Sortilin 1

SORT1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesSORT1, Gp95, LDLCQ6, NT3, NTR3, Sortilin 1
External IDsOMIM: 602458; MGI: 1338015; HomoloGene: 136097; GeneCards: SORT1; OMA:SORT1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

6272

20661

Ensembl

ENSG00000134243

ENSMUSG00000068747

UniProt

Q99523

Q6PHU5

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 MbChr 3: 108.19 – 108.27 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

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 hypertension, atherosclerosis, 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.