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Sortilin 1

SORT1
Protein SORT1 PDB 3F6K.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases SORT1, Gp95, LDLCQ6, NT3, NTR3, Sortilin 1
External IDs MGI: 1338015 HomoloGene: 136097 GeneCards: SORT1
Gene location (Human)
Chromosome 1 (human)
Chr. Chromosome 1 (human)
Chromosome 1 (human)
Genomic location for SORT1
Genomic location for SORT1
Band No data available Start 109,309,568 bp
End 109,397,951 bp
RNA expression pattern
PBB GE SORT1 212797 at fs.png

PBB GE SORT1 212807 s at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001205228
NM_002959

NM_001271599
NM_019972

RefSeq (protein)

NP_001192157
NP_002950

NP_001258528
NP_064356

Location (UCSC) Chr 1: 109.31 – 109.4 Mb Chr 1: 108.28 – 108.36 Mb
PubMed search

3F6K, 3G2U, 3G2V, 4MSL, 4N7E, 4PO7

NM_001205228
NM_002959

NM_001271599
NM_019972

NP_001192157
NP_002950

NP_001258528
NP_064356

Sortilin (SORT1) is a protein that in humans is encoded by the SORT1 gene on chromosome 1. This protein is a type I membrane glycoprotein in the vacuolar protein sorting 10 protein (Vps10p) family of sorting receptors. While it is ubiquitously expressed in many tissues, sortilin is most abundant in the central nervous system. At the cellular level, sortilin functions in protein transport between the Golgi apparatus, endosome, lysosome, and plasma membrane, leading to its involvement in multiple biological processes such as glucose and lipid metabolism as well as neural development and cell death. Moreover, the function and role of sortilin is now emerging in several major human diseases such as atherosclerosis and coronary artery disease, Alzheimer’s disease, and cancer. The SORT1 gene also contains one of 27 loci associated with increased risk of coronary artery disease.


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