The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| HCCSBA-20-REGO | 20 (40 μL) | 200 μL |
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| HCCSBA-20-REGR | 20 (40 μL) | 200 μL |
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| HCCSBA-20-ORGR | 20 (40 μL) | 200 μL |
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| HCCSBA-20-GOGR | 20 (40 μL) | 200 μL |
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| HCCSBA-20-GRRE | 20 (40 μL) | 200 μL |
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| HCCSBA-20-GROR | 20 (40 μL) | 200 μL |
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| HCCSBA-20-GRGO | 20 (40 μL) | 200 μL |
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| HCCSBA-20-AQOR | 20 (40 μL) | 200 μL |
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The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2010]
Gene Symbol : HCCS
Gene Name : Holocytochrome c synthase
Chromosome : CHR X: 111,112,85-111,230,85
Locus : Xp22.2
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