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LOC100533852 nuclear factor kappa B subunit 2 pseudogene [ Homo sapiens (human) ]

Gene ID: 100533852, updated on 10-Dec-2024

Summary

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Gene symbol
LOC100533852
Gene description
nuclear factor kappa B subunit 2 pseudogene
See related
Ensembl:ENSG00000267478
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See LOC100533852 in Genome Data Viewer
Location:
18p11.21
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 18 NC_000018.10 (12091518..12093086, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 18 NC_060942.1 (12254279..12255847, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (12091517..12093085, complement)

Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene single stranded DNA binding protein 4 pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 9305 Neighboring gene ADGRA3 pseudogene 1 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:12086167-12086899 Neighboring gene H3K27ac hESC enhancer GRCh37_chr18:12089047-12089547 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 13100 Neighboring gene ankyrin repeat domain 62 Neighboring gene RNA, U6 small nuclear 324, pseudogene Neighboring gene succinate dehydrogenase complex subunit D pseudogene 1

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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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)

See Variation Viewer (GRCh38)

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_028707.3 

    Range
    101..1669
    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_000018.10 Reference GRCh38.p14 Primary Assembly

    Range
    12091518..12093086 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060942.1 Alternate T2T-CHM13v2.0

    Range
    12254279..12255847 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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