amelogenesis imperfecta Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A dental enamel hypoplasia characterized by abnormal enamel formation. (Human Disease Ontology, DOID_2187)
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Genes

64 genes co-occuring with the disease amelogenesis imperfecta in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
AMELX amelogenin, X-linked 3.20021
ENAM enamelin 2.9334
AMELY amelogenin, Y-linked 2.91823
MMP20 matrix metallopeptidase 20 2.83537
AMBN ameloblastin (enamel matrix protein) 2.56943
FAM83H family with sequence similarity 83, member H 2.35976
KLK4 kallikrein-related peptidase 4 2.31018
TUFT1 tuftelin 1 2.24524
WDR72 WD repeat domain 72 2.05765
CNNM4 cyclin and CBS domain divalent metal cation transport mediator 4 1.91734
MMP25 matrix metallopeptidase 25 1.91033
DLX3 distal-less homeobox 3 1.90242
FAM20A family with sequence similarity 20, member A 1.89638
ROGDI rogdi homolog (Drosophila) 1.82233
C4ORF26 chromosome 4 open reading frame 26 1.66195
AMTN amelotin 1.55823
WDR7 WD repeat domain 7 1.27911
SLC24A4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 1.22865
ARHGAP6 Rho GTPase activating protein 6 1.19402
CNNM1 cyclin and CBS domain divalent metal cation transport mediator 1 1.16435
DSPP dentin sialophosphoprotein 1.15752
ATE1 arginyltransferase 1 1.15624
ITGB6 integrin, beta 6 1.01976
FAM20B family with sequence similarity 20, member B 0.993174
MSX2 msh homeobox 2 0.926692
SKP1 S-phase kinase-associated protein 1 0.855677
CNNM2 cyclin and CBS domain divalent metal cation transport mediator 2 0.842982
MSX1 msh homeobox 1 0.788033
COPB2 coatomer protein complex, subunit beta 2 (beta prime) 0.715618
LAMB3 laminin, beta 3 0.681894
RAB4A RAB4A, member RAS oncogene family 0.650508
HRAS Harvey rat sarcoma viral oncogene homolog 0.613183
CLCN5 chloride channel, voltage-sensitive 5 0.582773
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1 0.562946
DLX4 distal-less homeobox 4 0.551298
TRPV3 transient receptor potential cation channel, subfamily V, member 3 0.546256
AXIN2 axin 2 0.52729
FAM20C family with sequence similarity 20, member C 0.489311
COL17A1 collagen, type XVII, alpha 1 0.486266
KRT14 keratin 14, type I 0.480566
COL1A1 collagen, type I, alpha 1 0.479047
MNX1 motor neuron and pancreas homeobox 1 0.467684
COL1A2 collagen, type I, alpha 2 0.421016
CLCN7 chloride channel, voltage-sensitive 7 0.412779
GALNT3 polypeptide N-acetylgalactosaminyltransferase 3 0.390025
BACE1 beta-site APP-cleaving enzyme 1 0.375179
PCNT pericentrin 0.368518
KLK5 kallikrein-related peptidase 5 0.362978
CNGA3 cyclic nucleotide gated channel alpha 3 0.351923
MEPE matrix extracellular phosphoglycoprotein 0.347879
PAX9 paired box 9 0.334315
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit 0.32774
LAMC2 laminin, gamma 2 0.308842
KCNA5 potassium channel, voltage gated shaker related subfamily A, member 5 0.305948
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4 0.280439
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies) 0.26266
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2 0.25983
UROS uroporphyrinogen III synthase 0.248905
GALNS galactosamine (N-acetyl)-6-sulfatase 0.204263
SP6 Sp6 transcription factor 0.190476
IBSP integrin-binding sialoprotein 0.171535
FGF23 fibroblast growth factor 23 0.160021
RAC2 ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2) 0.157929
HPX hemopexin 0.157765