NP-C in Genomics Meaning
The NP-C meaning in Genomics terms is "Niemann-Pick Disease Type C". There are 1 related meanings of the NP-C Genomics abbreviation.
NP-C on Genomics Full Forms
- Niemann-Pick Disease Type C A type of Niemann-Pick disease inherited in an autosomal recessive manner, resulting in lipid storage in the brain and body. At the cellular level, the disorder is characterized by the accumulation of cholesterol and glycolipid. Most (about 95%) of NPC patients have mutations in the NPC1 gene in chromosome 18q11 which encodes a large membrane glycoprotein. The rest (about 5%) of NPC patients have mutations in the NPC2 gene in chromosome 14q24.3 which encodes a small cholesterol-binding protein.
Frequently Asked Questions (FAQ)
What does NP-C stand for Genomics?
NP-C stands for Niemann-Pick Disease Type C in Genomics terms.
What is the shortened form of Niemann-Pick Disease Type C in Genomics?
The short form of "Niemann-Pick Disease Type C" is NP-C for Genomics.
Citation
NP-C in Genomics. Acronym24.com. (2020, May 24). Retrieved November 26, 2024 from https://acronym24.com/np-c-meaning-in-genomics/
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