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Standards Ontologies Notations
mannose-P-dolichol utilization defect 1

Summary
Gene Symbol
  • MPDU1
Aliases
  • CDGIf
  • Lec35
  • PQLC5
  • SL15
  • SLC66A5
Organism
Homo sapiens (human)
External Links
NCBI Gene
9526
HGNC
7207
KEGG Gene ID
hsa:9526
PubChem
9526
Alliance of Genome Resources
Annotation
Keyword
  • Acetylation
  • Alternative splicing
  • Congenital disorder of glycosylation
  • Disease variant
  • Proteomics identification
  • Reference proteome
  • Repeat
  • Transmembrane helix
  • Transport
Proteins
Displaying all 4 entries
UniProt Protein Name
A0A0S2Z4W8
J3QW43
B4DLH7
O75352
  • Suppressor of Lec15 and Lec35 glycosylation mutation homolog
Annotation information from UniProt.
Gene Ontology (GO)
Displaying all 3 entries
GO Term Evidence Code PMID
oligosaccharide biosynthetic process
dolichol-linked oligosaccharide biosynthetic process
protein folding
GO Hierarchy
Displaying 1 entry
GO Term Evidence Code PMID
protein binding
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
KEGG BRITE Database
Orthology
K09660
Name
mannose-P-dolichol utilization defect 1
References
Disease
Disease Ontology
Displaying entries 21 - 30 of 35 in total
DO ID Disease Name Source
DOID:2738 pseudoxanthoma elasticum
DOID:2747 glycogen storage disease
DOID:2862 glucosephosphate dehydrogenase deficiency
DOID:2986 IgA glomerulonephritis
DOID:4702 mongolian spot
DOID:5212 congenital disorder of glycosylation
DOID:539 ophthalmoplegia
DOID:540 strabismus
DOID:5723 optic atrophy
DOID:9266 cystinuria
The Human Phenotype Ontology
Displaying entries 31 - 40 of 40 in total
HPO ID HPO Term
HP:0005478 Prominent frontal sinuses
HP:0007965 Undetectable visual evoked potentials
HP:0008064 Ichthyosis
HP:0008529 Absence of acoustic reflex
HP:0008947 Infantile muscular hypotonia
HP:0010864 Intellectual disability, severe
HP:0011344 Severe global developmental delay
HP:0011968 Feeding difficulties
HP:0012379 Abnormal circulating enzyme concentration or activity
HP:0012704 Widened subarachnoid space
Displaying all 2 entries
Disease ID Disease Name
ORPHA:79323
  • MPDU1-congenital disorder of glycosylation
OMIM:609180
  • MPDU1-congenital disorder of glycosylation
PubChem Disease
MedGen Diseases
OMIM Phenotypes
KEGG Diseases
Gene-Disease-Co-Occurrences-in-Literature (PubChem)
Ortholog
Displaying entries 1 - 10 of 76 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
179218 WB:WBGene00018181
33717 FB:FBgn0031662
415220 ZFIN:ZDB-GENE-040625-135 DANRE40069
447806 ZFIN:ZDB-GENE-040912-9
103045040 ASTMX05664
108268195 ICTPU32947
113580782 ELEEL27257
106577903 SALSA134091
106608952 SALSA134091
115194609 SALTR64854
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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