MN1 Chromosome 22
MN1 proto-oncogene, transcriptional regulator
Upload your DNA to see your personal genotypes for variants in MN1.
What This Gene Does
Meningioma 1 (MN1) contains two sets of CAG repeats. It is disrupted by a balanced translocation (4;22) in a meningioma, and its inactivation may contribute to meningioma 32 pathogenesis. [provided by RefSeq, Jul 2008]
Associated Conditions (8)
Inborn genetic diseases
CEBALID syndrome
MN1 C-terminal truncation (MCTT) syndrome
Familial meningioma
MN1-related disorder
Thyroid cancer
nonmedullary
1
Key Variants
RS147334255
Conflicting classifications of pathogenicity
Inborn genetic diseases, CEBALID syndrome, MN1 C-terminal truncation (MCTT) syndrome
Health Risk
RS1601319501
Conflicting classifications of pathogenicity
CEBALID syndrome, MN1 C-terminal truncation (MCTT) syndrome, Familial meningioma
Health Risk
RS1933302820
Conflicting classifications of pathogenicity
CEBALID syndrome, MN1 C-terminal truncation (MCTT) syndrome, CEBALID syndrome
Health Risk
RS200030766
Conflicting classifications of pathogenicity
MN1-related disorder, Inborn genetic diseases, MN1-related disorder
Health Risk
RS376119570
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS377232565
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS759786990
Conflicting classifications of pathogenicity
Inborn genetic diseases, Familial meningioma, CEBALID syndrome
Health Risk
RS769995080
Conflicting classifications of pathogenicity
Inborn genetic diseases, MN1-related disorder, Inborn genetic diseases
Health Risk
RS1932758837
Likely pathogenic
MN1 C-terminal truncation (MCTT) syndrome, MN1 C-terminal truncation (MCTT) syndrome
Health Risk
RS1932759453
Likely pathogenic
MN1 C-terminal truncation (MCTT) syndrome, MN1 C-terminal truncation (MCTT) syndrome
Health Risk
RS1933304057
Likely pathogenic
MN1 C-terminal truncation (MCTT) syndrome, MN1 C-terminal truncation (MCTT) syndrome
Health Risk
RS1933387717
Likely pathogenic
Health Risk
All Variants (31)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS147334255 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, CEBALID syndrome, MN1 C-terminal truncation (MCTT) syndrome |
| RS1601319501 | Health Risk | Conflicting classifications of pathogenicity | CEBALID syndrome, MN1 C-terminal truncation (MCTT) syndrome, Familial meningioma |
| RS1933302820 | Health Risk | Conflicting classifications of pathogenicity | CEBALID syndrome, MN1 C-terminal truncation (MCTT) syndrome, CEBALID syndrome |
| RS200030766 | Health Risk | Conflicting classifications of pathogenicity | MN1-related disorder, Inborn genetic diseases, MN1-related disorder |
| RS376119570 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS377232565 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS759786990 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Familial meningioma, CEBALID syndrome |
| RS769995080 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, MN1-related disorder, Inborn genetic diseases |
| RS1932758837 | Health Risk | Likely pathogenic | MN1 C-terminal truncation (MCTT) syndrome, MN1 C-terminal truncation (MCTT) syndrome |
| RS1932759453 | Health Risk | Likely pathogenic | MN1 C-terminal truncation (MCTT) syndrome, MN1 C-terminal truncation (MCTT) syndrome |
| RS1933304057 | Health Risk | Likely pathogenic | MN1 C-terminal truncation (MCTT) syndrome, MN1 C-terminal truncation (MCTT) syndrome |
| RS1933387717 | Health Risk | Likely pathogenic | — |
| RS1933401338 | Health Risk | Likely pathogenic | — |
| RS2123873148 | Health Risk | Likely pathogenic | CEBALID syndrome, CEBALID syndrome |
| RS2146315211 | Health Risk | Likely pathogenic | CEBALID syndrome, CEBALID syndrome |
| RS2517749386 | Health Risk | Likely pathogenic | CEBALID syndrome, CEBALID syndrome |
| RS2517771777 | Health Risk | Likely pathogenic | — |
| RS2517772878 | Health Risk | Likely pathogenic | CEBALID syndrome, CEBALID syndrome |
| RS761317200 | Health Risk | Likely pathogenic | CEBALID syndrome, MN1 C-terminal truncation (MCTT) syndrome, Thyroid cancer |
| RS891364169 | Health Risk | Likely pathogenic | CEBALID syndrome, CEBALID syndrome |
| RS1278300199 | Health Risk | Pathogenic | Inborn genetic diseases, Inborn genetic diseases |
| RS1601319584 | Health Risk | Pathogenic | CEBALID syndrome, CEBALID syndrome |
| RS1601319598 | Health Risk | Pathogenic | CEBALID syndrome, CEBALID syndrome |
| RS1601319615 | Health Risk | Pathogenic | CEBALID syndrome, MN1 C-terminal truncation (MCTT) syndrome, CEBALID syndrome |
| RS1932758693 | Health Risk | Pathogenic | CEBALID syndrome, CEBALID syndrome |
| RS1933308051 | Health Risk | Pathogenic | CEBALID syndrome, CEBALID syndrome |
| RS1933378166 | Health Risk | Pathogenic | CEBALID syndrome, CEBALID syndrome |
| RS2517749424 | Health Risk | Pathogenic | CEBALID syndrome, CEBALID syndrome |
| RS2517771244 | Health Risk | Pathogenic | CEBALID syndrome, CEBALID syndrome |
| RS1297805962 | Health Risk | Pathogenic/Likely pathogenic | CEBALID syndrome, CEBALID syndrome |
| RS1601319538 | Health Risk | Pathogenic/Likely pathogenic | CEBALID syndrome, MN1 C-terminal truncation (MCTT) syndrome, CEBALID syndrome |