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IGHV3OR16-17 immunoglobulin heavy variable 3/OR16-17 (non-functional) [ Homo sapiens (human) ]

Gene ID: 390714, updated on 10-Oct-2023

Summary

Official Symbol
IGHV3OR16-17provided by HGNC
Official Full Name
immunoglobulin heavy variable 3/OR16-17 (non-functional)provided by HGNC
Primary source
HGNC:HGNC:55105
See related
Ensembl:ENSG00000259680 AllianceGenome:HGNC:55105
Gene type
other
RefSeq status
MODEL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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

Location:
16p11.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (33844758..33845308, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (35417134..35417662, complement)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene ADAM metallopeptidase domain 21 pseudogene Neighboring gene immunoglobulin heavy variable 3/OR16-13 (non-functional) Neighboring gene immunoglobulin heavy variable 3/OR16-11 (pseudogene) Neighboring gene Rho GTPase activating protein 23 pseudogene 1

Genomic regions, transcripts, and products

General gene information

Other Names

  • IGHV3/OR16-17
  • immunoglobulin heavy chain variable region

NCBI Reference Sequences (RefSeq)

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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_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    33844758..33845308 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    35417134..35417662 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)