SERPINA5 (serpin family A member 5)

2007-02-01  

Identity

HGNC
LOCATION
14q32.13
LOCUSID
ALIAS
PAI-3,PAI3,PCI,PCI-B,PLANH3,PROCI
FUSION GENES

Other Information

Locus ID:

NCBI: 5104
MIM: 601841
HGNC: 8723
Ensembl: ENSG00000188488

Variants:

dbSNP: 5104
ClinVar: 5104
TCGA: ENSG00000188488
COSMIC: SERPINA5

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000188488ENST00000329597P05154
ENSG00000188488ENST00000329597A0A024R6N9
ENSG00000188488ENST00000553511G3V3F5
ENSG00000188488ENST00000553780P05154
ENSG00000188488ENST00000553780A0A024R6N9
ENSG00000188488ENST00000554220G3V264
ENSG00000188488ENST00000554276P05154
ENSG00000188488ENST00000554276A0A024R6N9
ENSG00000188488ENST00000554633G3V4B4
ENSG00000188488ENST00000554866P05154
ENSG00000188488ENST00000554866A0A024R6N9
ENSG00000188488ENST00000555681G3V482
ENSG00000188488ENST00000556064G3V3Y3
ENSG00000188488ENST00000556775G3V2M1
ENSG00000188488ENST00000557598G3V265

Expression (GTEx)

0
50
100
150
200
250
300
350
400
450
500

Pathways

PathwaySourceExternal ID
Complement and coagulation cascadesKEGGko04610
Complement and coagulation cascadesKEGGhsa04610
HemostasisREACTOMER-HSA-109582
Formation of Fibrin Clot (Clotting Cascade)REACTOMER-HSA-140877
Intrinsic Pathway of Fibrin Clot FormationREACTOMER-HSA-140837
Common Pathway of Fibrin Clot FormationREACTOMER-HSA-140875

PharmGKB

Entity IDNameTypeEvidenceAssociationPKPDPMIDs
PA443622Carcinoma, Non-Small-Cell LungDiseaseClinicalAnnotationassociatedPD31616045
PA445846ThrombocytopeniaDiseaseClinicalAnnotationassociatedPD31616045
PA448803carboplatinChemicalClinicalAnnotationassociatedPD31616045
PA449748gemcitabineChemicalClinicalAnnotationassociatedPD31616045

References

Pubmed IDYearTitleCitations
357170242023SERPINA5 may promote the development of preeclampsia by disruption of the uPA/uPAR pathway.1
373272672023The SERPINA5 coding variant E228Q does not contribute to clinicopathologic characteristics in Alzheimer's disease: A cross-sectional study.0
357170242023SERPINA5 may promote the development of preeclampsia by disruption of the uPA/uPAR pathway.1
373272672023The SERPINA5 coding variant E228Q does not contribute to clinicopathologic characteristics in Alzheimer's disease: A cross-sectional study.0
349643032022Proteomic analysis of human articular cartilage unravels the dyscoagulation in osteoarthritis and the potential value of serpinA5 as a biomarker for osteoarthritis.5
360005362022SERPINA5 promotes tumour cell proliferation by modulating the PI3K/AKT/mTOR signalling pathway in gastric cancer.7
361777952022ANXA2, SP17, SERPINA5, PRDX2 genes, and sperm DNA fragmentation differentially represented in male partners of infertile couples with normal and abnormal sperm parameters.3
349643032022Proteomic analysis of human articular cartilage unravels the dyscoagulation in osteoarthritis and the potential value of serpinA5 as a biomarker for osteoarthritis.5
360005362022SERPINA5 promotes tumour cell proliferation by modulating the PI3K/AKT/mTOR signalling pathway in gastric cancer.7
361777952022ANXA2, SP17, SERPINA5, PRDX2 genes, and sperm DNA fragmentation differentially represented in male partners of infertile couples with normal and abnormal sperm parameters.3
340096692021SERPIN A5 may have a potential as a biomarker in reflecting the improvement of semen quality in infertile men who underwent varicocele repair.2
348379232021Evaluation the Presence of SERPINA5 (Exon 3) and FTO rs9939609 Polymorphisms in Papillary Thyroid Cancer Patients.5
340096692021SERPIN A5 may have a potential as a biomarker in reflecting the improvement of semen quality in infertile men who underwent varicocele repair.2
348379232021Evaluation the Presence of SERPINA5 (Exon 3) and FTO rs9939609 Polymorphisms in Papillary Thyroid Cancer Patients.5
307155782020Genetic association in female stress urinary incontinence based on proteomic findings: a case-control study.1

Citation

Dessen P

SERPINA5 (serpin family A member 5)

Atlas Genet Cytogenet Oncol Haematol. 2007-02-01

Online version: http://atlasgeneticsoncology.org/gene/43985/serpina5