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Defective SLC26A2 causes chondrodysplasias
An instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-3560792)
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Statements
instance of
biological pathway
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3560792
part of
SLC transporter disorders
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3560792
Diseases associated with glycosaminoglycan metabolism
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3560792
found in taxon
Homo sapiens
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3560792
exact match
https://identifiers.org/reactome:R-HSA-3560792
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3560792
has part(s)
Defective SLC26A2 does not cotransport extracellular SO4(2-), H+ to cytosol
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3560792
cites work
Pathogenetics of the human SLC26 transporters
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3560792
Genotype-phenotype correlation in DTDST dysplasias: Atelosteogenesis type II and diastrophic dysplasia variant in one family
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3560792
Identifiers
Reactome ID
R-HSA-3560792
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3560792
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