Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12221 to 12230 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12221
Solute carrier family 35 member B3
C6orf196, CGI-19, PAPST2
Kidney disease, Diabetic neuropathy, Hearing loss, Orofacial cleft, Stevens-johnson syndrome, Toxic epidermal necrolysis

12222
Solute carrier family 35 member B4
YEA, YEA4
Insomnia

12223
Solute carrier family 35 member C1
CDG2C, FUCT1
Alzheimer disease, Attention deficit hyperactivity disorder, Congenital disorder of glycosylation, Desbuquois syndrome, Leukocyte adhesion deficiency, Diabetes mellitus type 2

12224
Solute carrier family 35 member D1
SHNKND, UGTREL7
Connective tissue disease, Craniofacial abnormalities, Desbuquois syndrome, Diverticular disease, Inflammatory bowel disease, Psoriasis

12225
Solute carrier family 35 member D2
HFRC1, SQV7L, UGTrel8, hfrc
Atrial fibrillation, Migraine, Non-small cell lung carcinoma

12226
Solute carrier family 35 member E1
-
Alzheimer disease

12227
Solute carrier family 35 member E2B
SLC35E2
Myopia

12228
Solute carrier family 35 member E3
BLOV1
Breast cancer, Uterine fibroid

12229
Solute carrier family 35 member E4
-
Atrial fibrillation

12230
Solute carrier family 35 member F1
C6orf169, dJ230I3.1
Aortic valve disease, Atrial fibrillation, Attention deficit hyperactivity disorder, Bipolar disorder, Bladder exstrophy, Coronary artery disease, Heart failure, Hypertension, Hypertrophic cardiomyopathy, Malunion fracture, Metabolic syndrome, Nephrotic syndrome, Neurodevelopmental disorder, Oligodendroglioma, Psychiatric disorders
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