Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
15061 to 15070 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

15061
Zinc finger FYVE-type containing 28
LST2, LYST2, lst-2
Alzheimer disease, Cervical cancer, Gastrointestinal disease, Schizophrenia, Diabetes mellitus, type 2

15062
Zymogen granule protein 16
JCLN, JCLN1, ZG16A
Alzheimer disease

15063
Zinc finger GATA like protein 1
GATAD3, GLP-1, GLP1
Eczema, Inflammatory skin disease, Psoriasis

15064
Zinc finger CCCH-type and G-patch domain containing
GPATC6, GPATCH6, KIAA1847, ZC3H9, ZC3HDC9, ZIP
Bell's palsy, Crohn disease, Diverticular disease, Inflammatory bowel disease, Metabolic syndrome, Prostate cancer, Diabetes mellitus, type 2, Ulcerative colitis

15065
Zinc finger GRF-type containing 1
C4orf21
Apraxia, Autism, Deglutition disorder, Dental caries, Dysarthria, Spastic paraplegia

15066
Zinc fingers and homeoboxes 2
AFR1, RAF
Major depressive disorder, Diabetes mellitus, type 2

15067
Zinc fingers and homeoboxes 3
TIX1
Androgenetic alopecia, Atrial fibrillation, Cancer, Coronary artery disease, Crohn disease, Diabetes mellitus, Diabetic eye disease, Heart failure, Hyperlipidemia, Inflammatory bowel disease, Major depressive disorder, Metabolic syndrome, Migraine, Mood disorder, Multiple sclerosis
View all (4 more)

15068
Zic family zinc finger 1
BAIDCS, CRS6, ZIC, ZNF201
Brachycephaly, Color vision deficiency, Craniosynostosis, Dandy-walker syndrome, Diabetic maculopathy, Insomnia, Metabolic syndrome, Turricephaly, Diabetes mellitus, type 2

15069
Zic family zinc finger 2
HPE5
Astrocytoma, Hepatocellular carcinoma, Congenital neurologic anomalies, Cyclocephaly, Holoprosencephaly, Microform holoprosencephaly, Syntelencephaly, Neural tube defect, Neural tube defects, x-linked, Orofacial cleft, Prostatic neoplasm, Schizophrenia, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly

15070
Zic family zinc finger 3
HTX, HTX1, VACTERLX, ZNF203
Bone disease, Congenital heart disease, Craniofacial abnormalities, Dextrocardia, Heterotaxy syndrome, Situs inversus, Tetralogy of fallot, Vacterl association