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    FAM230B family with sequence similarity 230 member B [ Homo sapiens (human) ]

    Gene ID: 642633, updated on 15-Jun-2019

    Summary

    Official Symbol
    FAM230Bprovided by HGNC
    Official Full Name
    family with sequence similarity 230 member Bprovided by HGNC
    Primary source
    HGNC:HGNC:32943
    See related
    Ensembl:ENSG00000215498
    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
    Restricted expression toward testis (RPKM 11.2) See more

    Genomic context

    See FAM230B in Genome Data Viewer
    Location:
    22q11.21
    Exon count:
    13
    Annotation release Status Assembly Chr Location
    109 current GRCh38.p12 (GCF_000001405.38) 22 NC_000022.11 (21166903..21192156)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (21522231..21538924)

    Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC112268299 Neighboring gene E2F transcription factor 6 pseudogene 2 Neighboring gene uncharacterized LOC105372935 Neighboring gene gamma-glutamyltransferase 2 Neighboring gene E2F transcription factor 6 pseudogene 3

    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

    Related articles in PubMed

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    General gene information

    Other Names

    • KB-1183D5.13
    • family with sequence similarity 230 member B (non-protein coding)

    Clone Names

    • FLJ46366

    NCBI Reference Sequences (RefSeq)

    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_108107.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AP000550
      Related
      ENST00000451257.5

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

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

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000022.11 Reference GRCh38.p13 Primary Assembly

      Range
      21166903..21192156
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_201565.1: Suppressed sequence

      Description
      NM_201565.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.
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