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
Showing genes starting with "Z"
481 to 490 of 517 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

481
Zona pellucida glycoprotein 3
OOMD3, OZEMA3, ZP3A, ZP3B, ZPC, Zp-3
Female infertility, Oocyte maturation defect, Parkinson disease

482
Zona pellucida glycoprotein 4
ZBP, ZP1, ZP1B, ZPB, ZPB2, Zp-4
Central nervous system cancer, Liver cirrhosis, Color vision deficiency, Glioblastoma, Glioma, Nonalcoholic fatty liver disease, Schizophrenia

483
Zona pellucida binding protein
SPGF66, ZPBP1
Insomnia, Major depressive disorder, Male infertility globozoospermia, Male infertility round headed spermatozoa, Neurotic disorder, Spermatogenic failure

484
Zona pellucida binding protein 2
ZPBPL
Ankylosing spondylitis, Asthma, Atrial fibrillation, Atrial flutter, Autoimmune disease, Autoimmune thyroid disease, B-cell acute lymphoblastic leukemia, Cardiovascular disease, Celiac disease, Cervical cancer, Common variable immunodeficiency, Crohn disease, Inflammatory bowel disease, Juvenile idiopathic arthritis, Biliary cholangitis
View all (9 more)

485
Zona pellucida like domain containing 1
-
Amblyopia, Bipolar disorder, Major depressive disorder, Multiple sclerosis, Schizophrenia, Scoliosis, Diabetes mellitus type 2

486
ZPR1 zinc finger
GKAF, ZNF259
Aneurysm, Aortic aneurysm, Atrial fibrillation, Cancer, Cardiovascular disease, Coronary artery disease, Diabetes mellitus, Hypertension, Hyperlipidemia, Lipoprotein lipase deficiency, Gallstones, Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies, Heart disease, Heart failure, Hypertriglyceridemia
View all (7 more)

487
Zinc finger RANBP2-type containing 1
TRABID
Hearing loss, Lung cancer, Squamous cell carcinoma

488
Zinc finger RANBP2-type containing 3
4933425L19Rik, AH2
Obesity, Diabetes mellitus type 2

489
Zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2
OFD21, U2AF1-RS2, U2AF1L2, U2AF1RS2, URP, ZC3H22
Congenital heart disease, Holoprosencephaly, Myelodysplastic syndrome, Orofaciodigital syndrome

490
Zinc finger and SCAN domain containing 10
OFNS, ZFP206, ZNF206
Global developmental delay, Otofacial neurodevelopmental syndrome, Hearing loss