Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Acetyl-CoA C-Acyltransferase [NCBI]


Gene


Gene Link Information
Gain
01
ZWS1 [NCBI] 0.000299491
ACAT1 [NCBI] 1.94994e-05
ACAA1 [NCBI] 1.62224e-05
SCP2 [NCBI] 1.53881e-05
HADHB [NCBI] 7.12804e-06
HADHA [NCBI] 6.69319e-06
HSD17B4 [NCBI] 6.10729e-06
ACAA2 [NCBI] 5.00637e-06
KAT2A [NCBI] 3.91805e-06
DECR1 [NCBI] 2.08968e-06
PEX7 [NCBI] 2.06221e-06
PEX14 [NCBI] 1.91531e-06
PEX1 [NCBI] 1.81579e-06
ABCD3 [NCBI] 1.75977e-06
OTC [NCBI] 1.67712e-06
OXCT2 [NCBI] 1.63436e-06
BNIP3 [NCBI] 1.59982e-06
KAT2B [NCBI] 1.53265e-06
PLTP [NCBI] 1.38979e-06
EP300 [NCBI] 1.28995e-06
MYOD1 [NCBI] 1.28635e-06
CS [NCBI] 1.2814e-06
ITPR1 [NCBI] 1.18391e-06
NR1H3 [NCBI] 1.08698e-06
CREBBP [NCBI] 1.07674e-06
CAT [NCBI] 7.99754e-07
VIP [NCBI] 6.95494e-07
APOE [NCBI] 6.86908e-07




OMIM


OMIM Link Information
gain
01
medium chain 3-ketoacyl-coa thiolase deficiency [NCBI] 0.003491
alpha-methylacetoacetic aciduria [NCBI] 0.00144526
d-bifunctional protein deficiency [NCBI] 0.000364074
hydroxyacyl-coa dehydrogenase ii deficiency [NCBI] 0.000271966
RCDP1 [NCBI] 0.000221788
ACAT1 [NCBI] 0.000195963
SCP2 [NCBI] 0.000160067
ZS [NCBI] 0.00014554
trifunctional protein deficiency [NCBI] 0.000101113
PEX7 [NCBI] 9.99605e-05
ALD [NCBI] 9.81696e-05
ACAA1 [NCBI] 8.80061e-05
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency [NCBI] 8.67029e-05
adrenoleukodystrophy, autosomal neonatal form [NCBI] 7.51836e-05
HADHB [NCBI] 7.41441e-05
HSD17B4 [NCBI] 6.28755e-05
ACAA2 [NCBI] 4.15969e-05
ACADM [NCBI] 3.93077e-05
SOAT1 [NCBI] 2.93539e-05
OTC [NCBI] 2.18177e-05
PPARA [NCBI] 2.12003e-05
PLTP [NCBI] 1.48221e-05
CAT [NCBI] 3.60463e-06
CF [NCBI] 3.3039e-06
APOE [NCBI] 3.09275e-06
VIP [NCBI] 1.9688e-06




Database Center for Life Science