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 6 920
NM_001008892.2 NP_001008892.1 5 784
NM_001008894.2 NP_001008894.1 4 727
NM_001184888.1 NP_001171817.1 5 875
NM_001184889.1 NP_001171818.1 9 1267
NM_030922.6 NP_112184.4 7 1042
XM_005272546.3 XP_005272603.1 7 1275
XM_005272547.4 XP_005272604.1 7 1059
XM_005272548.3 XP_005272605.1 6 889
XM_005272550.3 XP_005272607.1 6 727
XM_005272552.3 XP_005272609.1 5 989
XM_005272553.4 XP_005272610.1 5 793
XM_006720364.2 XP_006720427.1 8 1169
XM_006720365.2 XP_006720428.1 7 1014
XM_006720366.3 XP_006720429.1 6 880
XM_006720367.1 XP_006720430.1 6 1218
XM_011543877.2 XP_011542179.1 8 1402
XM_011543878.2 XP_011542180.1 8 1569
XM_011543879.2 XP_011542181.1 8 1140
XM_011543880.2 XP_011542182.1 6 1153
XM_017022645.1 XP_016878134.1 8 1463
XM_017022646.1 XP_016878135.1 8 1230
XM_017022647.1 XP_016878136.1 8 1178
XM_017022648.1 XP_016878137.1 8 1239
XM_017022649.1 XP_016878138.1 8 1373
XM_017022650.1 XP_016878139.1 8 1336
XM_017022651.1 XP_016878140.1 9 1757
XM_017022652.1 XP_016878141.1 8 1149
XM_017022653.1 XP_016878142.1 9 1463
XM_017022654.1 XP_016878143.1 7 987
XM_017022655.1 XP_016878144.1 6 985
XM_017022656.1 XP_016878145.1 6 995
XM_017022657.1 XP_016878146.1 7 1112
XM_017022658.1 XP_016878147.1 5 833
XM_017022659.1 XP_016878148.1 7 1083
XM_017022660.1 XP_016878149.1 5 1096
XM_017022661.1 XP_016878150.1 5 863
XM_017022662.1 XP_016878151.1 4 932
XM_017022663.1 XP_016878152.1 4 737
GenBank mRNA AK096305.1 - 6 901
AK300843.1 - 4 670
AK313584.1 - 5 859
AY732242.1 - 9 1188
BC000957.3 - 2 213
BC011775.2 - 5 696 3640970

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