thrombomodulin

Summary
Gene Symbol
  • THBD
Organism
Homo sapiens (human)
NCBI Gene
7056
PubChem
7056
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Direct protein sequencing
  • Disease variant
  • Disulfide bond
  • EGF-like domain
  • Hemolytic uremic syndrome
  • Hydroxylation
  • Proteoglycan
  • Receptor
  • Reference proteome
  • Repeat
  • Signal
  • Thrombophilia
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
P07204
  • Fetomodulin
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Kinase
Functional Category
  • J: Translation, ribosomal structure and biogenesis
  • K: Transcription
  • T: Signal transduction mechanisms
Displaying all 4 entries
Gene Ontology
ATP binding
kinase activity
nucleotide binding
phosphorylation
Disease
Disease Ontology
Displaying all 9 entries
DO ID Disease Name Source
DOID:0080301 atypical hemolytic-uremic syndrome
DOID:0111908 thrombophilia due to thrombomodulin defect
DOID:11247 disseminated intravascular coagulation
DOID:2841 asthma
DOID:3021 acute kidney failure
DOID:3410 carotid artery thrombosis
DOID:3526 cerebral infarction
DOID:409 liver disease
DOID:7148 rheumatoid arthritis

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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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