CRYBB3 Chromosome 22
Crystallin beta B3
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What This Gene Does
Crystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. Since lens central fiber cells lose their nuclei during development, these crystallins are made and then retained throughout life, making them extremely stable proteins. Mammalian lens crystallins are divided into alpha, beta, and gamma families; beta and gamma crystallins are also considered as a superfamily. Alpha and beta families are further divided into acidic and basic groups. Seven protein regions exist in crystallins: four homologous motifs, a connecting peptide, and N- and C-terminal extensions. Beta-crystallins, the most heterogeneous, differ by the presence of the C-terminal extension (present in the basic group, none in the acidic group). Beta-crystallins form aggregates of different sizes and are able to self-associate to form dimers or to form heterodimers with other beta-crystallins. This gene, a beta basic group member, is part of a gene cluster with beta-A4, beta-B1, and beta-B2. Mutations in this gene result in cataract congenital nuclear autosomal recessive type 2. [provided by RefSeq, Feb 2013]
Gene Info
Gene Group
Beta-gamma crystallins
Locus Type
gene with protein product
Location
22q11.23
Ensembl
ENSG00000100053
Associated Conditions (13)
Cataract 22 multiple types
Inborn genetic diseases
CRYBB3-related disorder
Gastric cancer
Ovarian serous cystadenocarcinoma
Thyroid cancer
nonmedullary
1
Hepatocellular carcinoma
Clear cell carcinoma of kidney
Developmental cataract
Microphthalmia
Cataract
Key Variants
RS113872601
Conflicting classifications of pathogenicity
Cataract 22 multiple types, Inborn genetic diseases, Cataract 22 multiple types
Health Risk
RS1203386884
Conflicting classifications of pathogenicity
Cataract 22 multiple types, Cataract 22 multiple types
Health Risk
RS142996620
Conflicting classifications of pathogenicity
Cataract 22 multiple types, Inborn genetic diseases, Cataract 22 multiple types
Health Risk
RS143187630
Conflicting classifications of pathogenicity
Cataract 22 multiple types, Cataract 22 multiple types
Health Risk
RS145770544
Conflicting classifications of pathogenicity
Cataract 22 multiple types, Inborn genetic diseases, Cataract 22 multiple types
Health Risk
RS147328317
Conflicting classifications of pathogenicity
Cataract 22 multiple types, CRYBB3-related disorder, Cataract 22 multiple types
Health Risk
RS147831812
Conflicting classifications of pathogenicity
Cataract 22 multiple types, Inborn genetic diseases, Gastric cancer
Health Risk
RS147937174
Conflicting classifications of pathogenicity
Cataract 22 multiple types, Cataract 22 multiple types
Health Risk
RS200457939
Conflicting classifications of pathogenicity
Cataract 22 multiple types, Inborn genetic diseases, Cataract 22 multiple types
Health Risk
RS201863246
Conflicting classifications of pathogenicity
Cataract 22 multiple types, Cataract 22 multiple types
Health Risk
RS199791142
Likely pathogenic
Cataract 22 multiple types, Cataract 22 multiple types
Health Risk
RS864309700
Likely pathogenic
Developmental cataract, Developmental cataract
Health Risk
All Variants (15)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS113872601 | Health Risk | Conflicting classifications of pathogenicity | Cataract 22 multiple types, Inborn genetic diseases, Cataract 22 multiple types |
| RS1203386884 | Health Risk | Conflicting classifications of pathogenicity | Cataract 22 multiple types, Cataract 22 multiple types |
| RS142996620 | Health Risk | Conflicting classifications of pathogenicity | Cataract 22 multiple types, Inborn genetic diseases, Cataract 22 multiple types |
| RS143187630 | Health Risk | Conflicting classifications of pathogenicity | Cataract 22 multiple types, Cataract 22 multiple types |
| RS145770544 | Health Risk | Conflicting classifications of pathogenicity | Cataract 22 multiple types, Inborn genetic diseases, Cataract 22 multiple types |
| RS147328317 | Health Risk | Conflicting classifications of pathogenicity | Cataract 22 multiple types, CRYBB3-related disorder, Cataract 22 multiple types |
| RS147831812 | Health Risk | Conflicting classifications of pathogenicity | Cataract 22 multiple types, Inborn genetic diseases, Gastric cancer |
| RS147937174 | Health Risk | Conflicting classifications of pathogenicity | Cataract 22 multiple types, Cataract 22 multiple types |
| RS200457939 | Health Risk | Conflicting classifications of pathogenicity | Cataract 22 multiple types, Inborn genetic diseases, Cataract 22 multiple types |
| RS201863246 | Health Risk | Conflicting classifications of pathogenicity | Cataract 22 multiple types, Cataract 22 multiple types |
| RS199791142 | Health Risk | Likely pathogenic | Cataract 22 multiple types, Cataract 22 multiple types |
| RS864309700 | Health Risk | Likely pathogenic | Developmental cataract, Developmental cataract |
| RS1432148373 | Health Risk | Pathogenic | Microphthalmia, Cataract, Microphthalmia |
| RS587777601 | Health Risk | Pathogenic | Cataract 22 multiple types, Cataract 22 multiple types |
| RS74315490 | Health Risk | Pathogenic | Developmental cataract, Cataract 22 multiple types, Developmental cataract |