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Gene

FAM20C

FAM20C golgi associated secretory pathway kinase

Summary

Cytogenetic location
7p22.3
Coordinates
Chromosome 7: 192,571–260,772 (GRCh38)
Exons
10 exons across 68.2 kb
Protein
584 amino acids
Also known as
IMAGE:4942737, DKFZp547D065, DMP4, G-CK
MANE Select transcript
ENST00000313766.6NM_020223.4
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 reports relevant to this gene

No Genome Test report reads FAM20C yet. The test sequences your whole genome, so your data includes it all the same.

How FAM20C 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 FAM20C sits. FAM20C and 3 genes near it on chromosome 7, from 1 to 726,671.Chromosome 77p22.3p22.3p22.2p22.1p21.3p21.2p21.1p15.3p15.2p15.1p14.3p14.2p14.1p13p12.3p12.2p12.1p11.2p11.1q11.1q11.21q11.22q11.23q21.11q21.12q21.13q21.2q21.3q22.1q22.2q22.3q31.1q31.2q31.31q31.32q31.33q32.1q32.2q32.3q33q34q35q36.1q36.2q36.30.1 Mb0.2 Mb0.3 Mb0.4 Mb0.5 Mb0.6 Mb0.7 MbFAM20C: 192,571–260,772, forward strandFAM20CFOXL3: 290,170–294,422, forward strandFOXL3PDGFA: 497,258–520,705, reverse strandPDGFAPRKAR1B: 549,195–728,268, reverse strandPRKAR1BDiagram of FAM20C: 10 exons on the forward strand of chromosome 7Exon 1: 2 known disease-causing sitesExon 7: 2 known disease-causing sitesExon 8: 1 known disease-causing siteExon 9: 1 known disease-causing siteExon 1: 192,571–193,804, 1,234 basesExon 2: 195,554–195,732, 179 basesExon 3: 208,898–208,976, 79 basesExon 4: 246,415–246,507, 93 basesExon 5: 248,315–248,430, 116 basesExon 6: 255,849–256,029, 181 basesExon 7: 256,654–256,763, 110 basesExon 8: 257,005–257,086, 82 basesExon 9: 258,646–258,705, 60 basesExon 10: 259,731–260,772, 1,042 bases12468105′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 68.2 kb; 1,755 of those bases code for the protein.

How a genome test reads FAM20C

6

positions in FAM20C 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 68.2 kb of FAM20C, introns included, not only the 3.2 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.
  • 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.). FAM20C gene: FAM20C golgi associated secretory pathway kinase. Retrieved 17 October 2026, from https://dantelabs.com/genes/fam20c

Vancouver

Dante Labs. FAM20C gene: FAM20C golgi associated secretory pathway kinase [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/fam20c

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