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PRECSIT p53 regulated carcinoma associated Stat3 activating long intergenic non-protein coding transcript [ Homo sapiens (human) ]

Gene ID: 283487, updated on 6-Nov-2022

Summary

Official Symbol
PRECSITprovided by HGNC
Official Full Name
p53 regulated carcinoma associated Stat3 activating long intergenic non-protein coding transcriptprovided by HGNC
Primary source
HGNC:HGNC:27492
See related
Ensembl:ENSG00000255874 AllianceGenome:HGNC:27492
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
C13orf29; LINC00346; NCRNA00346
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Genomic context

See PRECSIT in Genome Data Viewer
Location:
13q34
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (110863987..110870308, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (110094081..110100400, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (111516334..111522655, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370362 Neighboring gene uncharacterized LOC105370363 Neighboring gene ankyrin repeat domain 10 Neighboring gene poly(ADP-ribose) polymerase 1 pseudogene 1

Genomic regions, transcripts, and products

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Other Names

  • long intergenic non-protein coding RNA 346

Clone Names

  • FLJ97904

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_027701.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AJ295981, AL157875, BX647632
    Related
    ENST00000538077.3

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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    110863987..110870308 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    110094081..110100400 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_178514.3: Suppressed sequence

    Description
    NM_178514.3: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.