SMC1A Chromosome X

Structural maintenance of chromosomes 1A
225 variants 225 Health Risk

Upload your DNA to see your personal genotypes for variants in SMC1A.

What This Gene Does
Proper cohesion of sister chromatids is a prerequisite for the correct segregation of chromosomes during cell division. The cohesin multiprotein complex is required for sister chromatid cohesion. This complex is composed partly of two structural maintenance of chromosomes (SMC) proteins, SMC3 and either SMC1B or the protein encoded by this gene. Most of the cohesin complexes dissociate from the chromosomes before mitosis, although those complexes at the kinetochore remain. Therefore, the encoded protein is thought to be an important part of functional kinetochores. In addition, this protein interacts with BRCA1 and is phosphorylated by ATM, indicating a potential role for this protein in DNA repair. This gene, which belongs to the SMC gene family, is located in an area of the X-chromosome that escapes X inactivation. Mutations in this gene result in Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
Gene Info
Gene Group
"Structural maintenance of chromosomes proteins|Cohesin complex|MicroRNA protein coding host genes"
Locus Type
gene with protein product
Location
Xp11.22
Ensembl
ENSG00000072501
Associated Conditions (23)
Congenital muscular hypertrophy-cerebral syndrome
History of neurodevelopmental disorder
Developmental and epileptic encephalopathy
85
with or without midline brain defects
Inborn genetic diseases
Uterine corpus endometrial carcinoma
Thyroid cancer
nonmedullary
1
Abnormality of the nervous system
Cornelia de Lange syndrome 1
Posterior fossa group A ependymoma
Nonpapillary renal cell carcinoma
Epileptic encephalopathy
SMC1A-related cohesinopathy
SMC1A-related disorder
See cases
Seizure
6 conditions
+3 more conditions
Key Variants
RS1007398058
Conflicting classifications of pathogenicity
Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
Health Risk
RS1057521921
Conflicting classifications of pathogenicity
Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
Health Risk
RS112727682
Conflicting classifications of pathogenicity
History of neurodevelopmental disorder, History of neurodevelopmental disorder
Health Risk
RS1171109209
Conflicting classifications of pathogenicity
Congenital muscular hypertrophy-cerebral syndrome, Developmental and epileptic encephalopathy, 85
Health Risk
RS1312716558
Conflicting classifications of pathogenicity
Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
Health Risk
RS144354524
Conflicting classifications of pathogenicity
Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
Health Risk
RS1444762600
Conflicting classifications of pathogenicity
Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
Health Risk
RS147791932
Conflicting classifications of pathogenicity
Congenital muscular hypertrophy-cerebral syndrome, Inborn genetic diseases, Congenital muscular hypertrophy-cerebral syndrome
Health Risk
RS1556891104
Conflicting classifications of pathogenicity
Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
Health Risk
RS1602413408
Conflicting classifications of pathogenicity
Health Risk
RS183355603
Conflicting classifications of pathogenicity
Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
Health Risk
RS186510389
Conflicting classifications of pathogenicity
Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
Health Risk
All Variants (225)
RSID Category Clinical Significance Conditions
RS1556890139 Health Risk Likely pathogenic
RS1556891059 Health Risk Likely pathogenic
RS1556892359 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS1569351341 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS1569351534 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS1569358774 Health Risk Likely pathogenic
RS1569359535 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS1569359540 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Thyroid cancer, nonmedullary
RS1602409271 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS1602410098 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS1602413582 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS1602418853 Health Risk Likely pathogenic
RS2075588362 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS2075680329 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Thyroid cancer, nonmedullary
RS2075702300 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 85, with or without midline brain defects
RS2146582412 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS2146582443 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS2146582657 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 85, with or without midline brain defects
RS2146598341 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS2146599562 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Developmental and epileptic encephalopathy, 85
RS2146599602 Health Risk Likely pathogenic Abnormality of the nervous system, Abnormality of the nervous system
RS2146599714 Health Risk Likely pathogenic
RS2146599723 Health Risk Likely pathogenic
RS2146599836 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS2146604722 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS2146604738 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 85, with or without midline brain defects
RS2146606502 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS2520828084 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Developmental and epileptic encephalopathy, 85
RS2520828613 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 85, with or without midline brain defects
RS2520885299 Health Risk Likely pathogenic
RS2520920773 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Developmental and epileptic encephalopathy, 85
RS2520928997 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 85, with or without midline brain defects
RS2520930054 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS2520930073 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS2520930904 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS2520945062 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS2520958208 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS2520960923 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 85, with or without midline brain defects
RS2520970438 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS2520971102 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS2521010433 Health Risk Likely pathogenic
RS587784404 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS587784406 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS587784407 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS587784410 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS587784415 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS587784419 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS587784420 Health Risk Likely pathogenic Congenital muscular hypertrophy-cerebral syndrome, Congenital muscular hypertrophy-cerebral syndrome
RS727504164 Health Risk Likely pathogenic
RS781817340 Health Risk Likely pathogenic
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