Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Extrachromosomal Inheritance [NCBI]

Gene


 Gene Link Information
Gain		 01
TRNI [NCBI] 0.000157606
RNR2 [NCBI] 0.000141376
RAG1 [NCBI] 4.24148e-06
DUX4 [NCBI] 3.89584e-06
DHFR [NCBI] 3.89461e-06
MSTO1 [NCBI] 3.85026e-06
UQCRH [NCBI] 3.77088e-06
PATZ1 [NCBI] 3.70332e-06
KIF20B [NCBI] 3.54573e-06
KIN [NCBI] 3.48358e-06
ATP6 [NCBI] 3.46462e-06
SLIT2 [NCBI] 3.24732e-06
POLI [NCBI] 3.16342e-06
RPL14 [NCBI] 3.06096e-06
HLA-F [NCBI] 2.83172e-06
EGFR [NCBI] 2.8129e-06
PRL [NCBI] 2.78749e-06
TFAM [NCBI] 2.75152e-06
HEBP1 [NCBI] 2.7363e-06
CAD [NCBI] 2.57699e-06
ALB [NCBI] 2.03802e-06
MLL [NCBI] 1.9258e-06
HMOX1 [NCBI] 1.89971e-06
GJB2 [NCBI] 1.86675e-06
G6PD [NCBI] 1.75015e-06
HFE [NCBI] 1.66498e-06



OMIM


 OMIM Link Information
gain		 01
MAFD1 [NCBI] 0.00137138
myoclonic epilepsy, juvenile, 3 [NCBI] 0.000957753
leber optic atrophy [NCBI] 0.000411365
chloramphenicol toxicity [NCBI] 0.000380763
hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial [NCBI] 0.000170507
retinitis pigmentosa-deafness syndrome [NCBI] 0.000125454
hemochromatosis, neonatal [NCBI] 0.000113015
MTND2 [NCBI] 0.000108939
diabetes-deafness syndrome, maternally transmitted [NCBI] 9.43734e-05
CVS [NCBI] 8.08523e-05
HOS [NCBI] 6.95186e-05
MTND3 [NCBI] 6.82687e-05
MTCO1 [NCBI] 6.28066e-05
ABL1 [NCBI] 5.84159e-05
KSS [NCBI] 5.56019e-05
HD [NCBI] 5.18084e-05
MTTS2 [NCBI] 4.33758e-05
MTTI [NCBI] 3.48047e-05
MTND4L [NCBI] 3.24894e-05
MTTS1 [NCBI] 3.21179e-05
MTCO3 [NCBI] 2.95328e-05
MTRNR1 [NCBI] 2.80936e-05
MTND6 [NCBI] 2.79139e-05
MTND5 [NCBI] 2.79139e-05
MTTK [NCBI] 2.75701e-05
MTCO2 [NCBI] 2.74054e-05
ABO [NCBI] 2.69372e-05
MTCYB [NCBI] 2.6231e-05
factor x deficiency [NCBI] 2.57213e-05
MTND1 [NCBI] 2.51404e-05
MTND4 [NCBI] 2.42207e-05
RP [NCBI] 2.4008e-05
DHFR [NCBI] 2.08535e-05
PRNP [NCBI] 1.69737e-05
ALB [NCBI] 1.16261e-05
EGFR [NCBI] 9.07123e-06
PRL [NCBI] 7.7358e-06
G6PD [NCBI] 7.08854e-06



Database Center for Life Science