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    FAM86C2P family with sequence similarity 86 member C2, pseudogene [ Homo sapiens (human) ]

    Gene ID: 645332, updated on 17-Jun-2024

    Summary

    Official Symbol
    FAM86C2Pprovided by HGNC
    Official Full Name
    family with sequence similarity 86 member C2, pseudogeneprovided by HGNC
    Gene description
    family with sequence similarity 86, member A pseudogene
    Primary source
    HGNC:HGNC:42392
    See related
    Ensembl:ENSG00000290994 AllianceGenome:HGNC:42392
    Gene type
    pseudo
    RefSeq status
    PROVISIONAL
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Summary
    Predicted to enable methyltransferase activity. Predicted to be involved in methylation. [provided by Alliance of Genome Resources, Apr 2022]
    Expression
    Ubiquitous expression in thyroid (RPKM 3.6), kidney (RPKM 2.2) and 25 other tissues See more
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    Genomic context

    See FAM86C2P in Genome Data Viewer
    Location:
    11q13.2
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (67791767..67805336, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (67786963..67800535, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (67559238..67572807, complement)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr11:67525335-67525862 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:67525863-67526388 Neighboring gene uncharacterized LOC105369358 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:67526917-67527442 Neighboring gene EVA1C pseudogene 4 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:67555733-67556440 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:67559082-67559894 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:67560708-67561519 Neighboring gene ALG1 like 8, pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:67570465-67570966 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:67570967-67571466 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3650 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:67573265-67573766 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:67573767-67574266 Neighboring gene translation initiation factor IF-2-like Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:67593458-67593966 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:67593967-67594475 Neighboring gene ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 7 Neighboring gene NANOG hESC enhancer GRCh37_chr11:67610458-67611043 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr11:67624072-67624744 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:67640251-67640752 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:67640753-67641252 Neighboring gene long intergenic non-protein coding RNA 2754

    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

    General gene information

    Markers

    Other Names

    • Putative protein FAM86A-like 1
    • family with sequence similarity 86, member A pseudogene

    Clone Names

    • FLJ31209

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables methyltransferase activity IEA
    Inferred from Electronic Annotation
    more info
     
    Process Evidence Code Pubs
    involved_in methylation IEA
    Inferred from Electronic Annotation
    more info
     

    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_024249.1 RNA Sequence

      Status: PROVISIONAL

      Source sequence(s)
      AP003716
      Related
      ENST00000529253.5

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000011.10 Reference GRCh38.p14 Primary Assembly

      Range
      67791767..67805336 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060935.1 Alternate T2T-CHM13v2.0

      Range
      67786963..67800535 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NG_024379.1: Suppressed sequence

      Description
      NG_024379.1: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.