mineral metabolism disease Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An acquired metabolic disease that is characterized by abnormal mineral metabolism. (Human Disease Ontology, DOID_0050032)
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Genes

18 genes associated with the disease mineral metabolism disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PCSK7 proprotein convertase subtilisin/kexin type 7 1.65491
SIK3 SIK family kinase 3 1.57113
TF transferrin 1.06123
TMPRSS6 transmembrane protease, serine 6 0.724323
SRPRB signal recognition particle receptor, B subunit 0.63207
SLC17A3 solute carrier family 17 (organic anion transporter), member 3 0.5306
HIST1H2BJ histone cluster 1, H2bj 0.52461
HFE hemochromatosis 0.486425
BTN1A1 butyrophilin, subfamily 1, member A1 0.429338
LRRC16A leucine rich repeat containing 16A 0.345945
SLC17A1 solute carrier family 17 (organic anion transporter), member 1 0.311576
RSPO3 R-spondin 3 0.197766
KLHL13 kelch-like family member 13 0.197766
LUZP2 leucine zipper protein 2 0.197766
TRIM38 tripartite motif containing 38 0.126165
ARSB arylsulfatase B 0.052255
GHR growth hormone receptor 0.052255
SCGN secretagogin, EF-hand calcium binding protein 0.043246