Gene Gene information from NCBI Gene database.
Entrez ID 55848
Gene name Plasminogen receptor with a C-terminal lysine
Gene symbol PLGRKT
Synonyms (NCBI Gene)
AD025C9orf46MDS030PLG-RKTPlg-R(KT)
Chromosome 9
Chromosome location 9p24.1
miRNA miRNA information provided by mirtarbase database.
56
miRTarBase ID miRNA Experiments Reference
MIRT023956 hsa-miR-1-3p Proteomics 18668040
MIRT029997 hsa-miR-26b-5p Microarray 19088304
MIRT532464 hsa-miR-513b-3p PAR-CLIP 22012620
MIRT532463 hsa-miR-105-5p PAR-CLIP 22012620
MIRT532462 hsa-miR-7853-5p PAR-CLIP 22012620
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005886 Component Plasma membrane IEA
GO:0006935 Process Chemotaxis IEA
GO:0006954 Process Inflammatory response IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
618444 23633 ENSG00000107020
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9HBL7
Protein name Plasminogen receptor (KT) (Plg-R(KT))
Protein function Receptor for plasminogen. Regulates urokinase plasminogen activator-dependent and stimulates tissue-type plasminogen activator-dependent cell surface plasminogen activation. Proposed to be part of a local catecholaminergic cell plasminogen activ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10166 DUF2368 1 134 Uncharacterised conserved protein (DUF2368) Family
Tissue specificity TISSUE SPECIFICITY: Expressed in peripheral blood cells and monocytes. Expressed in adrenal medulla. {ECO:0000269|PubMed:21795689, ECO:0000269|PubMed:21940822}.
Sequence
Sequence length 147
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
AUTOIMMUNE THYROID DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPOTHYROIDISM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OBESITY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
POLYCYSTIC OVARY SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Alzheimer Disease Associate 28990359
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Associate 35454092
★☆☆☆☆
Found in Text Mining only
Lymphatic Metastasis Associate 17391312
★☆☆☆☆
Found in Text Mining only
Neoplasms Stimulate 35454092
★☆☆☆☆
Found in Text Mining only
Sexual Infantilism Associate 28990359
★☆☆☆☆
Found in Text Mining only
Squamous Cell Carcinoma of Head and Neck Associate 17391312, 35398964
★☆☆☆☆
Found in Text Mining only