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MAPT

protein-coding gene in the species Homo sapiens
Class type of: protein-coding gene Q14865307

Facts

13 properties
Instance of
gene
Subclass of
protein-coding gene
Chromosome
human chromosome 17
Cytogenetic location
17q21.31
Encodes
microtubule associated protein tau[9]
Expressed in
superior frontal gyrus, prefrontal cortex, right frontal lobe, right hemisphere of cerebellum, Brodmann area 9, primary visual cortex, anterior cingulate cortex, hypothalamus, hippocampus proper, temporal lobe
Found in taxon
Homo sapiens[10]
Genetic association
interstitial lung disease, progressive supranuclear palsy, Parkinson's disease, Pick disease, semantic dementia
Genomic end
46028334, 44105700[6][7]
Genomic start
43971748, 45894527[4][5]
HomoloGene ID
74962[3]
Ortholog
Mapt, Mapt[8]
Strand orientation
forward strand
🏷️ Also known as
en TAU en Tau proteins en tau-40 en DDPAC en FTDP-17 en MAPT en MAPTL en microtubule associated protein tau en MSTD en MTBT1 en MTBT2 en PPND en PPP1R103 ar بروتين تاو cs Tau (protein) el Πρωτεΐνη Tau fa پروتئین تاو he חלבון טאו id Protein tau it Proteina Tau
🔖 Identifiers · 11
Ensembl gene ID
ENSG00000186868, ENSG00000276155, ENSG00000277956
Ensembl transcript ID
ENST00000262410, ENST00000334239, ENST00000344290, ENST00000351559, ENST00000415613, ENST00000420682, ENST00000431008, ENST00000446361, ENST00000535772, ENST00000570299, ENST00000571311, ENST00000571987, ENST00000572440, ENST00000574436, ENST00000576518, ENST00000577017, ENST00000620070, ENST00000632500, ENST00000626880, ENST00000633054, ENST00000631447, ENST00000633801, ENST00000612872, ENST00000620981, ENST00000627800, ENST00000622106, ENST00000631701, ENST00000618029, ENST00000632122, ENST00000625417, ENST00000625688, ENST00000627711, ENST00000633415, ENST00000626571, ENST00000632975, ENST00000633047, ENST00000628393, ENST00000618825, ENST00000621329, ENST00000622728, ENST00000634049, ENST00000628437, ENST00000620818, ENST00000631918, ENST00000627067, ENST00000613360, ENST00000629368, ENST00000633409, ENST00000680542, ENST00000680674
Entrez Gene ID
4137
Exact match
identifiers.org
Google Knowledge Graph ID
/g/1218rvxg
HGNC ID
6893
HGNC gene symbol
MAPT
JSTOR topic ID (archived)
tau-proteins
OMIM ID
157140
RefSeq RNA ID
NM_001123066, NM_001123067, NM_001203251, NM_001203252, NM_005910, NM_016834, NM_016835, NM_016841, XM_005257362, XM_005257365, XM_005257366, XM_005257367, XM_005257368, XM_005257369, XM_005257370, XM_005257371, NM_001377265, NM_001377266, NM_001377267, NM_001377268, NR_165166, XM_047436074, XM_047436075, XM_047436076, XM_047436077, XM_047436078, XM_047436079, XM_047436080, XM_047436081
UMLS CUI
C1446659

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Summary

MAPT is a gene[1]. MAPT is a type of protein-coding gene[2].

References

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

Direct Wikidata claims

  1. [2] ↑ . NCBI homo sapiens annotation release 107. Retrieved . wikidata.org.
  2. [3] ↑ . NCBI Gene. Retrieved . wikidata.org.
  3. [4] ↑ . ensembl Release 106. wikidata.org.
  4. [5] ↑ . ensembl Release 106. wikidata.org.
  5. [6] ↑ . ensembl Release 106. wikidata.org.
  6. [7] ↑ . ensembl Release 106. wikidata.org.
  7. [8] ↑ . HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
  8. [9] ↑ . UniProt. Retrieved . wikidata.org.
  9. [10] ↑ . ensembl Release 106. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). MAPT. Retrieved November 7, 2026, from https://4ort.xyz/entity/mapt-q14865307
MLA “MAPT.” 4ort.xyz Knowledge Graph, 4ort.xyz, 7 Nov. 2026, https://4ort.xyz/entity/mapt-q14865307.
BibTeX @misc{4ortxyz_mapt-q14865307_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{MAPT}}, year = {2026}, url = {https://4ort.xyz/entity/mapt-q14865307}, note = {Accessed: 2026-11-07}}
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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. 25w ago · Mathieu Kappler · 2026-05-20 view diff on Wikidata ↗
    HGNC gene symbol → MAPT
    Genetic association → interstitial lung disease, progressive supranuclear palsy, Parkinson's disease +1
    RefSeq RNA ID → NM_001123066, NM_001123067, NM_001203251 +26
    Exact match → http://identifiers.org/ncbigene/4137
    + 23 other properties edited (see Wikidata diff for full list)
    "Changed [gsw] labels, descriptions or aliases: QuickStatements 3.0 batch #32527: human gene name and description in Alemannic"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.