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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Myotubularin-related protein 1
Summary
- UniProt ID
- Q13613
- Gene Symbol
-
- MTMR1
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- Q13613
- PubChem
- Q13613
- SwissLipids
- The Human Metabolome Database
- HMDBP11836
- The O-GlcNAc Database
- Q13613
- O-GlcNAcAtlas
- Q13613
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Cell membrane
- Cytoplasm
- Hydrolase
- Lipid metabolism
- Phosphoprotein
- Reference proteome
- Gene Ontology (GO)
| GO Term |
|---|
| regulation of phosphatidylinositol dephosphorylation |
| phosphatidylinositol dephosphorylation |
| phosphatidylinositol biosynthetic process |
| GO Term |
|---|
| cytoplasm |
| plasma membrane |
| membrane |
| cytosol |
Sequence
MDRPAAAAAAGCEGGGGPNPGPAGGRRPPRAAGGATAGSRQPSVETLDSPTGSHVEWCKQLIAATISSQISGSVTSENVSRDYKALRDGNKLAQMEEAPLFPGESIKAIVKDVMYICPFMGAVSGTLTVTDFKLYFKNVERDPHFILDVPLGVISRVEKIGAQSHGDNSCGIEIVCKDMRNLRLAYKQEEQSKLGIFENLNKHAFPLSNGQALFAFSYKEKFPINGWKVYDPVSEYKRQGLPNESWKISKINSNYEFCDTYPAIIVVPTSVKDDDLSKVAAFRAKGRVPVLSWIHPESQATITRCSQPLVGPNDKRCKEDEKYLQTIMDANAQSHKLIIFDARQNSVADTNKTKGGGYESESAYPNAELVFLEIHNIHVMRESLRKLKEIVYPSIDEARWLSNVDGTHWLEYIRMLLAGAVRIADKIESGKTSVVVHCSDGWDRTAQLTSLAMLMLDSYYRTIKGFETLVEKEWISFGHRFALRVGHGNDNHADADRSPIFLQFVDCVWQMTRQFPSAFEFNELFLITILDHLYSCLFGTFLCNCEQQRFKEDVYTKTISLWSYINSQLDEFSNPFFVNYENHVLYPVASLSHLELWVNYYVRWNPRMRPQMPIHQNLKELLAVRAELQKRVEGLQREVATRAVSSSSERGSSPSHSATSVHTSV
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 292 |
|
|||
| 664 |
|
G49108TO
G70994MS
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| RHOF GTPase cycle | Homo sapiens |
| Synthesis of PIPs at the plasma membrane | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050759 | myotonic dystrophy type 2 | |
| DOID:0110191 | Charcot-Marie-Tooth disease type 4B1 | |
| DOID:0111225 | centronuclear myopathy X-linked | |
| DOID:11722 | myotonic dystrophy type 1 | |
| DOID:14717 | centronuclear myopathy | |
| DOID:422 | congenital structural myopathy |
