Disease 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 [0-9]
Gene 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

Gene list (S)

SAMHD1
SAM domain and HD domain 1
SAR1B
SAR1 homolog B
SASH1
SAM and SH3 domain containing 1
SBF2
SET binding factor 2
SCN9A
sodium channel, voltage-gated, type IX, alpha subunit
SEC23B
Sec23 homolog B (S. cerevisiae)
SEPSECS
Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase
SGCA
sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)
SGCG
sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
SH3TC2
SH3 domain and tetratricopeptide repeats 2
SLC19A3
solute carrier family 19, member 3
SLC25A46
solute carrier family 25 member 46
SLC29A3
solute carrier family 29 (nucleoside transporters), member 3
SLC2A10
solute carrier family 2 (facilitated glucose transporter), member 10
SLC3A1
solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1
SLC45A2
solute carrier family 45, member 2
SLC7A7
solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
SMN1
survival of motor neuron 1, telomeric
SMPD1
sphingomyelin phosphodiesterase 1, acid lysosomal
SOST
sclerostin
SPG11
spastic paraplegia 11
SPG7
spastic paraplegia 7 (pure and complicated autosomal recessive)
SPTA1
spectrin, alpha, erythrocytic 1 (elliptocytosis 2)
SRD5A2
steroid-5-alpha-reductase, alpha polypeptide 2 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 2)