eating disorder Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A specific developmental disorder that is characterized by abnormal eating habits that may involve either insufficient or excessive food intake to the detriment of an individual's physical and emotional health. (Human Disease Ontology, DOID_8670)
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Genes

51 genes associated with the disease eating disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
RDH14 retinol dehydrogenase 14 (all-trans/9-cis/11-cis) 0.403461
TSHZ1 teashirt zinc finger homeobox 1 0.345945
ATP8A2 ATPase, aminophospholipid transporter, class I, type 8A, member 2 0.274608
CHODL chondrolectin 0.256228
FLNB filamin B, beta 0.256228
TSPAN7 tetraspanin 7 0.256228
SAYSD1 SAYSVFN motif domain containing 1 0.197766
FLG2 filaggrin family member 2 0.197766
PRM1 protamine 1 0.197766
PERP PERP, TP53 apoptosis effector 0.197766
GRID1 glutamate receptor, ionotropic, delta 1 0.197766
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila) 0.197766
ZNF804B zinc finger protein 804B 0.197766
CSRP2BP CSRP2 binding protein 0.197766
MTMR3 myotubularin related protein 3 0.197766
ROBO2 roundabout, axon guidance receptor, homolog 2 (Drosophila) 0.15771
CCNL1 cyclin L1 0.15771
PDE8A phosphodiesterase 8A 0.15771
C10ORF11 chromosome 10 open reading frame 11 0.15771
CATSPER3 cation channel, sperm associated 3 0.15771
RUFY1 RUN and FYVE domain containing 1 0.15771
MCTP1 multiple C2 domains, transmembrane 1 0.15771
TMEM106B transmembrane protein 106B 0.126165
MACROD2 MACRO domain containing 2 0.126165
CAMK1D calcium/calmodulin-dependent protein kinase ID 0.126165
ATOH7 atonal homolog 7 (Drosophila) 0.126165
IFI44 interferon-induced protein 44 0.126165
KLHL8 kelch-like family member 8 0.126165
EMP2 epithelial membrane protein 2 0.100789
SH2D3C SH2 domain containing 3C 0.100789
ASB3 ankyrin repeat and SOCS box containing 3 0.100789
AKAP6 A kinase (PRKA) anchor protein 6 0.080593
NTNG1 netrin G1 0.080593
PCDH7 protocadherin 7 0.080593
MAGI3 membrane associated guanylate kinase, WW and PDZ domain containing 3 0.080593
SHC4 SHC (Src homology 2 domain containing) family, member 4 0.080593
COL23A1 collagen, type XXIII, alpha 1 0.080593
SHFM1P1 split hand/foot malformation (ectrodactyly) type 1 pseudogene 1 0.064973
SGPP2 sphingosine-1-phosphate phosphatase 2 0.064973
WWOX WW domain containing oxidoreductase 0.064973
CCDC69 coiled-coil domain containing 69 0.064973
MSRA methionine sulfoxide reductase A 0.052255
GADL1 glutamate decarboxylase-like 1 0.052255
CDH9 cadherin 9, type 2 (T1-cadherin) 0.052255
SEMA6D sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D 0.052255
FAM155A family with sequence similarity 155, member A 0.052255
LRP2 low density lipoprotein receptor-related protein 2 0.043246
QSOX1 quiescin Q6 sulfhydryl oxidase 1 0.043246
ALDH4A1 aldehyde dehydrogenase 4 family, member A1 0.043246
OLIG2 oligodendrocyte lineage transcription factor 2 0.043246
VGLL4 vestigial-like family member 4 0.043246