Version 5.4
| Mus musculus Gene: Hs3st6 | |||||||
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| Summary | |||||||
| InnateDB Gene | IDBG-149307.6 | ||||||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||
| Gene Symbol | Hs3st6 | ||||||
| Gene Name | heparan sulfate (glucosamine) 3-O-sulfotransferase 6 | ||||||
| Synonyms | |||||||
| Species | Mus musculus | ||||||
| Ensembl Gene | ENSMUSG00000039628 | ||||||
| Encoded Proteins |
heparan sulfate (glucosamine) 3-O-sulfotransferase 6
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| Protein Structure |
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| Useful resources | Stemformatics EHFPI ImmGen | ||||||
| Entrez Gene | |||||||
| Summary |
This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000162040:
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| Gene Information | |||||||
| Type | Protein coding | ||||||
| Genomic Location | Chromosome 17:24753003-24758683 | ||||||
| Strand | Forward strand | ||||||
| Band | A3.3 | ||||||
| Transcripts |
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| Interactions | |||||||
| Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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| Gene Ontology | |||||||
Molecular Function |
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| Biological Process |
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| Cellular Component |
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| Orthologs | |||||||
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Species
Homo sapiens
Bos taurus
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Gene ID
Gene Order
Not yet available
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| Pathways | |||||||
| NETPATH | |||||||
| REACTOME |
Glycosaminoglycan metabolism pathway
Disease pathway
MPS IV - Morquio syndrome B pathway
MPS IV - Morquio syndrome A pathway
MPS IIIC - Sanfilippo syndrome C pathway
Metabolism pathway
MPS I - Hurler syndrome pathway
MPS IIID - Sanfilippo syndrome D pathway
Defective B4GALT7 causes EDS, progeroid type pathway
Diseases of glycosylation pathway
Defective CHSY1 causes TPBS pathway
Defective B3GAT3 causes JDSSDHD pathway
MPS II - Hunter syndrome pathway
Diseases associated with glycosaminoglycan metabolism pathway
HS-GAG biosynthesis pathway
Heparan sulfate/heparin (HS-GAG) metabolism pathway
MPS IX - Natowicz syndrome pathway
Glycogen storage diseases pathway
MPS VII - Sly syndrome pathway
Defective CHST14 causes EDS, musculocontractural type pathway
Defective CHST3 causes SEDCJD pathway
MPS VI - Maroteaux-Lamy syndrome pathway
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) pathway
MPS IIIB - Sanfilippo syndrome B pathway
MPS IIIA - Sanfilippo syndrome A pathway
Defective PAPSS2 causes SEMD-PA pathway
Defective EXT1 causes exostoses 1, TRPS2 and CHDS pathway
Mucopolysaccharidoses pathway
Defective CHST6 causes MCDC1 pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
Defective EXT2 causes exostoses 2 pathway
Defective SLC26A2 causes chondrodysplasias pathway
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| KEGG | |||||||
| INOH | |||||||
| PID NCI | |||||||
| Cross-References | |||||||
| SwissProt | Q5GFD5 | ||||||
| TrEMBL | A2RTI7 B7ZNT8 Q3UIC7 | ||||||
| UniProt Splice Variant | |||||||
| Entrez Gene | 328779 | ||||||
| UniGene | |||||||
| RefSeq | NM_001012402 | ||||||
| OMIM | |||||||
| CCDS | CCDS28496 | ||||||
| HPRD | |||||||
| IMGT | |||||||
| MGI ID | MGI:3580487 | ||||||
| MGI Symbol | Hs3st6 | ||||||
| EMBL | AK146974 AY574375 BC132520 BC138814 BC145424 CH466606 | ||||||
| GenPept | AAI32521 AAI38815 AAI45425 AAT84072 BAE27579 EDL22367 | ||||||
| RNA Seq Atlas | 328779 | ||||||