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    FAM95B1 family with sequence similarity 95 member B1 [ Homo sapiens (human) ]

    Gene ID: 100133036, updated on 19-Oct-2024

    Summary

    Official Symbol
    FAM95B1provided by HGNC
    Official Full Name
    family with sequence similarity 95 member B1provided by HGNC
    Primary source
    HGNC:HGNC:32318
    See related
    Ensembl:ENSG00000290718 AllianceGenome:HGNC:32318
    Gene type
    ncRNA
    RefSeq status
    PREDICTED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    PITAR
    Expression
    Biased expression in testis (RPKM 17.6), spleen (RPKM 1.7) and 3 other tissues See more
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    Genomic context

    See FAM95B1 in Genome Data Viewer
    Location:
    9p11.2
    Exon count:
    5
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (40323571..40329220)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (40338481..40344130)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (42468589..42474238)

    Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene ankyrin repeat domain 20 family member A2, pseudogene Neighboring gene RNA, U6 small nuclear 1269, pseudogene Neighboring gene sorting nexin 18 pseudogene 8 Neighboring gene zinc finger protein 114 pseudogene Neighboring gene calponin 2 pseudogene 2

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues 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

    • p53 Inactivating TRIM28 Associated RNA

    Clone Names

    • FLJ37619, DKFZp686P0734

    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_026759.1 RNA Sequence

      Status: PREDICTED

      Source sequence(s)
      BX664727
      Related
      ENST00000592053.5

    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_000009.12 Reference GRCh38.p14 Primary Assembly

      Range
      40323571..40329220
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060933.1 Alternate T2T-CHM13v2.0

      Range
      40338481..40344130
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)