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    BCDIN3D-AS1 BCDIN3D antisense RNA 1 [ Homo sapiens (human) ]

    Gene ID: 100286844, updated on 10-Dec-2024

    Summary

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    Official Symbol
    BCDIN3D-AS1provided by HGNC
    Official Full Name
    BCDIN3D antisense RNA 1provided by HGNC
    Primary source
    HGNC:HGNC:44113
    See related
    Ensembl:ENSG00000258057 AllianceGenome:HGNC:44113
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Expression
    Ubiquitous expression in brain (RPKM 2.2), prostate (RPKM 2.2) and 25 other tissues See more
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    Genomic context

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    See BCDIN3D-AS1 in Genome Data Viewer
    Location:
    12q13.12
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (49828543..49841154)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (49791557..49804166)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (50222326..50234937)

    Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid active region 6333 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 6334 Neighboring gene LSM6 homolog, U6 small nuclear RNA and mRNA degradation associated pseudogene 2 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:50184530-50185372 Neighboring gene NCK associated protein 5 like Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:50195140-50195640 Neighboring gene nuclear-encoded mitochondrial tRNA-Gln (TTG) 6-1 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr12:50218728-50219594 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr12:50219595-50220461 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 6335 Neighboring gene H3K27ac hESC enhancer GRCh37_chr12:50222070-50222648 Neighboring gene H3K27ac hESC enhancer GRCh37_chr12:50222649-50223227 Neighboring gene Sharpr-MPRA regulatory region 4864 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 6336 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 6337 Neighboring gene BCDIN3 domain containing RNA methyltransferase Neighboring gene ribosomal protein L35a pseudogene 28 Neighboring gene Fas apoptotic inhibitory molecule 2 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:50280844-50281632 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr12:50281633-50282421 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:50282422-50283210 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:50288891-50289470

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

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    Related articles in PubMed

    1. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Berndt SI, et al. Nat Genet, 2013 May. PMID 23563607, Free PMC Article
    2. Identification of intrahepatic cholangiocarcinoma related genes by comparison with normal liver tissues using expressed sequence tags. Wang AG, et al. Biochem Biophys Res Commun, 2006 Jul 7. PMID 16712791
    3. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. Kimura K, et al. Genome Res, 2006 Jan. PMID 16344560, Free PMC Article
    4. Complete sequencing and characterization of 21,243 full-length human cDNAs. Ota T, et al. Nat Genet, 2004 Jan. PMID 14702039

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Review eQTL and phenotype association data in this region using PheGenI

    EBI GWAS Catalog

    Description
    Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
    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

    Other Names

    • BCDIN3D antisense RNA 1 (non-protein coding)

    Clone Names

    • FLJ30580

    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_027499.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the longest transcript.
      Source sequence(s)
      AC131157, BC014925, DA122615
      Related
      ENST00000548872.5

    2. NR_027500.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (3) uses an alternate donor splice site in the 5' exon and lacks a segment in the 3' region, compared to variant 1.
      Source sequence(s)
      AC131157, AI193197, BC014925, CB153643

    3. NR_027501.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) uses an alternate donor splice site in the 5' exon and is shorter, compared to variant 1.
      Source sequence(s)
      AC131157, BC014925, CB153643

    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_000012.12 Reference GRCh38.p14 Primary Assembly

      Range
      49828543..49841154
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060936.1 Alternate T2T-CHM13v2.0

      Range
      49791557..49804166
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

    The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

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    Research Materials