Details for: FEZF2

Gene ID: 55079

Symbol: FEZF2

Ensembl ID: ENSG00000153266

Description: FEZ family zinc finger 2

Associated with

  • Axonal fasciculation
    (GO:0007413)
  • Cell dedifferentiation
    (GO:0043697)
  • Cerebral cortex gabaergic interneuron migration
    (GO:0021853)
  • Chromatin binding
    (GO:0003682)
  • Commitment of neuronal cell to specific neuron type in forebrain
    (GO:0021902)
  • Dendrite development
    (GO:0016358)
  • Dentate gyrus development
    (GO:0021542)
  • Dna-binding transcription activator activity, rna polymerase ii-specific
    (GO:0001228)
  • Dna-binding transcription repressor activity, rna polymerase ii-specific
    (GO:0001227)
  • Forebrain anterior/posterior pattern specification
    (GO:0021797)
  • Locomotory behavior
    (GO:0007626)
  • Metal ion binding
    (GO:0046872)
  • Negative regulation of cell population proliferation
    (GO:0008285)
  • Negative regulation of neuron differentiation
    (GO:0045665)
  • Negative regulation of transcription by rna polymerase ii
    (GO:0000122)
  • Neuron fate determination
    (GO:0048664)
  • Nucleus
    (GO:0005634)
  • Positive regulation of neuron differentiation
    (GO:0045666)
  • Positive regulation of transcription by rna polymerase ii
    (GO:0045944)
  • Regulation of axon guidance
    (GO:1902667)
  • Regulation of gene expression
    (GO:0010468)
  • Regulation of neurogenesis
    (GO:0050767)
  • Rna polymerase ii cis-regulatory region sequence-specific dna binding
    (GO:0000978)

Other Information

Genular Protein ID: 2683212799

Symbol: FEZF2_HUMAN

Name: Fez family zinc finger protein 2

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 21220648

Title: Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosis.

PubMed ID: 21220648

DOI: 10.1001/archneurol.2010.351

Sequence Information:

  • Length: 459
  • Mass: 48811
  • Checksum: F1C9A512C7F0FEAF
  • Sequence:
  • MASSASLETM VPPACPRAGA SPATSKTLAF SIERIMAKTS EPRAPFEPRP GALEADGSQG 
    KKLLNLCSPL PCMIPLQPLG YEVPSKTLLS YSELWKSSLR AGGGGGGGGG GGGGGGGAPV 
    CGASGLCKTN CGVCCKAELG LAPSALPAGR VIKPQVINQA VGLPASGSLY YFNYLDSTAY 
    PPSELLSGHL FPSGLLNAQA PAALAAHPKL FLLENAKLAG LAADKFPHPA PYPHKERLPA 
    PLEQVLKENS ALTAERGGVK GHSKLPGGSA DGKPKNFTCE VCGKVFNAHY NLTRHMPVHT 
    GARPFVCKVC GKGFRQASTL CRHKIIHTQE KPHKCNQCGK AFNRSSTLNT HIRIHAGYKP 
    FVCEFCGKGF HQKGNYKNHK LTHSGEKQYK CTICNKAFHQ VYNLTFHMHT HNDKKPFTCA 
    TCGKGFCRNF DLKKHVRKLH DSVGPAAPSA KDLTRTVQS

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.