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    ANOS2P anosmin 2, pseudogene [ Homo sapiens (human) ]

    Gene ID: 3734, updated on 17-Sep-2024

    Summary

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    Official Symbol
    ANOS2Pprovided by HGNC
    Official Full Name
    anosmin 2, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:6214
    See related
    AllianceGenome:HGNC:6214
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    KALP; ADMLY; KAL-Y
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    Genomic context

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    See ANOS2P in Genome Data Viewer
    Location:
    Yq11.221
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (13751706..13920022)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (14658336..14826674)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (15863586..16031902)

    Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene thymosin beta 4 Y-linked Neighboring gene PSIP1 pseudogene 2 Neighboring gene variable charge Y-linked Neighboring gene variable charge Y-linked 1B

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    Related articles in PubMed

    1. Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomes. Incerti B, et al. Nat Genet, 1992 Dec. PMID 1303285
    2. ANOS1: a unified nomenclature for Kallmann syndrome 1 gene (KAL1) and anosmin-1. de Castro F, et al. Brief Funct Genomics, 2017 Jul 1. PMID 27899353, Free PMC Article
    3. Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome. Montenegro LR, et al. Fertil Steril, 2013 Sep. PMID 23721716
    4. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Skaletsky H, et al. Nature, 2003 Jun 19. PMID 12815422
    5. Toward a complete human genome sequence. Sanger Center, et al. Genome Res, 1998 Nov. PMID 9847074

    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)

    General gene information

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    Markers

    Other Names

    • Kallmann syndrome sequence pseudogene
    • WUGSC:H_NH0304C24.2

    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_001153.5 

      Range
      101..168417
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    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_000024.10 Reference GRCh38.p14 Primary Assembly

      Range
      13751706..13920022
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060948.1 Alternate T2T-CHM13v2.0

      Range
      14658336..14826674
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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