Name

NIPA2 Gene

non imprinted in Prader-Willi/Angelman syndrome 2

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]

NIPA2P3 Gene

non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 3

NIPA2P2 Gene

non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 2

NIPA2P1 Gene

non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 1

NIPA2P5 Gene

non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 5

NIPA2P4 Gene

non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 4

nipa2 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term nipa2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

NIPA2 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for NIPA2 from the Pathway Commons Protein-Protein Interactions dataset.

nipa2l Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term nipa2l in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.