Version 5.4
Mus musculus Gene: Nipa2
Summary
InnateDB Gene IDBG-189285.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Nipa2
Gene Name non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human)
Synonyms 2600017P10Rik; 3830408P04Rik; AB041581
Species Mus musculus
Ensembl Gene ENSMUSG00000030452
Encoded Proteins
IDBP-189287
non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human)
IDBP-400624
non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human)
IDBP-400623
non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human)
IDBP-400622
non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human)
IDBP-535029
non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human)
IDBP-541811
non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human)
IDBP-533393
non imprinted in Prader-Willi/Angelman syndrome 2 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 ENSG00000140157:
This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.[provided by RefSeq, May 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 7:55931287-55962476
Strand Reverse strand
Band B5
Transcripts
ENSMUST00000032635 ENSMUSP00000032635
ENSMUST00000119201 ENSMUSP00000114020
ENSMUST00000117812 ENSMUSP00000113727
ENSMUST00000119041 ENSMUSP00000112394
ENSMUST00000147950
ENSMUST00000130239
ENSMUST00000152649 ENSMUSP00000120798
ENSMUST00000126604 ENSMUSP00000116219
ENSMUST00000135849
ENSMUST00000143325 ENSMUSP00000119946
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
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
ENSG00000140157
View Gene Order
ENSBTAG00000016895
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.333893 Mm.486878
RefSeq NM_001256130 NM_001256131 NM_001256132 NM_001256133 NM_023647 XM_006541324
OMIM
CCDS CCDS21316
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca