dental enamel hypoplasia Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

88 genes co-occuring with the disease dental enamel hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
AMELX amelogenin, X-linked 3.19382
AMELY amelogenin, Y-linked 2.94134
ENAM enamelin 2.86989
MMP20 matrix metallopeptidase 20 2.76291
AMBN ameloblastin (enamel matrix protein) 2.58446
FAM83H family with sequence similarity 83, member H 2.2993
KLK4 kallikrein-related peptidase 4 2.24842
TUFT1 tuftelin 1 2.18235
DLX3 distal-less homeobox 3 2.04506
WDR72 WD repeat domain 72 2.00424
FAM20A family with sequence similarity 20, member A 1.92295
CNNM4 cyclin and CBS domain divalent metal cation transport mediator 4 1.86323
MMP25 matrix metallopeptidase 25 1.85638
ROGDI rogdi homolog (Drosophila) 1.76954
C4ORF26 chromosome 4 open reading frame 26 1.60949
AMTN amelotin 1.50667
HEBP1 heme binding protein 1 1.27126
WDR7 WD repeat domain 7 1.22779
DSPP dentin sialophosphoprotein 1.21392
SLC24A4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 1.17808
DUSP23 dual specificity phosphatase 23 1.16949
ARHGAP6 Rho GTPase activating protein 6 1.1439
GJA1 gap junction protein, alpha 1, 43kDa 1.13755
CNNM1 cyclin and CBS domain divalent metal cation transport mediator 1 1.11435
ATE1 arginyltransferase 1 1.10678
MSX2 msh homeobox 2 1.00457
COL17A1 collagen, type XVII, alpha 1 0.98011
ITGB6 integrin, beta 6 0.97002
FAM20B family with sequence similarity 20, member B 0.944106
AIRE autoimmune regulator 0.924626
LAMB3 laminin, beta 3 0.907731
DLX4 distal-less homeobox 4 0.888438
HMGN2 high mobility group nucleosomal binding domain 2 0.833148
ODAM odontogenic, ameloblast asssociated 0.820437
DUSP26 dual specificity phosphatase 26 (putative) 0.808539
SKP1 S-phase kinase-associated protein 1 0.807718
FAM20C family with sequence similarity 20, member C 0.804436
CNNM2 cyclin and CBS domain divalent metal cation transport mediator 2 0.795002
MSX1 msh homeobox 1 0.739894
DEDD death effector domain containing 0.701124
GRHL2 grainyhead-like 2 (Drosophila) 0.683093
COPB2 coatomer protein complex, subunit beta 2 (beta prime) 0.668345
PDLIM1 PDZ and LIM domain 1 0.628065
LAMC2 laminin, gamma 2 0.626888
FLNB filamin B, beta 0.615138
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4 0.613574
RAB4A RAB4A, member RAS oncogene family 0.604591
MNX1 motor neuron and pancreas homeobox 1 0.575383
ITSN1 intersectin 1 (SH3 domain protein) 0.573828
HRAS Harvey rat sarcoma viral oncogene homolog 0.567609
CLCN5 chloride channel, voltage-sensitive 5 0.537344
ITGB4 integrin, beta 4 0.523816
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1 0.517649
TRPV3 transient receptor potential cation channel, subfamily V, member 3 0.500761
AXIN2 axin 2 0.482084
EVC2 Ellis van Creveld syndrome 2 0.465038
LUM lumican 0.453339
KRT14 keratin 14, type I 0.436026
COL1A1 collagen, type I, alpha 1 0.434899
OFD1 oral-facial-digital syndrome 1 0.402692
COL1A2 collagen, type I, alpha 2 0.377402
CLCN7 chloride channel, voltage-sensitive 7 0.369258
MMAA methylmalonic aciduria (cobalamin deficiency) cblA type 0.366301
GALNT3 polypeptide N-acetylgalactosaminyltransferase 3 0.346777
BACE1 beta-site APP-cleaving enzyme 1 0.332121
PCNT pericentrin 0.325187
KLK5 kallikrein-related peptidase 5 0.319726
ALPL alkaline phosphatase, liver/bone/kidney 0.31464
CNGA3 cyclic nucleotide gated channel alpha 3 0.309204
MEPE matrix extracellular phosphoglycoprotein 0.304864
PAX9 paired box 9 0.291898
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit 0.285086
KCNA5 potassium channel, voltage gated shaker related subfamily A, member 5 0.264077
HYLS1 hydrolethalus syndrome 1 0.257005
ALPPL2 alkaline phosphatase, placental-like 2 0.252774
ALPP alkaline phosphatase, placental 0.252422
TIPARP TCDD-inducible poly(ADP-ribose) polymerase 0.249257
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies) 0.221793
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2 0.219057
TRPV6 transient receptor potential cation channel, subfamily V, member 6 0.212945
UROS uroporphyrinogen III synthase 0.208579
ALB albumin 0.196459
GALNS galactosamine (N-acetyl)-6-sulfatase 0.169812
SP6 Sp6 transcription factor 0.160574
IBSP integrin-binding sialoprotein 0.141739
FGF23 fibroblast growth factor 23 0.141172
RAC2 ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2) 0.141032
HPX hemopexin 0.14102