Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
711 to 720 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

711
Solute carrier family 34 member 2
NAPI-3B, NAPI-IIb, NPTIIb, NaPi2b, PULAM
Non-small-cell lung carcinoma

712
Solute carrier family 34 member 3
HHRH, NPT2C, NPTIIc
Hypophosphatemic rickets, Desbuquois syndrome, Nephrolithiasis

713
Solute carrier family 35 member A1
CDG2F, CMPST, CST, hCST
Congenital disorder of glycosylation

714
Solute carrier family 35 member A2
CDG2M, CDGX, UDP-Gal-Tr, UGALT, UGAT, UGT, UGT1, UGT2, UGTL
Autism, Congenital disorder of glycosylation, Developmental and epileptic encephalopathy, X-linked complex neurodevelopmental disorder

715
Solute carrier family 35 member A3
AMRS
Arthrogryposis multiplex congenita, Arthrogryposis with neurodevelopmental impairment and seizures, Autism, Kidney disease

716
Solute carrier family 35 member B1
AXER, UGTREL1
Oligodendroglioma

717
Solute carrier family 35 member B2
HLD26, PAPST1, SLL, UGTrel4
Hypomyelinating leukodystrophy

718
Solute carrier family 35 member B3
C6orf196, CGI-19, PAPST2
Kidney disease, Diabetic neuropathy, Hearing loss, Orofacial cleft, Stevens-johnson syndrome, Toxic epidermal necrolysis

719
Solute carrier family 35 member B4
YEA, YEA4
Insomnia

720
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