Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
15081 to 15090 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

15081
Zinc finger matrin-type 1
-
Scoliosis

15082
Zinc finger matrin-type 2
Ptg-12, Snu23
Congenital radioulnar synostosis

15083
Zinc finger matrin-type 3
PAG608, WIG-1, WIG1
Central nervous system cancer, Glioblastoma, Glioma, Post-traumatic stress disorder, Throat disease

15084
Zinc finger matrin-type 4
-
Alzheimer disease, Behcet disease, Bladder exstrophy, Color vision deficiency, Congenital left-sided heart lesions, Eye disease, Oligodendroglioma, Schizophrenia, Scoliosis

15085
Zinc finger matrin-type 5
SNRNP20, U11/U12-20K, ZC3H19
Irritable bowel syndrome, Diabetes mellitus, type 2

15086
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 neoplasm, Common variable immunodeficiency, Neurodevelopmental disorder, Crohn disease
View all (33 more)

15087
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

15088
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

15089
Zinc finger MYM-type containing 2
FIM, MYM, NECRC, RAMP, SCLL, ZNF198
Alzheimer disease, Congenital anomalies of the kidney and urinary tract, Congenital anomalies of kidney and urinary tract, Intellectual developmental disorder, Myeloproliferative disorder, Neurodevelopmental disorder, Non-specific syndromic intellectual disability

15090
Zinc finger MYM-type containing 3
DXS6673E, MYM, XFIM, XLID112, ZNF198L2, ZNF261
Global developmental delay, Gout, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorder, Prostatic neoplasm