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IFNWP18 interferon omega 1 pseudogene 18 [ Homo sapiens (human) ]

Gene ID: 360001, updated on 10-Oct-2023

Summary

Official Symbol
IFNWP18provided by HGNC
Official Full Name
interferon omega 1 pseudogene 18provided by HGNC
Primary source
HGNC:HGNC:5450
See related
Ensembl:ENSG00000223684 AllianceGenome:HGNC:5450
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
LEIF-M
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Genomic context

Location:
9p21.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (21209173..21209899, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (21223030..21223756, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (21209172..21209898, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene interferon alpha 7 Neighboring gene interferon alpha 10 Neighboring gene interferon alpha 16 Neighboring gene interferon alpha 17

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • interferon, omega 18 (pseudogene)
  • pseudo-IFN-alpha-m processed pseudogene

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_002922.5 

    Range
    101..827
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    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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    21209173..21209899 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    21223030..21223756 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)