• Turnaround time:
    10–21 calendar days (14 days on average)
  • Preferred specimen:
    3mL whole blood in a purple-top tube
  • Alternate specimens:
    DNA or saliva/assisted saliva
  • Sample requirements
  • Request a sample kit




Associated disorders

The CRYGB gene currently has no well-established disease association; however, there is limited evidence supporting a correlation with autosomal dominant Congenital Cataracts (MedGen UID: 815130)

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Invitae tests that include this gene:

The CRYGB gene encodes the gamma-crystallin B protein. In the eye, crystallins are water soluble structural proteins accounting for 90% of lens proteins. Crystallins form protein-protein complexes with each other and with other crystallin proteins. These aggregates are crucial for the maintenance of lens clarity and refractive index/focusing of light by the lens. Alpha crystallins (CRYAA and CRYAB) are members of the small heat-shock protein family with chaperone-like properties that protect the eye by cellular tolerance to stress and damage (PMID: 17166758, 23288985).

Assay and technical information

Invitae is a College of American Pathologists (CAP)-accredited and Clinical Laboratory Improvement Amendments (CLIA)-certified clinical diagnostic laboratory performing full-gene sequencing and deletion/duplication analysis using next-generation sequencing technology (NGS).

Our sequence analysis covers clinically important regions of each gene, including coding exons, +/- 10 base pairs of adjacent intronic sequence in the transcript listed below. In addition, analysis covers the select non-coding variants specifically defined in the table below. Any variants that fall outside these regions are not analyzed. Any specific limitations in the analysis of these genes are also listed in the table below.

Our analysis detects most intragenic deletions and duplications at single exon resolution. However, in rare situations, single-exon copy number events may not be analyzed due to inherent sequence properties or isolated reduction in data quality. If you are requesting the detection of a specific single-exon copy number variation, please contact Client Services before placing your order.

Gene Transcript reference Sequencing analysis Deletion/Duplication analysis
CRYGB NM_005210.3