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MeSH keywords -> Related genes, diseases (OMIM)


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01 Sheep Diseases [NCBI]


Gene


Gene Link Information
Gain
01
MEG3 [NCBI] 0.000330389
CTSL1 [NCBI] 3.7434e-05
PRL [NCBI] 2.99906e-05
ACHE [NCBI] 2.19625e-05
GDF9 [NCBI] 2.11424e-05
ALB [NCBI] 1.24893e-05
TF [NCBI] 1.23076e-05
MCEE [NCBI] 1.20977e-05
HYAL2 [NCBI] 9.96529e-06
STOM [NCBI] 9.75058e-06
BMP15 [NCBI] 9.6846e-06
UROD [NCBI] 8.51273e-06
INSL3 [NCBI] 7.47111e-06
PLG [NCBI] 6.56092e-06
MAP2 [NCBI] 6.40287e-06
PCNA [NCBI] 6.13051e-06
SCGB1A1 [NCBI] 5.64222e-06
MATN1 [NCBI] 5.58912e-06
INS [NCBI] 5.16134e-06
IL2 [NCBI] 5.04437e-06
FGFR3 [NCBI] 4.71906e-06
PTGS1 [NCBI] 3.99488e-06
CCK [NCBI] 3.40706e-06
TLR4 [NCBI] 3.37722e-06
CAT [NCBI] 3.23209e-06
AVP [NCBI] 3.09224e-06
CD68 [NCBI] 2.98013e-06
TNF [NCBI] 2.72361e-06




OMIM


OMIM Link Information
gain
01
LIP [NCBI] 0.000830168
hyperbilirubinemia, conjugated, type iii [NCBI] 0.000140314
thyroid hormonogenesis, genetic defect in, 5 [NCBI] 9.37927e-05
neuraminidase deficiency with beta-galactosidase deficiency [NCBI] 8.47446e-05
PRL [NCBI] 8.03003e-05
ehlers-danlos syndrome, type vii, autosomal recessive [NCBI] 7.97164e-05
neural tube defects [NCBI] 7.10508e-05
gm1-gangliosidosis, type i [NCBI] 6.77584e-05
ACHE [NCBI] 6.48777e-05
HYAL2 [NCBI] 5.75277e-05
MEG3 [NCBI] 5.2444e-05
BMP15 [NCBI] 5.2444e-05
IL5 [NCBI] 4.40399e-05
ALB [NCBI] 4.21183e-05
TF [NCBI] 4.19159e-05
GLB1 [NCBI] 3.76234e-05
CCL2 [NCBI] 3.28373e-05
BWS [NCBI] 3.17359e-05
polycystic kidneys [NCBI] 2.87097e-05
GAL [NCBI] 2.57757e-05
PLG [NCBI] 2.33663e-05
INS [NCBI] 1.99248e-05
FGFR3 [NCBI] 1.90183e-05
IL2 [NCBI] 1.67218e-05
SHH [NCBI] 1.56569e-05
TLR4 [NCBI] 1.49384e-05
CJD [NCBI] 1.35487e-05
PCNA [NCBI] 8.72422e-06
CCK [NCBI] 5.63121e-06
CAT [NCBI] 5.24694e-06
CRH [NCBI] 3.69965e-06
AVP [NCBI] 2.56346e-06
VEGF [NCBI] 2.533e-06
TNF [NCBI] 1.94188e-06




Database Center for Life Science