glycoproteinosis

Summary
Synonym
  • Mucolipidosis type I
  • sialidosis
Definition
A mucolipidosis that is characterized by a deficiency of the enzyme alpha-N -acetyl neuraminidase (sialidase).
Super Class
mucolipidosis
Disease Ontology
DOID:3343
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 5 entries
Gene ID Gene Symbol Description Source
4758 NEU1 neuraminidase 1
55283 MCOLN3 mucolipin TRP cation channel 3
57192 MCOLN1 mucolipin TRP cation channel 1
79158 GNPTAB N-acetylglucosamine-1-phosphate transferase subunits alpha and beta
84572 GNPTG N-acetylglucosamine-1-phosphate transferase subunit gamma
Displaying all 4 entries
Gene ID Gene Symbol Description Source
18010 Neu1 neuraminidase 1
94178 Mcoln1 mucolipin 1
171166 Mcoln3 mucolipin 3
214505 Gnptg N-acetylglucosamine-1-phosphotransferase, gamma subunit
Displaying 1 entry
Gene ID Gene Symbol Description Source
176074 cup-5 Polycystin cation channel PKD1/PKD2 domain-containing protein
The Human Phenotype Ontology
Displaying entries 21 - 30 of 94 in total
HPO ID HPO Term
HP:0001337 Tremor
HP:0001350 Slurred speech
HP:0001744 Splenomegaly
HP:0002007 Frontal bossing
HP:0002167 Abnormality of speech or vocalization
HP:0002353 EEG abnormality
HP:0002650 Scoliosis
HP:0002652 Skeletal dysplasia
HP:0002750 Delayed skeletal maturation
HP:0002808 Kyphosis
Displaying 1 entry
Gene ID Gene Symbol Description
4758 NEU1 neuraminidase 1

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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: December 9, 2024