Annotation Detail

Information
Associated Genes
ARSA
Associated Variants
ARSA p.Ser98Leu (p.S98L) ( ENST00000216124.10, ENST00000356098.9, ENST00000395619.3, ENST00000395621.7, ENST00000453344.6 )
ARSA p.Ser98Leu (p.S98L) ( ENST00000216124.10, ENST00000356098.9, ENST00000395619.3, ENST00000395621.7, ENST00000453344.6 )
ARSA p.Thr276Met (p.T276M) ( ENST00000216124.10, ENST00000356098.9, ENST00000395619.3, ENST00000395621.7, ENST00000453344.6 )
ARSA p.Gln192His (p.Q192H) ( ENST00000216124.10, ENST00000356098.9, ENST00000395619.3, ENST00000395621.7, ENST00000453344.6 )
ARSA p.Thr276Met (p.T276M) ( ENST00000216124.10, ENST00000356098.9, ENST00000395619.3, ENST00000395621.7, ENST00000453344.6 )
ARSA p.Gln192His (p.Q192H) ( ENST00000216124.10, ENST00000356098.9, ENST00000395619.3, ENST00000395621.7, ENST00000453344.6 )
Associated Disease
Leukodystrophy, Metachromatic
Source Database
DisGeNET
Description
Metachromatic leukodystrophy is a lysosomal storage disorder caused by the deficiency of arylsulfatase A.
Pubmed
7825603
Original source reporting the Gene Disease association
UNIPROT
DisGENET score for the Gene Disease association
0.514051056554323
Year of publication
1995
Drugs