Table 1. Imprinted genes human and mouse.
Human
chr. |
Gene |
Parent |
Mouse chr(cM) |
Gene |
Parent |
1p | p73 | M | |||
1p | ARHI | P | |||
5q | U2AFBPL | NI | 11(12) | Irlgs2 | P |
6q | HYMAI | P | |||
6q | PLAGL1 | P | 10(15) | Zac1 | P |
6q | IGF2R | NI | 17(7) | Igf2r | M(AS) |
7p | GRB10 | M/P* | 11(8) | Grb10 | M |
7q | SGCE | no data | 6(1) | Sgce | P |
7q | MEST | P | 6(7) | Mest | P |
7q | COPG2 | P* | 6(7) | Copg2 | M(AS) |
7q | Hs.6421 | no data | 6(7) | Mit1 | P |
11p | H19 | M | 7(69) | H19 | M |
11p | IGF2 | P(AS) | 7(69) | Igf2 | P(AS) |
11p | INS | no data | 7(69) | Ins2 | P |
11p | ASCL2 | M | 7(69) | Mash2 | M |
11p | TSSC4 | NI | 7(69) | Tssc4 | M bias |
11p | MTR1 | P | |||
11p | KCNQ1 | M(AS) | 7(69) | Kcnq1 | M(AS) |
11p | CDKN1C | M | 7(69) | Cdnk1c | M |
11p | SLC22A1L | M | 7(69) | Orctl2 | M |
11p | TSSC3 | M | 7(69) | Tssc3 | M |
11p | ZNF215 | M | |||
11p | WT1 | M/P*(AS) | |||
13q | HTR2A | M* | 14(41) | Htr2a | M |
14q | DLK1 | NI | 12 | Dlk | P |
14q | MEG3 | M | 12(54) | Gtl2 | M |
15q | MKRN3 | P(AS) | 7(29) | Zfp127 | P |
15q | NDN | P | 7(28) | Ndn | P |
15q | MAGEL2 | P | 7(28) | Magel2 | P |
15q | SNRPN | P | 7(27) | Snrpn | P |
15q | IPW | P | 7(28) | Ipw | P |
15q | UBE3A | M(AS) | 7(28) | Ube3a | M |
15q | RASGRF1 | no data | 9(50) | Rasgrf1 | P |
18q | IMPACT | NI | 18 | Impact | P |
19q | PEG3 | no data | 7(4) | Peg3 | P |
19q | KIAA0972 | no data | 7(4) | Zim1 | M |
20q | GNAS1 | M/P(AS) | 2(104) | Gnas | M/P(AS) |
20q | NNAT | no data | 2(88) | Nnat | P |
Xq | XIST | P | X(42) | Xist | P |
X(57) | Esx1 | M | |||
19(49) | Ins1 | P |
Parent, parent-of-origin of expressed allele; P, paternal, M, maternal; AS, expression of an imprinted antisense transcript; NI, not imprinted; asterisk, conflicting data.