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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Uromodulin
Summary
- UniProt ID
- P07911
- Gene Symbol
-
- UMOD
- Organism
- Homo sapiens (human)
External Links
- GlycoProtDB
- GPDB0011425
- GlyConnect
- GlyGen
- P07911
- PubChem
- P07911
- RaftProt
- P07911
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Ciliopathy
- Cilium
- Direct protein sequencing
- Disease variant
- Disulfide bond
- EGF-like domain
- GPI-anchor
- Innate immunity
- Nephronophthisis
- Reference proteome
- Repeat
- Secreted
- Signal
- Gene Ontology (GO)
| GO Term |
|---|
| basolateral plasma membrane |
| apical plasma membrane |
| spindle pole |
| GO Term |
|---|
| calcium ion binding |
| IgG binding |
Sequence
MGQPSLTWMLMVVVASWFITTAATDTSEARWCSECHSNATCTEDEAVTTCTCQEGFTGDGLTCVDLDECAIPGAHNCSANSSCVNTPGSFSCVCPEGFRLSPGLGCTDVDECAEPGLSHCHALATCVNVVGSYLCVCPAGYRGDGWHCECSPGSCGPGLDCVPEGDALVCADPCQAHRTLDEYWRSTEYGEGYACDTDLRGWYRFVGQGGARMAETCVPVLRCNTAAPMWLNGTHPSSDEGIVSRKACAHWSGHCCLWDASVQVKACAGGYYVYNLTAPPECHLAYCTDPSSVEGTCEECSIDEDCKSNNGRWHCQCKQDFNITDISLLEHRLECGANDMKVSLGKCQLKSLGFDKVFMYLSDSRCSGFNDRDNRDWVSVVTPARDGPCGTVLTRNETHATYSNTLYLADEIIIRDLNIKINFACSYPLDMKVSLKTALQPMVSALNIRVGGTGMFTVRMALFQTPSYTQPYQGSSVTLSTEAFLYVGTMLDGGDLSRFALLMTNCYATPSSNATDPLKYFIIQDRCPHTRDSTIQVVENGESSQGRFSVQMFRFAGNYDLVYLHCEVYLCDTMNEKCKPTCSGTRFRSGSVIDQSRVLNLGPITRKGVQATVSRAFSSLGLLKVWLPLLLSATLTLTFQ
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 322 |
|
|
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Asparagine N-linked glycosylation | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:4989 | pancreatitis | |
| DOID:0110047 | Alzheimer's disease 14 | |
| DOID:0050576 | Senior-Loken syndrome | |
| DOID:0050741 | alcohol dependence | |
| DOID:0050745 | diffuse large B-cell lymphoma | |
| DOID:0060062 | familial juvenile hyperuricemic nephropathy | |
| DOID:0060239 | Van der Woude syndrome | |
| DOID:0060262 | gallbladder disease | |
| DOID:0060350 | adenine phosphoribosyltransferase deficiency | |
| DOID:0060357 | chylomicron retention disease |
