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VN2R1P vomeronasal 2 receptor 1 pseudogene [ Homo sapiens (human) ]

Gene ID: 344760, updated on 1-Jun-2020

Summary

Official Symbol
VN2R1Pprovided by HGNC
Official Full Name
vomeronasal 2 receptor 1 pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:30344
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
CASRL1; GPRC2B

Genomic context

See VN2R1P in Genome Data Viewer
Location:
3q25.31
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 3 NC_000003.12 (156033582..156037647)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (155751371..155755436)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene guanine monophosphate synthase Neighboring gene SET pseudogene 14 Neighboring gene ALG1 like 15, pseudogene Neighboring gene MRE11 homolog, double strand break repair nuclease pseudogene 1

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • calcium-sensing receptor like 1
  • seven transmembrane helix receptor

NCBI Reference Sequences (RefSeq)

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_006066.2 

    Range
    101..4166
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p13 Primary Assembly

    Range
    156033582..156037647
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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