Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Properdin [NCBI]


Gene


Gene Link Information
Gain
01
CFP [NCBI] 7.88919e-05
C3 [NCBI] 1.90951e-05
CFB [NCBI] 1.64627e-05
C4B [NCBI] 5.98121e-06
THBS1 [NCBI] 3.31891e-06
HEPACAM [NCBI] 2.31698e-06
HSD17B6 [NCBI] 2.28719e-06
B3GALTL [NCBI] 2.23604e-06
CFD [NCBI] 2.17399e-06
SEMA5A [NCBI] 2.12367e-06
BCAT1 [NCBI] 2.06859e-06
C4BPB [NCBI] 2.01264e-06
CTNND2 [NCBI] 2.00273e-06
C9 [NCBI] 1.94207e-06
THBS2 [NCBI] 1.92699e-06
SFRP4 [NCBI] 1.86804e-06
C2 [NCBI] 1.84015e-06
C4BPA [NCBI] 1.77889e-06
C4A [NCBI] 1.75092e-06
C5 [NCBI] 1.74344e-06
C5AR1 [NCBI] 1.6812e-06
CD55 [NCBI] 1.63076e-06
C3AR1 [NCBI] 1.59461e-06
FGA [NCBI] 1.51798e-06
ITGAM [NCBI] 1.45852e-06
CFH [NCBI] 1.40993e-06
CYP1B1 [NCBI] 1.40058e-06
MAOA [NCBI] 1.38665e-06
TLR3 [NCBI] 1.31785e-06
MMP2 [NCBI] 1.17926e-06
CD46 [NCBI] 1.15999e-06
MMP9 [NCBI] 1.13329e-06




OMIM


OMIM Link Information
gain
01
properdin deficiency, x-linked [NCBI] 0.00301229
IGAN1 [NCBI] 0.0019383
PFC [NCBI] 0.000698808
CFB [NCBI] 0.000303913
cirrhosis, familial [NCBI] 0.000125861
cri-du-chat syndrome [NCBI] 0.000118131
membranoproliferative glomerulonephritis, x-linked [NCBI] 0.000118131
complement factor i deficiency [NCBI] 9.79128e-05
complement component 2 deficiency [NCBI] 8.67144e-05
complement component 7 deficiency [NCBI] 8.15665e-05
SLE [NCBI] 7.26014e-05
SCIDX1 [NCBI] 7.05973e-05
C4B [NCBI] 5.1755e-05
C4A [NCBI] 5.15348e-05
SEMA5A [NCBI] 3.13477e-05
SYN1 [NCBI] 3.13477e-05
CFI [NCBI] 2.38602e-05
TIMP1 [NCBI] 2.35597e-05
C3 [NCBI] 2.08693e-05
MMP2 [NCBI] 2.01326e-05
MBL2 [NCBI] 1.16234e-05
RA [NCBI] 6.75645e-06
AVP [NCBI] 9.0489e-07
AD [NCBI] 5.38392e-09




Database Center for Life Science