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    IGKV7-3 immunoglobulin kappa variable 7-3 (pseudogene) [ Homo sapiens (human) ]

    Gene ID: 28905, updated on 10-Oct-2023

    Summary

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    Official Symbol
    IGKV7-3provided by HGNC
    Official Full Name
    immunoglobulin kappa variable 7-3 (pseudogene)provided by HGNC
    Primary source
    HGNC:HGNC:5839
    See related
    IMGT/GENE-DB:IGKV7-3; AllianceGenome:HGNC:5839
    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
    B1; IGKV73
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    Genomic context

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    See IGKV7-3 in Genome Data Viewer
    Location:
    2p11.2
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (88915080..88915678, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (88924076..88924674, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (89214596..89215194, complement)

    Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene immunoglobulin kappa variable 4-1 Neighboring gene immunoglobulin kappa variable 5-2 Neighboring gene piggyBac transposable element derived 4 pseudogene 5 Neighboring gene immunoglobulin kappa variable 2-4 (pseudogene) Neighboring gene immunoglobulin kappa locus

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    Related articles in PubMed

    1. The kappa gene repertoire of human neonatal B cells. Girschick HJ, et al. Mol Immunol, 2002 Jun. PMID 12044778
    2. The J kappa proximal region of the human K locus contains three uncommon V kappa genes which are arranged in opposite transcriptional polarities. Lorenz W, et al. Mol Immunol, 1988 May. PMID 3137458

    GeneRIFs: Gene References Into Functions

    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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    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_000834.1 

      Range
      426024..426622
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    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_000002.12 Reference GRCh38.p14 Primary Assembly

      Range
      88915080..88915678 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p14 PATCHES

    Genomic

    1. NW_012132915.1 Reference GRCh38.p14 PATCHES

      Range
      23906..24504 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060926.1 Alternate T2T-CHM13v2.0

      Range
      88924076..88924674 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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