Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| GSDME-20-RE | 20 (40 μL) | 200 μL |  |
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| GSDME-20-OR | 20 (40 μL) | 200 μL |  |
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| GSDME-20-GO | 20 (40 μL) | 200 μL |  |
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| GSDME-20-GR | 20 (40 μL) | 200 μL |  |
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| GSDME-20-AQ | 20 (40 μL) | 200 μL |  |
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Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Symbol : GSDME
Gene Name : Gasdermin E
Chromosome : CHR 7: 247,580,19-246,983,54
Locus : 7p15.3
Alt. Genes : FEM1B
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