Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12431 to 12440 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12431
Structural maintenance of chromosomes 4
CAP-C, CAPC, SMC-4, SMC4L1
Clonal hematopoiesis

12432
Structural maintenance of chromosomes 5
ATELS2, SMC5L1
Atelis syndrome, Liver cirrhosis, Mosaic variegated aneuploidy, Upper aerodigestive tract neoplasm

12433
Structural maintenance of chromosomes 6
SMC-6, SMC6L1, hSMC6
Benign prostatic hyperplasia, Hypothyroidism

12434
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

12435
Single-pass membrane protein with coiled-coil domains 1
C3orf43
Colorectal cancer

12436
Single-pass membrane protein with coiled-coil domains 2
C12orf70
Hyperopia, Lung cancer, Obstructive sleep apnea syndrome

12437
Single-pass membrane protein with coiled-coil domains 4
C11orf75, FN5
Metabolic syndrome, Diabetes mellitus type 2

12438
Sperm mitochondria associated cysteine rich protein
HSMCSGEN1, MCS, MCSP
Eczema, Scoliosis

12439
SMCR8-C9orf72 complex subunit
DENND8A
Neurodevelopmental disorder

12440
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
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