Gene: MAPT (microtubule-associated protein tau)  Homo sapiens

Symbol: MAPT
Name: microtubule-associated protein tau
Description: This gene encodes the microtubule-associated protein tau (MAPT) whose transcript undergoes complex, regulated alternative splicing, giving rise to several mRNA species. MAPT transcripts are differentially expressed in the nervous system, depending on stage of neuronal maturation and neuron type. MAPT gene mutations have been associated with several neurodegenerative disorders such as Alzheimer's disease, Pick's disease, frontotemporal dementia, cortico-basal degeneration and progressive supranuclear palsy. [provided by RefSeq, Jul 2008]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: DDPAC; FLJ31424; FTDP-17; G protein beta1/gamma2 subunit-interacting factor 1; MAPTL; MGC138549; microtubule-associated protein tau; microtubule-associated protein tau, isoform 4; MSTD; MTBT1; MTBT2; neurofibrillary tangle protein; OTTHUMP00000239567; OTTHUMP00000239568; OTTHUMP00000239569; OTTHUMP00000239570; OTTHUMP00000239571; paired helical filament-tau; PHF-tau; PPND; TAU
Orthologs: Mus musculus : Mapt (microtubule-associated protein tau)  MGI
Rattus norvegicus : Mapt (microtubule-associated protein tau)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_11745,168,771 - 45,302,704+NCBI
Human Genome Assembly HuRef1739,635,406 - 39,768,427+NCBI
Human Genome Assembly GRCh371743,971,748 - 44,105,700+NCBI
Human Genome Assembly Build 361741,327,624 - 41,461,547+NCBI
Human Cytogenetic Map17q21.1 NCBI
Human Genome Assembly1741,327,623 - 41,458,611 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on MAPT
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 736496
Created: 2004-02-06
Species: Homo sapiens
Last Modified: 2013-04-23
Status: ACTIVE