STH - saitohin Gene
Also Known as MAPTIT
Species: Homo sapiens
About STH
This gene has 1 transcript (splice variant), 1 gene allele and 2 orthologues.
Summary
Involved in positive regulation of mRNA splicing, via spliceosome. Located in nucleus and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]
STH Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_001007532.3 | NP_001007533.1 | saitohin |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
16186110 | GOA |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in positive regulation of mRNA splicing, via spliceosome |
IGI
IGI: Inferred from genetic interaction
|
16186110 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in cytoplasm |
IDA
IDA: Inferred from direct assay
|
16186110 | GOA |
| located in nucleus |
IDA
IDA: Inferred from direct assay
|
16186110 | GOA |
| located in perinuclear region of cytoplasm |
IDA
IDA: Inferred from direct assay
|
16186110 | GOA |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
saitohin |
|
STH Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
STH | Q8IWL8 | TFG | Homo sapiens | Q92734 | 32296183 | |
|
Intra
|
STH | Q8IWL8 | SMARCD1 | Homo sapiens | Q96GM5 | 32296183 | |
|
Intra
|
STH | Q8IWL8 | PEF1 | Homo sapiens | Q9UBV8 | 32296183 | |
|
Intra
|
STH | Q8IWL8 | NTAQ1 | Homo sapiens | Q96HA8 | 32296183 | |
|
Intra
|
STH | Q8IWL8 | CSTF2T | Homo sapiens | Q9H0L4 | 32296183 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Ascaris Lumbricoides Infection |
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| Dracunculiasis |
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| Filarial Elephantiasis |
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| Acidophil Adenoma |
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| Enterobiasis |
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| Loiasis |
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| Frontotemporal Dementia |
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| Taeniasis |
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| Elephantiasis |
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| Parasitic Helminthiasis Infectious Disease |
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| Yaws |
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| Urinary Schistosomiasis |
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| Podoconiosis |
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| Trichuriasis |
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| Hymenolepiasis |
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| Chromophobe Adenoma |
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| Chromosome 17q21.31 Duplication Syndrome |
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| Intestinal Schistosomiasis |
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| Gnathomiasis |
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| Trachoma |
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| Strongyloidiasis |
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| Ascaridiasis |
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| Dysbaric Osteonecrosis |
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| Onchocerciasis |
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| Scabies |
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| Paragonimiasis |
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| Mite Infestation |
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| Toxocariasis |
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| Koolen-De Vries Syndrome |
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| Filariasis |
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| Parkinson Disease, Late-Onset |
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| Clonorchiasis |
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| Hydrocele |
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| Loeffler Syndrome |
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| Cysticercosis |
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| Developmental And Epileptic Encephalopathy 24 |
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| Gastroduodenal Crohn'S Disease |
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| Giardiasis |
|
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| Alzheimer Disease, Familial, 1 |
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| Dysentery |
|
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| Acute Diarrhea |
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| Parasitic Ectoparasitic Infectious Disease |
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