IGHV3-69-1 immunoglobulin heavy variable 3-69-1 (pseudogene) [Homo sapiens (human)] - Gene

Summary

Official Symbol: IGHV3-69-1provided by HGNC
Official Full Name: immunoglobulin heavy variable 3-69-1 (pseudogene)provided by HGNC
Primary source: HGNC:HGNC:5631
See related: Ensembl:ENSG00000282600 IMGT/GENE-DB:IGHV3-69-1; AllianceGenome:HGNC:5631
Gene type: pseudo
RefSeq status: VALIDATED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: IGH; IGHM; IGHV; IgVH; IGHV3H; IGHV3-H; IGHV3-11
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Genomic context

Location:: 14q32.33

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	14	NC_000014.9 (106728163..106728615, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	14 (PATCHES)	NW_004166863.1 (1391330..1391782, complement)

Chromosome 14 - NC_000014.9 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?

IGHV3-H is a pseudogene incapable of being translated.
Title: Identification of two new alleles, IGHV3-23*04 and IGHJ6*04, and the complete sequence of the IGHV3-h pseudogene in the human immunoglobulin locus and their prevalences in Danish Caucasians.

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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)

General gene information

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Other Names

IGH c1906_heavy_IGHV3-11_IGHD3-22_IGHJ4
Ig heavy chain variable region
immunoglobulin heavy chain CDR3
immunoglobulin heavy chain variable region
immunoglobulin heavy variable 3-H (provisional) pseudogene
immunoglobulin heavy variable 3-H (pseudogene)
immunoglobulin heavy variable 3-H pseudogene (provisional)
immunoglobulin mu heavy chain variable region

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.