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
14911 to 14920 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14911
Zinc finger CCCH-type containing 18
NHN1
Color vision deficiency

14912
Zinc finger CCCH-type containing 4
C19orf7
Metabolic syndrome, Neurodevelopmental disorder, Obesity, Diabetes mellitus type 2

14913
Zinc finger CCCH-type containing 7A
HSPC055, ZC3H7, ZC3HDC7
Tourette syndrome, Oligodendroglioma

14914
Zinc finger CCCH-type containing 7B
ROXAN1, RoXaN
Alzheimer disease, Breast cancer, Hypothyroidism, Insomnia, Major depressive disorder, Neurotic disorder, Schizophrenia, Vitiligo

14915
Zinc finger CCCH-type containing 8
Fliz1, ZC3HDC8
Neurotic disorder

14916
Zinc finger CCCH-type containing, antiviral 1
ARTD13, FLB6421, PARP13, ZAP, ZC3H2, ZC3HDC2
Biliary cirrhosis, Multiple sclerosis, Biliary cholangitis

14917
ZC3HAV1 like
C7orf39
Oligodendroglioma

14918
Zinc finger C3HC-type containing 1
HSPC216, NIPA
Cardiovascular disease, Ischemic heart disease, Coronary artery disease, Diabetes mellitus type 2, Erectile dysfunction, Hypertension, Gallstones, Heart disease, Heart failure, Large artery stroke, Metabolic syndrome, Myocardial infarction, Myocardial ischemia, Stroke

14919
Zinc finger C4H2-type containing
HCA127, KIAA1166, MCS, MRXS4, WRWF, WRWFFR, WWS
Arthrogryposis multiplex congenita, Desbuquois syndrome, Hypogonadism, Microcephaly, Miles-carpenter syndrome, Neurodevelopmental disorder, Partington syndrome, Wieacker syndrome, Wieacker-wolff syndrome, X-linked intellectual disability

14920
Zinc finger CCHC-type containing 10
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Obstructive pulmonary disease, Metabolic syndrome, Diabetes mellitus type 2