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Protein Coding Gene : Nipa1 non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human)
Primary Identifier  MGI:2442058 Organism  mouse, laboratory
Chromosome  7 NCBI Gene Number  233280
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable magnesium ion transmembrane transporter activity. Involved in magnesium ion transport. Located in early endosome and plasma membrane. Is expressed in brain. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 6. Orthologous to human NIPA1 (NIPA magnesium transporter 1).
  • synonyms:
  • non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human),
  • Spg6,
  • RIKEN cDNA A830014A18 gene,
  • A830014A18Rik,
  • spastic paraplegia 6 homolog (human),
  • Nipa1,
  • 1110027G09Rik,
  • MGI:1915904,
  • RIKEN cDNA 1110027G09 gene
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0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

2 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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