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VN1R22P vomeronasal 1 receptor 22 pseudogene [ Homo sapiens (human) ]

Gene ID: 100312844, updated on 10-Oct-2023

Summary

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Official Symbol
VN1R22Pprovided by HGNC
Official Full Name
vomeronasal 1 receptor 22 pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:37337
See related
AllianceGenome:HGNC:37337
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:
4q25
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (107135657..107136055)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (110440564..110440962)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (108056814..108057212)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene ACTR6 pseudogene 1 Neighboring gene dickkopf WNT signaling pathway inhibitor 2 Neighboring gene H3K27ac hESC enhancer GRCh37_chr4:107898921-107899694 Neighboring gene H3K27ac hESC enhancer GRCh37_chr4:107899695-107900466 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:107994239-107994739 Neighboring gene vomeronasal 1 receptor 23 pseudogene Neighboring gene Sharpr-MPRA regulatory region 7463 Neighboring gene Rac family small GTPase 1 pseudogene 5

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_015702.1 

    Range
    101..499
    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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    107135657..107136055
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    110440564..110440962
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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