15q11.2 gene with protein product
HGNC:17043MonarchNCBI Gene 123606ENSG00000170113UniProt Q7RTP0OMIM 608145

Previous symbols: SPG6. Aliases: MGC35570, SLC57A1.

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

DisorderRelationshipWhere the gene appears
Hereditary Spastic Paraplegia causative
mechanism: Endosomal Membrane Trafficking and Sorting Defect (SPG6/SPG8/SPG80)
subtype: SPG6
scoped to subtype: SPG6
Prader-Willi Syndrome no genetic record
subtype: Type I Deletion
Mechanism modules · computed from kb/

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.