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VN1R112P vomeronasal 1 receptor 112 pseudogene [ Homo sapiens (human) ]

Gene ID: 100312854, updated on 10-Oct-2023

Summary

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Official Symbol
VN1R112Pprovided by HGNC
Official Full Name
vomeronasal 1 receptor 112 pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:37437
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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Location:
chromosome: 22
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Unplaced Scaffold NT_167214.1 (58708..58860, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (4750980..4751132, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Unplaced Scaffold NT_167214.1 (58708..58860, complement)

NT_167214.1Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC100507395 Neighboring gene uncharacterized LOC100507412 Neighboring gene RNA, 45S pre-ribosomal N5 Neighboring gene RNA, 18S ribosomal N5 Neighboring gene RNA, 5.8S ribosomal N5

NW_021160026.1Genomic Context describing neighboring genes Neighboring gene C-terminal-binding protein 2-like Neighboring gene uncharacterized LOC124905548 Neighboring gene uncharacterized LOC124905547

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. Extreme variability among mammalian V1R gene families. Young JM, et al. Genome Res, 2010 Jan. PMID 19952141, Free PMC Article

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)

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_015712.1 

    Range
    101..253
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    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. NT_167214.1 Reference GRCh38.p14 Primary Assembly

    Range
    58708..58860 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_021160026.1 Reference GRCh38.p14 PATCHES

    Range
    369546..369698 complement
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    4750980..4751132 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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