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PLAT (plasminogen activator, tissue type)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5327
Gene nameGene Name - the full gene name approved by the HGNC.
Plasminogen activator, tissue type
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
PLAT
SynonymsGene synonyms aliases
T-PA, TPA
ChromosomeChromosome number
8
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8p11.21
SummarySummary of gene provided in NCBI Entrez Gene.
This gene encodes tissue-type plasminogen activator, a secreted serine protease that converts the proenzyme plasminogen to plasmin, a fibrinolytic enzyme. The encoded preproprotein is proteolytically processed by plasmin or trypsin to generate heavy and l
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs114878147 G>A Conflicting-interpretations-of-pathogenicity Missense variant, coding sequence variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT005838 hsa-miR-204-5p Microarray 21282569
MIRT005953 hsa-miR-21-5p Luciferase reporter assay, Microarray, qRT-PCR 21131358
MIRT017829 hsa-miR-335-5p Microarray 18185580
MIRT735970 hsa-miR-142-5p Microarray, qRT-PCR 31552107
MIRT1239429 hsa-miR-1178 CLIP-seq
Transcription factors
Transcription factor Regulation Reference
ATF2 Activation 8647095
CREB1 Repression 8647095
CREM Unknown 9851700
JUN Activation 1963081
JUN Unknown 9851700
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004252 Function Serine-type endopeptidase activity IBA 21873635
GO:0004252 Function Serine-type endopeptidase activity IDA 1695900, 8508955
GO:0004252 Function Serine-type endopeptidase activity TAS
GO:0005102 Function Signaling receptor binding IPI 8186264
GO:0005515 Function Protein binding IPI 2503541, 10340997, 12694198, 24196407
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID P00750
Protein name Tissue-type plasminogen activator (t-PA) (t-plasminogen activator) (tPA) (EC 3.4.21.68) (Alteplase) (Reteplase) [Cleaved into: Tissue-type plasminogen activator chain A; Tissue-type plasminogen activator chain B]
Protein function Converts the abundant, but inactive, zymogen plasminogen to plasmin by hydrolyzing a single Arg-Val bond in plasminogen. By controlling plasmin-mediated proteolysis, it plays an important role in tissue remodeling and degradation, in cell migrat
PDB 1A5H , 1BDA , 1PK2 , 1PML , 1RTF , 1TPG , 1TPK , 1TPM , 1TPN , 5BRR , 5ZLZ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00039 fn1
41 78
Fibronectin type I domain
Domain
PF00008 EGF
86 117
EGF-like domain
Domain
PF00051 Kringle
127 208
Kringle domain
Domain
PF00051 Kringle
215 296
Kringle domain
Domain
PF00089 Trypsin
311 556
Trypsin
Domain
Sequence
Sequence length 562
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Apelin signaling pathway
Complement and coagulation cascades
Transcriptional misregulation in cancer
Prostate cancer
Fluid shear stress and atherosclerosis
  Signaling by PDGF
Dissolution of Fibrin Clot
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Cerebral infarction Cerebral Infarction rs2230500 9183334, 1899364, 1579960, 15502123, 18544249, 16148626
Dermatitis Dermatitis, Allergic Contact rs61816761, rs150597413, rs138726443, rs201356558, rs149484917, rs372754256, rs747301529, rs567795279, rs745915174 17374397
Hypertension Hypertensive disease rs13306026, rs13333226 22352330
Myocardial infarction Myocardial Infarction, Myocardial Failure rs12316150, rs41303970, rs909253, rs7291467, rs2234693 9183334, 12848087, 1430592, 10645301, 1899364, 20122609, 15215796, 2494454, 1898952, 7902905, 10914357, 8554022, 2521976, 8598594, 3121335, 7775709, 11382373, 11489769, 2105625, 12227717, 2505604, 1900011, 18195371, 7488445, 8328192, 3089627, 15301905, 10505926, 2104561, 19341228, 10171637, 1492007, 12074692, 22352330
Unknown
Disease name Disease term dbSNP ID References
Aphasia Aphasia, Aphasia, Acquired, Aphasia, Global, Aphasia, Progressive, Aphasia, Mixed 12690208
Arterial occlusive disease Arterial Occlusive Diseases 15557913
Atheromatous embolus Cholesterol Embolism 7939511
Atherosclerosis Atherosclerosis rs699947, rs59439148 12677255

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