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"
931 to 940 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

931
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

932
Single-pass membrane protein with coiled-coil domains 1
C3orf43
Colorectal cancer

933
Single-pass membrane protein with coiled-coil domains 2
C12orf70
Hyperopia, Lung cancer, Obstructive sleep apnea syndrome

934
Single-pass membrane protein with coiled-coil domains 4
C11orf75, FN5
Metabolic syndrome, Diabetes mellitus type 2

935
Sperm mitochondria associated cysteine rich protein
HSMCSGEN1, MCS, MCSP
Eczema, Scoliosis

936
SMCR8-C9orf72 complex subunit
DENND8A
Neurodevelopmental disorder

937
SMG6 nonsense mediated mRNA decay factor
C17orf31, EST1A, SMG-6, hEST1A, hSMG5/7a
Androgenetic alopecia, Atrial fibrillation, Attention deficit hyperactivity disorder, Bone fracture, Breast cancer, Obstructive pulmonary disease, Coronary artery disease, Diverticular disease, Esophageal cancer, Gastroesophageal reflux disease, Glaucoma, Heart failure, Hypertension, Irritable bowel syndrome, Metabolic syndrome
View all (13 more)

938
SMG7 nonsense mediated mRNA decay factor
C1orf16, EST1C, SGA56M
Autoimmune disease, Autoimmune musculoskeletal system disorder, Celiac disease, Myositis, Rheumatoid arthritis, Systemic lupus erythematosus, Systemic sclerosis

939
SMG8 nonsense mediated mRNA decay factor
ALKUS, C17orf71
Alzahrani-kuwahara syndrome, Retinitis pigmentosa

940
SMG9 nonsense mediated mRNA decay factor
C19orf61, F17127_1, HBMS, NEDITPO
Autism, Brainstem dysplasia, Global developmental delay, Neurodevelopmental disorder