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MeSH keywords -> Related genes, diseases (OMIM)


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01 Blood Bactericidal Activity [NCBI]


Gene


Gene Link Information
Gain
01
BPI [NCBI] 0.00048656
MPO [NCBI] 7.09953e-05
LBP [NCBI] 4.97893e-05
MS [NCBI] 4.84706e-05
CTSG [NCBI] 3.80195e-05
TNF [NCBI] 1.27968e-05
PPBP [NCBI] 6.51257e-06
CFH [NCBI] 5.6882e-06
C8A [NCBI] 5.40382e-06
DEFA3 [NCBI] 5.3719e-06
AZU1 [NCBI] 5.12613e-06
DEFA1 [NCBI] 4.79012e-06
C4BPA [NCBI] 4.77375e-06
GZMA [NCBI] 3.45134e-06
DEFA4 [NCBI] 3.05012e-06
DEFA6 [NCBI] 2.98492e-06
SPACA3 [NCBI] 2.79035e-06
C8B [NCBI] 2.57415e-06
IGH@ [NCBI] 2.5275e-06
FCGBP [NCBI] 2.5275e-06
GZMB [NCBI] 2.52638e-06
C8G [NCBI] 2.46544e-06
MARCO [NCBI] 2.29105e-06
PLUNC [NCBI] 2.21828e-06
CETP [NCBI] 2.18463e-06
C2 [NCBI] 2.12725e-06
CTSC [NCBI] 2.08362e-06
CXCL6 [NCBI] 2.07537e-06
VTN [NCBI] 1.90695e-06
PLA2G2A [NCBI] 1.90136e-06
CAMP [NCBI] 1.86923e-06
TREM1 [NCBI] 1.81569e-06
GNLY [NCBI] 1.7322e-06
CXCL5 [NCBI] 1.65221e-06
PADI4 [NCBI] 1.62444e-06
TIMP1 [NCBI] 1.55787e-06
C3 [NCBI] 1.55787e-06
LCN2 [NCBI] 1.51611e-06
IL13RA1 [NCBI] 1.4801e-06
C1QBP [NCBI] 1.41398e-06
CD93 [NCBI] 1.39935e-06
MAP2K2 [NCBI] 1.29995e-06
FASLG [NCBI] 1.20674e-06
SLC11A1 [NCBI] 1.10118e-06
HP [NCBI] 1.0732e-06
CALCA [NCBI] 1.00609e-06
IFNG [NCBI] 9.87055e-07
MAP2K1 [NCBI] 8.7389e-07
TF [NCBI] 8.52997e-07
IL1RN [NCBI] 5.89478e-07
CFTR [NCBI] 2.43363e-07
CASP3 [NCBI] 1.48976e-07




OMIM


OMIM Link Information
gain
01
MPO [NCBI] 0.00061975
CGD [NCBI] 0.000442906
myeloperoxidase deficiency [NCBI] 0.00030292
LAD [NCBI] 0.000213119
CHS [NCBI] 0.000209265
complement component 5 deficiency [NCBI] 0.00020376
SGD [NCBI] 0.000172737
properdin deficiency, x-linked [NCBI] 0.000162031
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant [NCBI] 0.000162031
OPTB1 [NCBI] 0.000145129
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i [NCBI] 0.000142188
LBP [NCBI] 0.000121138
whim syndrome [NCBI] 8.95276e-05
complement component 8 deficiency, type i [NCBI] 8.89545e-05
complement component 6 deficiency [NCBI] 8.27247e-05
complement factor i deficiency [NCBI] 8.0836e-05
CF [NCBI] 7.92912e-05
glutathione synthetase deficiency [NCBI] 7.48205e-05
ITGB2 [NCBI] 7.24088e-05
complement component 7 deficiency [NCBI] 7.1637e-05
PALS [NCBI] 7.02201e-05
blood group, p system [NCBI] 6.76611e-05
BPI [NCBI] 6.2383e-05
glycogen storage disease ib [NCBI] 6.06817e-05
kartagener syndrome [NCBI] 5.25996e-05
TNF [NCBI] 5.14588e-05
complement component 2 deficiency [NCBI] 4.86459e-05
DEFA6 [NCBI] 3.3854e-05
NAZC [NCBI] 3.3854e-05
DEFA3 [NCBI] 2.93122e-05
complement component 8 deficiency, type ii [NCBI] 2.93122e-05
RNASE3 [NCBI] 2.68847e-05
MARCO [NCBI] 2.67751e-05
C4BPA [NCBI] 2.50068e-05
PFC [NCBI] 2.50068e-05
DEFA1 [NCBI] 2.39602e-05
C9 [NCBI] 2.33536e-05
MBL2 [NCBI] 2.24272e-05
ELA2 [NCBI] 2.18387e-05
CYBB [NCBI] 2.02859e-05
CTSC [NCBI] 1.82889e-05
C3 [NCBI] 1.72952e-05
BTK [NCBI] 1.46031e-05
RNASE2 [NCBI] 1.30738e-05
RA [NCBI] 7.62751e-06
HP [NCBI] 5.66188e-06
TLR4 [NCBI] 4.93175e-06
TF [NCBI] 3.26282e-06
G6PD [NCBI] 1.49297e-06
SLE [NCBI] 2.643e-07
MDD [NCBI] 9.52705e-09




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