Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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15011 to 15020 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

15011
Zinc finger with KRAB and SCAN domains 7
ZFP, ZNF167, ZNF448, ZNF64, ZSCAN39
Major depressive disorder

15012
Zinc finger with KRAB and SCAN domains 8
LD5-1, ZNF192, ZSCAN40
Autism, Major depressive disorder, Rheumatoid arthritis, Diabetes mellitus type 1

15013
Zinc finger matrin-type 1
-
Scoliosis

15014
Zinc finger matrin-type 2
Ptg-12, Snu23
Congenital radioulnar synostosis

15015
Zinc finger matrin-type 3
PAG608, WIG-1, WIG1
Central nervous system cancer, Glioblastoma, Glioma, Post-traumatic stress disorder, Throat disease

15016
Zinc finger matrin-type 4
-
Alzheimer disease, Behcet disease, Bladder exstrophy, Color vision deficiency, Congenital left-sided heart lesions, Eye disease, Oligodendroglioma, Schizophrenia, Scoliosis

15017
Zinc finger matrin-type 5
SNRNP20, U11/U12-20K, ZC3H19
Irritable bowel syndrome, Diabetes mellitus type 2

15018
Zinc finger MIZ-type containing 1
MIZ, NEDDFSA, RAI17, TRAFIP10, ZIMP10
Ankylosing spondylitis, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Autoimmune disease, Autoimmune thyroid disease, Bipolar disorder, Breast cancer, Celiac disease, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Common variable immunodeficiency, Neurodevelopmental disorder, Crohn disease
View all (33 more)

15019
Zinc finger MIZ-type containing 2
NET27, TRAFIP20, ZIMP7, hZIMP7
Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Lung cancer, Metabolic syndrome, Diabetes mellitus type 2

15020
Zinc metallopeptidase STE24
FACE-1, FACE1, HGPS, PRO1, RSDM1, STE24, Ste24p
Craniofacial abnormalities, Desbuquois syndrome, Focal glomerulosclerosis, Lipodystrophy, Mandibuloacral dysostosis, Mandibuloacral dysplasia, Restrictive dermopathy, Tight skin contracture syndrome