HSPG2
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Homo sapiens |
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HSPG2 is differentially expressed in 277 experiments: 171 organism parts: bone marrow, cerebellum, ... (169 more);, 223 disease states: normal, glioblastoma, ... (221 more);, 96 cell types 427 cell lines 37 compound treatments and 72 other conditions. |
| Synonyms |
SJS1, PRCAN, perlecan |
| Orthologs |
HSPG2
(Gallus gallus)
Hspg2
(Mus musculus)
F1M566_RAT
(Rattus norvegicus)
hspg2
(Danio rerio)
HSPG2
(Bos taurus)
hspg2
(Xenopus laevis)
Q6TYZ5_CANFA
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology Term |
angiogenesis, plasma membrane, protein localization, protein binding, extracellular space, proteinaceous extracellular matrix, extracellular region, basal lamina, cardiac muscle tissue development, basement membrane, cell adhesion, lipid metabolic process, lipoprotein lipase activity, protein C-terminus binding, extracellular matrix organization, extracellular matrix, brain development, calcium ion binding, endochondral ossification, chondrocyte differentiation, embryonic skeletal system morphogenesis, cartilage development involved in endochondral bone morphogenesis, lipoprotein metabolic process |
| InterPro Term |
Ig_V-set, SEA, Ig_sub, EGF_laminin, Immunoglobulin, Laminin_B_type_IV, Laminin_G, Ig-like, EGF, Laminin_B_subgr, Ig_sub2, Laminin_G_2, EGF_3, EGF-like, Ig_I-set, Laminin_G_1, Ig_V-set_subgr, LDrepeatLR_classA_rpt, EGF-like_Ca-bd |
| InterPro ID |
IPR000082, IPR000034, IPR018031, IPR000742, IPR006209, IPR006210, IPR001791, IPR001881, IPR007110, IPR013151, IPR013106, IPR002172, IPR002049, IPR012680, IPR003598, IPR003599, IPR003596, IPR012679, IPR013098 |
| Gene Ontology ID |
GO:0008022, GO:0008104, GO:0007155, GO:0007420, GO:0048738, GO:0005615, GO:0005604, GO:0005605, GO:0005509, GO:0005515, GO:0005576, GO:0005578, GO:0004465, GO:0005886, GO:0006629, GO:0031012, GO:0001525, GO:0030198, GO:0060351, GO:0048704, GO:0002062, GO:0001958, GO:0042157 |
| EMBL-Bank ID |
L22078, X62515, AL445795, AL590556, M64283, AL590103, S76436, M85289 |
| UniProt Accession |
P98160, B6EU51, Q5SZI5, Q5SZI6, Q5SZI9, Q5SZI8, Q5SZJ2, Q5SZJ1, Q5SZJ0 |
| RefSeq ID |
NM_005529, NP_005520 |
| Ensembl Protein ID |
ENSP00000416385, ENSP00000405412, ENSP00000392022, ENSP00000396310, ENSP00000397573, ENSP00000395884, ENSP00000363827, ENSP00000363805, ENSP00000363808, ENSP00000436271 |
| UniGene ID |
Hs.562227 |
| HGNC Symbol |
HSPG2 |
| Description |
heparan sulfate proteoglycan 2 [Source:HGNC Symbol;Acc:5273] |
| Entrez Gene ID |
3339 |
| Ensembl Gene ID |
ENSG00000142798 |
| Gene-Disease Assocation |
SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1, DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH |
| Ensembl Transcript ID |
ENST00000480900, ENST00000426143, ENST00000493940, ENST00000469378, ENST00000471322, ENST00000412328, ENST00000374676, ENST00000374673, ENST00000374695, ENST00000430507, ENST00000453796, ENST00000481644, ENST00000486901, ENST00000427897, ENST00000439717, ENST00000498495 |
| Ensembl Family |
ENSFM00650001140070 |
| Ensembl Family Description |
BASEMENT MEMBRANE SPECIFIC HEPARAN SULFATE PROTEOGLYCAN CORE PRECURSOR HSPG PERLECAN PLC [CONTAINS ENDOREPELLIN; LG3 PEPTIDE] |
| Design Element |
g184426_3p_a_at, 201654_s_at, ENST00000480900, ENST00000471322, 32845_at, ENST00000430507, ENST00000469378, ENST00000481644, ENST00000426143, Hs.211573.0.S1_3p_a_at, ENST00000427897, ENST00000374695, 201655_s_at, M85289_at, ENST00000453796, ENST00000498495, 201655_3p_s_at, X62515_s_at, ENST00000412328, ENST00000493940, ENST00000486901, ENST00000439717, ENST00000374676, ENST00000374673 |
| Search EB-eye |
ENSG00000142798
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