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01 Rothmund-Thomson Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
RECQL4 [NCBI] 0.000415824
FERMT1 [NCBI] 0.000110541
RECQL [NCBI] 6.8623e-05
WRN [NCBI] 3.19773e-05
RECQL5 [NCBI] 2.69048e-05
RAD51 [NCBI] 1.33879e-05
UBR2 [NCBI] 1.27309e-05
UBR1 [NCBI] 1.0842e-05
NBN [NCBI] 5.34637e-06
PML [NCBI] 4.82538e-06
CASP3 [NCBI] 1.75762e-06



OMIM


 OMIM Link Information
gain		 01
RTS [NCBI] 0.00555486
PN [NCBI] 0.00266538
kindler syndrome [NCBI] 0.000827674
RECQL4 [NCBI] 0.00079693
RECQL3 [NCBI] 0.000124149
RECQL2 [NCBI] 0.00011941
spastic paraplegia with neuropathy and poikiloderma [NCBI] 0.00011797
parc syndrome [NCBI] 0.00011797
DKC [NCBI] 0.000107899
RECQL [NCBI] 9.68811e-05
poikiloderma, hereditary sclerosing [NCBI] 9.55083e-05
skeletal dysplasia with telangiectases and mesodermal dysgenesis of the iris [NCBI] 9.55083e-05
rapadilino syndrome [NCBI] 8.70372e-05
WRN [NCBI] 8.58501e-05
UBR2 [NCBI] 8.31009e-05
BGS [NCBI] 5.01747e-05
BLM [NCBI] 3.24965e-05



Database Center for Life Science