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MeSH keywords -> Related genes, diseases (OMIM)


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01 Arylsulfatases [NCBI]


Gene


Gene Link Information
Gain
01
ARSC2 [NCBI] 0.000494854
HDHD1CP [NCBI] 0.000243173
HDHD1BP [NCBI] 0.000208465
STSP [NCBI] 0.000208465
ARSE [NCBI] 4.92324e-05
STS [NCBI] 3.74977e-05
ARSD [NCBI] 1.07332e-05
ARSB [NCBI] 6.21787e-06
ARSA [NCBI] 5.4152e-06
ARSF [NCBI] 4.87817e-06
ARSG [NCBI] 4.79502e-06
GNS [NCBI] 4.38578e-06
SULF2 [NCBI] 4.38578e-06
SULF1 [NCBI] 4.05155e-06
GALNS [NCBI] 3.6349e-06
SHOX [NCBI] 3.20218e-06
FGFR3 [NCBI] 2.42065e-06
ARSJ [NCBI] 2.32808e-06
ARSK [NCBI] 2.32808e-06
ARSI [NCBI] 2.32808e-06
HDHD1A [NCBI] 2.12774e-06
ACP2 [NCBI] 1.9219e-06
SULT1B1 [NCBI] 1.85322e-06
ACO2 [NCBI] 1.82453e-06
SULT1E1 [NCBI] 1.78266e-06
IL1RN [NCBI] 1.72611e-06
GPR143 [NCBI] 1.70865e-06
TPSAB1 [NCBI] 1.69714e-06
SLCO1B3 [NCBI] 1.61535e-06
SLC26A2 [NCBI] 1.56974e-06
CTCF [NCBI] 1.55612e-06
CYP3A7 [NCBI] 1.54315e-06
KAL1 [NCBI] 1.4739e-06
PPOX [NCBI] 1.47147e-06
NAGA [NCBI] 1.46197e-06
PROC [NCBI] 1.32604e-06
SULT1A1 [NCBI] 1.30974e-06
DNASE2B [NCBI] 1.27403e-06
PSAP [NCBI] 1.23252e-06
MGP [NCBI] 1.21813e-06
SCP2 [NCBI] 1.20184e-06
CA9 [NCBI] 1.18899e-06
SOX9 [NCBI] 1.15971e-06
SRY [NCBI] 1.13953e-06
PAH [NCBI] 1.09028e-06
MATN1 [NCBI] 1.08571e-06
SELPLG [NCBI] 1.05933e-06
ALB [NCBI] 9.64061e-07
TTR [NCBI] 9.36973e-07
G6PD [NCBI] 8.36729e-07
PTHLH [NCBI] 8.36073e-07
CYP3A4 [NCBI] 7.09492e-07
AFP [NCBI] 6.12225e-07
MPO [NCBI] 5.88703e-07
CCK [NCBI] 5.38859e-07




OMIM


OMIM Link Information
gain
01
acroosteolysis with osteoporosis and changes in skull and mandible [NCBI] 0.00277021
ichthyosis, x-linked [NCBI] 0.0010406
metachromatic leukodystrophy [NCBI] 0.000841062
MSD [NCBI] 0.000398399
CDPX1 [NCBI] 0.000371061
ARSE [NCBI] 0.000270212
mucolipidosis iiia [NCBI] 0.000204383
mucopolysaccharidosis type vi [NCBI] 0.000182352
ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis [NCBI] 0.00017192
ARSA [NCBI] 0.000127034
xx male syndrome [NCBI] 0.000110375
CHS [NCBI] 0.000107242
DMC [NCBI] 0.000100472
NCIE1 [NCBI] 9.79464e-05
ISS [NCBI] 9.79464e-05
ichthyosis vulgaris [NCBI] 9.36131e-05
metachromatic leukodystrophy due to saposin b deficiency [NCBI] 9.36131e-05
ARSF [NCBI] 8.97157e-05
RCDP1 [NCBI] 8.28578e-05
CDPX2 [NCBI] 8.16698e-05
ARSD [NCBI] 7.94914e-05
mucopolysaccharidosis type iiia [NCBI] 7.94681e-05
mannosidosis, alpha b, lysosomal [NCBI] 6.58198e-05
hurler syndrome [NCBI] 6.47179e-05
mucolipidosis ii [NCBI] 6.07958e-05
alopecia, androgenetic [NCBI] 5.49422e-05
ARSB [NCBI] 4.969e-05
KAL1 [NCBI] 4.72403e-05
ARSC2 [NCBI] 4.48146e-05
dxf68s1e [NCBI] 4.48146e-05
ARSJ [NCBI] 3.73924e-05
ARSK [NCBI] 3.73924e-05
ARSI [NCBI] 3.73924e-05
ARSG [NCBI] 3.45916e-05
SULF2 [NCBI] 3.45916e-05
SLOS [NCBI] 3.36904e-05
SLC25A6 [NCBI] 3.14215e-05
SULF1 [NCBI] 3.14215e-05
PRPS2 [NCBI] 3.03444e-05
GNS [NCBI] 2.86826e-05
ACO2 [NCBI] 2.68826e-05
NAGA [NCBI] 2.51581e-05
MAN2B1 [NCBI] 2.33107e-05
OA1 [NCBI] 2.2361e-05
CTCF [NCBI] 2.03884e-05
SHOX [NCBI] 2.03884e-05
CF [NCBI] 1.58088e-05
mucopolysaccharidosis type ii [NCBI] 1.55031e-05
TTR [NCBI] 4.52488e-06
RNASE3 [NCBI] 3.83569e-06
VEGF [NCBI] 3.03338e-06
G6PD [NCBI] 2.59161e-06
AFP [NCBI] 4.32999e-07
MPO [NCBI] 2.99098e-07
CCK [NCBI] 4.31425e-08




Database Center for Life Science