Table 2.
Information of differentially expressed imprinted genes.
| Gene | p Value | Location | Full Name | Gene Type | Expression Allele | |
|---|---|---|---|---|---|---|
| Mouse | Human | |||||
| Kcnq1 | 0.003 | 7 69.3 cM | 11p15.5 | potassium voltage-gated channel, subfamily Q, member 1 | PC | M |
| Ntm | 0.026 | 9 AS | 11q25 | neurotrimin | PC | M |
| Peg10 | 0.030 | 6 0.5 cM | 7q21 | paternally expressed 10 | PC | P |
| Slc22a18 | 0.042 | 7 69.5 cM | 11p15.5 | solute carrier family 22 (organic cation transporter), member 18 | PC | M |
| Pwcr1 | 0.046 | 7 29.0 cM AS | 15q11.2 | Prader-Willi syndrome chromosome region 1 | NC | P |
| Gtl2 | 0.048 | 12 54.0 cM | 14q32 | gene trap locus 2 | NC | M |
| Nap1l5 | 0.005 | 6 C1 AS | 4q22.1 AS | nucleosome assembly protein 1-like 5 | PC | P |
| Peg3 | <0.001 | 7 6.5 cM AS | 19q13.4 AS | paternally expressed 3 | PC | P |
| Slc22a2 | 0.013 | 17 7.32 cM | 6q26 AS | solute carrier family 22 (organic cation transporter), member 2 | PC | M |
| Plagl1 | 0.019 | 10 15.0 cM | 6q24-q25 AS | pleiomorphic adenoma gene-like 1 | PC | P |
Note: PC, protein coding; NC, non-coding; P, Paternal; M, Maternal.