Mus musculus Gene: Nipa1
Summary
InnateDB Gene IDBG-189321.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Nipa1
Gene Name non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human)
Synonyms
Species Mus musculus
Ensembl Gene ENSMUSG00000047037
Encoded Proteins
non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human)
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000170113:
This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6. [provided by RefSeq, Nov 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 7:55977567-56019954
Strand Reverse strand
Band B5
Transcripts
ENSMUST00000052204 ENSMUSP00000053871
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0015095 magnesium ion transmembrane transporter activity
Biological Process
GO:0015693 magnesium ion transport
Cellular Component
GO:0005769 early endosome
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.389901
RefSeq NM_153578
OMIM
CCDS CCDS21317
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas