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FRMD8P1 FERM domain containing 8 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 83957, updated on 13-May-2022

Summary

Official Symbol
FRMD8P1provided by HGNC
Official Full Name
FERM domain containing 8 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:24690
See related
Ensembl:ENSG00000227942 AllianceGenome:HGNC:24690
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
Predicted to be involved in negative regulation of canonical Wnt signaling pathway. Predicted to be located in cytoskeleton. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

See FRMD8P1 in Genome Data Viewer
Location:
Xq12
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (65550622..65552421, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (63977061..63978860, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (64770502..64772301, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene zinc finger CCCH-type containing 12B Neighboring gene AP1M2 pseudogene 1 Neighboring gene LAS1 like ribosome biogenesis factor Neighboring gene moesin Neighboring gene Nanog homeobox pseudogene 9

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Other Names

  • FERM domain-containing protein 8 pseudogene
  • FKSG43
  • Putative FERM domain-containing protein FRMD8P1

Clone Names

  • MGC149236

Gene Ontology Provided by GOA

Process Evidence Code Pubs
involved_in negative regulation of canonical Wnt signaling pathway IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Component Evidence Code Pubs
located_in cytoskeleton IEA
Inferred from Electronic Annotation
more info
 
is_active_in plasma membrane IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 

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_033742.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL050306, BC128150
    Related
    ENST00000440433.1

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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    65550622..65552421 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    63977061..63978860 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_004716.3: Suppressed sequence

    Description
    NG_004716.3: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.
  2. NG_026711.1: Suppressed sequence

    Description
    NG_026711.1: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.
  3. NM_032033.1: Suppressed sequence

    Description
    NM_032033.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.