ENSG00000160202


Homo sapiens

Features
Gene ID: ENSG00000160202
  
Biological name :CRYAA
  
Synonyms : CRYAA / crystallin alpha A / P02489
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 21
Strand: 1
Band: q22.3
Gene start: 43169008
Gene end: 43172805
  
Corresponding Affymetrix probe sets: 210199_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000291554
Ensembl peptide - ENSP00000381201
Ensembl peptide - ENSP00000381200
NCBI entrez gene - 1409     See in Manteia.
OMIM - 123580
RefSeq - NM_000394
RefSeq - XM_005261093
RefSeq Peptide - NP_000385
swissprot - A0A140G945
swissprot - E9PHE4
swissprot - P02489
swissprot - E7EWH7
Ensembl - ENSG00000160202
  
Related genetic diseases (OMIM): 604219 - Cataract 9, multiple types, 604219
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
 cryaaENSDARG00000053502Danio rerio
 CRYAAENSGALG00000016199Gallus gallus
 CryaaENSMUSG00000024041Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
CRYAA2 / crystallin alpha A2ENSG00000276076100
CRYAB / P02511 / crystallin alpha BENSG0000010984653
HSPB6 / O14558 / heat shock protein family B (small) member 6ENSG0000000477640
HSPB1 / P04792 / heat shock protein family B (small) member 1ENSG0000010621139
HSPB2-C11orf52 / HSPB2-C11orf52 readthrough (NMD candidate)ENSG0000025444529
HSPB2 / Q16082 / heat shock protein family B (small) member 2ENSG0000017027629
HSPB8 / Q9UJY1 / heat shock protein family B (small) member 8ENSG0000015213725
HSPB3 / Q12988 / heat shock protein family B (small) member 3ENSG0000016927120


Protein motifs (from Interpro)
Interpro ID Name
 IPR001436  Alpha crystallin/Heat shock protein
 IPR002068  Alpha crystallin/Hsp20 domain
 IPR003090  Alpha-crystallin, N-terminal
 IPR008978  HSP20-like chaperone
 IPR012274  Alpha-crystallin, subunit A
 IPR031107  Small heat shock protein HSP20


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007601 visual perception IMP
 biological_processGO:0032387 negative regulation of intracellular transport IDA
 biological_processGO:0043066 negative regulation of apoptotic process IDA
 biological_processGO:0050821 protein stabilization IMP
 biological_processGO:0050896 response to stimulus IEA
 biological_processGO:0051260 protein homooligomerization IDA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005654 nucleoplasm IDA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005829 cytosol IDA
 cellular_componentGO:0070062 extracellular exosome HDA
 molecular_functionGO:0005212 structural constituent of eye lens IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0042802 identical protein binding IPI
 molecular_functionGO:0046872 metal ion binding IEA
 molecular_functionGO:0051082 unfolded protein binding IPI


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]
Show

 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]
Show

 HP:0000486 Strabismus "Strabismus (also known as squint) is a condition in which the eyes are not properly aligned with each other." [HPO:curators]
Show

 HP:0000501 Glaucoma "Glaucoma refers loss of retinal ganglion cells in a characteristic pattern of optic neuropathy usually associated with increased intraocular pressure." [HPO:curators]
Show

 HP:0000505 Impaired vision 
Show

 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]
Show

 HP:0000519 Congenital cataract "A congenital `cataract` (HP:0000518)." [HPO:probinson]
Show

 HP:0000545 Myopia 
Show

 HP:0000568 Microphthalmos "A developmental anomaly characterized by abnormal smallness of one or both eyes." [HPO:curators]
Show

 HP:0000612 Iris coloboma "A `coloboma` (HP:0000589) of the `iris` (FMA:58235)." [HPO:probinson]
Show

 HP:0000639 Nystagmus "Rhythmic, involuntary oscillations of one or both eyes related to abnormality in fixation, conjugate gaze, or vestibular mechanisms." [HPO:curators]
Show

 HP:0000646 Amblyopia "Reduced visual acuity that is uncorrectable by lenses in the absence of detectable anatomic defects in the eye or visual pathways. Ambylopia can result from visual deprivation during the critical period of development of visual abilities which lasts to about the age of 8 years. Thus, ambylopia can result from strabismus, anisometropia, or high hypermetropia in there is a failure to form a focused image in one or both eyes." [HPO:curators]
Show

 HP:0001131 Corneal dystrophy 
Show

 HP:0007834 Progressive cataracts 
Show

 HP:0007957 Variable degree of corneal opacities 
Show

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

0 s.

 
External programs and data are copyrighted by and are the property of their respective authors.
The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation


                   


© Olivier Tassy / Olivier Pourquie 2007-2024
contact: otassy@igbmc.fr