Mutations in this gene cause the X-linked Kallmann syndrome. The encoded protein is similar in sequence to proteins known to function in neural cell adhesion and axonal migration. In addition, this cell surface protein is N-glycosylated and may have anti-protease activity. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ANOS1BA-20-REGO | 20 (40 μL) | 200 μL |
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| ANOS1BA-20-REGR | 20 (40 μL) | 200 μL |
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| ANOS1BA-20-ORGR | 20 (40 μL) | 200 μL |
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| ANOS1BA-20-GOGR | 20 (40 μL) | 200 μL |
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| ANOS1BA-20-GRRE | 20 (40 μL) | 200 μL |
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| ANOS1BA-20-GROR | 20 (40 μL) | 200 μL |
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| ANOS1BA-20-GRGO | 20 (40 μL) | 200 μL |
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| ANOS1BA-20-AQOR | 20 (40 μL) | 200 μL |
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Mutations in this gene cause the X-linked Kallmann syndrome. The encoded protein is similar in sequence to proteins known to function in neural cell adhesion and axonal migration. In addition, this cell surface protein is N-glycosylated and may have anti-protease activity. [provided by RefSeq, Jul 2008]
Gene Symbol : ANOS1
Gene Name : Anosmin 1
Chromosome : CHR X: 873,218,6-852,887,3
Locus : Xp22.31
Alt. Genes : LRPPRC
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