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POMT1

protein-coding gene in the species Homo sapiens
Gene gene Q18035505
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POMT1

Summary

POMT1 is a gene[1].

Key Facts

  • POMT1's instance of is recorded as gene[2].
  • POMT1 is a type of protein-coding gene[3].
  • POMT1's HomoloGene ID is recorded as 68548[4].
  • POMT1's ortholog is recorded as Pomt1[5].
  • POMT1's ortholog is recorded as Pomt1[6].
  • POMT1's ortholog is recorded as PMT4[7].
  • POMT1's ortholog is recorded as rt[8].
  • POMT1's ortholog is recorded as pomt1[9].
  • POMT1's encodes is recorded as Protein O-mannosyltransferase 1[10].
  • POMT1's encodes is recorded as Protein O-mannosyl-transferase 1[11].
  • POMT1's found in taxon is recorded as Homo sapiens[12].
  • POMT1's genetic association is recorded as Walker–Warburg syndrome[13].
  • POMT1's genetic association is recorded as autosomal recessive limb-girdle muscular dystrophy type 2K[14].
  • POMT1's exact match is recorded as http://identifiers.org/ncbigene/10585[15].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Ensembl Release 87. wikidata.org.
  3. [4] ↑ . Q20641742. Retrieved . wikidata.org.
  4. [5] ↑ . HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
  5. [6] ↑ . HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
  6. [7] ↑ . HomoloGene build68. wikidata.org.
  7. [8] ↑ . HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
  8. [9] ↑ . HomoloGene build68. wikidata.org.
  9. [10] ↑ . Q905695. Retrieved . wikidata.org.
  10. [11] ↑ . Q905695. Retrieved . wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  13. [14] ↑ . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  14. [15] ↑ . Identifiers.org. ebi.ac.uk. Provenance: wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

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). POMT1. Retrieved May 3, 2026, from https://4ort.xyz/entity/pomt1-q18035505
MLA “POMT1.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/pomt1-q18035505.
BibTeX @misc{4ortxyz_pomt1-q18035505_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{POMT1}}, year = {2026}, url = {https://4ort.xyz/entity/pomt1-q18035505}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): POMT1 — https://4ort.xyz/entity/pomt1-q18035505 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/pomt1-q18035505 · Last refreshed:

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 18d ago · Mathieu Kappler · 2026-05-20 view diff on Wikidata ↗
    Hgnc gene symbol → POMT1
    Genetic association → Walker–Warburg syndrome, autosomal recessive limb-girdle muscular dystrophy type 2K
    Refseq rna id → XR_929703, NM_001077365, NM_001077366 +24
    Exact match → http://identifiers.org/ncbigene/10585
    + 14 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||gsw */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/32527|batch #32527]]: human gene name and description in Alemannic"
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