This gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19. [provided by RefSeq, Oct 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| LETM1BA-20-REGO | 20 (40 μL) | 200 μL |
|
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| LETM1BA-20-REGR | 20 (40 μL) | 200 μL |
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| LETM1BA-20-ORGR | 20 (40 μL) | 200 μL |
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| LETM1BA-20-GOGR | 20 (40 μL) | 200 μL |
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| LETM1BA-20-GRRE | 20 (40 μL) | 200 μL |
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| LETM1BA-20-GROR | 20 (40 μL) | 200 μL |
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| LETM1BA-20-GRGO | 20 (40 μL) | 200 μL |
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| LETM1BA-20-AQOR | 20 (40 μL) | 200 μL |
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This gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19. [provided by RefSeq, Oct 2009]
Gene Symbol : LETM1
Gene Name : Leucine zipper and EF-hand containing transmembrane protein 1
Chromosome : CHR 4: 185,624,6-181,147,8
Locus : 4p16.3
Alt. Genes : YAF2
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