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01 Olivopontocerebellar Atrophies [NCBI]

Gene


 Gene Link Information
Gain		 01
ITPR1 [NCBI] 3.09082e-05
RABEP1 [NCBI] 1.40278e-05
SLC1A6 [NCBI] 1.36821e-05
SNCA [NCBI] 1.23333e-05
SLC1A1 [NCBI] 1.09805e-05
GNAI2 [NCBI] 1.08556e-05
SLC1A2 [NCBI] 1.03847e-05
SLC1A3 [NCBI] 1.03395e-05
SLC18A2 [NCBI] 9.68155e-06
GFAP [NCBI] 9.34638e-06
ATXN2 [NCBI] 8.19521e-06
NEFL [NCBI] 7.65438e-06
ATXN1 [NCBI] 7.61771e-06
CDK5 [NCBI] 7.50369e-06
PARK2 [NCBI] 5.58316e-06
CHAT [NCBI] 5.54551e-06
VHL [NCBI] 5.37145e-06
FMR1 [NCBI] 5.13106e-06
TRH [NCBI] 4.74326e-06
TH [NCBI] 4.40841e-06
MBP [NCBI] 3.9852e-06
BAX [NCBI] 3.53444e-06
FASLG [NCBI] 3.43314e-06
CASP3 [NCBI] 2.91434e-06



OMIM


 OMIM Link Information
gain		 01
cerebellar atrophy with progressive microcephaly [NCBI] 0.00236517
pontocerebellar hypoplasia, type 1 [NCBI] 0.00107364
pontocerebellar hypoplasia, type 2 [NCBI] 0.000991404
SCAX1 [NCBI] 0.000840405
MJD [NCBI] 0.000434922
CDG1A [NCBI] 0.000317221
encephalopathy, fatal infantile, with olivopontocerebellar hypoplasia [NCBI] 0.000269279
SCA2 [NCBI] 0.000118376
SCA1 [NCBI] 0.000110727
branchial myoclonus with spastic paraparesis and cerebellar ataxia [NCBI] 9.3728e-05
DSMA1 [NCBI] 7.47703e-05
FXTAS [NCBI] 7.2683e-05
SCA6 [NCBI] 5.60054e-05
SCA7 [NCBI] 5.28878e-05
GFAP [NCBI] 4.26686e-05
DRPLA [NCBI] 3.70749e-05
CHAT [NCBI] 2.57724e-05
HD [NCBI] 2.54263e-05
TH [NCBI] 1.90138e-05
CRH [NCBI] 1.78773e-05
MBP [NCBI] 1.70458e-05
CJD [NCBI] 8.9227e-06



Database Center for Life Science