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PFN1P2 profilin 1 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 767846, updated on 13-May-2022

Summary

Official Symbol
PFN1P2provided by HGNC
Official Full Name
profilin 1 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:24298
See related
Ensembl:ENSG00000270392 MIM:608609; AllianceGenome:HGNC:24298
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
COAS3; C1orf152
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Genomic context

See PFN1P2 in Genome Data Viewer
Location:
1p11.2
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (120432204..120434109, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (120445504..120447409, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (148735239..148737141, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene U1 spliceosomal RNA Neighboring gene uncharacterized LOC101929788 Neighboring gene NBPF member 8 Neighboring gene PDE4DIP pseudogene 2 Neighboring gene uncharacterized LOC107985524 Neighboring gene U2 spliceosomal RNA

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_003242.3 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC241952, BC137262
    Related
    ENST00000604437.2

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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    120432204..120434109 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_025791753.1 Reference GRCh38.p14 PATCHES

    Range
    49541..51445 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    120445504..120447409 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)