Gene Transcripts

Gene Symbol
NIPA2
Entrez Gene ID
81614
Gene Name
non imprinted in Prader-Willi/Angelman syndrome 2
Gene Aliases
Chromosome Location
Chr. 15: 22838641 - 22868384 on Build GRCh38
UniGene ID
Hs.591003
Species
Homo sapiens
Interrogated Sequence Translated Protein Targeted Exon(s) siRNA Location IMAGE Clone ID
RefSeq NM_001008860.2 NP_001008860.1 7 1207
NM_001008892.2 NP_001008892.1 6 1071
NM_001008894.2 NP_001008894.1 5 1014
NM_001184888.1 NP_001171817.1 6 1162
NM_001184889.1 NP_001171818.1 10 1554
NM_030922.6 NP_112184.4 8 1329
XM_005272546.3 XP_005272603.1 8 1562
XM_005272547.4 XP_005272604.1 8 1346
XM_005272548.3 XP_005272605.1 7 1176
XM_005272550.3 XP_005272607.1 7 1014
XM_005272552.3 XP_005272609.1 6 1276
XM_005272553.4 XP_005272610.1 6 1080
XM_006720364.2 XP_006720427.1 9 1456
XM_006720365.2 XP_006720428.1 8 1301
XM_006720366.3 XP_006720429.1 7 1167
XM_006720367.1 XP_006720430.1 7 1505
XM_011543877.2 XP_011542179.1 9 1689
XM_011543878.2 XP_011542180.1 9 1856
XM_011543879.2 XP_011542181.1 9 1427
XM_011543880.2 XP_011542182.1 7 1440
XM_017022645.1 XP_016878134.1 9 1750
XM_017022646.1 XP_016878135.1 9 1517
XM_017022647.1 XP_016878136.1 9 1465
XM_017022648.1 XP_016878137.1 9 1526
XM_017022649.1 XP_016878138.1 9 1660
XM_017022650.1 XP_016878139.1 9 1623
XM_017022651.1 XP_016878140.1 10 2044
XM_017022652.1 XP_016878141.1 9 1436
XM_017022653.1 XP_016878142.1 10 1750
XM_017022654.1 XP_016878143.1 8 1274
XM_017022655.1 XP_016878144.1 7 1272
XM_017022656.1 XP_016878145.1 7 1282
XM_017022657.1 XP_016878146.1 8 1399
XM_017022658.1 XP_016878147.1 6 1120
XM_017022659.1 XP_016878148.1 8 1370
XM_017022660.1 XP_016878149.1 6 1383
XM_017022661.1 XP_016878150.1 6 1150
XM_017022662.1 XP_016878151.1 5 1219
XM_017022663.1 XP_016878152.1 5 1024
GenBank mRNA AK096305.1 - 7 1188
AK300843.1 - 5 957
AK313584.1 - 6 1146
AY732242.1 - 10 1475
BC000957.3 - 3 500
BC011775.2 - 6 983 3640970
U90904.1 - 1 163

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