inability to walk Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Incapability to ambulate. (Human Phenotype Ontology, HP_0002540)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002540
Similar Terms
Downloads & Tools

Genes

19 genes associated with the inability to walk phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAR adenosine deaminase, RNA-specific
ADSL adenylosuccinate lyase
AP4S1 adaptor-related protein complex 4, sigma 1 subunit
ATP8A2 ATPase, aminophospholipid transporter, class I, type 8A, member 2
C10ORF2 chromosome 10 open reading frame 2
CDKL5 cyclin-dependent kinase-like 5
CLN3 ceroid-lipofuscinosis, neuronal 3
ERBB4 erb-b2 receptor tyrosine kinase 4
FAM126A family with sequence similarity 126, member A
GDAP1 ganglioside induced differentiation associated protein 1
MEF2C myocyte enhancer factor 2C
PGAP3 post-GPI attachment to proteins 3
POMT1 protein-O-mannosyltransferase 1
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
SLC17A5 solute carrier family 17 (acidic sugar transporter), member 5
SLC19A3 solute carrier family 19 (thiamine transporter), member 3
SLC9A6 solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6
SUCLA2 succinate-CoA ligase, ADP-forming, beta subunit
TK2 thymidine kinase 2, mitochondrial