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"
921 to 930 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

921
Structural maintenance of chromosomes 2
CAP-E, CAPE, SMC-2, SMC2L1
Alzheimer disease, Aortic stenosis, Basal cell carcinoma, Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Keratinocyte carcinoma, Lung cancer
View all (13 more)

922
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 disorder, Neuromuscular disease, Wiedemann-steiner syndrome

923
Structural maintenance of chromosomes 4
CAP-C, CAPC, SMC-4, SMC4L1
Clonal hematopoiesis

924
Structural maintenance of chromosomes 5
ATELS2, SMC5L1
Atelis syndrome, Mosaic variegated aneuploidy, Upper aerodigestive tract neoplasm

925
Structural maintenance of chromosomes 6
SMC-6, SMC6L1, hSMC6
Benign prostatic hyperplasia, Hypothyroidism

926
Structural maintenance of chromosomes flexible hinge domain containing 1
BAMS, FSHD2
Arhinia-choanal atresia-microphthalmia syndrome, Atrial fibrillation, Bosma arhinia microphthalmia syndrome, Chediak-higashi syndrome, Conotruncal cardiac defect, Crohn disease, Cryptorchidism, Facial nerve disorder, Facioscapulohumeral muscular dystrophy, Inflammatory bowel disease, Male infertility single gene azoospermia, Muscular dystrophy, Myopathy, Diabetes mellitus type 2, Ulcerative colitis

927
Single-pass membrane protein with coiled-coil domains 1
C3orf43
Colorectal cancer

928
Single-pass membrane protein with coiled-coil domains 2
C12orf70
Hyperopia, Lung cancer, Obstructive sleep apnea syndrome

929
Single-pass membrane protein with coiled-coil domains 4
C11orf75, FN5
Metabolic syndrome, Diabetes mellitus type 2

930
Sperm mitochondria associated cysteine rich protein
HSMCSGEN1, MCS, MCSP
Eczema, Scoliosis