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    ADAM6 ADAM metallopeptidase domain 6 (pseudogene) [ Homo sapiens (human) ]

    Gene ID: 8755, updated on 8-Nov-2023

    Summary

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    Official Symbol
    ADAM6provided by HGNC
    Official Full Name
    ADAM metallopeptidase domain 6 (pseudogene)provided by HGNC
    Primary source
    HGNC:HGNC:213
    See related
    Ensembl:ENSG00000290844 AllianceGenome:HGNC:213
    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
    tMDCIV; C14orf96
    Summary
    Predicted to be located in external side of plasma membrane and sperm head plasma membrane. Predicted to be part of protein-containing complex. [provided by Alliance of Genome Resources, Apr 2022]
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    Genomic context

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    Location:
    14q32.33
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (105969729..105972269, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (100240816..100243356, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (106435818..106438358, complement)

    Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene immunoglobulin heavy locus Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr14:106445918-106447117 Neighboring gene immunoglobulin heavy variable (II)-1-1 (pseudogene) Neighboring gene immunoglobulin heavy variable 6-1 Neighboring gene immunoglobulin heavy variable 1-2 Neighboring gene ribosomal protein S8 pseudogene 1

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • 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

    Bibliography

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    Related articles in PubMed

    1. Comparative genomic analysis of human and chimpanzee proteases. Puente XS, et al. Genomics, 2005 Dec. PMID 16162398
    2. The complete nucleotide sequence of the human immunoglobulin heavy chain variable region locus. Matsuda F, et al. J Exp Med, 1998 Dec 7. PMID 9841928, Free PMC Article
    3. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. Kimura K, et al. Genome Res, 2006 Jan. PMID 16344560, Free PMC Article
    4. Complete sequencing and characterization of 21,243 full-length human cDNAs. Ota T, et al. Nat Genet, 2004 Jan. PMID 14702039

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Review eQTL and phenotype association data in this region using PheGenI

    Variation

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    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    Genotypes

    General gene information

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    Markers

    Other Names

    • a disintegrin and metalloproteinase domain 6
    • anti-peanut 2S albumin immunoglobulin heavy chain variable region
    • metalloprotease-like, disintegrin-like protein pseudogene

    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.

    Genomic

    1. NG_001019.6 

      Range
      908076..910616
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. NR_002224.2 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AA609214, AC246787, AK093400, DB059945
      Related
      ENST00000606026.2

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000014.9 Reference GRCh38.p14 Primary Assembly

      Range
      105969729..105972269 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p14 ALT_REF_LOCI_1

    Genomic

    1. NT_187600.1 Reference GRCh38.p14 ALT_REF_LOCI_1

      Range
      437498..440038 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060938.1 Alternate T2T-CHM13v2.0

      Range
      100240816..100243356 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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