MAPT

GENERAL INFORMATION

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Gene name

MAPT

Gene description

Microtubule-associated protein tau

Protein class

Candidate cardiovascular disease genes
Disease related genes
FDA approved drug targets
Plasma proteins
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

13
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (cerebral cortex)
GTEx:Group enriched (cerebellum, cerebral cortex, hippocampus, skeletal muscle)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression in CNS, peripheral ganglia and nerves, kidney, skeletal and heart muscle.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data.

Data reliability

Supportive based on 3 antibodies.
HPA069524 , HPA069570 , CAB000151
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Cerebellum

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (cerebral cortex)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (cerebellum, cerebral cortex, hippocampus, skeletal muscle)

Organ

Expression



GENE INFORMATION

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Gene name

MAPT (HGNC Symbol)

Synonyms

DDPAC, FLJ31424, FTDP-17, MAPTL, MGC138549, MSTD, MTBT1, MTBT2, PPND, PPP1R103, tau

Description

Microtubule-associated protein tau (HGNC Symbol)

Entrez gene summary

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]

Chromosome

17

Cytoband

q21.31

Chromosome location (bp)

45894382 - 46028334

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000186868 (version 78.38)

Entrez gene

4137

UniProt

P10636 (UniProt - Evidence at protein level)

neXtProt

NX_P10636

Antibodypedia

MAPT antibodies


PROTEIN BROWSER

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ENST00000262410
 
ENST00000334239
 
ENST00000340799
 
ENST00000344290
 
ENST00000351559
 
ENST00000415613
 
ENST00000420682
 
ENST00000431008
 
ENST00000446361
 
ENST00000535772
 
ENST00000571987
 
ENST00000574436
 
ENST00000576518
 
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PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

MAPT-001 ENSP00000334886
ENST00000334239
P10636
Show all »
Show » Show » 352 36.8 No 0
MAPT-002 ENSP00000408975
ENST00000446361
P10636
Show all »
Show » Show » 383 40 No 0
MAPT-003 ENSP00000413056
ENST00000420682
P10636
Show all »
Show » Show » 412 43 No 0
MAPT-004 ENSP00000410838
ENST00000415613
P10636
Show all »
Show » Show » 776 80.9 No 0
MAPT-006 ENSP00000389250
ENST00000431008
P10636
Show all »
Show » Show » 410 42.6 No 0
MAPT-007 ENSP00000460965
ENST00000574436
P10636
Show all »
Show » Show » 441 45.8 No 0
MAPT-008 ENSP00000458742
ENST00000571987
P10636
Show all »
Show » Show » 758 78.9 No 0
MAPT-009 ENSP00000458621
ENST00000576518
I3L170
Show all »
Show » Show » 341 35.7 No 0
MAPT-201 ENSP00000262410
ENST00000262410
P10636
Show all »
Show » Show » 758 78.9 No 0
MAPT-202 ENSP00000340438
ENST00000340799
P10636
Show all »
Show » Show » 412 43 No 0
MAPT-203 ENSP00000340820
ENST00000344290
P10636
Show all »
Show » Show » 776 80.9 No 0
MAPT-204 ENSP00000303214
ENST00000351559
P10636
Show all »
Show » Show » 441 45.8 No 0
MAPT-205 ENSP00000443028
ENST00000535772
P10636
Show all »
Show » Show » 410 42.6 No 0