Homo sapiens Gene: HYAL2
Summary
InnateDB Gene IDBG-36557.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol HYAL2
Gene Name hyaluronoglucosaminidase 2
Synonyms LUCA2
Species Homo sapiens
Ensembl Gene ENSG00000068001
Encoded Proteins
hyaluronoglucosaminidase 2
hyaluronoglucosaminidase 2
hyaluronoglucosaminidase 2
hyaluronoglucosaminidase 2
hyaluronoglucosaminidase 2
hyaluronoglucosaminidase 2
hyaluronoglucosaminidase 2
hyaluronoglucosaminidase 2
hyaluronoglucosaminidase 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a weak acid-active hyaluronidase. The encoded protein is similar in structure to other more active hyaluronidases. Hyaluronidases degrade hyaluronan, one of the major glycosaminoglycans of the extracellular matrix. Hyaluronan and fragments of hyaluronan are thought to be involved in cell proliferation, migration and differentiation. Although it was previously thought to be a lysosomal hyaluronidase that is active at a pH below 4, the encoded protein is likely a GPI-anchored cell surface protein. This hyaluronidase serves as a receptor for the oncogenic virus Jaagsiekte sheep retrovirus. The gene is one of several related genes in a region of chromosome 3p21.3 associated with tumor suppression. This gene encodes two alternatively spliced transcript variants which differ only in the 5' UTR.[provided by RefSeq, Mar 2010]
This gene encodes a weak acid-active hyaluronidase. The encoded protein is similar in structure to other more active hyaluronidases. Hyaluronidases degrade hyaluronan, one of the major glycosaminoglycans of the extracellular matrix. Hyaluronan and fragments of hyaluronan are thought to be involved in cell proliferation, migration and differentiation. Although it was previously thought to be a lysosomal hyaluronidase that is active at a pH below 4, the encoded protein is likely a GPI-anchored cell surface protein. This hyaluronidase serves as a receptor for the oncogenic virus Jaagsiekte sheep retrovirus. The gene is one of several related genes in a region of chromosome 3p21.3 associated with tumor suppression. This gene encodes two alternatively spliced transcript variants which differ only in the 5\' UTR.[provided by RefSeq, Mar 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 3:50317790-50322906
Strand Reverse strand
Band p21.31
Transcripts
ENST00000357750 ENSP00000350387
ENST00000395139 ENSP00000378571
ENST00000447092 ENSP00000401853
ENST00000442581 ENSP00000406657
ENST00000458018 ENSP00000399677
ENST00000424190 ENSP00000398714
ENST00000426286 ENSP00000409642
ENST00000428028 ENSP00000414656
ENST00000415028 ENSP00000405855
ENST00000481597
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0001618 virus receptor activity
GO:0004415 hyalurononglucosaminidase activity
GO:0005515 protein binding
GO:0005540 hyaluronic acid binding
GO:0019899 enzyme binding
GO:0030294 receptor signaling protein tyrosine kinase inhibitor activity
GO:0030971 receptor tyrosine kinase binding
GO:0033906 hyaluronoglucuronidase activity
GO:0050431 transforming growth factor beta binding
Biological Process
GO:0000302 response to reactive oxygen species
GO:0001822 kidney development
GO:0002244 hematopoietic progenitor cell differentiation
GO:0005975 carbohydrate metabolic process
GO:0006027 glycosaminoglycan catabolic process
GO:0009615 response to virus
GO:0010259 multicellular organismal aging
GO:0010764 negative regulation of fibroblast migration
GO:0019064 fusion of virus membrane with host plasma membrane
GO:0019087 transformation of host cell by virus
GO:0030203 glycosaminoglycan metabolic process
GO:0030212 hyaluronan metabolic process
GO:0030214 hyaluronan catabolic process
GO:0030308 negative regulation of cell growth
GO:0035810 positive regulation of urine volume
GO:0042117 monocyte activation
GO:0042307 positive regulation of protein import into nucleus
GO:0043407 negative regulation of MAP kinase activity
GO:0044281 small molecule metabolic process
GO:0044344 cellular response to fibroblast growth factor stimulus
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0046677 response to antibiotic
GO:0046718 viral entry into host cell
GO:0048705 skeletal system morphogenesis
GO:0050729 positive regulation of inflammatory response
GO:0051216 cartilage development
GO:0051607 defense response to virus
GO:0051898 negative regulation of protein kinase B signaling
GO:0060586 multicellular organismal iron ion homeostasis
GO:0061099 negative regulation of protein tyrosine kinase activity
GO:0070295 renal water absorption
GO:0071347 cellular response to interleukin-1
GO:0071356 cellular response to tumor necrosis factor
GO:0071493 cellular response to UV-B
GO:0071560 cellular response to transforming growth factor beta stimulus
GO:2000484 positive regulation of interleukin-8 secretion
GO:2000778 positive regulation of interleukin-6 secretion
GO:2001238 positive regulation of extrinsic apoptotic signaling pathway
Cellular Component
GO:0000139 Golgi membrane
GO:0005737 cytoplasm
GO:0005764 lysosome
GO:0005783 endoplasmic reticulum
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0005902 microvillus
GO:0009986 cell surface
GO:0016023 cytoplasmic membrane-bounded vesicle
GO:0016324 apical plasma membrane
GO:0030139 endocytic vesicle
GO:0031362 anchored component of external side of plasma membrane
GO:0031410 cytoplasmic vesicle
GO:0045121 membrane raft
GO:0046658 anchored component of plasma membrane
GO:0048471 perinuclear region of cytoplasm
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Hyaluronan uptake and degradation pathway
Mucopolysaccharidoses pathway
Myoclonic epilepsy of Lafora pathway
Defective B4GALT7 causes EDS, progeroid type pathway
Defective CHST6 causes MCDC1 pathway
MPS VI - Maroteaux-Lamy syndrome pathway
Defective PAPSS2 causes SEMD-PA pathway
Metabolism of carbohydrates pathway
MPS IIID - Sanfilippo syndrome D pathway
Defective SLC26A2 causes chondrodysplasias pathway
MPS IX - Natowicz syndrome pathway
Defective EXT1 causes exostoses 1, TRPS2 and CHDS pathway
Defective CHST14 causes EDS, musculocontractural type pathway
MPS IV - Morquio syndrome B pathway
Defective B3GAT3 causes JDSSDHD pathway
Defective CHST3 causes SEDCJD pathway
MPS IV - Morquio syndrome A pathway
Defective EXT2 causes exostoses 2 pathway
Diseases associated with glycosaminoglycan metabolism pathway
MPS II - Hunter syndrome pathway
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) pathway
Glycosaminoglycan metabolism pathway
Diseases of glycosylation pathway
MPS VII - Sly syndrome pathway
Defective CHSY1 causes TPBS pathway
Metabolism pathway
MPS I - Hurler syndrome pathway
MPS IIIA - Sanfilippo syndrome A pathway
Hyaluronan metabolism pathway
MPS IIIC - Sanfilippo syndrome C pathway
Disease pathway
Glycogen storage diseases pathway
MPS IIIB - Sanfilippo syndrome B pathway
KEGG
Glycosaminoglycan degradation pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.76873
RefSeq NM_003773 NM_033158
HUGO
OMIM
CCDS CCDS2818
HPRD 04649
IMGT
EMBL
GenPept
RNA Seq Atlas