Imprinting Data
For each cell up to a maximum of 4 samples were analysed, two undifferentiated
Time points (Undiff T1 and Undiff T2) and two differentiated times points (Diff T1
and Diff T2).
11 imprinted loci were examined. For each loci there are two columns of data.
DNA
DNA indicates the sequence obtained at each loci.
e.g. A/G: Alleles are heterozygous (A/G); A: Alleles are homozygous (A/A); G:
Alleles are homozygous (G/G).
RNA
RNA indicates the sequence of the transcribes alleles
e.g. A/G: Minor allele contributes 30-50% of total expression; A>G: Minor allele
contributes 15-29% of total expression; A: Minor allele contributes 0-14% to total
expression.
n.s. - no sample; X - reaction failed.
H19
NESP55
GNAS
11p15.5
20q13.2
SLC22A18
BWSCR1A 11p15.5
GTL2
IGF2
IPW
MEG3
14q32.3
11p15.5
15q11-q13
KCNQ10T1 1
11p15.5
KCNQ10T1 2
11p15.5
PEG1
PEG3
SNRPN
7q32
15q12
GUANINE NUCLEOTIDE BINDING
PROTEIN
BECKWITH-WIEDEMANN
SYNDROME CHROMOSOME REGION
1, CANDIDATE A
MATERNALLY EXPRESSED GENE 3
INSULIN-LIKE GROWTH FACTOR II
IMPRINTED IN PRADER-WILLI
SYNDROME
KCNQ1-OVERLAPPING TRANSCRIPT
1
KCNQ1-OVERLAPPING TRANSCRIPT
2
PATERNALLY EXPRESSED GENE 1
PATERNALLY EXPRESSED GENE 3
SMALL NUCLEAR
RIBONUCLEOPROTEIN
POLYPEPTIDE N