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Gene

FKBP14

FKBP prolyl isomerase 14

Summary

Cytogenetic location
7p14.3
Coordinates
Chromosome 7: 30,010,587–30,026,702 (GRCh38)
Exons
4 exons across 16.1 kb
Protein
211 amino acids
Also known as
FLJ20731, FKBP22
MANE Select transcript
ENST00000222803.10NM_017946.4
Locus type
gene with protein product
  • Very high
  • Confident
  • Low
  • Very low

Reference genomeGRCh38

Positions on gene and variant pages follow this choice, in this browser.

Curated report relevant to this gene

How FKBP14 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 7, with a bracket where FKBP14 sits. FKBP14 and 10 genes near it on chromosome 7, from 29,518,645 to 30,518,644.Chromosome 77p14.3p22.3p22.2p22.1p21.3p21.2p21.1p15.3p15.2p15.1p14.3p14.2p14.1p13p12.3p12.2p12.1p11.2p11.1q11.1q11.21q11.22q11.23q21.11q21.12q21.13q21.2q21.3q22.1q22.2q22.3q31.1q31.2q31.31q31.32q31.33q32.1q32.2q32.3q33q34q35q36.1q36.2q36.329.6 Mb29.8 Mb30 Mb30.2 Mb30.4 MbPRR15: 29,563,775–29,568,145, forward strandPRR15WIPF3: 29,806,447–29,917,061, forward strandWIPF3SCRN1: 29,920,103–29,990,289, reverse strandSCRN1FKBP14: 30,010,587–30,026,702, reverse strandFKBP14PLEKHA8: 30,027,404–30,130,483, forward strandPLEKHA8MTURN: 30,134,728–30,162,765, forward strandMTURNZNRF2: 30,284,413–30,371,239, forward strandZNRF2: 30,362,400–30,412,502, forward strandNOD1: 30,424,527–30,478,914, reverse strandNOD1GGCT: 30,496,616–30,504,866, reverse strandGGCT: 30,497,077–30,550,761, reverse strandDiagram of FKBP14: 4 exons on the reverse strand of chromosome 7Exon 4: 3 known disease-causing sitesExon 3: 3 known disease-causing sitesExon 2: 3 known disease-causing sitesExon 1: 6 known disease-causing sitesExon 4: 30,010,587–30,014,893, 4,307 basesExon 3: 30,018,996–30,019,123, 128 basesExon 2: 30,022,665–30,022,816, 152 basesExon 1: 30,026,312–30,026,702, 391 bases43215′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 5 kb of the gene's 16.1 kb; 636 of those bases code for the protein.

How a genome test reads FKBP14

18

positions in FKBP14 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 16.1 kb of FKBP14, introns included, not only the 5 kb of exons.

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.
  • GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
  • The ACMG secondary findings list, SF v3.2.
  • ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
  • The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
  • Data release 2026.10.16-c6eea6bf.

Cite this page

APA

Dante Labs. (n.d.). FKBP14 gene: FKBP prolyl isomerase 14. Retrieved 16 October 2026, from https://dantelabs.com/genes/fkbp14

Vancouver

Dante Labs. FKBP14 gene: FKBP prolyl isomerase 14 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/fkbp14

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