Table 3 Imprinted genes located within the UPD regions detected in our study.
From: Genome-wide uniparental disomy screen in human discarded morphologically abnormal embryos
Case No. | SNP microarray karyotype | Imprinted gene |
|---|---|---|
1 | Arr UPD(12)(q13.13–q23.1) | RBP5 |
2 | Arr −16,UPD(10)(q21.2–q22.2),UPD(22)(q13.1-qter) | NA |
3 | Arr UPD(3)(p21.33–p21.1) | NA |
4A | Arr −1,−4,+8,−13,−15,−16,−19,−21,UPD(3)(p21.31-p21.1),UPD(17)(p12-pter) | NA |
4B | Arr –Y,−2,−7,−8,−11,−13,−22,UPD(1)(p36.13-pter)(q21.3–q42.2),UPD(3)(p26.6-p13)(q24),UPD(4)(p15.31–q21.3),UPD(6)(pter-q23.3),UPD(9)(q21.2–q34.11),UPD(14)(q21.2–q21.3)(q22.3–q32.2),UPD(15)(q15–q15.3),UPD(16)(p12.2–pter)(q22.1–q22.2)(q23.3–q24.1),UPD(17) | TP73, AIM1, LIN28B, GLIS3, DLK1, MEG3, ZNF597, NAA60, RTL1 |
5 | Arr−7,−12,−13,UPD(21) | NA |
6 | Arr UPD(1)(p32.2-p32.1),UPD(3)(pter-p26.2)(p24.3-p13)(q12.3-qter) | NA |
7 | Arr UPD(20)(q11.22) | BLCAP, NNAT |
8 | Arr UPD(1–22,X) | ALL |
