ARSE Products

Description

Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene.

Bioinformatics

Entrez	415 Human
Uniprot	NP_000038 Human P51690 Human
Product By Gene ID	415
Alternate Names	MGC163310 EC 3.1.6.2 CDPX EC 3.1.6 CDPXR EC 3.1.6.- CDPX1 chondrodysplasia punctata 1 ASE arylsulfatase E arylsulfatase E (chondrodysplasia punctata 1)

Diseases related to ARSE

Discover more about diseases related to ARSE.

Chondrodysplasia Punctata
Dwarfism
Steroid Sulfatase Deficiency Disease
Hypoplasia
Madelung's Deformity
Osteochondrodysplasias
Developmental Delay (disorder)
Genetic Diseases, X-linked
Ichthyoses
Fetal Warfarin Syndrome
Leri-weill Dyschondrosteosis
Sex Chromosome Aberrations
Cytogenetic Abnormality
Mild Mental Retardation
Developmental Disabilities
Embryopathies
Learning Disabilities
Chromosome Breakage

Pathways for ARSE

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Bone Development
Localization
Methylation
Cartilage Development
Male Meiosis
Dna Methylation
Meiosis
Bone Mineralization

Research Areas for ARSE

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Lipid and Metabolism

PTMs for ARSE

Learn more about PTMs related to ARSE.

Glycosylation
Methylation

Bioinformatics Tool for ARSE

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