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LOC100419041 sorting nexin 18 pseudogene [ Homo sapiens (human) ]

Gene ID: 100419041, updated on 17-Sep-2024

Summary

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Gene symbol
LOC100419041
Gene description
sorting nexin 18 pseudogene
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Annotation information
Annotation category: not annotated on reference assembly
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Genomic context

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See LOC100419041 in Genome Data Viewer
Location:
chromosome: 22
Annotation release Status Assembly Chr Location
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (3749962..3751099, complement)

Chromosome 22 - NC_060946.1Genomic Context describing neighboring genes Neighboring gene putative ankyrin repeat domain-containing protein 20A2 Neighboring gene putative double homeobox protein 3 Neighboring gene uncharacterized LOC124908455 Neighboring gene putative ankyrin repeat domain-containing protein 20A2 Neighboring gene uncharacterized LOC100287610 Neighboring gene ASNS pseudogene 5

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_060946.1 Chromosome 22 Alternate T2T-CHM13v2.0

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • sorting nexin 18 pseudogene 12

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_025020.3 

    Range
    101..1238
    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

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    3749962..3751099 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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