MT-TY
Basic information
Region (hg38): M:5826-5891
Previous symbols: [ "MTTY" ]
Links
Phenotypes
GenCC
Source:
- mitochondrial disease (Definitive), mode of inheritance: Mitochondrial
ClinVar
This is a list of variants' phenotypes submitted to
Variants pathogenicity by type
Statistics on ClinVar variants can assist in determining whether a specific variant type in the MT-TY gene is commonly pathogenic or not.
In the table, we include only reliable ClinVar variants with their consequences to MANE Select, Mane Plus Clinical transcripts, or transcripts with TSL equals 1. Click the count to view the source variants.
Warning: slight differences between displayed counts and the number of variants in ClinVar may occur, primarily due to (1) the application of a different transcript and/or consequence by our variant effect predictor or (2) differences in clinical significance: we classify Benign/Likely benign variants as Likely benign and Pathogenic/Likely pathogenic variants as Likely pathogenic.
Variant type | Pathogenic | Likely pathogenic | VUS | Likely benign | Benign | Sum |
---|---|---|---|---|---|---|
synonymous | 0 | |||||
missense | 0 | |||||
nonsense | 0 | |||||
start loss | 0 | |||||
frameshift | 0 | |||||
inframe indel | 0 | |||||
splice donor/acceptor (+/-2bp) | 0 | |||||
splice region | 0 | |||||
non coding | 0 | |||||
Total | 0 | 0 | 0 | 0 | 0 |
Variants in MT-TY
This is a list of pathogenic ClinVar variants found in the MT-TY region.
You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.
Position | Type | Phenotype | Significance | ClinVar |
---|---|---|---|---|
M-5836-A-G | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Benign (Jul 12, 2019) | ||
M-5837-G-A | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Uncertain significance (Jul 12, 2019) | ||
M-5839-C-T | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Benign (Jul 12, 2019) | ||
M-5840-C-A | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Uncertain significance (Jul 12, 2019) | ||
M-5840-C-T | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Likely benign (Jul 12, 2019) | ||
M-5841-T-C | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Uncertain significance (Jul 12, 2019) | ||
M-5843-A-G | Focal segmental glomerulosclerosis and dilated cardiomyopathy • Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Benign (Jul 12, 2019) | ||
M-5846-C-T | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Benign (Jul 12, 2019) | ||
M-5852-T-C | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Uncertain significance (Jul 12, 2019) | ||
M-5855-A-G | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Likely benign (Jul 12, 2019) | ||
M-5858-T-C | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Uncertain significance (Jul 12, 2019) | ||
M-5864-G-A | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Uncertain significance (Jul 12, 2019) | ||
M-5865-T-C | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Uncertain significance (Jul 12, 2019) | ||
M-5867-C-T | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Likely benign (Jul 12, 2019) | ||
M-5874-T-C | Exercise intolerance and complex III deficiency, somatic | Pathogenic (Oct 24, 2000) | ||
M-5875-C-T | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Likely benign (Jul 12, 2019) | ||
M-5876-A-G | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Likely benign (Jul 12, 2019) | ||
M-5877-C-T | Kearns-Sayre syndrome | Pathogenic (Oct 01, 2001) | ||
M-5884-AT-A | Kearns-Sayre syndrome | Pathogenic (Dec 26, 2001) | ||
M-5885-T-C | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke • See cases | Uncertain significance (Mar 25, 2020) | ||
M-5889-A-G | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke | Uncertain significance (Jul 12, 2019) |
GnomAD
Source:
dbNSFP
Source:
- Pathway
- Aminoacyl-tRNA biosynthesis - Homo sapiens (human)
(Consensus)
Mouse Genome Informatics
- Gene name
- mt-Ty
- Phenotype