Protein Ontology Report - hNIPA1 PR:Q7RTP0 - http://purl.obolibrary.org/obo/PR_Q7RTP0

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)
Synonyms	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 Organism-Specific Category Number of Terms organism-gene 1 organism-sequence 2 organism-modification 0
Term Hierarchy Visualization	DAG     OLS     Cytoscape

Related Cross References
DB identifiers	HGNC:17043, Reactome:R-HSA-5215946, UniProtKB:Q7RTP0

Interactive Sequence View Select/align proteoforms across species

Protein Forms Display Category: All All organism-gene organism-sequence
PRO ID & Category Annotation Complex Name Short Label Definition & Comment

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