gene,0,0 GSM1416388,0,0 GSM1416389,0,0 GSM1416390,0,0 GSM1416391,0,0 GSM1416392,0,0 GSM1416393,0,0 GSM1416394,0,0 GSM1416395,0,0 GSM1416396,0,0 GSM1416397,0,0 GSM1416398,0,0.139 GSM1416399,0,0 GSM1416400,0,0 GSM1416401,0,0 GSM1416402,0,0 GSM1416403,0,0 GSM1416404,0,0 GSM1416405,0,0 GSM1416406,0,0 GSM1416407,0,0 GSM1416408,0,0 GSM1416409,0,0 GSM1416410,0,0 GSM1416411,0,0 GSM1416412,0,0 GSM1416413,0,0 GSM1416414,0,0 GSM1416437,0,0 GSM1416438,0,0 GSM1416439,0,0 GSM1416440,0,0 GSM1416441,0,0 GSM1416442,0,0 GSM1416443,0,0 GSM1416444,0,0 GSM1416445,0,0 GSM1416446,0,0 GSM1416447,0,0 GSM1416448,0,0 GSM1416449,0,0 GSM1416450,0,0 GSM1416451,0,0
Synonyms | NCRNA00002 |
Description | imprinted in Prader-Willi syndrome (non-protein coding) |
---|---|
Chromosome | 15q11.2 |
Database Reference | MIM:601491 HGNC:6109 |
See related | THE HUMAN PROTEIN ATLAS |
Dataset | GSE58652 |
IPW expression in each cell group | Minimum Value (TPM) | Median Value (TPM) | Maximum Value (TPM) |
---|---|---|---|
HEK293T | 0 | 0 | 0.139 |