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IFNA22P interferon alpha 22, pseudogene [ Homo sapiens (human) ]

Gene ID: 3453, updated on 10-Dec-2024

Summary

Official Symbol
IFNA22Pprovided by HGNC
Official Full Name
interferon alpha 22, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:5431
See related
AllianceGenome:HGNC:5431
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
IFNAP22
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Genomic context

See IFNA22P in Genome Data Viewer
Location:
9p21.3
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (21277688..21278563, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (21291856..21292731, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (21277687..21278562, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene interferon omega 1 pseudogene 5 Neighboring gene interferon alpha 14 Neighboring gene uncharacterized LOC107987053 Neighboring gene interferon alpha 5 Neighboring gene interferon alpha 20, pseudogene

Genomic regions, transcripts, and products

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.

RNA

  1. NR_036676.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL162420, V00539

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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    21277688..21278563 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    21291856..21292731 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_005640.4: Suppressed sequence

    Description
    NG_005640.4: This RefSeq was permanently suppressed because it is now thought that this gene is a transcribed pseudogene.