MGP Database

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MGP005443

Ontology/Pathway Information

Entrez Gene ID55576
Gene Namestabilin 2
Gene Symbol STAB2
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005737 IDA:HPACcytoplasm
GO:0030666 TAS:ReactomeCendocytic vesicle membrane
GO:0009897 ISS:UniProtKBCexternal side of plasma membrane
GO:0005887 IDA:UniProtKBCintegral component of plasma membrane
GO:0005886 TAS:ReactomeCplasma membrane
GO:0005540 ISS:UniProtKBFhyaluronic acid binding
GO:0030169 IDA:UniProtKBFlow-density lipoprotein particle binding
GO:0005041 IDA:UniProtKBFlow-density lipoprotein receptor activity
GO:0015035 NAS:UniProtKBFprotein disulfide oxidoreductase activity
GO:0005044 IDA:UniProtKBFscavenger receptor activity
GO:0001525 NAS:UniProtKBPangiogenesis
GO:0005975 TAS:ReactomePcarbohydrate metabolic process
GO:0007155 NAS:UniProtKBPcell adhesion
GO:0042742 IDA:UniProtKBPdefense response to bacterium
GO:0006897 ISS:UniProtKBPendocytosis
GO:0030203 TAS:ReactomePglycosaminoglycan metabolic process
GO:0030214 TAS:ReactomePhyaluronan catabolic process
GO:0030212 TAS:ReactomePhyaluronan metabolic process
GO:0055114 NAS:GOCPoxidation-reduction process
GO:0006898 TAS:UniProtKBPreceptor-mediated endocytosis
GO:0030193 IMP:UniProtKBPregulation of blood coagulation
GO:0010468 IMP:UniProtKBPregulation of gene expression
GO:0044281 TAS:ReactomePsmall molecule metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_160300Binding and Uptake of Ligands by Scavenger Receptors
REACT_268678Defective B3GAT3 causes JDSSDHD
REACT_268431Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
REACT_268749Defective B4GALT7 causes EDS, progeroid type
REACT_267917Defective CHST14 causes EDS, musculocontractural type
REACT_267648Defective CHST3 causes SEDCJD
REACT_268786Defective CHST6 causes MCDC1
REACT_268113Defective CHSY1 causes TPBS
REACT_267942Defective EXT1 causes exostoses 1, TRPS2 and CHDS
REACT_267741Defective EXT2 causes exostoses 2
REACT_268843Defective PAPSS2 causes SEMD-PA
REACT_268059Defective SLC26A2 causes chondrodysplasias
REACT_116125Disease
REACT_268624Diseases associated with glycosaminoglycan metabolism
REACT_268324Diseases of glycosylation
REACT_264090Glycogen storage diseases
REACT_121315Glycosaminoglycan metabolism
REACT_121083Hyaluronan metabolism
REACT_120996Hyaluronan uptake and degradation
REACT_111217Metabolism
REACT_474Metabolism of carbohydrates
REACT_147857MPS I - Hurler syndrome
REACT_147734MPS II - Hunter syndrome
REACT_147753MPS IIIA - Sanfilippo syndrome A
REACT_147788MPS IIIB - Sanfilippo syndrome B
REACT_147860MPS IIIC - Sanfilippo syndrome C
REACT_147749MPS IIID - Sanfilippo syndrome D
REACT_147825MPS IV - Morquio syndrome A
REACT_147798MPS IV - Morquio syndrome B
REACT_147739MPS IX - Natowicz syndrome
REACT_147759MPS VII - Sly syndrome
REACT_147719MPS VI - Maroteaux-Lamy syndrome
REACT_147853Mucopolysaccharidoses
REACT_264430Myoclonic epilepsy of Lafora
REACT_164002Scavenging by Class H Receptors
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