dyscalculia Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A learning disability involving a math disability can cause such difficulties as learning math concepts (such as quantity, place value, and time), difficulty memorizing math facts, difficulty organizing numbers, and understanding how problems are organized on the page. (Human Disease Ontology, DOID_12568)
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Genes

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

Symbol Name Standardized Value
GLRA2 glycine receptor, alpha 2 1.31886
GYLTL1B glycosyltransferase-like 1B 1.28872
SLC7A11 solute carrier family 7 (anionic amino acid transporter light chain, xc- system), member 11 1.28304
ADD3 adducin 3 (gamma) 1.15368
ADRA2A adrenoceptor alpha 2A 0.952438
CEBPD CCAAT/enhancer binding protein (C/EBP), delta 0.876148
TBX1 T-box 1 0.818385
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein 0.615138
SMPD1 sphingomyelin phosphodiesterase 1, acid lysosomal 0.604981
VCP valosin containing protein 0.590558
PSEN2 presenilin 2 0.543155
NF1 neurofibromin 1 0.53657
TARDBP TAR DNA binding protein 0.534635
CD6 CD6 molecule 0.526904
GRN granulin 0.526904
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4 0.510344
APOH apolipoprotein H (beta-2-glycoprotein I) 0.386679
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13 0.379626
PSEN1 presenilin 1 0.334315