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Gene

FEZF2

FEZ family zinc finger 2

Summary

Cytogenetic location
3p14.2
Coordinates
Chromosome 3: 62,369,681–62,373,550 (GRCh38)
Exons
5 exons across 3.9 kb
Protein
459 amino acids
Also known as
FLJ10142, FKSG36, TOF, FEZL, Zfp312
Previous symbols
ZNF312
MANE Select transcript
ENST00000283268.8NM_018008.4
Locus type
Protein-coding
  • Very high
  • Confident
  • Low
  • Very low

Curated reports relevant to this gene

No Genome Test report reads FEZF2 yet. The test sequences your whole genome, so your data includes it all the same.

How FEZF2 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
Chromosome 3, with a bracket where FEZF2 sits. FEZF2 and 3 genes near it on chromosome 3, from 61,871,616 to 62,871,615.Chromosome 33p14.2p26.3p26.2p26.1p25.3p25.2p25.1p24.3p24.2p24.1p23p22.3p22.2p22.1p21.33p21.32p21.31p21.2p21.1p14.3p14.2p14.1p13p12.3p12.2p12.1p11.2p11.1q11.1q11.2q12.1q12.2q12.3q13.11q13.12q13.13q13.2q13.31q13.32q13.33q21.1q21.2q21.3q22.1q22.2q22.3q23q24q25.1q25.2q25.31q25.32q25.33q26.1q26.2q26.31q26.32q26.33q27.1q27.2q27.3q28q2962 Mb62.2 Mb62.4 Mb62.6 Mb62.8 MbPTPRG: 61,561,569–62,297,609, forward strandPTPRGCEP15: 62,319,001–62,336,213, forward strandCEP15FEZF2: 62,369,681–62,373,550, reverse strandFEZF2CADPS: 62,398,346–62,875,563, reverse strandCADPSDiagram of FEZF2: 5 exons on the reverse strand of chromosome 3Exon 5: 1 known disease-causing siteExon 5: 62,369,681–62,370,342, 662 basesExon 4: 62,371,217–62,371,349, 133 basesExon 3: 62,371,533–62,371,667, 135 basesExon 2: 62,372,017–62,372,926, 910 basesExon 1: 62,373,279–62,373,550, 272 bases543215′3′

Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.

Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).

Nearby genes from Ensembl release 116, on GRCh38.

Exons make up 2.1 kb of the gene's 3.9 kb; 1,380 of those bases code for the protein.

Sequencing FEZF2

5Low

How hard FEZF2 is to sequence with short reads, out of 100

  • Mappability0%
  • Homology0%
  • Repeats3.9%
  • GC content43%
  • Reference coverage0%

1

position in FEZF2 where ClinVar classes a change as pathogenic or likely pathogenic

None of them falls in a region short reads find hard.

A whole genome covers all 3.9 kb of FEZF2, introns included, not only the 2.1 kb of exons.

External links

Where this comes from

  • HGNC: the gene's symbol, name, other symbols and location.
  • MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
  • ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
  • The Genome in a Bottle genome stratifications, from NIST: the sequencing difficulty score.
  • Data release 2026.10.17-8666dff2.

Cite this page

APA

Dante Labs. (n.d.). FEZF2 gene: FEZ family zinc finger 2. Retrieved 17 October 2026, from https://dantelabs.com/genes/fezf2

Vancouver

Dante Labs. FEZF2 gene: FEZ family zinc finger 2 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/fezf2

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