Ambox notice.png

GONUTS is under stress! The website is currently experiencing long-wait times and frequent time-outs due to the record number of students, groups, and annotations related to CACAO this semester. We are currently working on increasing performance -- please accept our apologies for the technical difficulties.

You can help reduce stress on the server by:

  1. not reloading pages frequently - this just adds
  2. opening links in new windows (so you can read the old page)

MGI:Lyst

From GONUTS
Jump to: navigation, search

Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Lyst ( synonyms: D13Sfk13 )
Protein Name(s) lysosomal trafficking regulator,
External Links
MGI MGI:107448

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0002446

neutrophil mediated immunity

MGI:MGI:68578
PMID:7988496[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0002456

T cell mediated immunity

MGI:MGI:55165
PMID:6977094[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0005623

cell

MGI:MGI:54067
PMID:408[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

C

From MGI

GO:0005623

cell

MGI:MGI:55273
PMID:7089489[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0963

C

From MGI

GO:0005829

cytosol

MGI:MGI:1099544
PMID:9368050[5]

IDA: Inferred from Direct Assay

C

From MGI

GO:0006644

phospholipid metabolic process

MGI:MGI:54469
PMID:580786[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0006810

transport

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0813

P

From MGI

GO:0007017

microtubule-based process

MGI:MGI:54205
PMID:187062[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0007040

lysosome organization

MGI:MGI:1099544
PMID:9368050[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968
MGI:MGI:1855969

P

From MGI

GO:0007040

lysosome organization

MGI:MGI:53816
PMID:4697831[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0007040

lysosome organization

MGI:MGI:53992
PMID:1113502[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0007040

lysosome organization

MGI:MGI:55104
PMID:6170520[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0007040

lysosome organization

MGI:MGI:56449
PMID:4031470[11]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0007596

blood coagulation

MGI:MGI:55798
PMID:6696991[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0015031

protein transport

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0653

P

From MGI

GO:0015630

microtubule cytoskeleton

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99698

C

From MGI

GO:0030595

leukocyte chemotaxis

MGI:MGI:53883
PMID:4589319[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0032438

melanosome organization

MGI:MGI:3618562
PMID:16518687[14]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3620573

P

From MGI

GO:0032438

melanosome organization

MGI:MGI:53824
PMID:4634048[15]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0032510

endosome to lysosome transport via multivesicular body sorting pathway

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99698

P

From MGI

GO:0032816

positive regulation of natural killer cell activation

MGI:MGI:55273
PMID:7089489[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0033299

secretion of lysosomal enzymes

MGI:MGI:54067
PMID:408[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0033299

secretion of lysosomal enzymes

MGI:MGI:55273
PMID:7089489[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0033364

mast cell secretory granule organization

MGI:MGI:54412
PMID:624833[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0042267

natural killer cell mediated cytotoxicity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99698

P

From MGI

GO:0042493

response to drug

MGI:MGI:77039
PMID:2513223[17]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0042742

defense response to bacterium

MGI:MGI:53883
PMID:4589319[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0042742

defense response to bacterium

MGI:MGI:53949
PMID:4601767[18]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0042742

defense response to bacterium

MGI:MGI:68578
PMID:7988496[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0042832

defense response to protozoan

MGI:MGI:55417
PMID:6218091[19]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0043473

pigmentation

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445970

P

From MGI

GO:0043473

pigmentation

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99698

P

From MGI

GO:0043473

pigmentation

MGI:MGI:55273
PMID:7089489[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0043473

pigmentation

MGI:MGI:56449
PMID:4031470[11]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0043473

pigmentation

MGI:MGI:73117
PMID:13943454[20]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2660913

P

From MGI

GO:0043473

pigmentation

MGI:MGI:77039
PMID:2513223[17]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0048753

pigment granule organization

MGI:MGI:54133
PMID:1278263[21]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0051607

defense response to virus

MGI:MGI:55120
PMID:6272291[22]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI

GO:0055091

phospholipid homeostasis

MGI:MGI:54469
PMID:580786[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1855968

P

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. 1.0 1.1 Tanaka E et al. (1994) Effects of the beige mutation on respiratory tract infection with Pseudomonas aeruginosa in mice. Exp Lung Res 20: 351-66 PubMed GONUTS page
  2. Saxena RK et al. (1982) Defective T-cell response in beige mutant mice. Nature 295: 240-1 PubMed GONUTS page
  3. 3.0 3.1 Brandt EJ et al. (1975) Defective lysosomal enzyme secretion in kidneys of Chediak-Higashi (beige) mice. J Cell Biol 67: 774-88 PubMed GONUTS page
  4. 4.0 4.1 4.2 4.3 Orn A et al. (1982) Pigment mutations in the mouse which also affect lysosomal functions lead to suppressed natural killer cell activity. Scand J Immunol 15: 305-10 PubMed GONUTS page
  5. 5.0 5.1 Perou CM et al. (1997) The Beige/Chediak-Higashi syndrome gene encodes a widely expressed cytosolic protein. J Biol Chem 272: 29790-4 PubMed GONUTS page
  6. 6.0 6.1 Prueitt JL et al. (1978) Pulmonary surface-active materials in the Chediak-Higashi syndrome. J Lipid Res 19: 410-5 PubMed GONUTS page
  7. Oliver JM (1976) Impaired microtubule function correctable by cyclic GMP and cholinergic agonists in the Chediak-Higashi syndrome. Am J Pathol 85: 395-418 PubMed GONUTS page
  8. Oliver C & Essner E (1973) Distribution of anomalous lysosomes in the beige mouse: a homologue of Chediak-Higashi syndrome. J Histochem Cytochem 21: 218-28 PubMed GONUTS page
  9. Oliver C & Essner E (1975) Formation of anomalous lysosomes in monocytes, neutrophils, and eosinophils from bone marrow of mice with Chédiak-Higashi syndrome. Lab Invest 32: 17-27 PubMed GONUTS page
  10. Willingham MC et al. (1981) The origin and fate of large dense bodies in beige mouse fibroblasts. Lysosomal fusion and exocytosis. Exp Cell Res 136: 157-68 PubMed GONUTS page
  11. 11.0 11.1 Ahmed F & Shire JG (1985) Lysosomal mutations inhibit lipofuscinosis of the spleen in C57BL mice. J Hered 76: 311-2 PubMed GONUTS page
  12. Novak EK et al. (1984) Platelet storage pool deficiency in mouse pigment mutations associated with seven distinct genetic loci. Blood 63: 536-44 PubMed GONUTS page
  13. 13.0 13.1 Gallin JI et al. (1974) Granulocyte function in the Chediak-Higashi syndrome of mice. Blood 43: 201-6 PubMed GONUTS page
  14. Runkel F et al. (2006) Grey, a novel mutation in the murine Lyst gene, causes the beige phenotype by skipping of exon 25. Mamm Genome 17: 203-10 PubMed GONUTS page
  15. Hearing VJ et al. (1973) The fine structure of melanogenesis in coat color mutants of the mouse. J Ultrastruct Res 43: 88-106 PubMed GONUTS page
  16. Chi EY et al. (1978) Mast cell granule formation in the beige mouse. J Histochem Cytochem 26: 131-7 PubMed GONUTS page
  17. 17.0 17.1 Ahmed F et al. (1989) Lysosomal mutations increase susceptibility to anaesthetics. Experientia 45: 1133-5 PubMed GONUTS page
  18. Elin RJ et al. (1974) Infection and immunoglobulin concentrations in Chediak-Higashi mice. Infect Immun 10: 88-91 PubMed GONUTS page
  19. Kirkpatrick CE & Farrell JP (1982) Leishmaniasis in beige mice. Infect Immun 38: 1208-16 PubMed GONUTS page
  20. PIERRO LJ & CHASE HB (1963) Slate--a new coat color mutant in the mouse. J Hered 54: 47-50 PubMed GONUTS page
  21. Robison WG Jr & Kuwabara T (1976) Light-induced alterations of retinal pigment epithelium in black, albino, and beige mice. Exp Eye Res 22: 549-57 PubMed GONUTS page
  22. Shellam GR et al. (1981) Increased susceptibility to cytomegalovirus infection in beige mutant mice. Proc Natl Acad Sci U S A 78: 5104-8 PubMed GONUTS page
Personal tools
Namespaces
Variants
Actions
Navigation
Cacao
Journal Clubs
page contributors
Toolbox