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MTTP (NM_001300785) - microsomal triglyceride transfer protein
Microsomal Triglyceride Transfer Protein Large Subunit Isoform 2
Legend
Mutation impacts
direct
network-rewiring
motif-changing
proximal
distal
none
Sites
multiple types
acetylation
methylation
succinylation
sumoylation
ubiquitination
glycosylation
- C-linked
- N-linked
- O-linked
- S-linked
phosphorylation
- SARS-CoV-2
Others
Exact position of a PTM site
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Mutations Visualisation
Protein summary
This is an alternative isoform of MTTP protein.
View all 2 isoforms
MTTP:
microsomal triglyceride transfer protein large subunit isoform 2
Description:
MTP encodes the large subunit of the heterodimeric microsomal triglyceride transfer protein. Protein disulfide isomerase (PDI) completes the heterodimeric microsomal triglyceride transfer protein, which has been shown to play a central role in lipoprotein assembly. Mutations in MTP can cause abetalipoproteinemia. [provided by RefSeq, Jul 2008].
- Strand
- +
- Chromosome
- 4
- Protein
- 921 residues
- All mutations
- 187
- PTM sites
- 4
- CDS
- 100,485,252 - 100,544,005
- Transcription
- 100,485,234 - 100,545,154
External references
Mappings retrieved from NCBI & UniProt.