XB-FEAT-6049176: Difference between revisions
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= | =arse= | ||
This is the community wiki page for the gene '' | This is the community wiki page for the gene ''arse'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase. | ||
=nomenclature changes= | |||
06.05.2018 | |||
Human name has changed for Entrez Gene: 415. From arylsulfatase E (chondrodysplasia punctata 1) to arylsulfatase E | |||
08/23.2019 | |||
Human symbol has changed for genepage ID: 6049176 From arse to ARSL | |||
Human symbol has changed for Entrez Gene: 415. From ARSE to ARSL | |||
=Summary from NCBi for human ARSL= | |||
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. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome. [provided by RefSeq, Sep 2013] | |||
Latest revision as of 11:30, 28 August 2019
arse
This is the community wiki page for the gene arse please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
06.05.2018
Human name has changed for Entrez Gene: 415. From arylsulfatase E (chondrodysplasia punctata 1) to arylsulfatase E
08/23.2019
Human symbol has changed for genepage ID: 6049176 From arse to ARSL
Human symbol has changed for Entrez Gene: 415. From ARSE to ARSL
Summary from NCBi for human ARSL
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. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome. [provided by RefSeq, Sep 2013]