gptkbp:instanceOf
|
gptkb:gene
|
gptkbp:alias
|
gptkb:MTPPT
gptkb:solute_carrier_family_25_member_19
|
gptkbp:associatedWith
|
gptkb:Amish_lethal_microcephaly
gptkb:thiamine_metabolism_dysfunction_syndrome_4
|
gptkbp:encodes
|
gptkb:mitochondrial_thiamine_pyrophosphate_carrier_protein
|
gptkbp:Entrez_Gene_ID
|
gptkb:ENSG00000170291
51006
|
gptkbp:function
|
transports thiamine pyrophosphate into mitochondria
|
gptkbp:HGNC_ID
|
HGNC:10990
|
https://www.w3.org/2000/01/rdf-schema#label
|
SLC25A19
|
gptkbp:locatedOnChromosome
|
gptkb:chromosome_17
|
gptkbp:location
|
mitochondrial inner membrane
|
gptkbp:OMIM
|
606521
|
gptkbp:orthologInMouse
|
gptkb:Slc25a19
|
gptkbp:product
|
gptkb:Mitochondrial_thiamine_pyrophosphate_carrier
|
gptkbp:proteinFamily
|
gptkb:solute_carrier_family_25
|
gptkbp:species
|
gptkb:Homo_sapiens
|
gptkbp:UniProtID
|
gptkb:Q9H2D1
|
gptkbp:bfsParent
|
gptkb:Alzheimer's_disease_pathway
gptkb:SLC_family
|
gptkbp:bfsLayer
|
7
|