transaldolase 1

Summary
Gene Symbol
  • TALDO1
Organism
Homo sapiens (human)
External Links
NCBI Gene
6888
HGNC
11559
KEGG Gene ID
hsa:6888
PubChem
6888
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Acetylation
  • Alternative initiation
  • Cytoplasm
  • Disease variant
  • Nucleus
  • Pentose shunt
  • Phosphoprotein
  • Reference proteome
  • Schiff base
  • Transferase
Proteins
Displaying all 2 entries
UniProt Protein Name
A0A140VK56
P37837
Gene Ontology (GO)
GO Hierarchy
KEGG BRITE Database
Orthology
K00616
Name
transaldolase [EC:2.2.1.2]
References
Disease
Disease Ontology
Displaying entries 1 - 10 of 73 in total
DO ID Disease Name Source
DOID:0110114 atrial heart septal defect 9
DOID:0014667 disease of metabolism
DOID:0050427 xeroderma pigmentosum
DOID:0050865 tongue squamous cell carcinoma
DOID:0060262 gallbladder disease
DOID:0060891 Parkinson's disease 19A
DOID:0060895 Parkinson's disease 4
DOID:0060896 Parkinson's disease 23
DOID:0080145 childhood T-cell acute lymphoblastic leukemia
DOID:0110106 atrial heart septal defect 1
The Human Phenotype Ontology
Displaying entries 1 - 10 of 45 in total
HPO ID HPO Term
HP:0000007 Autosomal recessive inheritance
HP:0000056 Abnormal clitoris morphology
HP:0000077 Abnormality of the kidney
HP:0000154 Wide mouth
HP:0000233 Thin vermilion border
HP:0000260 Wide anterior fontanel
HP:0000322 Short philtrum
HP:0000325 Triangular face
HP:0000369 Low-set ears
HP:0000470 Short neck
Displaying all 2 entries
Disease ID Disease Name
OMIM:606003
  • transaldolase deficiency
ORPHA:101028
  • transaldolase deficiency

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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