Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
3021 to 3030 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3021
Crystallin gamma C
CCL, CRYG3, CTRCT2
Attention deficit hyperactivity disorder, Cataract, Cataract-microcornea syndrome, Congenital cataract, Lamellar cataract, Nuclear cataract

3022
Crystallin gamma D
CACA, CCA3, CCP, CRYG4, CTRCT4, PCC, cry-g-D
Cataract, Cataract-microcornea syndrome, Congenital cataract, Coralliform cataract, Lamellar cataract, Nuclear cataract, Hepatomegaly, Myopia

3023
Crystallin gamma N
-
Coronary artery disease

3024
Crystallin gamma S
CRYG8, CTRCT20
Cataract, Congenital cataract, Lamellar cataract, Sutural cataract, Retinitis pigmentosa

3025
Crystallin lambda 1
GDH, HEL30, gul3DH, lambda-CRY
Astrocytoma, Breast cancer, Central nervous system cancer, Deafness, Glioblastoma, Glioma, Hearing loss, Obesity, Prostatic neoplasms

3026
Crystallin mu
DFNA40, THBP
Isolated sensorineural deafness, Nonsyndromic hearing loss, Congestive heart failure, Deafness, Heart failure, Pelvic organ prolapse

3027
Crystallin zeta
-
Autism

3028
Crystallin zeta like 1
4P11, FERRY4, Fy-4, QOH-1
Crohn disease, Inflammatory bowel disease

3029
CRYZL2P-SEC16B readthrough
-
Breast cancer, Color vision deficiency, Insomnia, Metabolic syndrome, Osteoarthritis, Scoliosis, Diabetes mellitus type 2

3030
Citrate synthase
-
Eczema, Cardiomyopathy, Dilated cardiomyopathy, Congestive heart failure, Heart failure, Hypertrophic cardiomyopathy, Hypoxia, Inflammatory skin disease, Obesity, Psoriasis