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    LINC02903 long intergenic non-protein coding RNA 2903 [ Homo sapiens (human) ]

    Gene ID: 154907, updated on 10-Dec-2024

    Summary

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    Official Symbol
    LINC02903provided by HGNC
    Official Full Name
    long intergenic non-protein coding RNA 2903provided by HGNC
    Primary source
    HGNC:HGNC:33712
    See related
    Ensembl:ENSG00000205174 AllianceGenome:HGNC:33712
    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
    C7orf66
    Expression
    Low expression observed in reference dataset See more
    Orthologs
    all
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    Genomic context

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    See LINC02903 in Genome Data Viewer
    Location:
    7q31.1
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (108883975..108884587, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (110208148..110208759, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (108524032..108524644, complement)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene sorbitol dehydrogenase pseudogene Neighboring gene uncharacterized LOC107986836 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr7:108465150-108466349 Neighboring gene BUB3 mitotic checkpoint protein pseudogene 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:108852947-108853448 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:108853449-108853948 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr7:108871548-108872106 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:109237086-109237867 Neighboring gene NANOG hESC enhancer GRCh37_chr7:109251582-109252157 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr7:109287079-109288278 Neighboring gene immunoglobulin binding protein 1 pseudogene

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • 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

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    Related articles in PubMed

    1. Large-scale genome-wide association study of Asian population reveals genetic factors in FRMD4A and other loci influencing smoking initiation and nicotine dependence. Yoon D, et al. Hum Genet, 2012 Jun. PMID 22006218, Free PMC Article
    2. Analysis of heavy and light chain pairings indicates that receptor editing shapes the human antibody repertoire. de Wildt RM, et al. J Mol Biol, 1999 Jan 22. PMID 9887257
    3. A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variants. Tao S, et al. Carcinogenesis, 2012 Mar. PMID 22219177, Free PMC Article
    4. Creation of genome-wide protein expression libraries using random activation of gene expression. Harrington JJ, et al. Nat Biotechnol, 2001 May. PMID 11329013
    5. Human chromosome 7: DNA sequence and biology. Scherer SW, et al. Science, 2003 May 2. PMID 12690205, Free PMC Article

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Find tests for this gene in the NIH Genetic Testing Registry (GTR)

    Review eQTL and phenotype association data in this region using PheGenI

    EBI GWAS Catalog

    Description
    A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variants.
    EBI GWAS Catalog
    Large-scale genome-wide association study of Asian population reveals genetic factors in FRMD4A and other loci influencing smoking initiation and nicotine dependence.
    EBI GWAS Catalog

    Variation

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    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    General gene information

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    Markers

    Homology

    Other Names

    • uncharacterized protein C7orf66

    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_171002.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC004014
      Related
      ENST00000624695.1

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    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
      108883975..108884587 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      110208148..110208759 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001024607.3: Suppressed sequence

      Description
      NM_001024607.3: This RefSeq was removed because it is now thought that this gene does not encode a protein.
    Nucleotide Protein
    Heading Accession and Version

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