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    MANCR mitotically associated long non coding RNA [ Homo sapiens (human) ]

    Gene ID: 100216001, updated on 22-Oct-2024

    Summary

    Official Symbol
    MANCRprovided by HGNC
    Official Full Name
    mitotically associated long non coding RNAprovided by HGNC
    Primary source
    HGNC:HGNC:44678
    See related
    Ensembl:ENSG00000231298 AllianceGenome:HGNC:44678
    Gene type
    ncRNA
    RefSeq status
    PREDICTED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    LINC00704
    Expression
    Biased expression in spleen (RPKM 1.8), colon (RPKM 0.5) and 5 other tissues See more
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    Genomic context

    See MANCR in Genome Data Viewer
    Location:
    10p15.1
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (4650185..4678070, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (4652609..4678492, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (4692377..4720262, complement)

    Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 7156 Neighboring gene uncharacterized LOC105376372 Neighboring gene long intergenic non-protein coding RNA 703 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr10:4449652-4450851 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr10:4473152-4474351 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2922 Neighboring gene RNA, U6 small nuclear 163, pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:4599913-4600414 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:4649568-4650068 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:4703529-4704512 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr10:4704879-4706078 Neighboring gene long intergenic non-protein coding RNA 705 Neighboring gene uncharacterized LOC105376373 Neighboring gene uncharacterized LOC105376375 Neighboring gene uncharacterized LOC107984197 Neighboring gene uncharacterized LOC105376374

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues 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
    Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus.
    EBI GWAS Catalog
    Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
    EBI GWAS Catalog

    General gene information

    Markers

    Other Names

    • long intergenic non-protein coding RNA 704

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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_024475.1 RNA Sequence

      Status: PREDICTED

      Source sequence(s)
      BC048320
      Related
      ENST00000430998.8

    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_000010.11 Reference GRCh38.p14 Primary Assembly

      Range
      4650185..4678070 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060934.1 Alternate T2T-CHM13v2.0

      Range
      4652609..4678492 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)