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CFL1P1 cofilin 1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 142913, updated on 25-Oct-2022

Summary

Official Symbol
CFL1P1provided by HGNC
Official Full Name
cofilin 1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:28560
See related
Ensembl:ENSG00000290782 AllianceGenome:HGNC:28560
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
CFLP1
Expression
Low expression observed in reference dataset See more
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Genomic context

See CFL1P1 in Genome Data Viewer
Location:
10q23.31
Exon count:
4
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (87818313..87845612)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (88702221..88729514)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (89578070..89605369)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene 3'-phosphoadenosine 5'-phosphosulfate synthase 2 Neighboring gene uncharacterized LOC124902476 Neighboring gene ATPase family AAA domain containing 1 Neighboring gene Sharpr-MPRA regulatory region 3344 Neighboring gene RNA, 7SL, cytoplasmic 78, pseudogene Neighboring gene killin, p53 regulated DNA replication inhibitor Neighboring gene phosphatase and tensin homolog Neighboring gene ribosomal protein L11 pseudogene 3

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

General gene information

Markers

Other Names

  • cofilin 1 (non-muscle) pseudogene 1
  • cofilin pseudogene 1

Clone Names

  • MGC35136

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_028492.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    BC031631
    Related
    ENST00000438248.1

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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    87818313..87845612
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_013171807.1 Reference GRCh38.p14 PATCHES

    Range
    34135..61434
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    88702221..88729514
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_004788.2: Suppressed sequence

    Description
    NG_004788.2: This RefSeq was permanently suppressed because it is now thought that this gene is a transcribed pseudogene.
  2. NM_152427.1: Suppressed sequence

    Description
    NM_152427.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.