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
14971 to 14980 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14971
Zinc finger CCCH-type containing 12A
MCPIP, MCPIP-1, MCPIP1, Reg1, dJ423B22.1
Arterial occlusive disease, Hepatitis b

14972
Zinc finger CCCH-type containing 12B
CXorf32, MCPIP2
Androgenetic alopecia, Autism, Erectile dysfunction, Hypogonadism, Insomnia, Prostate cancer

14973
Zinc finger CCCH-type containing 12C
MCPIP3
Psoriasis

14974
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

14975
Zinc finger CCCH-type containing 13
KIAA0853, Xio
Crohn disease, Inflammatory bowel disease, Myopia, Diabetes mellitus type 2, Ulcerative colitis

14976
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

14977
Zinc finger CCCH-type containing 15
DFRP1, HT010, LEREPO4, MSTP012
Color vision deficiency

14978
Zinc finger CCCH-type containing 18
NHN1
Color vision deficiency

14979
Zinc finger CCCH-type containing 4
C19orf7
Metabolic syndrome, Neurodevelopmental disorder, Obesity, Diabetes mellitus type 2

14980
Zinc finger CCCH-type containing 7A
HSPC055, ZC3H7, ZC3HDC7
Tourette syndrome, Oligodendroglioma