Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Adenine Nucleotide Translocator 1 [NCBI]

Gene


 Gene Link Information
Gain		 01
LOC392301 [NCBI] 0.000299491
SLC25A4 [NCBI] 4.45371e-05
POLG [NCBI] 1.54903e-05
C10orf2 [NCBI] 1.45248e-05
SLC25A6 [NCBI] 9.9934e-06
UCP3 [NCBI] 2.86434e-06
MTCH2 [NCBI] 2.40177e-06
POLG2 [NCBI] 2.37199e-06
SLC25A17 [NCBI] 2.32083e-06
SLC25A5 [NCBI] 2.1795e-06
FRG1 [NCBI] 2.15337e-06
PRPF6 [NCBI] 2.12957e-06
PPID [NCBI] 2.0192e-06
AGFG1 [NCBI] 1.82453e-06
PPIB [NCBI] 1.6836e-06
GADD45A [NCBI] 1.63467e-06
LRRK2 [NCBI] 1.54321e-06
GPX1 [NCBI] 1.46365e-06
DIABLO [NCBI] 1.42757e-06
RELA [NCBI] 1.34596e-06
ATR [NCBI] 1.33296e-06
PARP1 [NCBI] 1.30713e-06
ATM [NCBI] 1.27649e-06
CREBBP [NCBI] 1.18009e-06
BRCA1 [NCBI] 1.17273e-06
CASP9 [NCBI] 9.55517e-07
BAX [NCBI] 8.27171e-07
AR [NCBI] 8.13642e-07
CASP3 [NCBI] 6.68893e-07



OMIM


 OMIM Link Information
gain		 01
cataract and cardiomyopathy [NCBI] 0.00254657
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 2 [NCBI] 0.000403834
SLC25A4 [NCBI] 0.000343436
SANDO [NCBI] 0.000174453
alpers diffuse degeneration of cerebral gray matter with hepatic cirrhosis [NCBI] 0.000171597
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive [NCBI] 0.000162803
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1 [NCBI] 0.000156475
mitochondrial dna depletion syndrome, hepatocerebral form [NCBI] 0.000155135
POLG [NCBI] 0.000141459
SLC25A5 [NCBI] 3.76507e-05
C10ORF2 [NCBI] 3.45931e-05
ANKRD1 [NCBI] 3.2048e-05
AGER [NCBI] 2.00401e-05
AR [NCBI] 5.98125e-06



Database Center for Life Science