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MGI:Als2

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Als2 ( synonyms: Als2cr6, Alsin )
Protein Name(s) amyotrophic lateral sclerosis 2 (juvenile) homolog (human),
External Links
MGI MGI:1921268

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0001662

behavioral fear response

MGI:MGI:3588008
PMID:16107644[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3522476

P

From MGI

GO:0001726

ruffle

MGI:MGI:3759339
PMID:15033976[2]

IDA: Inferred from Direct Assay

C

From MGI

GO:0001881

receptor recycling

MGI:MGI:3690398
PMID:17093100[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3522476

P

From MGI

GO:0001934

positive regulation of protein phosphorylation

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

P

From MGI

GO:0005085

guanyl-nucleotide exchange factor activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0344

F

From MGI

GO:0005089

Rho guanyl-nucleotide exchange factor activity

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR000219

F

From MGI

GO:0005097

Rab GTPase activator activity

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

EMBL:AB053305

F

From MGI

GO:0005515

protein binding

MGI:MGI:3690398
PMID:17093100[3]

IPI: Inferred from Physical Interaction

UniProtKB:Q925T6

F

From MGI

GO:0005543

phospholipid binding

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001849

F

From MGI

GO:0005622

intracellular

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR000219

C

From MGI

GO:0005622

intracellular

MGI:MGI:3611988
PMID:16321985[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3612978

C

From MGI

GO:0005622

intracellular

MGI:MGI:3652645
PMID:16769894[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3653518

C

From MGI

GO:0005634

nucleus

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

EMBL:AB053306

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:3590026
PMID:16085057[6]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_001013431

C

From MGI

GO:0005769

early endosome

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

EMBL:AB053305

C

From MGI

GO:0005769

early endosome

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

C

From MGI

GO:0005792

microsome

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_001013431

C

From MGI

GO:0005813

centrosome

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

C

From MGI

GO:0005829

cytosol

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

EMBL:AB053305
EMBL:AB053306

C

From MGI

GO:0005829

cytosol

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

C

From MGI

GO:0006979

response to oxidative stress

MGI:MGI:3588008
PMID:16107644[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3522476

P

From MGI

GO:0007032

endosome organization

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

P

From MGI

GO:0007041

lysosomal transport

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

EMBL:AB053305

P

From MGI

GO:0007409

axonogenesis

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_001013431

P

From MGI

GO:0007528

neuromuscular junction development

MGI:MGI:3611988
PMID:16321985[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3612978

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:3588008
PMID:16107644[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3522476

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:3652645
PMID:16769894[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3653518

P

From MGI

GO:0008104

protein localization

MGI:MGI:3690398
PMID:17093100[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3522476

P

From MGI

GO:0008219

cell death

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_001013431

P

From MGI

GO:0014069

postsynaptic density

MGI:MGI:3690398
PMID:17093100[3]

IDA: Inferred from Direct Assay

C

From MGI

GO:0016020

membrane

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_001013431

C

From MGI

GO:0016050

vesicle organization

MGI:MGI:3590026
PMID:16085057[6]

IDA: Inferred from Direct Assay

P

From MGI

GO:0016197

endosome transport

MGI:MGI:3611988
PMID:16321985[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3612978

P

From MGI

GO:0016197

endosome transport

MGI:MGI:3652645
PMID:16769894[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3653518

P

From MGI

GO:0016601

Rac protein signal transduction

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_001013431

P

From MGI

GO:0017112

Rab guanyl-nucleotide exchange factor activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

F

From MGI

GO:0017137

Rab GTPase binding

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

EMBL:AB053305

F

From MGI

GO:0017137

Rab GTPase binding

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

F

From MGI

GO:0019717

synaptosome

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_001013431

C

From MGI

GO:0030027

lamellipodium

MGI:MGI:3759339
PMID:15033976[2]

IDA: Inferred from Direct Assay

C

From MGI

GO:0030424

axon

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_001013431

C

From MGI

GO:0030425

dendrite

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_001013431

C

From MGI

GO:0030425

dendrite

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

C

From MGI

GO:0030426

growth cone

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_001013431

C

From MGI

GO:0030675

Rac GTPase activator activity

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

EMBL:AB053305

F

From MGI

GO:0030676

Rac guanyl-nucleotide exchange factor activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

F

From MGI

GO:0032313

regulation of Rab GTPase activity

MGI:MGI:3590026
PMID:16085057[6]

IDA: Inferred from Direct Assay

P

From MGI

GO:0032851

positive regulation of Rab GTPase activity

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

EMBL:AB053305

P

From MGI

GO:0032855

positive regulation of Rac GTPase activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

P

From MGI

GO:0035023

regulation of Rho protein signal transduction

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR000219

P

From MGI

GO:0035249

synaptic transmission, glutamatergic

MGI:MGI:3690398
PMID:17093100[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3522476

P

From MGI

GO:0042598

vesicular fraction

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

C

From MGI

GO:0042802

identical protein binding

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

EMBL:AB053305

F

From MGI

GO:0042803

protein homodimerization activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

F

From MGI

GO:0043025

neuronal cell body

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_001013431

C

From MGI

GO:0043197

dendritic spine

MGI:MGI:3690398
PMID:17093100[3]

IDA: Inferred from Direct Assay

C

From MGI

GO:0043234

protein complex

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

C

From MGI

GO:0043539

protein serine/threonine kinase activator activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

F

From MGI

GO:0045860

positive regulation of protein kinase activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

P

From MGI

GO:0048365

Rac GTPase binding

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

EMBL:AB053305

F

From MGI

GO:0048812

neuron projection morphogenesis

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

P

From MGI

GO:0050790

regulation of catalytic activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0344

P

From MGI

GO:0050790

regulation of catalytic activity

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR000219

P

From MGI

GO:0051260

protein homooligomerization

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

EMBL:AB053305

P

From MGI

GO:0071902

positive regulation of protein serine/threonine kinase activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q96Q42

P

From MGI

colocalizes_with

GO:0005813

centrosome

MGI:MGI:3590026
PMID:16085057[6]

IDA: Inferred from Direct Assay

C

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. 1.0 1.1 1.2 Cai H et al. (2005) Loss of ALS2 function is insufficient to trigger motor neuron degeneration in knock-out mice but predisposes neurons to oxidative stress. J Neurosci 25: 7567-74 PubMed GONUTS page
  2. 2.0 2.1 Topp JD et al. (2004) Alsin is a Rab5 and Rac1 guanine nucleotide exchange factor. J Biol Chem 279: 24612-23 PubMed GONUTS page
  3. 3.0 3.1 3.2 3.3 3.4 3.5 Lai C et al. (2006) Amyotrophic lateral sclerosis 2-deficiency leads to neuronal degeneration in amyotrophic lateral sclerosis through altered AMPA receptor trafficking. J Neurosci 26: 11798-806 PubMed GONUTS page
  4. 4.0 4.1 4.2 Hadano S et al. (2006) Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking. Hum Mol Genet 15: 233-50 PubMed GONUTS page
  5. 5.0 5.1 5.2 Devon RS et al. (2006) Als2-deficient mice exhibit disturbances in endosome trafficking associated with motor behavioral abnormalities. Proc Natl Acad Sci U S A 103: 9595-600 PubMed GONUTS page
  6. 6.0 6.1 6.2 6.3 Millecamps S et al. (2005) Alsin is partially associated with centrosome in human cells. Biochim Biophys Acta 1745: 84-100 PubMed GONUTS page
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