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MYT1L

protein-coding gene in the species Homo sapiens
Gene gene Q18036678
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MYT1L

Summary

MYT1L is a gene[1]. MYT1L ranks in the top 2% of gene entities by monthly Wikipedia readership (15 views/month).[2]

Key Facts

  • MYT1L's instance of is recorded as gene[3].
  • MYT1L is a type of protein-coding gene[4].
  • MYT1L's HomoloGene ID is recorded as 7435[5].
  • MYT1L's genomic start is recorded as 1789113[6].
  • MYT1L's genomic start is recorded as 1792885[7].
  • MYT1L's genomic end is recorded as 2335032[8].
  • MYT1L's genomic end is recorded as 2331664[9].
  • MYT1L's ortholog is recorded as Myt1l[10].
  • MYT1L's ortholog is recorded as Myt1l[11].
  • MYT1L's ortholog is recorded as myt1la[12].
  • MYT1L's encodes is recorded as Myelin transcription factor 1 like[13].
  • MYT1L's found in taxon is recorded as Homo sapiens[14].

Why It Matters

MYT1L ranks in the top 2% of gene entities by monthly Wikipedia readership (15 views/month).[2] MYT1L is known by 7 alternative names across languages and contexts.[15]

References

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

Direct Wikidata claims

  1. [3] ↑ . ensembl Release 106. wikidata.org.
  2. [4] ↑ . Ensembl Release 87. wikidata.org.
  3. [5] ↑ . Q20641742. Retrieved . wikidata.org.
  4. [6] ↑ . ensembl Release 106. wikidata.org.
  5. [7] ↑ . ensembl Release 106. wikidata.org.
  6. [8] ↑ . ensembl Release 106. wikidata.org.
  7. [9] ↑ . ensembl Release 106. wikidata.org.
  8. [10] ↑ . HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
  9. [11] ↑ . HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
  10. [12] ↑ . HomoloGene build68. wikidata.org.
  11. [13] ↑ . Q905695. Retrieved . wikidata.org.
  12. [14] ↑ . ensembl Release 106. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [15] ↑ . Wikidata aliases. 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). MYT1L. Retrieved May 3, 2026, from https://4ort.xyz/entity/myt1l
MLA “MYT1L.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/myt1l.
BibTeX @misc{4ortxyz_myt1l_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{MYT1L}}, year = {2026}, url = {https://4ort.xyz/entity/myt1l}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): MYT1L — https://4ort.xyz/entity/myt1l (retrieved 2026-05-03)

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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. 12d ago · Mathieu Kappler · 2026-05-20 view diff on Wikidata ↗
    Genetic association → attention deficit hyperactivity disorder, autosomal dominant non-syndromic intellectual disability 39, syndromic intellectual disability
    Subclass of → —
    Chromosome → human chromosome 2
    Strand orientation → reverse strand
    + 8 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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