Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
1131 to 1140 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1131
Solute carrier family 39 member 13
EDSSPD3, LZT-Hs9, SCDEDS, ZIP13
Bone disease, Connective tissue disease, Cutis laxa, Desbuquois syndrome, Ehlers-danlos syndrome, Mitral valve prolapse, Myopia, Scleroderma, Spondyloepimetaphyseal dysplasia, Stroke, Tooth abnormalities

1132
Structural maintenance of chromosomes 3
BAM, BMH, CDLS3, CSPG6, HCAP, SMC3L1
Autism, Cornelia de lange syndrome, De lange syndrome, Desbuquois syndrome, Intellectual developmental disorder, Myeloid leukemia, Neurodevelopmental disorders, Neuromuscular diseases, Wiedemann-steiner syndrome

1133
SEC14 and spectrin domain containing 1
Solo
Atrial fibrillation, Bipolar disorder, Dental caries, Alzheimer disease, Migraine, Scoliosis

1134
Synaptogyrin 2
-
Lung cancer, Squamous cell carcinoma, Vitiligo

1135
Synaptogyrin 1
-
Biliary cirrhosis, Bipolar disorder, Crohn disease, Hypothyroidism, Inflammatory bowel disease, Myeloid leukemia, Systemic lupus erythematosus, Ovarian cancer, Biliary cholangitis, Rheumatoid arthritis, Schizophrenia, Ulcerative colitis

1136
Solute carrier family 6 member 5
GLYT-2, GLYT2, HKPX3, NET1
Apnea, Brain disease, Hereditary hyperekplexia, Hyperekplexia, Hyperexplexia hereditary, Obesity, Psoriasis, Schizophrenia, Diabetes mellitus, type 1, Diabetes mellitus, type 2

1137
Solute carrier family 28 member 1
CNT1, HCNT1, URCTU
Alzheimer disease, Breast neoplasm, Cerebral amyloid angiopathy, Color vision deficiency, Nephrolithiasis, Psoriasis, Retinal degeneration, Myopia

1138
Single-pass membrane protein with aspartate rich tail 1
C22orf32, DDDD, EMRE

1139
SR-related CTD associated factor 11
CASP11, SFRS2IP, SIP1, SRRP129, SRSF2IP
Coronary artery disease, Rheumatoid arthritis

1140
Solute carrier family 24 member 1
CSNB1D, HsT17412, NCKX, NCKX1, RODX
Moyamoya angiopathy, Night blindness, congenital stationary, Oguchi disease, Optic atrophy, Retinitis pigmentosa