|
gptkbp:instanceOf
|
gptkb:gene
|
|
gptkbp:alias
|
gptkb:VLDL_receptor
gptkb:VLDL-R
gptkb:VLDLR1
|
|
gptkbp:alternativeSplicing
|
yes
|
|
gptkbp:associatedWith
|
gptkb:Reelin_signaling_pathway
cerebellar hypoplasia and mental retardation
|
|
gptkbp:encodes
|
gptkb:VLDLR_protein
|
|
gptkbp:Entrez_Gene_ID
|
gptkb:ENSG00000147852
7436
|
|
gptkbp:expressedIn
|
gptkb:adipose_tissue
gptkb:skeletal_muscle
brain
heart
|
|
gptkbp:fullName
|
gptkb:very_low_density_lipoprotein_receptor
|
|
gptkbp:function
|
mediates endocytosis of VLDL
involved in neuronal migration
lipoprotein receptor activity
|
|
gptkbp:HGNC_ID
|
HGNC:12698
|
|
gptkbp:interactsWith
|
gptkb:ApoE
gptkb:ApoE-containing_lipoproteins
gptkb:Reelin
|
|
gptkbp:locatedOnChromosome
|
gptkb:chromosome_9
gptkb:9p24.2
|
|
gptkbp:memberOf
|
gptkb:low_density_lipoprotein_receptor_family
|
|
gptkbp:mutationAssociatedWith
|
gptkb:VLDLR-associated_cerebellar_hypoplasia
|
|
gptkbp:OMIM
|
192977
|
|
gptkbp:organism
|
gptkb:Homo_sapiens
|
|
gptkbp:orthologInMouse
|
gptkb:Vldlr
|
|
gptkbp:product
|
single-pass type I membrane protein
|
|
gptkbp:UniProtID
|
P98155
|
|
gptkbp:bfsParent
|
gptkb:chromosome_9
|
|
gptkbp:bfsLayer
|
6
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
VLDLR
|