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VN1R18P vomeronasal 1 receptor 18 pseudogene [ Homo sapiens (human) ]

Gene ID: 100133087, updated on 10-Dec-2024

Summary

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Official Symbol
VN1R18Pprovided by HGNC
Official Full Name
vomeronasal 1 receptor 18 pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:37334
See related
Ensembl:ENSG00000275423 AllianceGenome:HGNC:37334
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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See VN1R18P in Genome Data Viewer
Location:
2p16.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (47989625..47990561)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (47995591..47996527)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (48216764..48217700)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105374592 Neighboring gene uncharacterized LOC105374591 Neighboring gene peptidylprolyl isomerase A pseudogene 62 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:48274138-48274662 Neighboring gene uncharacterized LOC124907765 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:48274663-48275186 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr2:48333670-48334869 Neighboring gene uncharacterized LOC105374593 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11474 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11475 Neighboring gene Sharpr-MPRA regulatory region 12235 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:48383419-48383918

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)

General gene information

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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_014058.1 

    Range
    101..1037
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    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_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    47989625..47990561
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    47995591..47996527
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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