Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4941 to 4950 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4941
Frizzled class receptor 9
CD349, FZD3
Gout

4942
Fizzy and cell division cycle 20 related 1
CDC20C, CDH1, DEE109, FZR, FZR2, HCDH, HCDH1
Autism, Cerebellar ataxia, Developmental and epileptic encephalopathy, Global developmental delay

4943
G0/G1 switch 2
-
Carcinoma, Liver cirrhosis

4944
G2/M-phase specific E3 ubiquitin protein ligase
KIAA1333, PHF7B
Amyotrophic lateral sclerosis, Frontotemporal dementia, Urinary bladder cancer

4945
G3BP stress granule assembly factor 1
G3BP, HDH-VIII
Alzheimer disease, Astrocytoma, Basal cell carcinoma, Central nervous system cancer, Glioblastoma, Glioma

4946
G3BP stress granule assembly factor 2
-
Alzheimer disease

4947
Glucose-6-phosphatase catalytic subunit 1
G6PC, G6PT, G6Pase, GSD1, GSD1a
Glycogen storage disease, Gout, Hypoglycemia, Liver cirrhosis

4948
Glucose-6-phosphatase catalytic subunit 2
IGRP
Carbohydrate metabolism disease, Intestinal disaccharide malabsorption, Metabolic syndrome, Osteoarthritis, Diabetes mellitus type 2

4949
Glucose-6-phosphatase catalytic subunit 3
SCN4, UGRP
Severe congenital neutropenia, Dursun syndrome, Congenital neutropenia

4950
Glucose-6-phosphate dehydrogenase
CNSHA1, G6PD1
Anemia, Congenital nonspherocytic hemolytic anemia, Hemolytic anemia, Anhidrotic ectodermal dysplasia with immunodeficiency, osteopetrosis, and lymphedema, Autoinflammatory disease, systemic, x-linked, Bipolar disorder, Bloch sulzberger syndrome, Cerebrovascular disorder, Granulomatous disease, Glucose-6-phosphate dehydrogenase deficiency, Contact dermatitis, Diabetes mellitus, Hemolysis, Hyper-igm immunodeficiency syndrome, Immunodeficiency
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