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01 Pseudohypoparathyroidism [NCBI]

Gene


 Gene Link Information
Gain		 01
PTH [NCBI] 0.000821133
GNAS [NCBI] 0.000807263
HPT [NCBI] 0.000341765
PTH1R [NCBI] 1.43319e-05
GHRH [NCBI] 1.23557e-05
GNG4 [NCBI] 1.13121e-05
GNG3 [NCBI] 1.07289e-05
STX16 [NCBI] 1.07289e-05
GNB5 [NCBI] 1.07289e-05
GNB4 [NCBI] 1.07289e-05
GNG11 [NCBI] 1.02954e-05
GNAI3 [NCBI] 9.95e-06
GNB2 [NCBI] 9.95e-06
GNB1 [NCBI] 9.41701e-06
GNA13 [NCBI] 8.83966e-06
TRPV5 [NCBI] 8.54077e-06
NNAT [NCBI] 8.06523e-06
TRH [NCBI] 4.68765e-06
GNB3 [NCBI] 4.21924e-06
FGF23 [NCBI] 3.32718e-06
ACP5 [NCBI] 2.07952e-06
PTHLH [NCBI] 1.53772e-06
AVP [NCBI] 1.00438e-06
PRL [NCBI] 2.6774e-07



OMIM


 OMIM Link Information
gain		 01
AHO [NCBI] 0.00747098
PTH [NCBI] 0.00318124
pseudohypoparathyroidism, type ii [NCBI] 0.00243653
pseudohypoparathyroidism, type ib [NCBI] 0.00201939
GNAS [NCBI] 0.00178175
amelogenesis imperfecta, hypoplastic type [NCBI] 0.000898321
brachydactyly-mental retardation syndrome [NCBI] 0.000844965
IBGC1 [NCBI] 0.000560268
STX16 [NCBI] 0.000208273
BDE [NCBI] 0.00014868
osseous heteroplasia, progressive [NCBI] 0.000144342
SLE [NCBI] 0.00014353
CHNG1 [NCBI] 0.000124022
PTHR1 [NCBI] 0.000119924
albright hereditary osteodystrophy 2 [NCBI] 0.000110667
MAS [NCBI] 0.000106707
gnas complex locus, antisense transcript [NCBI] 6.93505e-05
AIH2 [NCBI] 5.99137e-05
thyrotropin deficiency, isolated [NCBI] 5.50618e-05
NDP [NCBI] 2.42502e-05
KSS [NCBI] 1.56245e-05
PRL [NCBI] 6.12025e-06
AVP [NCBI] 1.45669e-06



Database Center for Life Science