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    MTRNR2L11 MT-RNR2 like 11 [ Homo sapiens (human) ]

    Gene ID: 100463489, updated on 17-Jun-2019

    Summary

    Official Symbol
    MTRNR2L11provided by HGNC
    Official Full Name
    MT-RNR2 like 11provided by HGNC
    Primary source
    HGNC:HGNC:37168
    Gene type
    pseudo
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    HN11

    Genomic context

    See MTRNR2L11 in Genome Data Viewer
    Location:
    1q43
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (237943724..237945213, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (238107024..238108513, complement)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene nuclear-encoded mitochondrial tRNA-Pro (TGG) 1-1 Neighboring gene MT-ND1 pseudogene 25 Neighboring gene nuclear-encoded mitochondrial tRNA-Leu (TAA) 3-1 Neighboring gene MT-CYB pseudogene 15 Neighboring gene MT-ND6 pseudogene 15

    Genomic regions, transcripts, and products

    General gene information

    Other Names

    • MT-RNR2-like 11 (pseudogene)

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    receptor antagonist activity IBA
    Inferred from Biological aspect of Ancestor
    more info
    PubMed 
    Process Evidence Code Pubs
    negative regulation of execution phase of apoptosis IBA
    Inferred from Biological aspect of Ancestor
    more info
    PubMed 
    negative regulation of signaling receptor activity IEA
    Inferred from Electronic Annotation
    more info
     
    Component Evidence Code Pubs
    cytoplasm IEA
    Inferred from Electronic Annotation
    more info
     
    extracellular region IEA
    Inferred from Electronic Annotation
    more info
     

    NCBI Reference Sequences (RefSeq)

    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_023152.1 

      Range
      101..1590
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

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

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000001.11 Reference GRCh38.p13 Primary Assembly

      Range
      237943724..237945213 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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