(Q50289013)

English

Defective SLC26A2 does not cotransport extracellular SO4(2-), H+ to cytosol

An instance of the biological reaction in Homo sapiens with Reactome ID (R-HSA-3560789)

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Statements

biological process

1 reference

8 July 2022

Defective SLC26A2 causes chondrodysplasias

1 reference

8 July 2022

1 reference

8 July 2022

https://identifiers.org/reactome:R-HSA-3560789

1 reference

8 July 2022

2

object has role

1 reference

8 July 2022

1

object has role

1 reference

8 July 2022

SLC26A2 mutants [plasma membrane]

1

object has role

1 reference

8 July 2022

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

1 reference

8 July 2022

Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene

1 reference

8 July 2022

Mutations in the diastrophic dysplasia sulfate transporter (DTDST) gene: correlation between sulfate transport activity and chondrodysplasia phenotype.

1 reference

8 July 2022

Identifiers

1 reference

8 July 2022

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