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LINC-PINT long intergenic non-protein coding RNA, p53 induced transcript [ Homo sapiens (human) ]

Gene ID: 378805, updated on 7-Aug-2022

Summary

Official Symbol
LINC-PINTprovided by HGNC
Official Full Name
long intergenic non-protein coding RNA, p53 induced transcriptprovided by HGNC
Primary source
HGNC:HGNC:26885
See related
Ensembl:ENSG00000231721 MIM:618212; AllianceGenome:HGNC:26885
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
PINT; MKLN1-AS1; LincRNA-Pint
Summary
Predicted to act upstream of or within several processes, including adipose tissue development; adult somatic muscle development; and hair follicle development. [provided by Alliance of Genome Resources, Apr 2022]
Expression
Ubiquitous expression in bone marrow (RPKM 3.9), brain (RPKM 3.1) and 24 other tissues See more
Orthologs
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Genomic context

See LINC-PINT in Genome Data Viewer
Location:
7q32.3
Exon count:
18
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (130877562..131109925, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (132195054..132427432, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (130562321..130794684, complement)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 2521 Neighboring gene Sharpr-MPRA regulatory region 8443 Neighboring gene microRNA 29b-1 Neighboring gene microRNA 29a Neighboring gene long intergenic non-protein coding RNA 513 Neighboring gene Sharpr-MPRA regulatory region 13565 Neighboring gene Sharpr-MPRA regulatory region 6658 Neighboring gene RNA, U6 small nuclear 1010, pseudogene Neighboring gene MKLN1 intron CAGE-defined mid-level expression enhancer Neighboring gene muskelin 1 Neighboring gene ribosomal protein L27 pseudogene 11

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Phenotypes

EBI GWAS Catalog

Description
Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium.
EBI GWAS Catalog
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer.
EBI GWAS Catalog
Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.
EBI GWAS Catalog

General gene information

Markers

Homology

Other Names

  • MKLN1 antisense RNA 1 (head to head)
  • p53 induced noncoding transcript

Clone Names

  • FLJ38230, FLJ43663, hCG_2038586

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

RNA

  1. NR_015431.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) is the reference variant.
    Source sequence(s)
    AA281849, AC013434, AK125651, AL569506, AL713664, BC130416, BX451434, CA412672, DB472406, R67739
  2. NR_024153.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) differs in the 5' and 3' exon structure and lacks an alternate internal exon, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    AL569506, BC039420, CA412672, R67739
    Related
    ENST00000433079.5
  3. NR_034120.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (9) uses an alternate promoter and represents an alternate exon structure, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    AC016831, AK095549
  4. NR_109850.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) contains an alternate internal exon, resulting in a longer transcript, compared to variant 1.
    Source sequence(s)
    AA281849, AC058791, AK125651, AL569506, AL713664, BC130416, BX451434, CA412672, DB472406, R67739
    Related
    ENST00000451786.6
  5. NR_109851.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (4) contains an alternate internal exon, resulting in a longer transcript, compared to variant 1.
    Source sequence(s)
    AA281849, AK125651, AL569506, AL713664, BC130416, BI833488, BX451434, CA412672, DB472406, R67739
  6. NR_109852.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (5) contains an alternate internal exon, resulting in a longer transcript, compared to variant 1.
    Source sequence(s)
    AA281849, AK125651, AL569506, AL713664, BC130416, BI914823, BX451434, CA412672, DB472406, R67739
  7. NR_109853.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (6) differs in the 3' exon structure, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    AL569506, BC130416, BG706681, CA412672, DB472406, R67739
  8. NR_109854.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (7) differs in the 3' exon structure, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    AL569506, AV727262, BC047367, BC130416, CA412672, DB472406, R67739
  9. NR_109855.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (8) lacks an alternate internal exon and differs in the 3' exon structure, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    BC130416, DA321983, DB472406
  10. NR_110472.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (10) uses an alternate promoter and represents an alternate exon structure, resulting in a shorter transcript, compared to variant 1. It uses an alternate splice site in the 3' terminal exon, compared to variant 9.
    Source sequence(s)
    AC016831
  11. NR_110473.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (11) uses an alternate promoter and represents an alternate exon structure, resulting in a shorter transcript, compared to variant 1. It uses an alternate 3' terminal exon, compared to variant 9.
    Source sequence(s)
    AC016831, AK095549, GU321462
  12. NR_170175.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC013434, AC016831, AC058791
  13. NR_170176.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC013434, AC016831, AC058791

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    130877562..131109925 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    132195054..132427432 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001085379.1: Suppressed sequence

    Description
    NM_001085379.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.