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)
Sequence
MGQPSLTWMLMVVVASWFITTAATDTSEARWCSECHSNATCTEDEAVTTCTCQEGFTGDGLTCVDLDECAIPGAHNCSANSSCVNTPGSFSCVCPEGFRLSPGLGCTDVDECAEPGLSHCHALATCVNVVGSYLCVCPAGYRGDGWHCECSPGSCGPGLDCVPEGDALVCADPCQAHRTLDEYWRSTEYGEGYACDTDLRGWYRFVGQGGARMAETCVPVLRCNTAAPMWLNGTHPSSDEGIVSRKACAHWSGHCCLWDASVQVKACAGGYYVYNLTAPPECHLAYCTDPSSVEGTCEECSIDEDCKSNNGRWHCQCKQDFNITDISLLEHRLECGANDMKVSLGKCQLKSLGFDKVFMYLSDSRCSGFNDRDNRDWVSVVTPARDGPCGTVLTRNETHATYSNTLYLADEIIIRDLNIKINFACSYPLDMKVSLKTALQPMVSALNIRVGGTGMFTVRMALFQTPSYTQPYQGSSVTLSTEAFLYVGTMLDGGDLSRFALLMTNCYATPSSNATDPLKYFIIQDRCPHTRDSTIQVVENGESSQGRFSVQMFRFAGNYDLVYLHCEVYLCDTMNEKCKPTCSGTRFRSGSVIDQSRVLNLGPITRKGVQATVSRAFSSLGLLKVWLPLLLSATLTLTFQ
Glycosylation Sites
Displaying entries 1 - 10 of 18 in total
Position Description PubMed ID GlyTouCan ID Source
38 N-linked (GlcNAc...) asparagine
76 N-linked (GlcNAc...) asparagine
80 N-linked (GlcNAc...) asparagine
89
154
225
232 N-linked (GlcNAc...) (complex) asparagine
252
275 N-linked (GlcNAc...) (high mannose) asparagine
277
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying 1 entry
Pathway Name Organism
Asparagine N-linked glycosylation Homo sapiens
Disease
Displaying entries 1 - 10 of 156 in total
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

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024