poor speech Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002465
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21 genes associated with the poor speech phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADK adenosine kinase
CHKB choline kinase beta
CHMP1A charged multivesicular body protein 1A
DLAT dihydrolipoamide S-acetyltransferase
GJC2 gap junction protein, gamma 2, 47kDa
KANSL1 KAT8 regulatory NSL complex subunit 1
KIF4A kinesin family member 4A
LINS lines homolog (Drosophila)
MID2 midline 2
MTO1 mitochondrial tRNA translation optimization 1
POMK protein-O-mannose kinase
RNASET2 ribonuclease T2
RTTN rotatin
SMARCA2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2
SOBP sine oculis binding protein homolog (Drosophila)
TAF2 TAF2 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 150kDa
TUBB4A tubulin, beta 4A class IVa
UBE2A ubiquitin-conjugating enzyme E2A
UQCC2 ubiquinol-cytochrome c reductase complex assembly factor 2
VLDLR very low density lipoprotein receptor
WDR45 WD repeat domain 45