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VN1R9P vomeronasal 1 receptor 9 pseudogene [ Homo sapiens (human) ]

Gene ID: 317691, updated on 13-May-2022

Summary

Official Symbol
VN1R9Pprovided by HGNC
Official Full Name
vomeronasal 1 receptor 9 pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:20257
See related
AllianceGenome:HGNC:20257
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
VN1R22-1P
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Genomic context

See VN1R9P in Genome Data Viewer
Location:
22q11.1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (17021355..17022270, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (17698026..17698941, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (17502245..17503160, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene GRB2 associated binding protein family member 4 Neighboring gene interleukin 9 receptor pseudogene Neighboring gene cat eye syndrome chromosome region, candidate 7 Neighboring gene interleukin 17 receptor A Neighboring gene ribosomal protein L31 pseudogene 62

Genomic regions, transcripts, and products

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_015792.1 

    Range
    101..1016
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    17021355..17022270 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    17698026..17698941 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)