OR52V1P olfactory receptor family 52 subfamily V member 1 pseudogene [Homo sapiens (human)] - Gene

Summary

Official Symbol: OR52V1Pprovided by HGNC
Official Full Name: olfactory receptor family 52 subfamily V member 1 pseudogeneprovided by HGNC
Primary source: HGNC:HGNC:15238
See related: Ensembl:ENSG00000249633 AllianceGenome:HGNC:15238
Gene type: pseudo
RefSeq status: INFERRED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary: Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]
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Genomic context

Location:: 11p15.4

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	11	NC_000011.10 (5527223..5528126, complement)
RS_2023_10	current	T2T-CHM13v2.0 (GCF_009914755.1)	11	NC_060935.1 (5586598..5587501, complement)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	11	NC_000011.9 (5548453..5549356, complement)

Chromosome 11 - NC_000011.10 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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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

ECD16470 (e-PCR)
- UniSTS:297485

ECD04962 (e-PCR)
- UniSTS:286030

stSG611035 (e-PCR)
- UniSTS:449144

stSG611036 (e-PCR)
- UniSTS:449145

stSG611037 (e-PCR)
- UniSTS:449146

ECD14816 (e-PCR)
- UniSTS:295836

REN98552 (e-PCR)
- UniSTS:423349

REN98553 (e-PCR)
- UniSTS:423350

REN98554 (e-PCR)
- UniSTS:423351

REN98555 (e-PCR)
- UniSTS:423352

REN98556 (e-PCR)
- UniSTS:423353

REN98557 (e-PCR)
- UniSTS:423354

REN98558 (e-PCR)
- UniSTS:423355

REN98559 (e-PCR)
- UniSTS:423356

REN98560 (e-PCR)
- UniSTS:423357

REN98561 (e-PCR)
- UniSTS:423358

REN98562 (e-PCR)
- UniSTS:423359

REN98563 (e-PCR)
- UniSTS:423360

REN98564 (e-PCR)
- UniSTS:423361

REN98565 (e-PCR)
- UniSTS:423362

REN98566 (e-PCR)
- UniSTS:423363

ECD05387 (e-PCR)
- UniSTS:286453

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.