QuickView for SPTLC1;jsessionid=20FBE4840BC175A90D7789FAEE71BD1F;jsessionid=1DA8D782EAEAC9BB499968958EA1779B;jsessionid=E2A1472434F1A7350D130C7FBF7ED56E (gene)

Summary
General Info

Body Atlas

Most Correlated Tissues

Colon mucosa
Ileum mucosa
Monocyte of peripheral blood
Skin
Conjunctiva

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Disease Atlas

Most Correlated Diseases

Amyotrophic lateral sclerosis
Motor neuron disease
Complications of pregnancy, childbirth and the puerperium
Disease due to Adenovirus
Varicella-zoster virus infection

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Pharmaco Atlas

Most Correlated Compounds

ginkgolide A
Synephrine
Bacitracin
hexachlorobutadiene
Pyrilamine

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Knockdown Atlas

Most Correlated Gene Perturbations

SPTLC3
SPTLC1
SPTLC2
ADIPOQ
CAV1

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Curated Studies

Most Correlated Studies

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Literature

Most Relevant Literature

The ORMs interact with transmembrane domain 1 of Lcb1 and regulate serine palmitoyltransferase oligo…
Ultrapotent miniproteins targeting the SARS-CoV-2 receptor-binding domain protect against infection …
Specific Deoxyceramide Species Correlate with Expression of Macular Telangiectasia Type 2 (MacTel2) …
Description of a patient cohort with Hereditary Sensory Neuropathy type 1 without retinal disease Ma…
SPTLC1 p.Leu38Arg, a novel mutation associated with childhood ALS.

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Clinical Trials

Most Relevant Clinical Trials

There were no clinical trials for SPTLC1;jsessionid=20FBE4840BC175A90D7789FAEE71BD1F;jsessionid=1DA8D782EAEAC9BB499968958EA1779B;jsessionid=E2A1472434F1A7350D130C7FBF7ED56E

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