Display Settings:

Format

Send to:

Choose Destination

    MT1DP metallothionein 1D, pseudogene [ Homo sapiens ]

    Gene ID: 326343, updated on 11-May-2012

    Summary

    Official Symbol
    MT1DPprovided by HGNC
    Official Full Name
    metallothionein 1D, pseudogeneprovided by HGNC
    Primary source
    HGNC:7396
    See related
    HPRD:17610
    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
    MTM

    Genomic context

    Location :
    16q13
    Sequence :
    Chromosome: 16; NC_000016.9 (56677599..56678853)
    See MT1DP in Epigenomics, MapViewer

    Chromosome 16 - NC_000016.9Genomic Context describing neighboring genes Neighboring gene metallothionein 1J, pseudogene Neighboring gene metallothionein 1A Neighboring gene metallothionein 1C, pseudogene Neighboring gene metallothionein 1B

    Genomic regions, transcripts, and products

    HIV-1 protein interactions

    Protein Gene Interaction Pubs
    Tat tat Microarray analysis indicates HIV-1 Tat upregulates the interferon-responsive gene expression of many proteins, including Metallothionein, in immature dendritic cells, an effect that likely facilitates the expansion of HIV-1 infection PubMed

    Go to the HIV-1, Human Protein Interaction Database

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description
    BioGRID:130579 BioGRID:113164 UBC    BioGRID  PubMed Affinity Capture-MS 

    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.

    RNA

    1. NR_003658.2 RNA Sequence

      Description
      Transcript Variant: This variant (1) represents the longer transcript.
      Source sequence(s)
      AC026461, BG181336
    2. NR_027781.1 RNA Sequence

      Description
      Transcript Variant: This variant (2) differs at the 5' end and is shorter compared to variant 1.
      Source sequence(s)
      AF348999, BC130317, BG181336

    RefSeqs of Annotated Genomes: Build 37.3

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

    Reference GRCh37.p5 Primary Assembly

    Genomic

    1. NC_000016.9 Reference GRCh37.p5 Primary Assembly

      Range
      56677599..56678853
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate HuRef

    Genomic

    1. AC_000148.1 Alternate HuRef

      Range
      42547053..42548307
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_175620.1: Suppressed sequence

      Description
      NM_175620.1: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.

    Related Sequences

    Nucleotide Protein
    Heading Accession and Version
    genomic AC026461.11 (42522..44085) None
    genomic CH471092.1 EAW82877.1
      EAW82878.1
    mRNA AF348999.2 AAO32959.2
    mRNA BC130315.1 None
    mRNA BC130317.1 None
    mRNA BG181336.1 None
    Protein Accession Links
    GenPept Link UniProtKB Link
    A1L3X4.1 GenPept UniProtKB/Swiss-Prot:A1L3X4

      Supplemental Content