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    FAM47B family with sequence similarity 47 member B [ Homo sapiens (human) ]

    Gene ID: 170062, updated on 10-Dec-2024

    Summary

    Official Symbol
    FAM47Bprovided by HGNC
    Official Full Name
    family with sequence similarity 47 member Bprovided by HGNC
    Primary source
    HGNC:HGNC:26659
    See related
    Ensembl:ENSG00000189132 AllianceGenome:HGNC:26659
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Orthologs
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    Genomic context

    See FAM47B in Genome Data Viewer
    Location:
    Xp21.1
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (34942796..34944915)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (34537453..34539572)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (34960913..34963032)

    Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene SRSF2 pseudogene 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:34499547-34500046 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:34575763-34576344 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chrX:34577375-34577902 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:34577903-34578428 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:34578429-34578954 Neighboring gene NANOG hESC enhancer GRCh37_chrX:34611791-34612292 Neighboring gene transmembrane protein 47 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:34782794-34783536 Neighboring gene ReSE screen-validated silencer GRCh37_chrX:35063242-35063449 Neighboring gene MAGE family member B18 pseudogene Neighboring gene Sharpr-MPRA regulatory region 13056 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29517 Neighboring gene RNA, U6 small nuclear 1087, pseudogene

    Genomic regions, transcripts, and products

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    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.

    Genomic

    1. NG_021372.1 RefSeqGene

      Range
      5001..7120
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_152631.3NP_689844.2  protein FAM47B

      See identical proteins and their annotated locations for NP_689844.2

      Status: VALIDATED

      Source sequence(s)
      AL043092, AL043093, BC035026
      Consensus CDS
      CCDS14236.1
      UniProtKB/Swiss-Prot
      Q5JQN5, Q6PIG3, Q8NA70
      Related
      ENSP00000328307.5, ENST00000329357.6
      Conserved Domains (2) summary
      pfam06346
      Location:189328
      Drf_FH1; Formin Homology Region 1
      pfam14642
      Location:1258
      FAM47; FAM47 family

    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_000023.11 Reference GRCh38.p14 Primary Assembly

      Range
      34942796..34944915
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060947.1 Alternate T2T-CHM13v2.0

      Range
      34537453..34539572
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)