Language Disorders Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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15 genes associated with the Language Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
ATP2C2 ATPase, Ca++ transporting, type 2C, member 2
BCL2 B-cell CLL/lymphoma 2
BRAF B-Raf proto-oncogene, serine/threonine kinase
CMIP c-Maf inducing protein
CNTNAP2 contactin associated protein-like 2
DCDC2 doublecortin domain containing 2
FOXP2 forkhead box P2
GCFC2 GC-rich sequence DNA-binding factor 2
IRGM immunity-related GTPase family, M
KIAA0319 KIAA0319
MRPL19 mitochondrial ribosomal protein L19
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
SOS1 son of sevenless homolog 1 (Drosophila)