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GENE AND PROTEIN SUMMARY

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Gene name

IDS

Description

iduronate 2-sulfatase

Protein class

Enzymes, Mapped to UniProt SWISS-PROT, Potential transmembrane proteins, Potentially secreted proteins

Protein evidence

Medium

Entrez gene summary

Iduronate-2-sulfatase is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this X-chromosome gene that result in enzymatic deficiency lead to the sex-linked Mucopolysaccharidosis Type II, also known as Hunter Syndrome. Iduronate-2-sulfatase has a strong sequence similarity with human arylsulfatases A, B, and C, and human glucosamine-6-sulfatase. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Oct 2009]

External links

Ensembl, UniProt, Entrez gene, neXtProt, Antibodypedia

No of splice variants

9 in total
0 with predicted TM region
6 with predicted signal peptide

SUBCELLULAR LOCATION SUMMARY

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Pending subcellular analysis

NORMAL TISSUE & ORGAN SUMMARY

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Pending normal tissue analysis

CANCER TISSUE SUMMARY

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Pending cancer tissue analysis

CELL LINE SUMMARY

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RNA evidence

High
 

Cell line

Cell origin

RNA abundance

IH staining

IF intensity

A-431 Skin High

-

-

A-549 Lung High

-

-

CACO-2 Colon Medium

-

-

HEK 293 Embryonal kidney High

-

-

HeLa Cervix Medium

-

-

Hep-G2 Liver Medium

-

-

MCF-7 Pleural effusion High

-

-

PC-3 Bone marrow High

-

-

RT-4 Urinary bladder Medium

-

-

U-2 OS Bone High

-

-

U-251 MG Brain High

-

-

ANTIBODY SUMMARY

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Pending antibodies