UNIPROT:Q16637 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:Q16637 (SMA)
8,107 document(s) hit in 31,850,051 MEDLINE articles (0.01 seconds)

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Concepts found in the documents ranked by [ Frequency | Pointwise Mutual Information | Symmetric Conditional Probability ] .

Human Gene/Protein
SMA	11.9
PLS3 protein	11.9
ZNF297B	11.9
regulator of G protein signalling 5	11.9
CTNNBIP1 protein	11.9
NRK2	11.9
TAOK1 protein	11.9
SMN2	11.5
SMA3	11.4
SMN	11.1
OTU domain-containing protein 4	10.9
HCAM1	10.9
actin, alpha 2, smooth muscle, aorta	10.9
OR52E2	10.9
GUSBP1	10.9
C3orf62	10.9
V-ATPase B2 subunit	10.9
SR-like splicing factor	10.7
neuronal apoptosis inhibitory protein	10.6
bicaudal D homolog 2	10.6
GTF2H2	10.5
CAPN7	10.4
Nicotinamide riboside kinase	10.4
Gemin8	10.2
SMN-interacting protein 1	10.1
SMA4	10.1
survival of motor neuron	10.1
plastin 3	10.0
Serine-threonine kinase receptor-associated protein	10.0
FSP1	10.0
tetraspanin 12	9.9
F-box protein 31	9.9
SRY-box 7	9.9
hCD	9.9
HECTD1 protein	9.9
HDAC10 protein	9.9
Tudor domain-containing protein 3	9.9
ACINUS	9.9
CCT-beta	9.9
enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase	9.9

Disease
Combined valvular disease	11.9
SMA II	11.5
Spinal muscular atrophy	11.1
Benign monomelic amyotrophy	10.9
SMAX2	10.9
Uterine fibrosis	10.9
Kugelberg-Welander	10.5
Excessive skin	10.4
Anterior horn cell disease	10.4
Anterior capsule opacification	10.4
SMA4	10.1
Varicose veins of lower extremities	9.9
Infection by Opisthorchis viverrini	9.9
Subcapsular cataracts	9.9
Werdnig-Hoffmann disease	9.9
Renal interstitial fibrosis	9.8
Gastrointestinal stromal sarcoma	9.6
Liver cholestasis	9.6
Potassium retention	9.4
Metanephric adenofibroma	9.4
Scapuloperoneal spinal muscular atrophy	9.4
Ossifying renal tumor	9.4
ECL cell carcinoid	9.4
SMARD1	9.3
Myolipoma	9.1
Giant cell reaction	9.1
Intravascular leiomyomatosis	9.1
Autoimmune myocarditis	9.0
Peritoneal fibrosis	9.0
Renal fibrosis	9.0
Bulbar weakness	8.9
Wilkie syndrome	8.9
PCH1	8.8
Hepatic schistosomiasis	8.8
Biliary fibrosis	8.8
Periodic catatonia	8.8
IGDS	8.6
Verocay body	8.5
Congenital Myasthenic Syndromes	8.5
Secondary biliary cirrhosis	8.4

Enzyme
beta-alanine-pyruvate aminotransferase	9.4
carboxypeptidase 1	8.4
creatinine iminohydrolase	7.5
HK2	7.3
PME	6.7
creatininase	6.1
ceramidase	5.5
CYP8B1	5.4
STK2	5.4
AST	5.4
prolyl-tRNA synthetase	5.3
MMP	5.0
GAR	5.0
lysyl hydroxylase	5.0
lysyl oxidase	5.0
glycyl-tRNA synthetase	5.0
aspartate aminotransferase	4.9
matrix metalloproteinase 2	4.8
p80	4.8
guanidinoacetate methyltransferase	4.8
calpain 3	4.7
alanine aminotransferase	4.7
CD10	4.6
proteinase A	4.4
GD3 synthase	4.4
sphingosine kinase	4.4
legumain	4.3
tryptase	4.3
phosphatidylinositol-4,5-bisphosphate 3-kinase	4.3
collagenase	4.3
galactocerebrosidase	4.2
GSK	4.2
calpain 3	4.2
dihydrodiol dehydrogenase	4.1
glutamic dehydrogenase	4.1
inositol 3-kinase	4.1
methylthioadenosine phosphorylase	4.1
AMP-activated kinase	4.1
Rex	4.1
3-mercaptopyruvate sulfurtransferase	4.1