RPL17-C18orf32 (RPL17-C18orf32 readthrough)

Gene Gene information from NCBI Gene database.
Gene miRNA Other IDs Pathways Associated diseases
Entrez ID 100526842
Gene name RPL17-C18orf32 readthrough
Gene symbol RPL17-C18orf32
Synonyms (NCBI Gene)
PD-1RPL17
Chromosome 18
Chromosome location 18q21.1
Summary This locus represents naturally occurring read-through transcription between the neighboring RPL17 (ribosomal protein L17) and C18orf32 (chromosome 18 open reading frame 32) genes. Alternative splicing results in multiple transcript variants. The encoded
miRNA miRNA information provided by mirtarbase database.
112
Gene miRNA Other IDs Pathways Associated diseases
Show/Hide all (112)
miRTarBase ID miRNA Experiments Reference
MIRT571733 hsa-miR-3609 PAR-CLIP 20371350
MIRT571732 hsa-miR-548ah-5p PAR-CLIP 20371350
MIRT571731 hsa-miR-106a-5p PAR-CLIP 20371350
MIRT571730 hsa-miR-106b-5p PAR-CLIP 20371350
MIRT571729 hsa-miR-17-5p PAR-CLIP 20371350
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Other IDs Pathways Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
Gene miRNA Other IDs Pathways Associated diseases
  KEGG 
  Ribosome
Coronavirus disease - COVID-19 		 
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
Gene miRNA Other IDs Pathways Associated diseases
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)
Show/Hide Unknown Diseases (5)
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
ANEMIA, MACROCYTIC — Disgenet
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATTENTION DEFICIT HYPERACTIVITY DISORDER — Disgenet
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTISTIC DISORDER — Disgenet
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 25 — Disgenet
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations