Version 5.4
Homo sapiens Gene: NIPA2
Summary
InnateDB Gene IDBG-3989.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol NIPA2
Gene Name non imprinted in Prader-Willi/Angelman syndrome 2
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000140157
Encoded Proteins
IDBP-3991
non imprinted in Prader-Willi/Angelman syndrome 2
IDBP-3993
non imprinted in Prader-Willi/Angelman syndrome 2
IDBP-234071
non imprinted in Prader-Willi/Angelman syndrome 2
IDBP-234073
non imprinted in Prader-Willi/Angelman syndrome 2
IDBP-583125
non imprinted in Prader-Willi/Angelman syndrome 2
IDBP-598907
non imprinted in Prader-Willi/Angelman syndrome 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary 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 15:22838641-22868384
Strand Forward strand
Band q11.2
Transcripts
ENST00000337451 ENSP00000337618
ENST00000359727 ENSP00000352762
ENST00000398014 ENSP00000381096
ENST00000398013 ENSP00000381095
ENST00000539711 ENSP00000437746
ENST00000560039 ENSP00000453700
ENST00000561072
ENST00000559571
ENST00000560205
ENST00000560762
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
Mus musculus
Bos taurus
Gene ID
Gene Order
ENSMUSG00000030452
View Gene Order
ENSBTAG00000016895
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene
RefSeq NM_001008860 NM_001008892 NM_001008894 NM_001184888 NM_001184889 NM_030922 XM_005272546 XM_005272547 XM_005272548 XM_005272549 XM_005272550 XM_005272553 XM_006720365 XM_006720368
HUGO
OMIM
CCDS CCDS73693 CCDS73694
HPRD 16290
IMGT
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