Mitochondrial thiamine pyrophosphate carrier

Summary
UniProt ID
Q9HC21
Gene Symbol
SLC25A19 DNC MUP1
Gene ID
60386
Organism
Homo sapiens (human)
GlyGen
Q9HC21
PubChem
Q9HC21
The Human Metabolome Database
HMDBP11980
Re-Glyco
Q9HC21
Annotation
Keyword
Alternative splicing Antiport Disease variant Mitochondrion Neuropathy Phosphoprotein Proteomics identification Reference proteome Repeat Transmembrane helix
Gene Ontology (GO)
GO Hierarchy
Sequence
MVGYDPKPDGRNNTKFQVAVAGSVSGLVTRALISPFDVIKIRFQLQHERLSRSDPSAKYHGILQASRQILQEEGPTAFWKGHVPAQILSIGYGAVQFLSFEMLTELVHRGSVYDAREFSVHFVCGGLAACMATLTVHPVDVLRTRFAAQGEPKVYNTLRHAVGTMYRSEGPQVFYKGLAPTLIAIFPYAGLQFSCYSSLKHLYKWAIPAEGKKNENLQNLLCGSGAGVISKTLTYPLDLFKKRLQVGGFEHARAAFGQVRRYKGLMDCAKQVLQKEGALGFFKGLSPSLLKAALSTGFMFFSYEFFCNVFHCMNRTASQR
Glycosylation Sites
Displaying 1 entry
Position Description PubMed ID GlyTouCan ID Source
12
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying 1 entry
Pathway Name Organism
Vitamin B1 (thiamin) metabolism Homo sapiens
Disease
Displaying all 2 entries
DO ID Disease Name Source
DOID:655 inherited metabolic disorder
DOID:10907 microcephaly

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026