Gene: EPHB1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2047
Gene Symbol: EPHB1
EPHB1 		0.100 CausalMutation phenotype CLINVAR Progressive hereditary spastic paraplegia caused by a homozygous KY mutation. 28488683 2017