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    FAM95A family with sequence similarity 95 member A [ Homo sapiens (human) ]

    Gene ID: 90499, updated on 17-Sep-2024

    Summary

    Official Symbol
    FAM95Aprovided by HGNC
    Official Full Name
    family with sequence similarity 95 member Aprovided by HGNC
    Primary source
    HGNC:HGNC:28069
    See related
    Ensembl:ENSG00000289811 AllianceGenome:HGNC:28069
    Gene type
    ncRNA
    RefSeq status
    PREDICTED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Expression
    Biased expression in testis (RPKM 8.0), thyroid (RPKM 3.5) and 2 other tissues See more
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    Genomic context

    See FAM95A in Genome Data Viewer
    Location:
    2q11.1
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (94755326..94761184, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (95261845..95267703, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (95421071..95426929, complement)

    Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene MPRA-validated peak3791 silencer Neighboring gene calponin 2 pseudogene 8 Neighboring gene zinc finger protein 114 pseudogene Neighboring gene ankyrin repeat domain 20 family member A8, pseudogene Neighboring gene cytochrome P450 family 4 subfamily F member 32, pseudogene Neighboring gene sorting nexin 18 pseudogene 14 Neighboring gene RNA, U6 small nuclear 1320, pseudogene

    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

    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_038409.1 RNA Sequence

      Status: PREDICTED

      Source sequence(s)
      AL137712
      Related
      ENST00000700700.1

    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_000002.12 Reference GRCh38.p14 Primary Assembly

      Range
      94755326..94761184 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060926.1 Alternate T2T-CHM13v2.0

      Range
      95261845..95267703 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)