CRYBA1 Gene Summary [Human]

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 acidic group member, encodes two proteins (crystallin, beta A3 and crystallin, beta A1) from a single mRNA, the latter protein is 17 aa shorter than crystallin, beta A3 and is generated by use of an alternate translation initiation site. Deletion of exons 3 and 4 causes the autosomal dominant disease 'zonular cataract with sutural opacities'. [provided by RefSeq, Jul 2008]

Details

Type
Protein Coding
Official Symbol
CRYBA1
Official Name
crystallin beta A1 [Source:HGNC Symbol;Acc:HGNC:2394]
Ensembl ID
ENSG00000108255
Bio databases IDs NCBI: 1411 Ensembl: ENSG00000108255
Aliases crystallin beta A1, eye lens structural protein
Synonyms BA3/A1, BA3A1C, beta-A3, CCZS, Cryb, CRYB1, crystallin beta A1, crystallin, beta A1, crystallin β A1, crystallin, β A1, Crystallin β A3, CTRCT10, β-A3
Species
Human, Homo sapiens
OrthologiesMouseRat

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in human CRYBA1 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • structural constituent of eye lens
  • greek key motif
  • protein binding
  • identical protein binding
  • Beta/Gamma crystallin

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • high myopia
  • hereditary disorder
  • congenital zonular cataract with sutural opacities 10
  • cataract disease
  • exfoliative glaucoma
  • major depression
  • multiple types cataract 10
  • congenital cataract
regulated by
role in cell
  • apoptosis
  • autophagy by
  • phagocytosis by

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Cytoplasm

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the human CRYBA1 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • negative regulation of ERK1 and ERK2 cascade
  • regulation of autophagy
  • phagocytosis
  • positive regulation of anoikis
  • negative regulation of TOR signaling cascade
  • visual perception
  • negative regulation of cytokine production
  • lens development in camera-type eye
  • negative regulation of protein kinase B signaling cascade

Cellular Component

Where in the cell the gene product is active
  • nucleus
  • cytoplasm

Molecular Function

What the gene product does at the molecular level
  • protein binding
  • structural constituent of eye lens

Gene-Specific Assays for Results You Can Trust

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