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PTMS (Parathymosin) is a Protein Coding gene. Diseases associated with PTMS include Muscular Dystrophy, Congenital, Lmna-Related and Hyperoxaluria, Primary, Type I.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005634 | nucleus | TAS | 10854063 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0002376 | immune system process | IEA | -- |
GO:0006260 | DNA replication | TAS | 10854063 |
Name | Status | Disease Links | Group | Role | Mechanism of Action | Clinical Trials |
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This gene was present in the common ancestor of mammals.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
Chimpanzee (Pan troglodytes) |
Mammalia | PTMS 31 |
|
OneToOne | |
Cow (Bos Taurus) |
Mammalia | PTMS 31 |
|
OneToOne | |
Dog (Canis familiaris) |
Mammalia | PTMS 30 31 |
|
OneToOne |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
dgv2323n54 | CNV | loss | 21841781 |
esv27720 | CNV | loss | 19812545 |
esv3580394 | CNV | gain | 25503493 |
nsv1071006 | CNV | deletion | 25765185 |
nsv1126309 | CNV | deletion | 24896259 |
nsv557257 | CNV | loss | 21841781 |
nsv557258 | CNV | loss | 21841781 |
nsv832323 | CNV | loss | 17160897 |
Disorder | Aliases | PubMed IDs |
---|---|---|
muscular dystrophy, congenital, lmna-related |
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hyperoxaluria, primary, type i |
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primary hyperoxaluria |
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carbohydrate metabolic disorder |
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cardiomyopathy, familial hypertrophic, 4 |
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