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Gene

FRMD7

FERM domain containing 7

Summary

Cytogenetic location
Xq26.2
Coordinates
Chromosome X: 132,076,990–132,128,020 (GRCh38)
Exons
12 exons across 51 kb
Protein
714 amino acids
Also known as
FLJ43346
Previous symbols
NYS, NYS1
MANE Select transcript
ENST00000298542.9NM_194277.3
Locus type
Protein-coding
  • Very high
  • Confident
  • Low
  • Very low

Curated reports relevant to this gene

No Genome Test report reads FRMD7 yet. The test sequences your whole genome, so your data includes it all the same.

How FRMD7 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome X, with a bracket where FRMD7 sits. FRMD7 and 3 genes near it on chromosome X, from 131,602,505 to 132,602,504.Chromosome XXq26.2p22.33p22.32p22.31p22.2p22.13p22.12p22.11p21.3p21.2p21.1p11.4p11.3p11.23p11.22p11.21p11.1q11.1q11.2q12q13.1q13.2q13.3q21.1q21.2q21.31q21.32q21.33q22.1q22.2q22.3q23q24q25q26.1q26.2q26.3q27.1q27.2q27.3q28131.8 Mb132 Mb132.2 Mb132.4 Mb132.6 MbSTK26: 132,023,223–132,075,948, forward strandSTK26FRMD7: 132,076,990–132,128,020, reverse strandFRMD7RAP2C: 132,202,882–132,219,627, reverse strandRAP2CMBNL3: 132,369,320–132,490,155, reverse strandMBNL3Diagram of FRMD7: 12 exons on the reverse strand of chromosome XExon 12: 3 known disease-causing sitesExon 11: 1 known disease-causing siteExon 10: 1 known disease-causing siteExon 9: 6 known disease-causing sitesExon 7: 3 known disease-causing sitesExon 6: 1 known disease-causing siteExon 2: 1 known disease-causing siteExon 12: 132,076,990–132,078,966, 1,977 basesExon 11: 132,080,006–132,080,081, 76 basesExon 10: 132,080,198–132,080,266, 69 basesExon 9: 132,082,363–132,082,526, 164 basesExon 8: 132,084,490–132,084,585, 96 basesExon 7: 132,085,581–132,085,728, 148 basesExon 6: 132,085,920–132,086,034, 115 basesExon 5: 132,094,042–132,094,139, 98 basesExon 4: 132,097,266–132,097,344, 79 basesExon 3: 132,099,468–132,099,510, 43 basesExon 2: 132,100,612–132,100,716, 105 basesExon 1: 132,127,788–132,128,020, 233 bases1210864215′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 3.2 kb of the gene's 51 kb; 2,145 of those bases code for the protein.

Sequencing FRMD7

18

positions in FRMD7 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 51 kb of FRMD7, introns included, not only the 3.2 kb of exons.

Traits linked to FRMD7

The Human Phenotype Ontology lists these as features of the rare conditions FRMD7 can cause. Each trait's page lists the other genes linked to it.

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 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.). FRMD7 gene: FERM domain containing 7. Retrieved 17 October 2026, from https://dantelabs.com/genes/frmd7

Vancouver

Dante Labs. FRMD7 gene: FERM domain containing 7 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/frmd7

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