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Gene Gene information from NCBI Gene database.
Entrez ID 5555
Gene name Proline rich protein HaeIII subfamily 2
Gene symbol PRH2
Synonyms (NCBI Gene)
PRP-1/PRP-2Prpr1/Pr2
Chromosome 12
Chromosome location 12p13.2
Summary This gene encodes a member of the heterogeneous family of proline-rich salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature isoforms before secretion from the parotid and submandibular/sublingua
miRNA miRNA information provided by mirtarbase database.
65 Show/Hide all (65)
miRTarBase ID miRNA Experiments Reference
MIRT018946 hsa-miR-335-5p Microarray 18185580
MIRT1261272 hsa-miR-1238 CLIP-seq
MIRT1261273 hsa-miR-1273d CLIP-seq
MIRT1261274 hsa-miR-1279 CLIP-seq
MIRT1261275 hsa-miR-150 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16203048, 26091039
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space TAS 2993301
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
168790 9367 ENSG00000134551
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
KEGG Pathway
Salivary secretion
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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 Reference Evidence Score
Malignant tumor of urinary bladder Uncertain significance ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (24)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Arthrogryposis Arthrogryposis multiplex congenita BEFREE 26287277
★★★★★
★☆☆☆☆
Found in Text Mining only
Blood Coagulation Disorders Blood Coagulation Disorders BEFREE 30159948
★★★★★
★☆☆☆☆
Found in Text Mining only
Cardiomyopathies Cardiomyopathy BEFREE 24736382
★★★★★
★☆☆☆☆
Found in Text Mining only
Cardiomyopathy, Hypertrophic, Familial Cardiomyopathy BEFREE 10024460, 9140840, 9218526, 9503187
★★★★★
★☆☆☆☆
Found in Text Mining only
Cerebral Palsy Cerebral palsy BEFREE 30965088
★★★★★
★☆☆☆☆
Found in Text Mining only
Cerebrovascular accident Stroke BEFREE 15574195
★★★★★
★☆☆☆☆
Found in Text Mining only
Dental Caries Dental caries Pubtator 29191562 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Disseminated Intravascular Coagulation Disseminated Intravascular Coagulation BEFREE 22728069
★★★★★
★☆☆☆☆
Found in Text Mining only
Fibrosis, Liver Liver Fibrosis BEFREE 29704446
★★★★★
★☆☆☆☆
Found in Text Mining only
Hyperlipoproteinemia Type IIa Hyperlipoproteinemia BEFREE 10024460
★★★★★
★☆☆☆☆
Found in Text Mining only