LINC-PINT (long intergenic non-protein coding RNA, p53 induced transcript)

Gene Gene information from NCBI Gene database.
Gene miRNA Other IDs Protein Associated diseases
Entrez ID 378805
Gene name Long intergenic non-protein coding RNA, p53 induced transcript
Gene symbol LINC-PINT
Synonyms (NCBI Gene)
LincRNA-PintMKLN1-AS1PINTPINT87aaTISPL
Chromosome 7
Chromosome location 7q32.3
miRNA miRNA information provided by mirtarbase database.
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Gene miRNA Other IDs Protein Associated diseases
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miRTarBase ID miRNA Experiments Reference
MIRT737321 hsa-miR-21-3p qRT-PCR 32401035
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
618212 26885 ENSG00000231721
Protein Protein information from UniProt database.
Gene miRNA Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
A0A455ZAR2
Protein name Transcriptional regulator PINT87aa
Protein function Enhances the binding of the PAF1 complex to target gene promoters and plays a role in negative regulation of transcription (PubMed:30367041). May function as an anchor to keep the PAF1 complex on target gene promoters, sequentially pausing RNA p
Family and domains
Tissue specificity TISSUE SPECIFICITY: Expressed in brain, liver, kidney and stomach with lower levels in breast, intestine, thyroid and pancreas. {ECO:0000269|PubMed:30367041}.
Sequence 


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Sequence length
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Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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Gene miRNA Other IDs Protein Associated diseases
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Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
LINC-PINT-related disorder Likely benign; Benign rs573515445, rs190124113, rs1877727, rs3800567, rs558233368 RCV003902320
RCV003904504
RCV003979845
RCV003981976
RCV003969134