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MeSH keywords -> Related genes, diseases (OMIM)


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01 Elastic Tissue [NCBI]


Gene


Gene Link Information
Gain
01
FBLN5 [NCBI] 0.00010872
ABCC6 [NCBI] 3.93755e-05
ELN [NCBI] 3.67928e-05
LOXL1 [NCBI] 3.62597e-05
TNXB [NCBI] 3.06066e-05
FBLN1 [NCBI] 2.16235e-05
GLB1 [NCBI] 1.76946e-05
FBN1 [NCBI] 1.62445e-05
MFAP5 [NCBI] 1.61093e-05
CD68 [NCBI] 1.55167e-05
VCAN [NCBI] 1.30386e-05
LTBP2 [NCBI] 1.23412e-05
MMP2 [NCBI] 1.15014e-05
LTBP1 [NCBI] 1.04179e-05
LOX [NCBI] 1.00931e-05
MMP12 [NCBI] 9.53105e-06
MFAP4 [NCBI] 7.02683e-06
PROM2 [NCBI] 6.85922e-06
MFAP1 [NCBI] 6.71574e-06
MMP9 [NCBI] 6.5911e-06
TGFB1 [NCBI] 6.24679e-06
MFAP2 [NCBI] 6.20406e-06
LTBP4 [NCBI] 6.05549e-06
FBLN2 [NCBI] 5.98874e-06
FBN2 [NCBI] 5.8673e-06
KRT15 [NCBI] 5.75904e-06
NID2 [NCBI] 5.70901e-06
LEMD3 [NCBI] 5.70901e-06
LYZ [NCBI] 5.57241e-06
ZMPSTE24 [NCBI] 5.57241e-06
SLC4A3 [NCBI] 5.49073e-06
NEU1 [NCBI] 5.16e-06
COL4A2 [NCBI] 4.93427e-06
COL4A4 [NCBI] 4.82794e-06
COL4A3 [NCBI] 4.7884e-06
COL4A1 [NCBI] 4.6113e-06
BMP2 [NCBI] 4.53042e-06
BGN [NCBI] 4.46103e-06
HAS2 [NCBI] 4.36793e-06
CD55 [NCBI] 4.36793e-06
TNC [NCBI] 4.29453e-06
DCN [NCBI] 4.17265e-06
COL3A1 [NCBI] 4.112e-06
PDGFB [NCBI] 4.09258e-06
COL1A2 [NCBI] 4.04563e-06
CSF2 [NCBI] 3.94131e-06
MMP7 [NCBI] 3.87742e-06
SPP1 [NCBI] 3.60258e-06
TGFBI [NCBI] 3.36033e-06
MGP [NCBI] 3.32008e-06
IGF2 [NCBI] 3.14789e-06
DEFB4 [NCBI] 3.13694e-06
CLU [NCBI] 2.84754e-06
CNN1 [NCBI] 2.69396e-06
IBSP [NCBI] 2.47621e-06
IL6 [NCBI] 1.97397e-06
VEGFA [NCBI] 1.10296e-06
EGF [NCBI] 9.84868e-07
FASLG [NCBI] 9.39468e-07
NGF [NCBI] 3.84549e-07




OMIM


OMIM Link Information
gain
01
AKE [NCBI] 0.00357597
PXE [NCBI] 0.00276376
EPS [NCBI] 0.00211333
facial ectodermal dysplasia [NCBI] 0.00189459
focal facial dermal dysplasia [NCBI] 0.00101143
cutis laxa, autosomal recessive, type i [NCBI] 0.000978677
collagenosis, familial reactive perforating [NCBI] 0.00095499
aortic aneurysm, familial thoracic 1 [NCBI] 0.000910064
skin creases, multiple benign ring-shaped, of limbs [NCBI] 0.000840831
SVAS [NCBI] 0.000571409
cutis laxa, autosomal dominant [NCBI] 0.000549855
MFS [NCBI] 0.000402108
RA [NCBI] 0.000266888
WSS [NCBI] 0.000243315
buschke-ollendorff syndrome [NCBI] 0.000220333
ATS [NCBI] 0.000214388
temporal arteritis [NCBI] 0.000168828
tracheobronchomegaly [NCBI] 0.000141472
takayasu arteritis [NCBI] 0.000141472
AMVC [NCBI] 0.000141472
epidermolysis bullosa pruriginosa [NCBI] 0.000126695
acrogeria, gottron type [NCBI] 0.000126695
ELN [NCBI] 0.000111079
ehlers-danlos syndrome, type iii [NCBI] 0.000110004
FBLN5 [NCBI] 9.98349e-05
sulfocysteinuria [NCBI] 9.96511e-05
pseudoxanthoma elasticum, forme fruste [NCBI] 9.96511e-05
LOXL1 [NCBI] 9.71799e-05
EMILIN1 [NCBI] 9.71799e-05
CF [NCBI] 9.57805e-05
cutis laxa, autosomal recessive, type ii [NCBI] 9.56376e-05
morquio syndrome b [NCBI] 9.21347e-05
ABCC6 [NCBI] 7.77799e-05
GACI [NCBI] 7.54371e-05
GLB1 [NCBI] 7.30302e-05
EFE [NCBI] 6.91225e-05
LOX [NCBI] 6.37655e-05
microfibril-associated glycoprotein 2 [NCBI] 6.35432e-05
gm1-gangliosidosis, type i [NCBI] 6.28937e-05
ehlers-danlos syndrome, type i [NCBI] 6.28937e-05
costello syndrome [NCBI] 5.78709e-05
SLE [NCBI] 5.50939e-05
LSA [NCBI] 5.44596e-05
MFAP4 [NCBI] 5.35606e-05
hurler syndrome [NCBI] 5.07576e-05
EFEMP2 [NCBI] 4.97933e-05
LTBP4 [NCBI] 4.97933e-05
MFAP1 [NCBI] 4.73473e-05
TNXB [NCBI] 3.66197e-05
homocystinuria [NCBI] 2.80087e-05
SMS [NCBI] 2.58558e-05
PI [NCBI] 2.12875e-05
NF1 [NCBI] 1.91501e-05
WBS [NCBI] 1.88196e-05
VEGF [NCBI] 1.57519e-05
GJA1 [NCBI] 1.45485e-05
CEACAM5 [NCBI] 4.0235e-06
CRC [NCBI] 9.99704e-07
EGF [NCBI] 5.44209e-07
NGFB [NCBI] 5.10727e-08




Database Center for Life Science