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

Gene ID: 3734, updated on 10-Oct-2023

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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Location:
Yq11.221
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (13751706..13920022)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (14658336..14826674)
105.20220307 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_2023_10

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

Gene LinkOut

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