Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Acidosis, Renal Tubular [NCBI]

Gene


 Gene Link Information
Gain		 01
SLC4A1 [NCBI] 0.000363913
SLC4A4 [NCBI] 0.000217443
CA2 [NCBI] 0.000206546
ATP6V1B1 [NCBI] 0.000124379
ATP6V0A4 [NCBI] 0.000103625
SLC9A3 [NCBI] 2.98925e-05
UMOD [NCBI] 2.28477e-05
OCRL [NCBI] 1.6194e-05
ATP6V1C2 [NCBI] 1.54911e-05
ATP6V0E2 [NCBI] 1.54911e-05
ATP6V1G1 [NCBI] 1.54911e-05
ATP6V0D2 [NCBI] 1.54911e-05
SLC26A1 [NCBI] 1.31108e-05
ATP6V1H [NCBI] 1.31108e-05
SLC4A1AP [NCBI] 1.31108e-05
ATP6V1G3 [NCBI] 1.31108e-05
SLC9A8 [NCBI] 1.31108e-05
CA14 [NCBI] 1.22125e-05
ATP6V1G2 [NCBI] 1.16292e-05
LDHD [NCBI] 1.11955e-05
SLC12A7 [NCBI] 1.085e-05
FOXI1 [NCBI] 1.05627e-05
AMBP [NCBI] 1.04745e-05
CA4 [NCBI] 1.03167e-05
CLDN16 [NCBI] 1.03167e-05
RHAG [NCBI] 1.03167e-05
SLC4A2 [NCBI] 1.01017e-05
SLC9A2 [NCBI] 1.01017e-05
SP7 [NCBI] 1.01017e-05
CA1 [NCBI] 9.91073e-06
SLC26A6 [NCBI] 9.73893e-06
SLC4A3 [NCBI] 9.43975e-06
ATP6 [NCBI] 8.67733e-06
TCIRG1 [NCBI] 8.3577e-06
ATF4 [NCBI] 7.30437e-06
SLC22A12 [NCBI] 6.88849e-06
SGK1 [NCBI] 5.74828e-06
B2M [NCBI] 5.73273e-06
AGXT2L1 [NCBI] 5.64237e-06
RUNX2 [NCBI] 5.48842e-06
PTH [NCBI] 5.14219e-06
NAT1 [NCBI] 4.73809e-06
PRL [NCBI] 3.42584e-06
TROVE2 [NCBI] 3.09208e-06
EPO [NCBI] 9.5644e-07



OMIM


 OMIM Link Information
gain		 01
OPTB3 [NCBI] 0.00173067
renal tubular acidosis, distal, autosomal dominant [NCBI] 0.00160992
renal tubular acidosis, distal, with progressive nerve deafness [NCBI] 0.00127609
glomerulopathy with fibronectin deposits [NCBI] 0.00092257
SLC4A1 [NCBI] 0.000874593
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation [NCBI] 0.000774688
renal tubular acidosis, distal, with hemolytic anemia [NCBI] 0.000552505
RTADR [NCBI] 0.000552505
SRS [NCBI] 0.000460245
CA2 [NCBI] 0.00040148
renal tubular acidosis, proximal [NCBI] 0.000331004
OCRL [NCBI] 0.000242559
ATP6V0A4 [NCBI] 0.00023749
renal tubular acidosis iii [NCBI] 0.000220505
SLC4A4 [NCBI] 0.000215133
HOMG3 [NCBI] 0.00021328
PHA2 [NCBI] 0.000194257
RA [NCBI] 0.000173485
carnitine palmitoyltransferase i deficiency [NCBI] 0.000147685
fructose intolerance, hereditary [NCBI] 0.000133277
ATP6V1B1 [NCBI] 0.000130575
CA1 [NCBI] 0.000130575
thyrotoxic periodic paralysis [NCBI] 0.000127644
pyruvate carboxylase deficiency [NCBI] 0.000110727
hyperparathyroidism, neonatal self-limited primary, with hypercalciuria [NCBI] 0.00011017
hypomagnesemia, renal, with ocular involvement [NCBI] 7.92517e-05
KCNK5 [NCBI] 7.89672e-05
ATP6V0E2 [NCBI] 7.89672e-05
SLC12A7 [NCBI] 7.89672e-05
say syndrome [NCBI] 7.37614e-05
hawkinsinuria [NCBI] 6.96835e-05
arthrogryposis, renal dysfunction, and cholestasis [NCBI] 6.14354e-05
VPS33B [NCBI] 5.66176e-05
FOXI1 [NCBI] 5.66176e-05
TINU [NCBI] 5.60292e-05
HHRH [NCBI] 5.60292e-05
3-@methylglutaconic aciduria, type i [NCBI] 5.32371e-05
AUH [NCBI] 5.04502e-05
xanthinuria, type i [NCBI] 4.98027e-05
dent disease 1 [NCBI] 4.98027e-05
CLDN16 [NCBI] 4.90287e-05
TCIRG1 [NCBI] 4.56908e-05
OPTB1 [NCBI] 4.07231e-05
glycogen storage disease iii [NCBI] 3.71729e-05
hyperoxaluria, primary, type i [NCBI] 3.71729e-05
mitochondrial complex iv deficiency [NCBI] 3.67278e-05
FIH [NCBI] 3.62955e-05
glycogen storage disease ixa [NCBI] 3.45327e-05
UGB [NCBI] 3.1673e-05
B2M [NCBI] 2.91191e-05
glycogen storage disease i [NCBI] 2.87802e-05
wilson disease [NCBI] 1.96747e-05
SLE [NCBI] 1.38802e-05
PTH [NCBI] 7.31143e-06
NPPA [NCBI] 4.7623e-06
PRL [NCBI] 4.25045e-06
AVP [NCBI] 9.48422e-07
EPO [NCBI] 2.10149e-07



Database Center for Life Science