Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5091 to 5100 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5091
Glial cells missing transcription factor 2
FIH2, GCMB, HRPT4, hGCMb
Desbuquois syndrome, Eye disease, Hyperparathyroidism, Hypoparathyroidism, Visual disorder

5092
GCN1 activator of EIF2AK4
GCN1L, GCN1L1, PRIC295
Arthrogryposis multiplex congenita, Obesity, Pena-shokeir syndrome

5093
Germ cell nuclear acidic peptidase
ACRC, NAAR1, SPGFX4
Azoospermia, Male infertility single gene azoospermia, Spermatogenic failure, x-linked, Testicular azoospermia

5094
Glucosaminyl (N-acetyl) transferase 1
C2GNT, C2GNT-L, C2GNT1, C2GlcNAcT, G6NT, NACGT2, NAGCT2
Central nervous system cancer, Kidney disease, Glioblastoma, Glioma, Liver cirrhosis, Prostatic neoplasms

5095
Glucosaminyl (N-acetyl) transferase 2 (I blood group)
CCAT, CTRCT13, GCNT2C, GCNT5, IGNT, II, NACGT1, NAGCT1, ULG3, bA360O19.2, bA421M1.1
Cataract, Congenital cataract, Congenital total cataract, Gout

5096
Glucosaminyl (N-acetyl) transferase 4
C2GNT3, LINC01336
Metabolic syndrome, Diabetes mellitus type 2

5097
Glucosaminyl (N-acetyl) transferase family member 7
C20orf105, dJ1153D9.2, gcnt
Alzheimer disease, Gastroesophageal reflux disease

5098
GCOM1, MYZAP-POLR2M combined locus
GRINL1A, Gcom2, MYZAP, MYZAP-POLR2M, gcom
Astrocytoma, Atrial fibrillation, Dilated cardiomyopathy, Substance abuse

5099
Germinal center associated signaling and motility like
C1orf150
Lymphoblastic leukemia, Hemorrhagic disease, Thrombocytopenia, Urticaria

5100
Glycine cleavage system protein H
GCE, MMDS7, NKH
Glycine encephalopathy