ENSG00000244752


Homo sapiens

Features
Gene ID: ENSG00000244752
  
Biological name :CRYBB2
  
Synonyms : CRYBB2 / crystallin beta B2 / P43320
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 22
Strand: 1
Band: q11.23
Gene start: 25219522
Gene end: 25231869
  
Corresponding Affymetrix probe sets: 206777_s_at (Human Genome U133 Plus 2.0 Array)   206778_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000381273
NCBI entrez gene - 1415     See in Manteia.
OMIM - 123620
RefSeq - XM_011529900
RefSeq - NM_000496
RefSeq - XM_006724141
RefSeq Peptide - NP_000487
swissprot - R4UMM2
swissprot - P43320
Ensembl - ENSG00000244752
  
Related genetic diseases (OMIM): 601547 - Cataract 3, multiple types, 601547
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 crybb2ENSDARG00000053512Danio rerio
 CRYBB2ENSGALG00000026086Gallus gallus
 Crybb2ENSMUSG00000042240Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
CRYBB3 / P26998 / crystallin beta B3ENSG0000010005355
CRYBB1 / P53674 / crystallin beta B1ENSG0000010012253
CRYBA1 / P05813 / crystallin beta A1ENSG0000010825541
CRYBA4 / P53673 / crystallin beta A4ENSG0000019643138
CRYBA2 / P53672 / crystallin beta A2ENSG0000016349935
CRYGC / P07315 / crystallin gamma CENSG0000016325431
CRYGS / P22914 / crystallin gamma SENSG0000021313931
CRYGD / P07320 / crystallin gamma DENSG0000011823130
CRYGA / P11844 / crystallin gamma AENSG0000016858230
CRYGB / P07316 / crystallin gamma BENSG0000018218730
CRYGN / Q8WXF5 / crystallin gamma NENSG0000012737721


Protein motifs (from Interpro)
Interpro ID Name
 IPR001064  Beta/gamma crystallin
 IPR011024  Gamma-crystallin-like
 IPR033058  Beta-crystallin B2


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007601 visual perception TAS
 biological_processGO:0043010 camera-type eye development IEA
 biological_processGO:0050896 response to stimulus IEA
 molecular_functionGO:0005198 structural molecule activity NAS
 molecular_functionGO:0005212 structural constituent of eye lens IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0042802 identical protein binding IPI
 molecular_functionGO:0042803 protein homodimerization activity IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
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 HP:0000482 Microcornea "A congenital abnormality of the `cornea` (FMA:58238) in which the cornea and the anterior segment of the eye are smaller than normal. The horizontal diameter of the cornea does not reach 10 mm even in adulthood." [HPO:probinson]
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 HP:0000518 Cataract "A cataract is an opacity or clouding that develops in the crystalline `lens` (FMA:58241) of the eye or in its `capsule` (FMA:58881)." [HPO:probinson]
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 HP:0000519 Congenital cataract "A congenital `cataract` (HP:0000518)." [HPO:probinson]
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 HP:0000545 Myopia 
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 HP:0000612 Iris coloboma "A `coloboma` (HP:0000589) of the `iris` (FMA:58235)." [HPO:probinson]
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 HP:0000639 Nystagmus "Rhythmic, involuntary oscillations of one or both eyes related to abnormality in fixation, conjugate gaze, or vestibular mechanisms." [HPO:curators]
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 HP:0001131 Corneal dystrophy 
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 HP:0007957 Variable degree of corneal opacities 
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 HP:0007976 Cerulean cataracts "Cerulean cataracts are a kind of `congenital cataract` (HP:0000519) having peripheral bluish and white opacifications in concentric layers with occasional central lesions arranged radially. Although the opacities may be observed during fetal development and childhood, usually visual acuity is only mildly reduced until adulthood, when lens extraction is generally necessary." [HPO:probinson, pmid:19496508, pmid:9158139]
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 HP:0010695 Sutural cataract "A type of `congenital cataract` (HP:0000519) in which the opacity follows the anterior or posterior Y suture." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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