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LOC100421910 olfactory receptor family 8 subfamily U member 3 pseudogene [ Homo sapiens (human) ]

Gene ID: 100421910, updated on 17-Sep-2024

Summary

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Gene symbol
LOC100421910
Gene description
olfactory receptor family 8 subfamily U member 3 pseudogene
See related
Ensembl:ENSG00000230973
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 LOC100421910 in Genome Data Viewer
Location:
Xq26.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (131437064..131437690, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (129761173..129761799, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (130571038..130571664, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC102723546 Neighboring gene uncharacterized LOC107985705 Neighboring gene olfactory receptor family 5 subfamily BH member 1 pseudogene Neighboring gene olfactory receptor family 1 subfamily AA member 1 pseudogene Neighboring gene Sharpr-MPRA regulatory region 3295 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:130611149-130611726 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:130611727-130612303 Neighboring gene NLRP7 pseudogene 1 Neighboring gene olfactory receptor family 13 subfamily H member 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_026763.1 

    Range
    101..727
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    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    131437064..131437690 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    129761173..129761799 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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