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Symbol Name ID |
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| STS | D14Nds1 | |||||||||||||||||||||||||||||||||
| Synonyms | uPA, u-PA, urokinase-type plasminogen activator | |||||||||||||||||||||||||||||||||
| Feature Type | protein coding gene | |||||||||||||||||||||||||||||||||
| Genetic Map | ||||||||||||||||||||||||||||||||||
| Sequence Map |
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Mammalian homology |
human;
rat;
cattle;
chimpanzee;
dog, domestic;
pig, domestic
(Mammalian Orthology) Comparative Map (Mouse/Human Plau ± 2 cM)
Protein SuperFamily: urokinase-type plasminogen activator |
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Humanortholog |
PLAU plasminogen activator, urokinase
NCBI Gene ID 5328 Human Synonyms: ATF, BDPLT5, QPD, u-PA, UPA, URK Human Chr10:75670862-75677259 bp, + strand Reference GRCh37.p2 Primary Assembly Human Diseases Associated with Human PLAU (2) | |||||||||||||||||||||||||||||||||
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Alleles and phenotypes |
All alleles(6) :
Targeted(6)
Homozygotes show occasional fibrin deposits in non-healing ulcerations and reduced neointima formation after arterial injury. They are susceptible to thrombosis after traumatic or inflammatory challenge and appear to be immunologically hyporesponsive displaying characteristics of functional anergy. Human Diseases Modeled Using Mouse Plau (1) Alleles Annotated to Human Diseases(1) |
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Gene Ontology (GO) classifications |
All GO classifications: (31 annotations)
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| Expression |
Literature Summary: (24 records) Data Summary: Results (188) Tissues (158) Images (31) Theiler Stages: 1, 2, 3, 4, 7, 9, 11, 13, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 28
External Resources: Allen Institute GEO ArrayExpress |
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Molecular reagents |
All nucleic(24)
cDNA(14)
Primer pair(8)
Other(2)
Microarray probesets(3) |
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Other database links |
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| Sequences |
All sequences(18) RefSeq(2) UniProt(3) |
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| Polymorphisms | All PCR and RFLP(14) : PCR(7) RFLP(7) SNPs(48 from dbSNP Build 128) | |||||||||||||||||||||||||||||||||
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Protein-related information |
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| References |
(Earliest) J:7809
Belin D, et al., Cloning, nucleotide sequencing and expression of cDNAs encoding mouse urokinase-type plasminogen activator. Eur J Biochem. 1985 Apr 15;148(2):225-32 (Latest) J:184521 Koss M, et al., Congenital Asplenia in Mice and Humans with Mutations in a Pbx/Nkx2-5/p15 Module. Dev Cell. 2012 May 15;22(5):913-26 All references(206) |
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Other accession IDs |
MGD-MRK-13347 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 04/03/2013 MGI 5.12 |
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