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
12161 to 12170 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12161
Solute carrier family 35 member B1
AXER, UGTREL1
Oligodendroglioma

12162
Solute carrier family 35 member B2
HLD26, PAPST1, SLL, UGTrel4
Hypomyelinating leukodystrophy

12163
Solute carrier family 35 member B3
C6orf196, CGI-19, PAPST2
Kidney disease, Diabetic neuropathy, Hearing loss, Orofacial cleft, Stevens-johnson syndrome, Toxic epidermal necrolysis

12164
Solute carrier family 35 member B4
YEA, YEA4
Insomnia

12165
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

12166
Solute carrier family 35 member D1
SHNKND, UGTREL7
Connective tissue disease, Craniofacial abnormalities, Desbuquois syndrome, Diverticular disease, Inflammatory bowel disease, Psoriasis

12167
Solute carrier family 35 member D2
HFRC1, SQV7L, UGTrel8, hfrc
Atrial fibrillation, Migraine, Non-small cell lung carcinoma

12168
Solute carrier family 35 member E1
-
Alzheimer disease

12169
Solute carrier family 35 member E2B
SLC35E2
Myopia

12170
Solute carrier family 35 member E3
BLOV1
Breast cancer, Uterine fibroid