Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
501 to 510 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

501
230
Aldolase, fructose-bisphosphate C
ALDC
Autoimmune nervous system disorder

502
ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase
CDG1K, HMAT1, HMT-1, HMT1, MT-1, Mat-1, hMat-1
Congenital disorder of glycosylation

503
ALG10 alpha-1,2-glucosyltransferase
ALG10A, DIE2, KCR1
Congenital disorder of glycosylation

504
ALG10 alpha-1,2-glucosyltransferase B
ALG10, KCR1
Atypical femoral fracture, Long qt syndrome, Diabetes mellitus, type 2

505
ALG11 alpha-1,2-mannosyltransferase
CDG1P, GT8
Congenital disorder of glycosylation, Crohn disease, Hepatolenticular degeneration, Inflammatory bowel disease, Ulcerative colitis

506
ALG12 alpha-1,6-mannosyltransferase
CDG1G, ECM39, PP14673, hALG12
Congenital disorder of glycosylation, Desbuquois syndrome, Osteoarthritis, Schizophrenia

507
ALG13 UDP-N-acetylglucosaminyltransferase subunit
CDG1S, CXorf45, DEE36, EIEE36, GLT28D1, MDS031, TDRD13, YGL047W
Congenital disorder of glycosylation, Developmental and epileptic encephalopathy, Epilepsy, Focal glomerulosclerosis, Intellectual developmental disorder, Intellectual developmental disorder, x-linked, Neurodevelopmental disorder, X-linked intellectual disability, Scoliosis

508
ALG14 UDP-N-acetylglucosaminyltransferase subunit
CMS15, IDDEBF, MEPCA
Bipolar disorder, Congenital disorder of glycosylation, Congenital myasthenic syndrome, Congenital myopathy, Intellectual developmental disorder seizures behavioral, Myasthenic syndrome, Scoliosis, Tourette syndrome

509
ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase like 2
-
Autism

510
ALG2 alpha-1,3/1,6-mannosyltransferase
CDG1I, CDGIi, CMS14, CMSTA3, NET38, hALPG2
Congenital disorder of glycosylation, Congenital myasthenic syndrome, Myasthenic syndrome