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ZNF322P1 zinc finger protein 322 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 387328, updated on 13-May-2022

Summary

Official Symbol
ZNF322P1provided by HGNC
Official Full Name
zinc finger protein 322 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:14003
See related
AllianceGenome:HGNC:14003
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
ZNF322; ZNF322B
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Genomic context

See ZNF322P1 in Genome Data Viewer
Location:
9q22.33
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (97195351..97200145, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (109367122..109371915, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (99957633..99962427, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC112268050 Neighboring gene Sharpr-MPRA regulatory region 737 Neighboring gene ankyrin repeat domain 18C, pseudogene Neighboring gene RNA, U6 small nuclear 798, pseudogene Neighboring gene uncharacterized LOC107987025 Neighboring gene uncharacterized LOC124902224

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.

Genomic

  1. NG_032063.1 

    Range
    101..4895
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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
    97195351..97200145 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    109367122..109371915 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_199005.1: Suppressed sequence

    Description
    NM_199005.1: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.
  2. NR_002831.2: Suppressed sequence

    Description
    NR_002831.2: This RefSeq was permanently suppressed because it was primarily UTR sequence.