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MGI:Ppt1

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Ppt1 ( synonyms: CLN1, D4Ertd184e )
Protein Name(s) palmitoyl-protein thioesterase 1,
External Links
MGI MGI:1298204

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0002084

protein depalmitoylation

MGI:MGI:2154013
PMID:11717424[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176390

P

From MGI

GO:0002084

protein depalmitoylation

MGI:MGI:3608104
PMID:16242638[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176390

P

From MGI

GO:0002084

protein depalmitoylation

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0005576

extracellular region

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

C

From MGI

GO:0005615

extracellular space

MGI:MGI:1276629
PMID:9685319[3]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005624

membrane fraction

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P45479

C

From MGI

GO:0005634

nucleus

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

C

From MGI

GO:0005764

lysosome

MGI:MGI:1276629
PMID:9685319[3]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005764

lysosome

MGI:MGI:3608104
PMID:16242638[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176390

C

From MGI

GO:0005764

lysosome

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P45479

C

From MGI

GO:0005764

lysosome

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

C

From MGI

GO:0005794

Golgi apparatus

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

C

From MGI

GO:0006309

DNA fragmentation involved in apoptotic nuclear change

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0006464

protein modification process

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR002472

P

From MGI

GO:0006898

receptor-mediated endocytosis

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0006907

pinocytosis

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0007040

lysosome organization

MGI:MGI:3612221
PMID:16368712[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176390

P

From MGI

GO:0007040

lysosome organization

MGI:MGI:3654230
PMID:16542649[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3527191

P

From MGI

GO:0007042

lysosomal lumen acidification

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0007269

neurotransmitter secretion

MGI:MGI:3608104
PMID:16242638[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176390

P

From MGI

GO:0007399

nervous system development

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0007420

brain development

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0007601

visual perception

MGI:MGI:3526470
PMID:15649713[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3527191

P

From MGI

GO:0007625

grooming behavior

MGI:MGI:2154013
PMID:11717424[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176390

P

From MGI

GO:0008021

synaptic vesicle

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P45479

C

From MGI

GO:0008021

synaptic vesicle

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

C

From MGI

GO:0008306

associative learning

MGI:MGI:3580037
PMID:15885820[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176390

P

From MGI

GO:0008344

adult locomotory behavior

MGI:MGI:2154013
PMID:11717424[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176390

P

From MGI

GO:0008344

adult locomotory behavior

MGI:MGI:3526470
PMID:15649713[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3527191

P

From MGI

GO:0008474

palmitoyl-(protein) hydrolase activity

MGI:MGI:2154013
PMID:11717424[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176390

F

From MGI

GO:0008474

palmitoyl-(protein) hydrolase activity

MGI:MGI:3608104
PMID:16242638[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176390

F

From MGI

GO:0008474

palmitoyl-(protein) hydrolase activity

MGI:MGI:3655641
PMID:12483688[8]

IDA: Inferred from Direct Assay

F

From MGI

GO:0008474

palmitoyl-(protein) hydrolase activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

F

From MGI

GO:0015031

protein transport

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0016042

lipid catabolic process

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0016290

palmitoyl-CoA hydrolase activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

F

From MGI

GO:0016787

hydrolase activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0378

F

From MGI

GO:0030308

negative regulation of cell growth

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0030424

axon

MGI:MGI:3655641
PMID:12483688[8]

IDA: Inferred from Direct Assay

C

From MGI

GO:0030424

axon

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

C

From MGI

GO:0030425

dendrite

MGI:MGI:1351142
PMID:10611498[9]

IDA: Inferred from Direct Assay

C

From MGI

GO:0031579

membrane raft organization

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0032429

regulation of phospholipase A2 activity

MGI:MGI:3711639
PMID:17341491[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176390

P

From MGI

GO:0043005

neuron projection

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P45479

C

From MGI

GO:0043025

neuronal cell body

MGI:MGI:1351142
PMID:10611498[9]

IDA: Inferred from Direct Assay

C

From MGI

GO:0043025

neuronal cell body

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P45479

C

From MGI

GO:0043066

negative regulation of apoptotic process

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0043524

negative regulation of neuron apoptotic process

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0044257

cellular protein catabolic process

MGI:MGI:3612221
PMID:16368712[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176390

P

From MGI

GO:0044265

cellular macromolecule catabolic process

MGI:MGI:3656423
PMID:15647513[11]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176390

P

From MGI

GO:0045121

membrane raft

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

C

From MGI

GO:0045202

synapse

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P45479

C

From MGI

GO:0048260

positive regulation of receptor-mediated endocytosis

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0048549

positive regulation of pinocytosis

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0051181

cofactor transport

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI

GO:0051186

cofactor metabolic process

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P50897

P

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. 1.0 1.1 1.2 1.3 Gupta P et al. (2001) Disruption of PPT1 or PPT2 causes neuronal ceroid lipofuscinosis in knockout mice. Proc Natl Acad Sci U S A 98: 13566-71 PubMed GONUTS page
  2. 2.0 2.1 2.2 2.3 Virmani T et al. (2005) Progressively reduced synaptic vesicle pool size in cultured neurons derived from neuronal ceroid lipofuscinosis-1 knockout mice. Neurobiol Dis 20: 314-23 PubMed GONUTS page
  3. 3.0 3.1 Salonen T et al. (1998) Mouse palmitoyl protein thioesterase: gene structure and expression of cDNA. Genome Res 8: 724-30 PubMed GONUTS page
  4. 4.0 4.1 Zhang Z et al. (2006) Palmitoyl-protein thioesterase-1 deficiency mediates the activation of the unfolded protein response and neuronal apoptosis in INCL. Hum Mol Genet 15: 337-46 PubMed GONUTS page
  5. Ahtiainen L et al. (2006) Palmitoyl protein thioesterase 1 (PPT1) deficiency causes endocytic defects connected to abnormal saposin processing. Exp Cell Res 312: 1540-53 PubMed GONUTS page
  6. 6.0 6.1 Jalanko A et al. (2005) Mice with Ppt1Deltaex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons. Neurobiol Dis 18: 226-41 PubMed GONUTS page
  7. Wendt KD et al. (2005) Behavioral assessment in mouse models of neuronal ceroid lipofuscinosis using a light-cued T-maze. Behav Brain Res 161: 175-82 PubMed GONUTS page
  8. 8.0 8.1 Ahtiainen L et al. (2003) Palmitoyl protein thioesterase 1 is targeted to the axons in neurons. J Comp Neurol 455: 368-77 PubMed GONUTS page
  9. 9.0 9.1 Isosomppi J et al. (1999) Developmental expression of palmitoyl protein thioesterase in normal mice. Brain Res Dev Brain Res 118: 1-11 PubMed GONUTS page
  10. Zhang Z et al. (2007) Production of lysophosphatidylcholine by cPLA2 in the brain of mice lacking PPT1 is a signal for phagocyte infiltration. Hum Mol Genet 16: 837-47 PubMed GONUTS page
  11. Cho SK et al. (2005) Characterization of lipid-linked oligosaccharide accumulation in mouse models of Batten disease. Glycobiology 15: 637-48 PubMed GONUTS page
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