Dyscalculia Gene Set

Dataset DisGeNET Gene-Disease Associations
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)
External Link https://www.disgenet.org/browser/0/1/0/C0869474
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Genes

20 genes associated with the disease Dyscalculia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APP amyloid beta (A4) precursor protein
C9ORF72 chromosome 9 open reading frame 72
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CHCHD10 coiled-coil-helix-coiled-coil-helix domain containing 10
CHMP2B charged multivesicular body protein 2B
FUS FUS RNA binding protein
GRN granulin
HNRNPA1 heterogeneous nuclear ribonucleoprotein A1
HNRNPA2B1 heterogeneous nuclear ribonucleoprotein A2/B1
MAPT microtubule-associated protein tau
PNKP polynucleotide kinase 3'-phosphatase
PSEN1 presenilin 1
SQSTM1 sequestosome 1
SRY sex determining region Y
TARDBP TAR DNA binding protein
TBK1 TANK-binding kinase 1
TERT telomerase reverse transcriptase
TMEM106B transmembrane protein 106B
TREM2 triggering receptor expressed on myeloid cells 2
VCP valosin containing protein