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FBXW4P1 F-box and WD repeat domain containing 4 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 26226, updated on 13-May-2022

Summary

Official Symbol
FBXW4P1provided by HGNC
Official Full Name
F-box and WD repeat domain containing 4 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:13609
See related
Ensembl:ENSG00000230701 AllianceGenome:HGNC:13609
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
FBW3; FBXW3; SHFM3P1
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Genomic context

See FBXW4P1 in Genome Data Viewer
Location:
22q11.23
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (23262767..23265005)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (23685630..23687868)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (23604954..23607192)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene BCR activator of RhoGEF and GTPase Neighboring gene BCR-ABL minor-breakpoint cluster region Neighboring gene Sharpr-MPRA regulatory region 5876 Neighboring gene RNA, 7SL, cytoplasmic 263, pseudogene Neighboring gene BCR-ABL p195 breakpoint cluster region Neighboring gene BCR-ABL p200 breakpoint cluster region

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Other Names

  • F-box and WD-40 domain protein 3
  • split hand/foot malformation (ectrodactyly) type 3 pseudogene 1

Clone Names

  • FLJ94893

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_033408.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AF174606, AI432341, BP385887, BX091573, U07000
    Related
    ENST00000426721.2

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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    23262767..23265005
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    23685630..23687868
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_005085.3: Suppressed sequence

    Description
    NG_005085.3: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.
  2. NG_027469.1: Suppressed sequence

    Description
    NG_027469.1: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.
  3. NM_012165.1: Suppressed sequence

    Description
    NM_012165.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.