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Gene

CRYGC

crystallin gamma C

Summary

Cytogenetic location
2q33.3
Coordinates
Chromosome 2: 208,128,137–208,129,828 (GRCh38)
Exons
3 exons across 1.7 kb
Protein
174 amino acids
Previous symbols
CRYG3
MANE Select transcript
ENST00000282141.4NM_020989.4
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 CRYGC yet. The test sequences your whole genome, so your data includes it all the same.

How CRYGC is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
Chromosome 2, with a bracket where CRYGC sits. CRYGC and 10 genes near it on chromosome 2, from 207,628,983 to 208,628,982.Chromosome 22q33.3p25.3p25.2p25.1p24.3p24.2p24.1p23.3p23.2p23.1p22.3p22.2p22.1p21p16.3p16.2p16.1p15p14p13.3p13.2p13.1p12p11.2p11.1q11.1q11.2q12.1q12.2q12.3q13q14.1q14.2q14.3q21.1q21.2q21.3q22.1q22.2q22.3q23.1q23.2q23.3q24.1q24.2q24.3q31.1q31.2q31.3q32.1q32.2q32.3q33.1q33.2q33.3q34q35q36.1q36.2q36.3q37.1q37.2q37.3207.8 Mb208 Mb208.2 Mb208.4 Mb208.6 MbCCNYL1: 207,711,515–207,761,839, forward strandCCNYL1FZD5: 207,762,598–207,769,914, reverse strandFZD5PLEKHM3: 207,821,288–208,025,846, reverse strandPLEKHM3CRYGD: 208,121,607–208,124,595, reverse strandCRYGDCRYGC: 208,128,137–208,129,828, reverse strandCRYGCCRYGB: 208,142,573–208,146,163, reverse strandCRYGBCRYGA: 208,160,740–208,163,589, reverse strandCRYGAC2orf80: 208,165,343–208,190,245, reverse strandIDH1: 208,236,224–208,266,095, reverse strandIDH1PIKFYVE: 208,266,229–208,358,755, forward strandPIKFYVEPTH2R: 208,359,714–208,854,503, forward strandPTH2RDiagram of CRYGC: 3 exons on the reverse strand of chromosome 2Exon 3: 4 known disease-causing sitesExon 3: 208,128,137–208,128,475, 339 basesExon 2: 208,129,441–208,129,683, 243 basesExon 1: 208,129,784–208,129,828, 45 bases3215′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 0.6 kb of the gene's 1.7 kb; 525 of those bases code for the protein.

How a genome test reads CRYGC

4

positions in CRYGC 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 1.7 kb of CRYGC, introns included, not only the 0.6 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.). CRYGC gene: crystallin gamma C. Retrieved 17 October 2026, from https://dantelabs.com/genes/crygc

Vancouver

Dante Labs. CRYGC gene: crystallin gamma C [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/crygc

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