Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3021 to 3030 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3021
Cryptochrome circadian regulator 2
HCRY2, PHLL2
Alzheimer disease, Bipolar disorder, Major depressive disorder, Seasonal affective disorder, Diabetes mellitus type 2

3022
Crystallin alpha A
CRYA1, CTRCT9, HSPB4
Androgenetic alopecia, Ankylosing spondylitis, Autoimmune disease, Cataract, Cataract-microcornea syndrome, Congenital cataract, Congenital total cataract, Anterior polar cataract, Lamellar cataract, Nuclear cataract, Schizophrenia, Uveitis

3023
Crystallin alpha B
CMD1II, CRYA2, CTPP2, CTRCT16, HEL-S-101, HSPB5, MFM2, MFM2A, MFM2B
Renal cell carcinoma, Squamous cell carcinoma, Cardiomyopathy, Dilated cardiomyopathy, Cataract, Colonic neoplasms, Congenital cataract, Degenerative disorder, Lamellar cataract, Nuclear cataract, Posterior polar cataract, Esophageal neoplasms, Hypertrophic cardiomyopathy, Liver cirrhosis, Mouth neoplasms
View all (5 more)

3024
Crystallin beta A1
CRYB1, CTRCT10
Cataract, Congenital cataract, Lamellar cataract, Nuclear cataract, Posterior polar cataract, Sutural cataract, Major depressive disorder, Posterior subcapsular cataract, Diabetes mellitus type 2

3025
Crystallin beta A2
CTRCT42
Cataract, Congenital cataract, Coronary artery disease, Anterior polar cataract, Nuclear cataract, Diabetes mellitus type 2

3026
Crystallin beta A4
CTRCT23, CYRBA4, MCOPCT4
Anophthalmia/microphthalmia-esophageal atresia syndrome, Cataract-microcornea syndrome, Cataract, Congenital cataract, Crohn disease, Lamellar cataract, Inflammatory bowel disease, Schizophrenia, Ulcerative colitis

3027
Crystallin beta B1
CATCN3, CTRCT17
Bipolar disorder, Cataract, Cataract-microcornea syndrome, Congenital cataract, Nuclear cataract, Major depressive disorder, Schizophrenia, Specific language disorder

3028
Crystallin beta B2
CCA2, CRYB2, CRYB2A, CTRCT3, D22S665
Alzheimer disease, Ankylosing spondylitis, Autoimmune disease, Cataract-microcornea syndrome, Cataract, Congenital cataract, Color vision deficiency, Congenital total cataract, Cystitis, Nuclear cataract, Posterior subcapsular cataract, Sutural cataract, Uveitis

3029
Crystallin beta B3
CATCN2, CRYB3, CTRCT22
Cataract, Congenital cataract, Cystitis, Anterior polar cataract, Non-syndromic cataract, Nuclear cataract, Embryonal nuclear cataract, Microphthalmos

3030
Crystallin beta-gamma domain containing 1
AIM1, ST4
Alzheimer disease, Exostoses, Melanoma, Stroke