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MeSH keywords -> Related genes, diseases (OMIM)


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01 Myofibrils [NCBI]


Gene


Gene Link Information
Gain
01
MYOM2 [NCBI] 0.000174844
MYOT [NCBI] 9.39785e-05
TTN [NCBI] 8.70327e-05
PLN [NCBI] 4.86256e-05
TRIM63 [NCBI] 3.60295e-05
CSRP3 [NCBI] 3.33754e-05
TMOD1 [NCBI] 2.41328e-05
TCAP [NCBI] 2.34954e-05
TRIM54 [NCBI] 2.28771e-05
TRIM55 [NCBI] 2.22549e-05
CRYAB [NCBI] 1.96911e-05
NEBL [NCBI] 1.91103e-05
OBSCN [NCBI] 1.89221e-05
LDB3 [NCBI] 1.84194e-05
ACTA1 [NCBI] 1.77809e-05
FLNC [NCBI] 1.7279e-05
CDH15 [NCBI] 1.47826e-05
NRAP [NCBI] 1.24345e-05
UCP3 [NCBI] 1.24212e-05
NEB [NCBI] 1.04707e-05
MYOD1 [NCBI] 1.01377e-05
FBXO32 [NCBI] 9.8802e-06
ACTC1 [NCBI] 9.50066e-06
PAX7 [NCBI] 9.38868e-06
DES [NCBI] 9.35272e-06
FHL2 [NCBI] 9.05533e-06
ACTN1 [NCBI] 8.99488e-06
TNNI3 [NCBI] 8.90752e-06
MYH7 [NCBI] 8.7175e-06
CAPN3 [NCBI] 8.69178e-06
PPP1R2 [NCBI] 8.27814e-06
MYOG [NCBI] 7.33879e-06
MSTN [NCBI] 6.90178e-06
CTSL1 [NCBI] 6.83397e-06
NEURL2 [NCBI] 6.75612e-06
LMNA [NCBI] 6.51922e-06
USP13 [NCBI] 6.50323e-06
ASB15 [NCBI] 6.50323e-06
TBPL2 [NCBI] 6.50323e-06
MYF6 [NCBI] 6.30173e-06
LMOD1 [NCBI] 6.13419e-06
TNN [NCBI] 6.13419e-06
MYL7 [NCBI] 6.13419e-06
KBTBD10 [NCBI] 5.99077e-06
SPEG [NCBI] 5.8654e-06
TAF3 [NCBI] 5.8654e-06
PLVAP [NCBI] 5.75404e-06
CS [NCBI] 5.74695e-06
TBX20 [NCBI] 5.65386e-06
MYOM1 [NCBI] 5.56283e-06
LIM2 [NCBI] 5.47941e-06
SGCA [NCBI] 5.40243e-06
CFL2 [NCBI] 5.40243e-06
HSPB1 [NCBI] 5.37622e-06
CNN1 [NCBI] 5.33456e-06
GMEB1 [NCBI] 5.33097e-06
CACNB1 [NCBI] 5.33097e-06
CKMT2 [NCBI] 5.26429e-06
TNNT3 [NCBI] 5.26429e-06
CKMT1A [NCBI] 5.20179e-06
MYL2 [NCBI] 5.08744e-06
CKMT1B [NCBI] 5.08744e-06
TNNI2 [NCBI] 5.03484e-06
DGKZ [NCBI] 5.03484e-06
SGCB [NCBI] 5.03484e-06
TNNT1 [NCBI] 4.9373e-06
SEPN1 [NCBI] 4.89189e-06
HSPB6 [NCBI] 4.72852e-06
MCTS1 [NCBI] 4.72852e-06
ANKRD1 [NCBI] 4.58823e-06
TNNC1 [NCBI] 4.55605e-06
MYBPC3 [NCBI] 4.52487e-06
S100A1 [NCBI] 4.49465e-06
SLC16A1 [NCBI] 4.46532e-06
GAPDH [NCBI] 4.36004e-06
ANK2 [NCBI] 4.28119e-06
TLN1 [NCBI] 4.23431e-06
CALM3 [NCBI] 4.18954e-06
PSMB10 [NCBI] 4.18954e-06
PRKCH [NCBI] 4.10566e-06
MYF5 [NCBI] 4.08576e-06
ANK1 [NCBI] 4.08576e-06
ACTN2 [NCBI] 3.99184e-06
FABP3 [NCBI] 3.79731e-06
OXCT2 [NCBI] 3.6731e-06
VCL [NCBI] 3.6731e-06
PSME1 [NCBI] 3.66021e-06
KCNE1 [NCBI] 3.59823e-06
NAIP [NCBI] 3.58629e-06
TNC [NCBI] 3.57449e-06
PLEC1 [NCBI] 3.32713e-06
MYO6 [NCBI] 3.30019e-06
MYH9 [NCBI] 3.29137e-06
FLNA [NCBI] 3.24008e-06
AQP4 [NCBI] 3.14498e-06
NFATC2 [NCBI] 3.05838e-06
SLC6A6 [NCBI] 3.01782e-06
PSMB8 [NCBI] 2.94763e-06
ACTB [NCBI] 2.88798e-06
PRKCZ [NCBI] 2.85948e-06
PSMB9 [NCBI] 2.78914e-06
NKX2-5 [NCBI] 2.72363e-06
SMN1 [NCBI] 2.72363e-06
BCAR1 [NCBI] 2.69484e-06
UBE2I [NCBI] 2.63977e-06
MB [NCBI] 2.61338e-06
EIF4EBP1 [NCBI] 2.56273e-06
PRKD1 [NCBI] 2.41471e-06
DAG1 [NCBI] 2.36348e-06
IAPP [NCBI] 2.35356e-06
CLU [NCBI] 2.14541e-06
FGF2 [NCBI] 2.14018e-06
IL1B [NCBI] 1.94604e-06
SRF [NCBI] 1.94184e-06
PDGFA [NCBI] 1.67472e-06
ACHE [NCBI] 1.47236e-06
SNCA [NCBI] 1.44615e-06
PRKCB [NCBI] 1.41727e-06
PRKCA [NCBI] 1.39599e-06
CTGF [NCBI] 1.38392e-06
CXCL12 [NCBI] 1.02679e-06
TNF [NCBI] 9.81061e-07
CD68 [NCBI] 9.03136e-07
CASP3 [NCBI] 8.68969e-07
CTNNB1 [NCBI] 6.57966e-07
HGF [NCBI] 5.21093e-07
PCNA [NCBI] 4.26191e-07




OMIM


OMIM Link Information
gain
01
WDM [NCBI] 0.00201127
myopathy, distal, with onset in infancy [NCBI] 0.00154746
NEM3 [NCBI] 0.00133097
NEM6 [NCBI] 0.00123667
myopathy, hyaline body, autosomal recessive [NCBI] 0.0011195
carnitine deficiency, myopathic [NCBI] 0.000844839
NLS [NCBI] 0.000711442
MTM1 [NCBI] 0.000460406
RSMD1 [NCBI] 0.00042361
CD [NCBI] 0.000422141
myopathy, centronuclear, autosomal dominant [NCBI] 0.000421833
myopathy with storage of glycoproteins and glycosaminoglycans [NCBI] 0.000316957
central core disease of muscle [NCBI] 0.000294579
cardiomyopathy, infantile histiocytoid [NCBI] 0.000262975
LGMD1A [NCBI] 0.000252566
myopathy, myosin storage [NCBI] 0.000229563
tibial muscular dystrophy, tardive [NCBI] 0.000204658
CFTD [NCBI] 0.00019716
dystonia with ringbinden [NCBI] 0.000185316
NEM7 [NCBI] 0.000185316
myopathy, myofibrillar, desmin-related [NCBI] 0.00017221
TMOD [NCBI] 0.000163656
pleoconial myopathy with salt craving [NCBI] 0.000146079
filaminopathy, autosomal dominant [NCBI] 0.000146079
ophthalmoplegic neuromuscular disorder with abnormal mitochondria [NCBI] 0.000146079
myopathy with giant abnormal mitochondria [NCBI] 0.000131295
alpha-b crystallinopathy [NCBI] 0.000121708
spinal muscular atrophy, proximal, adult, autosomal dominant [NCBI] 0.00011459
DES [NCBI] 0.000104366
mitochondrial myopathy [NCBI] 9.6691e-05
KSS [NCBI] 9.26123e-05
myotonia congenita, autosomal dominant [NCBI] 9.07797e-05
LGMD2D [NCBI] 9.07797e-05
COFS1 [NCBI] 8.37771e-05
DMD [NCBI] 8.25962e-05
UCMD [NCBI] 8.17922e-05
SMA3 [NCBI] 8.17922e-05
abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism [NCBI] 7.82114e-05
CF [NCBI] 7.39516e-05
HYPP [NCBI] 6.84743e-05
glycogen storage disease v [NCBI] 6.62411e-05
SJS1 [NCBI] 6.32115e-05
CMT1B [NCBI] 5.44106e-05
RSTS [NCBI] 5.44106e-05
EDMD [NCBI] 5.00726e-05
CACNB1 [NCBI] 4.60671e-05
TRIM32 [NCBI] 4.36217e-05
CFL2 [NCBI] 4.18038e-05
glycogen storage disease ii [NCBI] 4.07502e-05
ADSS [NCBI] 4.03555e-05
FLNC [NCBI] 3.91513e-05
TTID [NCBI] 3.91513e-05
SEPN1 [NCBI] 3.91513e-05
BCAR1 [NCBI] 3.64199e-05
SLE [NCBI] 3.54153e-05
SGCA [NCBI] 3.50464e-05
RYR3 [NCBI] 3.50464e-05
CMH [NCBI] 3.41145e-05
ACTC1 [NCBI] 3.33815e-05
PTK2 [NCBI] 3.11085e-05
CLCN1 [NCBI] 2.96207e-05
CRYAB [NCBI] 2.96207e-05
MTM1 [NCBI] 2.96207e-05
MSTN [NCBI] 2.67707e-05
RUNX1 [NCBI] 2.67707e-05
CSF3 [NCBI] 2.639e-05
DSTN [NCBI] 2.62071e-05
BIRC1 [NCBI] 2.50444e-05
RYR1 [NCBI] 2.34122e-05
AQP4 [NCBI] 2.30573e-05
GAPDH [NCBI] 2.30274e-05
UCP3 [NCBI] 2.14201e-05
FGF2 [NCBI] 1.69088e-05
GPI [NCBI] 1.52148e-05
MB [NCBI] 1.42983e-05
PDCD8 [NCBI] 1.29861e-05
IAPP [NCBI] 1.29348e-05
NPPA [NCBI] 1.26433e-05
SRF [NCBI] 9.86124e-06
XDH [NCBI] 7.31896e-06
RNASE3 [NCBI] 5.78795e-06
ACHE [NCBI] 3.88513e-06
TNF [NCBI] 1.1003e-06
HGF [NCBI] 1.02091e-06
MG [NCBI] 6.36224e-07
PCNA [NCBI] 5.6791e-07




Database Center for Life Science