1.1.1.102: 3-dehydrosphinganine reductase
This is an abbreviated version!
For detailed information about 3-dehydrosphinganine reductase, go to the full flat file.
Word Map on EC 1.1.1.102
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1.1.1.102
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sphingolipids
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ceramide
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nadph-dependent
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phytosphingosine
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sphingomyelin
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inositolphosphorylceramide
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palmitoyl-coa
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food industry
- 1.1.1.102
- sphingolipids
- ceramide
-
nadph-dependent
- phytosphingosine
- sphingomyelin
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inositolphosphorylceramide
- palmitoyl-coa
- food industry
Reaction
Synonyms
3-KDS reductase, 3-ketodihydrosphingosine reductase, 3-ketosphinganine reductase, 3-oxosphinganine reductase, 3-oxosphinganine:NADPH oxidoreductase, 3KDSR, D-3-dehydrosphinganine reductase, D-3-oxosphinganine reductase, D-3-oxosphinganine:B-NADPH oxidoreductase, DSR, FVT-1, Fvt1, h-FTV-1, KDS reductase, Ksr1p, KsrA, m-FTV-1, More, TSC10, TSC10A, Tsc10p
ECTree
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Disease
Disease on EC 1.1.1.102 - 3-dehydrosphinganine reductase
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Carcinogenesis
Identification of target genes regulated by FOXC1 using nickel agarose-based chromatin enrichment.
Ichthyosis
Progressive symmetrical erythrokeratoderma manifesting as harlequin-like ichthyosis with severe thrombocytopenia secondary to a homozygous 3-ketodihydrosphingosine reductase mutation.
Leukemia
3-Ketodihydrosphingosine reductase maintains ER homeostasis and unfolded protein response in leukemia.
Lymphoma, Follicular
FVT-1, a novel human transcription unit affected by variant translocation t(2;18)(p11;q21) of follicular lymphoma.
Muscular Atrophy, Spinal
A missense mutation in the 3-ketodihydrosphingosine reductase FVT1 as candidate causal mutation for bovine spinal muscular atrophy.
Neoplasms
FVT-1, a novel human transcription unit affected by variant translocation t(2;18)(p11;q21) of follicular lymphoma.
Thrombocytopenia
Progressive symmetrical erythrokeratoderma manifesting as harlequin-like ichthyosis with severe thrombocytopenia secondary to a homozygous 3-ketodihydrosphingosine reductase mutation.
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