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    KRT10-AS1 KRT10 antisense RNA 1 [ Homo sapiens (human) ]

    Gene ID: 147184, updated on 10-Dec-2024

    Summary

    Official Symbol
    KRT10-AS1provided by HGNC
    Official Full Name
    KRT10 antisense RNA 1provided by HGNC
    Primary source
    HGNC:HGNC:28305
    See related
    Ensembl:ENSG00000167920 AllianceGenome:HGNC:28305
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    TMEM99
    Summary
    Predicted to be located in membrane. [provided by Alliance of Genome Resources, Dec 2024]
    Annotation information
    Note: Multiple studies indicate that this gene exhibits elevated expression in various types of cancers. [20 Feb 2019]
    Expression
    Biased expression in skin (RPKM 53.2), testis (RPKM 22.6) and 5 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See KRT10-AS1 in Genome Data Viewer
    Location:
    17q21.2
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (40819145..40836274)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (41683465..41700595)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (38975397..38992526)

    Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr17:38954190-38955389 Neighboring gene uncharacterized LOC105371776 Neighboring gene keratin 28 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr17:38975907-38977106 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr17:38983418-38984617 Neighboring gene keratin 10 Neighboring gene uncharacterized LOC105371777 Neighboring gene Sharpr-MPRA regulatory region 3631 Neighboring gene keratin 12 Neighboring gene keratin 20

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    General gene information

    Markers

    Other Names

    • transmembrane protein 99 (putative)

    Clone Names

    • MGC21518

    Gene Ontology Provided by GOA

    Component Evidence Code Pubs
    located_in membrane 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_160886.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC090283
    2. NR_160887.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC090283
    3. NR_160888.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC090283
      Related
      ENST00000301665.10

    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_000017.11 Reference GRCh38.p14 Primary Assembly

      Range
      40819145..40836274
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060941.1 Alternate T2T-CHM13v2.0

      Range
      41683465..41700595
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NG_033147.1: Suppressed sequence

      Description
      NG_033147.1: This RefSeq was removed because it is now thought that this gene does not encode a protein.
    2. NM_001195386.1: Suppressed sequence

      Description
      NM_001195386.1: This RefSeq was removed because it is now thought that this gene does not encode a protein.
    3. NM_001195387.1: Suppressed sequence

      Description
      NM_001195387.1: This RefSeq was removed because it is now thought that this gene does not encode a protein.
    4. NM_145274.3: Suppressed sequence

      Description
      NM_145274.3: This RefSeq was removed because it is now thought that this gene does not encode a protein.