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IGHV3OR16-13 immunoglobulin heavy variable 3/OR16-13 (non-functional) [ Homo sapiens (human) ]

Gene ID: 100287372, updated on 2-Nov-2024

Summary

Official Symbol
IGHV3OR16-13provided by HGNC
Official Full Name
immunoglobulin heavy variable 3/OR16-13 (non-functional)provided by HGNC
Primary source
HGNC:HGNC:5637
See related
IMGT/GENE-DB:IGHV3/OR16-13; AllianceGenome:HGNC:5637
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
IGHV3OR1613
Summary
Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Nov 2024]
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Genomic context

See IGHV3OR16-13 in Genome Data Viewer
Location:
16p11.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (33827366..33827659)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (35399742..35400035)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (33629833..33630126)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene immunoglobulin heavy variable 3/OR16-12 (non-functional) Neighboring gene ADAM metallopeptidase domain 21 pseudogene Neighboring gene immunoglobulin heavy variable 3/OR16-17 (non-functional) Neighboring gene immunoglobulin heavy variable 3/OR16-11 (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_011771.1 

    Range
    101..394
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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
    33827366..33827659
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    35399742..35400035
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)