Mannose-P-dolichol utilization defect 1

mammalian protein found in Homo sapiens
Protein protein Q21120860
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Summary

Mannose-P-dolichol utilization defect 1 is a protein[1].

Key Facts

  • Mannose-P-dolichol utilization defect 1's instance of is recorded as protein[2].
  • Mannose-P-dolichol utilization defect 1's UniProt protein ID is recorded as O75352[3].
  • Mannose-P-dolichol utilization defect 1's part of is recorded as Mannose-P-dolichol utilization defect 1 protein[4].
  • Mannose-P-dolichol utilization defect 1's part of is recorded as PQ-loop repeat, protein family[5].
  • Mannose-P-dolichol utilization defect 1's has part is recorded as PQ-loop repeat[6].
  • Mannose-P-dolichol utilization defect 1's RefSeq protein ID is recorded as NP_001317002[7].
  • Mannose-P-dolichol utilization defect 1's RefSeq protein ID is recorded as NP_004861[8].
  • Mannose-P-dolichol utilization defect 1's RefSeq protein ID is recorded as XP_006721660[9].
  • Mannose-P-dolichol utilization defect 1's RefSeq protein ID is recorded as XP_006721661[10].
  • Mannose-P-dolichol utilization defect 1's RefSeq protein ID is recorded as XP_011522383[11].
  • Mannose-P-dolichol utilization defect 1's RefSeq protein ID is recorded as XP_024306808[12].
  • Mannose-P-dolichol utilization defect 1's molecular function is recorded as protein binding[13].
  • Mannose-P-dolichol utilization defect 1's cell component is recorded as integral component of membrane[14].
  • Mannose-P-dolichol utilization defect 1's cell component is recorded as extracellular exosome[15].
  • Mannose-P-dolichol utilization defect 1's cell component is recorded as endoplasmic reticulum membrane[16].
  • Mannose-P-dolichol utilization defect 1's cell component is recorded as membrane[17].
  • Mannose-P-dolichol utilization defect 1's cell component is recorded as membrane[18].
  • Mannose-P-dolichol utilization defect 1's biological process is recorded as dolichol-linked oligosaccharide biosynthetic process[19].
  • Mannose-P-dolichol utilization defect 1's biological process is recorded as oligosaccharide biosynthetic process[20].
  • Mannose-P-dolichol utilization defect 1's biological process is recorded as protein folding[21].
  • Mannose-P-dolichol utilization defect 1's biological process is recorded as transport[22].
  • Mannose-P-dolichol utilization defect 1's biological process is recorded as oligosaccharide biosynthetic process[23].
  • Mannose-P-dolichol utilization defect 1's encoded by is recorded as MPDU1[24].
  • Mannose-P-dolichol utilization defect 1's found in taxon is recorded as Homo sapiens[25].
  • Mannose-P-dolichol utilization defect 1's Ensembl protein ID is recorded as ENSP00000250124[26].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . UniProt. Retrieved . wikidata.org.
  2. [3] ↑ . UniProt. Retrieved . wikidata.org.
  3. [4] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  6. [7] ↑ . Q20641742. Retrieved . wikidata.org.
  7. [8] ↑ . Q20641742. Retrieved . wikidata.org.
  8. [9] ↑ . Q20641742. Retrieved . wikidata.org.
  9. [10] ↑ . Q20641742. Retrieved . wikidata.org.
  10. [11] ↑ . Q20641742. Retrieved . wikidata.org.
  11. [12] ↑ . Q20641742. Retrieved . wikidata.org.
  12. [13] ↑ . Screening of hepatocyte proteins binding to F protein of hepatitis C virus by yeast two-hybrid system. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  13. [14] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  14. [15] ↑ . Proteomic analysis of podocyte exosome-enriched fraction from normal human urine. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  15. [16] ↑ . Requirement of the Lec35 gene for all known classes of monosaccharide-P-dolichol-dependent glycosyltransferase reactions in mammals. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  16. [17] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] ↑ . MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] ↑ . MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  20. [21] ↑ . Requirement of the Lec35 gene for all known classes of monosaccharide-P-dolichol-dependent glycosyltransferase reactions in mammals. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  21. [22] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] ↑ . MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  23. [24] ↑ . UniProt. Retrieved . wikidata.org.
  24. [25] ↑ . UniProt. Retrieved . wikidata.org.
  25. [26] ↑ . Ensembl Release 99. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). Mannose-P-dolichol utilization defect 1. Retrieved May 3, 2026, from https://4ort.xyz/entity/mannose-p-dolichol-utilization-defect-1-q21120860
MLA “Mannose-P-dolichol utilization defect 1.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/mannose-p-dolichol-utilization-defect-1-q21120860.
BibTeX @misc{4ortxyz_mannose-p-dolichol-utilization-defect-1-q21120860_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Mannose-P-dolichol utilization defect 1}}, year = {2026}, url = {https://4ort.xyz/entity/mannose-p-dolichol-utilization-defect-1-q21120860}, note = {Accessed: 2026-05-03}}
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