Gene: glucosidase, beta, acid; GBA


Gene Symbol: GBA
OMIM: 606463
Chromosome location: 1q22

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Gaucher disease, type I || c.1226A>G

Phenotype:    Gaucher disease, type I
Dna Change:    c.1226A>G
Protein Change:    p.Asn409Ser (N370S)
Mutation Type:    Substitution
Mutation Effect:    Missense
Location:    exon 10
Transcript:    NM_001005741.2

PopulationEthnic GroupRegionMutation FrquencyCoalescence TimeReference
ItalyNANANANAFilocamo M et al., 2000Filocamo M, Bonuccelli G, Mazzotti R, Giona F, Gatti R, . Identification of a novel recombinant allele in three unrelated Italian Gaucher patients: implications for prognosis and genetic counseling.. Blood Cells Mol. Dis.. 2000; 26(4):307-11

References

Filocamo M, Bonuccelli G, Mazzotti R, Giona F, Gatti R, Identification of a novel recombinant allele in three unrelated Italian Gaucher patients: implications for prognosis and genetic counseling.Blood Cells Mol. Dis.. 2000; 26(4):307-11