CRYAA2 (crystallin alpha A2)

2018-11-01  

Identity

HGNC
CRYAA2
LOCATION
21q22.3
LOCUSID
102724652
ALIAS
CRYAA

Other Information

Locus ID:

NCBI: 102724652
HGNC: 51901
Ensembl: ENSG00000276076

Variants:

dbSNP: 102724652
ClinVar: 102724652
TCGA: ENSG00000276076
COSMIC: CRYAA2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000276076ENST00000619537A0A140G945
ENSG00000276076ENST00000624019A0A096LPJ9
ENSG00000276076ENST00000624932A0A140G945

Pathways

PathwaySourceExternal ID
Protein processing in endoplasmic reticulumKEGGko04141
Protein processing in endoplasmic reticulumKEGGhsa04141

Protein levels (Protein atlas)

Not detected
Low
Medium
High
cerebral cortex
cerebellum
hippocampus
caudate
eye
thyroid gland
parathyroid gland
adrenal gland
nasopharynx
bronchus
lung
oral mucosa
salivary gland
esophagus
stomach 1
stomach 2
duodenum
small intestine
colon
rectum
liver
gallbladder
pancreas
kidney
urinary bladder
testis
epididymis
seminal vesicle
prostate
vagina
ovary
fallopian tube
endometrium 1
endometrium 2
cervix, uterine
placenta
breast
heart muscle
smooth muscle
skeletal muscle
soft tissue 1
soft tissue 2
adipose tissue
skin 1
skin 2
appendix
spleen
lymph node
tonsil
bone marrow

References

Pubmed IDYearTitleCitations
284757012017CRISPR/Cas9-Mediated Mutation of αA-Crystallin Gene Induces Congenital Cataracts in Rabbits.0

Citation

Dessen P

CRYAA2 (crystallin alpha A2)

Atlas Genet Cytogenet Oncol Haematol. 2018-11-01

Online version: http://atlasgeneticsoncology.org/gene/80435/cryaa2