The protein encoded by this gene is a single-pass type I membrane protein of unknown function that contains several EGF-like domains, Kelch repeats, and PSI domains. Defects in this gene are a cause of Carpenter syndrome 2. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MEGF8BA-20-REGO | 20 (40 μL) | 200 μL |
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| MEGF8BA-20-REGR | 20 (40 μL) | 200 μL |
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| MEGF8BA-20-ORGR | 20 (40 μL) | 200 μL |
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| MEGF8BA-20-GOGR | 20 (40 μL) | 200 μL |
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| MEGF8BA-20-GRRE | 20 (40 μL) | 200 μL |
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| MEGF8BA-20-GROR | 20 (40 μL) | 200 μL |
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| MEGF8BA-20-GRGO | 20 (40 μL) | 200 μL |
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| MEGF8BA-20-AQOR | 20 (40 μL) | 200 μL |
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The protein encoded by this gene is a single-pass type I membrane protein of unknown function that contains several EGF-like domains, Kelch repeats, and PSI domains. Defects in this gene are a cause of Carpenter syndrome 2. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]
Gene Symbol : MEGF8
Gene Name : Multiple EGF like domains 8
Chromosome : CHR 19: 423,256,08-423,787,68
Locus : 19q13.2
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