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. 2012 Jun 19;13:257. doi: 10.1186/1471-2164-13-257

Table 1.

Breed and genotype of individuals sequenced for the presence ofFGF20c.535A > T

Breed Genotype No. of individuals c.496 (rs14481412) c.535 c.552 (rs14481413)
UC Davis (low line)
sc/sc
10
CC
TT
AA
UC Davis (high line)
sc/sc
10
CC
TT
AA
Storrs, Connecticut (low line)
sc/sc
2
CC
TT
AA
Israeli experimental line
sc/sc
16
CC
TT
AA
Israeli experimental line
sc/+
3
CC
AT
AA
Israeli experimental line
sc/+
6
CC
AT
AG
New Hampshire (IFAG, Germany)
WT
6
CC
AA
AA
New Hampshire (IFAG, Germany)
WT
4
CT
AA
AG
New Hampshire, UK
WT
2
TT
AA
GG
New Hampshire, UK
WT
1
CT
AA
AG
Black Leghorn
WT
1
CC
AA
AA
Araucana
WT
1
CC
AA
AA
Old English Pheasant Fowl
WT
1
CC
AA
AA
Langshan
WT
1
CT
AA
AG
Silver Appenzeller
WT
1
CC
AA
AA
Roslin Institute experimental
WT
2
CC
AA
AA
Roslin Institute experimental
WT
1
CT
AA
AG
ISA Brown
WT
2
CC
AA
AA
Outbred, Mexico
WT
7
CC
AA
AA
Outbred, Mexico
WT
2
TT
AA
GG
Outbred, Mexico
WT
1
CT
AA
AG
Cream Legbar
WT
1
CC
AA
AA
Dorking
WT
1
CC
AA
AA
Campine
WT
1
CC
AA
AA
Naked Neck, Wernlas collection
WT
1
TT
AA
GG
Hungarian AVIANDIV Naked Neck
WT
1
TT
AA
GG
Naked Neck, English
WT
1
CC
AA
AA
Scots Grey WT 1 TT AA GG

Results from sequencing FGF20 exon 3 in 38 sc/sc individuals, 9 sc/+ individuals and 40 WT birds. The FGF20 c.535A > T mutation was found in all of the sc/sc and none of the WT samples sequenced. The genotype of the two flanking SNPs (rs14481412 and rs14481413) revealed that 25/40 WT individuals were homozygous for the same haplotype as scaleless, indicating that the FGF20 c.535A > T mutation does not lie within a rare haplotype.