HPN (hepsin)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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3249 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Hepsin |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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HPN |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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TMPRSS1 |
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Chromosome
Chromosome number
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19 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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19q13.11 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a type II transmembrane serine protease that may be involved in diverse cellular functions, including blood coagulation and the maintenance of cell morphology. Expression of the encoded protein is associated with the growth and progressi |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | ||||||||||||||||
| UniProt ID | P05981 | |||||||||||||||
| Protein name | Serine protease hepsin (EC 3.4.21.106) (Transmembrane protease serine 1) [Cleaved into: Serine protease hepsin non-catalytic chain; Serine protease hepsin catalytic chain] | |||||||||||||||
| Protein function | Serine protease that cleaves extracellular substrates, and contributes to the proteolytic processing of growth factors, such as HGF and MST1/HGFL (PubMed:15839837, PubMed:21875933). Plays a role in cell growth and maintenance of cell morphology | |||||||||||||||
| PDB | 1O5E , 1O5F , 1P57 , 1Z8G , 3T2N , 5CE1 | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Detected in liver and kidney. {ECO:0000269|PubMed:21875933}. | |||||||||||||||
| Sequence | ||||||||||||||||
| Sequence length | 417 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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