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ZNRF2P1 zinc and ring finger 2 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 441208, updated on 13-May-2022

Summary

Official Symbol
ZNRF2P1provided by HGNC
Official Full Name
zinc and ring finger 2 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:42792
See related
AllianceGenome:HGNC:42792
Gene type
pseudo
RefSeq status
PROVISIONAL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See ZNRF2P1 in Genome Data Viewer
Location:
7p14.3
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (32727950..32729983)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (32867570..32869576)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (32767562..32769595)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene LSM5 homolog, U6 small nuclear RNA and mRNA degradation associated Neighboring gene AVL9 cell migration associated Neighboring gene DPY19L1 pseudogene 1 Neighboring gene microRNA 550a-2 Neighboring gene microRNA 550b-2 Neighboring gene long intergenic non-protein coding RNA 997

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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_003502.2 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC018645

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_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    32727950..32729983
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    32867570..32869576
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001013723.1: Suppressed sequence

    Description
    NM_001013723.1: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.