Gene Gene information from NCBI Gene database.
Entrez ID 692312
Gene name PPAN-P2RY11 readthrough
Gene symbol PPAN-P2RY11
Synonyms (NCBI Gene)
BXDC3P2RY11P2Y11PPANSSF1Ssf-1
Chromosome 19
Chromosome location 19p13.2
Summary This locus represents naturally occurring read-through transcription between the adjacent PPAN and P2RY11 genes. Alternative splicing results in two transcript variants, one of which encodes a fusion protein that shares sequence identity with each individ
miRNA miRNA information provided by mirtarbase database.
105
miRTarBase ID miRNA Experiments Reference
MIRT051844 hsa-let-7c-5p CLASH 23622248
MIRT512604 hsa-miR-1273a PAR-CLIP 23446348
MIRT453182 hsa-miR-4699-5p PAR-CLIP 23592263
MIRT453181 hsa-miR-3665 PAR-CLIP 23592263
MIRT453180 hsa-miR-657 PAR-CLIP 23592263
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
4
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
PPAN-P2RY11-related disorder Likely benign rs376693285, rs147142449, rs760333567, rs200987497 RCV003949612
RCV003924212
RCV003932280
RCV003962079