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
14901 to 14910 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14901
Zinc finger CCCH-type containing 10
ZC3HDC10
Hyperglycemia, Diabetes mellitus type 2, Obesity, Systemic sclerosis

14902
Zinc finger CCCH-type containing 11A
ZC3HDC11A
Androgenetic alopecia, Breast cancer, Breast neoplasms, Coronary artery disease

14903
Zinc finger CCCH-type containing 11B
ZC3HDC11B
Corneal astigmatism, Diabetes mellitus, Hypertension, Metabolic syndrome, Open angle glaucoma, Osteoarthritis, Otosclerosis, Diabetes mellitus type 2

14904
Zinc finger CCCH-type containing 12A
MCPIP, MCPIP-1, MCPIP1, Reg1, dJ423B22.1
Arterial occlusive disease

14905
Zinc finger CCCH-type containing 12B
CXorf32, MCPIP2
Androgenetic alopecia, Autism, Erectile dysfunction, Hypogonadism, Insomnia, Prostate cancer

14906
Zinc finger CCCH-type containing 12C
MCPIP3
Psoriasis

14907
Zinc finger CCCH-type containing 12D
C6orf95, MCPIP4, TFL, dJ281H8.1, p34
Asthma, Hepatocellular carcinoma, Coronary artery disease, Dupuytren contracture, Stevens-johnson syndrome, Toxic epidermal necrolysis

14908
Zinc finger CCCH-type containing 13
KIAA0853, Xio
Crohn disease, Inflammatory bowel disease, Myopia, Diabetes mellitus type 2, Ulcerative colitis

14909
Zinc finger CCCH-type containing 14
MRT56, MSUT-2, NY-REN-37, SUT2, UKp68
Alzheimer disease, Amyotrophic lateral sclerosis, Nonsyndromic intellectual disability, Intellectual developmental disorder

14910
Zinc finger CCCH-type containing 15
DFRP1, HT010, LEREPO4, MSTP012
Color vision deficiency