|
1031
|
|
|
Solute carrier family 25 member 32 |
GLYB, MFT, MFTC, RREI |
|
|
1032
|
|
|
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 |
HsT19690, SIAT8-B, SIAT8B, ST8SIA-II, ST8SiaII, STX |
|
|
1033
|
|
|
Solute carrier family 7 member 5 |
4F2LC, CD98, D16S469E, E16, LAT1, MPE16 |
|
|
1034
|
|
|
Sorting nexin 27 |
MRT1, MY014 |
|
|
1035
|
|
|
Solute carrier family 14 member 2 |
HUT2, UT-A2, UT2, UTA, UTR, hUT-A6 |
|
|
1036
|
|
|
Solute carrier organic anion transporter family member 5A1 |
OATP-J, OATP-RP4, OATP5A1, OATPJ, OATPRP4, SLC21A15 |
|
|
1037
|
|
|
SET binding factor 2 |
CMT4B2, DENND7B, MTMR13 |
Acquired kyphoscoliosis, Charcot-marie-tooth disease, Charcot-marie-tooth disease with glaucoma, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Congenital clubfoot, Congenital kyphoscoliosis, Distal amyotrophy, Glaucoma, Hearing loss, Leukemia, Moyamoya disease, Pancreatic carcinoma, Pancreatic cancer |
|
1038
|
|
|
Sprouty RTK signaling antagonist 4 |
HH17 |
Anxiety disorder, Congenital camptodactyly, Breast hypoplasia, Hypoplasia of the ovary, Congenital sensorineural hearing loss, Cryptorchidism, Dysarthria, Erectile dysfunction, Female hypogonadism syndrome, Gynecomastia, Hearing loss, Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism with or without anosmia, Hypopituitarism, Ichthyosis, Kallmann syndrome, Leukemia, Mental depression, Mirror movements, Myeloid leukemia, Non-obstructive azoospermia, Non-seminomatous tumor of testis, Normosmic congenital hypogonadotropic hypogonadism, Nystagmus, Obesity, Osteochondrodysplasia, Osteopenia, Osteoporosis, Paraplegia, Penis agenesis, Physiologic amenorrhea, Ptosis, Renal agenesis, Secondary physiologic amenorrhea, Skeletal dysplasia, Testicular hypogonadismView all (21 more) |
|
1039
|
|
|
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 |
SIAT7-E, SIAT7E, ST6GalNAcV |
|
|
1040
|
|
|
SHANK associated RH domain interactor |
AIFID, SIPL1 |
|
