Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10717
Gene Symbol: AP4B1
AP4B1
0.100 CausalMutation phenotype CLINVAR Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47) . 22290197 2012
Entrez Id: 10717
Gene Symbol: AP4B1
AP4B1
0.100 CausalMutation phenotype CLINVAR Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature. 21620353 2011
Entrez Id: 10717
Gene Symbol: AP4B1
AP4B1
0.100 CausalMutation phenotype CLINVAR A new locus (SPG47) maps to 1p13.2-1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosum. 21440262 2011