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IGHV2OR16-5 immunoglobulin heavy variable 2/OR16-5 (non-functional) [ Homo sapiens (human) ]

Gene ID: 100129631, updated on 13-May-2022

Summary

Official Symbol
IGHV2OR16-5provided by HGNC
Official Full Name
immunoglobulin heavy variable 2/OR16-5 (non-functional)provided by HGNC
Primary source
HGNC:HGNC:5579
See related
Ensembl:ENSG00000259303 IMGT/GENE-DB:IGHV2/OR16-5; AllianceGenome:HGNC:5579
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
IGHV2OR165
Summary
Predicted to enable antigen binding activity and immunoglobulin receptor binding activity. Predicted to be involved in several processes, including activation of immune response; defense response to other organism; and phagocytosis. Predicted to be part of immunoglobulin complex, circulating. Predicted to be active in external side of plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

See IGHV2OR16-5 in Genome Data Viewer
Location:
16p11.2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (32847713..32848254)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (33436419..33436960, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (32859034..32859575)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene HERC2 pseudogene 5 Neighboring gene uncharacterized LOC101060048 Neighboring gene B cell receptor associated protein 31 pseudogene 2 Neighboring gene solute carrier family 6 member 10, pseudogene

Genomic regions, transcripts, and products

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_065965.1 

    Range
    101..642
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    32847713..32848254
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    33436419..33436960 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)