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Protein Ontology Report - hNIPA1

This page represents a class of proteins encompassing all the protein products of the NIPA1 gene in human.
Ontology Information
PRO ID PR:Q7RTP0 Show OBO stanza
PRO name magnesium transporter NIPA1 (human)
PRO-short-label: hNIPA1
EXACT: non-imprinted in Prader-Willi/Angelman syndrome region protein 1 (human); spastic paraplegia 6 protein (human)
Gene-based: NIPA1; SPG6
Definition A magnesium transporter NIPA1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q7RTP0]
PRO Category organism-gene
Parent PR:000011217 magnesium transporter NIPA1
Terms by PRO Category Retrieve All terms OBO Stanza / PAF
Category Number of Terms
organism-gene 1
organism-sequence 2
organism-modification 0
Term Hierarchy Visualization DAG     OLS     Cytoscape

Interactive Sequence View Select/align proteoforms across species

Protein Forms
PRO ID & Category Annotation Complex Name Short Label Definition & Comment