Non-imprinted in Prader-Willi/Angelman syndrome region protein 2 is a protein that in humans is encoded by the NIPA2 gene.[5][6]
^ abcGRCh38: Ensembl release 89: ENSG00000140157 – Ensembl, May 2017
^ abcGRCm38: Ensembl release 89: ENSMUSG00000030452 – Ensembl, May 2017
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^Chai JH, Locke DP, Greally JM, Knoll JH, Ohta T, Dunai J, Yavor A, Eichler EE, Nicholls RD (Sep 2003). "Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons". Am J Hum Genet. 73 (4): 898–925. doi:10.1086/378816. PMC 1180611. PMID 14508708.
^"Entrez Gene: NIPA2 non imprinted in Prader-Willi/Angelman syndrome 2".
syndrome region protein 2 is a protein that in humans is encoded by the NIPA2 gene. GRCh38: Ensembl release 89: ENSG00000140157 – Ensembl, May 2017 GRCm38:...
encodes Non-imprinted in Prader-Willi/Angelman syndrome region protein 1 NIPA2, a gene in humans that encodes Non-imprinted in Prader-Willi/Angelman syndrome...
encoding protein MicroRNA 627 MIR9-3HG: encoding protein MIR9-3 host gene NIPA2: encoding protein Non-imprinted in Prader-Willi/Angelman syndrome region...