Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 D-Amino-Acid Oxidase [NCBI]

Gene


 Gene Link Information
Gain		 01
G30 [NCBI] 0.000424532
DAO [NCBI] 9.46033e-05
DAOA [NCBI] 3.14626e-05
SRR [NCBI] 2.25689e-05
DDO [NCBI] 1.82331e-05
DTNBP1 [NCBI] 9.81591e-06
NRG1 [NCBI] 3.07162e-06
ITGBL1 [NCBI] 2.46605e-06
NALCN [NCBI] 2.34458e-06
CPZ [NCBI] 2.14696e-06
ACAA1 [NCBI] 2.08492e-06
CCBL1 [NCBI] 2.08492e-06
FGF14 [NCBI] 2.06707e-06
PIPOX [NCBI] 2.00564e-06
SLC10A2 [NCBI] 1.88597e-06
ABP1 [NCBI] 1.83071e-06
LDHD [NCBI] 1.6941e-06
RGS4 [NCBI] 1.63658e-06
DISC1 [NCBI] 1.49731e-06
AGXT2L1 [NCBI] 1.38662e-06
DPEP1 [NCBI] 1.37995e-06
HDC [NCBI] 1.2283e-06
CAT [NCBI] 7.31299e-07
AKT1 [NCBI] 6.65841e-07



OMIM


 OMIM Link Information
gain		 01
DAO [NCBI] 0.00226757
SCZD7 [NCBI] 0.00188466
MAFD6 [NCBI] 0.00102383
d-bifunctional protein deficiency [NCBI] 0.000285167
leukocyte nuclear appendages, hereditary prevalence of [NCBI] 0.000213124
hydroxyprolinemia [NCBI] 0.000156115
DDO [NCBI] 0.000114676
adrenoleukodystrophy, autosomal neonatal form [NCBI] 0.000104968
SCZD [NCBI] 9.81062e-05
g30 gene [NCBI] 7.63504e-05
g72 gene [NCBI] 7.31789e-05
HSD17B4 [NCBI] 5.58496e-05
SRR [NCBI] 3.35063e-05
RGS4 [NCBI] 2.71281e-05
DTNBP1 [NCBI] 2.55332e-05
PRODH [NCBI] 2.17522e-05
AKT1 [NCBI] 1.91411e-05
NRG1 [NCBI] 1.4976e-05
HDC [NCBI] 9.27862e-06
COMT [NCBI] 5.25417e-06
CAT [NCBI] 1.29598e-06



Database Center for Life Science