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Table 1 Intron-exon structure of GOLAG8E

From: Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region

Exon

Exon (bp)

Intron (kb)

Intron

Exon

Exon

Intron

1

146

  

AGTCGC

AGAAAG

tggctc

2

120

1.7

tggctc

TTAAAA

GGAGAT

tgacag

3

60

0.5

tgacag

TCAGCA

CTGGAG

ttgtag

4

81

0.2

ttgtag

AGCCCG

TCTTTG

ctcag

5

360

0.9

ctcag

AAACAA

CTAGAG

ccacag'

6

85

0.1

ccacag'

GTTCAA

TTGAAG

ccaaag

7

110

0.1

ccaaag

AAGAGT

GAGAGG

ttacag

8

90

1.1

ttacag

CAGTTC

ACACAG

ttgcag

9

108

0.1

ttgcag

TTGAAG

CAGGAG

gggcag

10

88

0.2

gggcag

GTTTGC

AGATGG

tctcag

11

257

0.4

tctcag

CTGAAC

GAGCTG

gtccag

12

69

0.3

gtccag

AACAAT

GGCAAG

ccttag

13

66

1.4

ccttag

GAGCGC

GGGAAG

caacag

14

92

0.4

caacag

GACACG

GCCATG

ctccag

15

101

0.6

ctccag

AGCGGC

CCATCA

ccgcag

16

101

0.1

ccgcag

GAAAGT

ATGAAG

ctccag

17

152

0.1

ctccag

GTGAAG

ATGGTG

ccaaag

18

1200

0.1

ccaaag

ATCTTT

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