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WB:C02C6.1b

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Contents

Species (Taxon ID) Caenorhabditis elegans (nematode) (taxon:6239)
Gene Name(s) C02C6.1b ( synonyms: C02C6.1, dyn1 )
Protein Name(s) No Information Provided.
External Links
WB WBGene00001130

Annotations

Qualifier GO ID GO term name Reference(s) Evidence Code with/from Aspect Notes Status
GO:0000003

reproduction

WB:WBPaper00002892
PMID:9294229[1]

IMP: Inferred from Mutant Phenotype

WB:WBVar00088400
WB:WBPhenotype:0001384

P

From WB

GO:0000003

reproduction

WB:WBPaper00025054
PMID:15791247[2]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00039407
WB:WBPhenotype:0000689

P

From WB

GO:0000003

reproduction

WB:WBPerson48

IMP: Inferred from Mutant Phenotype

WB:WBVar00249878
WB:WBPhenotype:0000688

P

From WB

GO:0001891

phagocytic cup

WB:WBPaper00031805
PMID:18425118[3]

IDA: Inferred from Direct Assay

C

From WB

GO:0002119

nematode larval development

WB:WBPaper00006395
PMID:14551910[4]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00024449
WB:WBPhenotype:0000059

P

From WB

GO:0002119

nematode larval development

WB:WBPaper00024497
PMID:15489339[5]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00028338
WB:WBPhenotype:0000054

P

From WB

GO:0002119

nematode larval development

WB:WBPaper00024497
PMID:15489339[5]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00028338
WB:WBPhenotype:0000059

P

From WB

GO:0003924

GTPase activity

PMID:12520011[6]
PMID:12654719[7]

IEA: Inferred from Electronic Annotation

INTERPRO:IPR001401

F

From WB

GO:0003924

GTPase activity

PMID:12520011[6]
PMID:12654719[7]

IEA: Inferred from Electronic Annotation

INTERPRO:IPR003130

F

From WB

GO:0003924

GTPase activity

WB:WBPaper00002892
PMID:9294229[1]

ISS: Inferred from Sequence or Structural Similarity

F

From WB

GO:0005525

GTP binding

PMID:12520011[6]
PMID:12654719[7]

IEA: Inferred from Electronic Annotation

INTERPRO:IPR000375

F

From WB

GO:0005525

GTP binding

PMID:12520011[6]
PMID:12654719[7]

IEA: Inferred from Electronic Annotation

INTERPRO:IPR001401

F

From WB

GO:0005525

GTP binding

PMID:12520011[6]
PMID:12654719[7]

IEA: Inferred from Electronic Annotation

INTERPRO:IPR003130

F

From WB

GO:0005876

spindle microtubule

WB:WBPaper00005664
PMID:12498685[8]

IDA: Inferred from Direct Assay

C

From WB

GO:0006897

endocytosis

WB:WBPaper00002892
PMID:9294229[1]

IMP: Inferred from Mutant Phenotype

P

From WB

GO:0006898

receptor-mediated endocytosis

WB:WBPaper00003831
PMID:10588660[9]

IMP: Inferred from Mutant Phenotype

P

From WB

GO:0006898

receptor-mediated endocytosis

WB:WBPaper00027659
PMID:16740477[10]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00065880
WB:WBPhenotype:0001425

P

From WB

GO:0006898

receptor-mediated endocytosis

WB:WBPaper00030951
PMID:17704769[11]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00071641
WB:WBPhenotype:0001425

P

From WB

GO:0007281

germ cell development

WB:WBPaper00005664
PMID:12498685[8]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00064262
WB:WBPhenotype:0000812

P

From WB

GO:0008219

cell death

WB:WBPaper00027659
PMID:16740477[10]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00065879
WB:WBPhenotype:0000729

P

From WB

GO:0009790

embryo development

WB:WBPaper00004812
PMID:11483962[12]

IMP: Inferred from Mutant Phenotype

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00003831
PMID:10588660[9]

IMP: Inferred from Mutant Phenotype

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00003831
PMID:10588660[9]

IMP: Inferred from Mutant Phenotype

WB:WBVar00088400
WB:WBPhenotype:0000050

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00005194
PMID:11922622[13]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00024283
WB:WBPhenotype:0000050

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00005654
PMID:12529635[14]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00008324
WB:WBPhenotype:0000050

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00006395
PMID:14551910[4]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00024449
WB:WBPhenotype:0000050

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00024200
PMID:15166316[15]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00080545
WB:WBPhenotype:0000050

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00034638
PMID:19531359[16]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00080726
WB:WBPhenotype:0000050

P

From WB

GO:0018996

molting cycle, collagen and cuticulin-based cuticle

WB:WBPaper00005654
PMID:12529635[14]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00008324
WB:WBPhenotype:0000638

P

From WB

GO:0018996

molting cycle, collagen and cuticulin-based cuticle

WB:WBPaper00026763
PMID:16122351[17]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00066834
WB:WBPhenotype:0000638

P

From WB

GO:0030496

midbody

WB:WBPaper00005664
PMID:12498685[8]

IDA: Inferred from Direct Assay

C

From WB

GO:0031143

pseudopodium

WB:WBPaper00027659
PMID:16740477[10]

IDA: Inferred from Direct Assay

C

From WB

GO:0031410

cytoplasmic vesicle

WB:WBPaper00005664
PMID:12498685[8]

IDA: Inferred from Direct Assay

C

From WB

GO:0032154

cleavage furrow

WB:WBPaper00005664
PMID:12498685[8]

IDA: Inferred from Direct Assay

C

From WB

GO:0040007

growth

WB:WBPaper00006395
PMID:14551910[4]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00024449
WB:WBPhenotype:0000059

P

From WB

GO:0040007

growth

WB:WBPaper00024497
PMID:15489339[5]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00028338
WB:WBPhenotype:0000059

P

From WB

GO:0040010

positive regulation of growth rate

WB:WBPaper00002892
PMID:9294229[1]

IMP: Inferred from Mutant Phenotype

WB:WBVar00088400
WB:WBPhenotype:0000031

P

From WB

GO:0040011

locomotion

WB:WBPaper00002892
PMID:9294229[1]

IMP: Inferred from Mutant Phenotype

P

From WB

GO:0040011

locomotion

WB:WBPaper00005654
PMID:12529635[14]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00008324
WB:WBPhenotype:0000643

P

From WB

GO:0040011

locomotion

WB:WBPaper00006395
PMID:14551910[4]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00024449
WB:WBPhenotype:0000643

P

From WB

GO:0040011

locomotion

WB:WBPaper00024200
PMID:15166316[15]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00080545
WB:WBPhenotype:0000643

P

From WB

GO:0040011

locomotion

WB:WBPaper00030848
PMID:17629760[18]

IMP: Inferred from Mutant Phenotype

WB:WBVar00088400
WB:WBPhenotype:0000643

P

From WB

GO:0040039

inductive cell migration

WB:WBPaper00028783
PMID:17090602[19]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00065691
WB:WBPhenotype:0000195

P

From WB

GO:0043652

engulfment of apoptotic cell

WB:WBPaper00027659
PMID:16740477[10]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00065881
WB:WBPhenotype:0000885

P

From WB

GO:0045202

synapse

WB:WBPaper00004812
PMID:11483962[12]

IDA: Inferred from Direct Assay

C

From WB

GO:0045335

phagocytic vesicle

WB:WBPaper00027659
PMID:16740477[10]

IDA: Inferred from Direct Assay

C

From WB

GO:0045335

phagocytic vesicle

WB:WBPaper00031805
PMID:18425118[3]

IDA: Inferred from Direct Assay

C

From WB


Notes

References

See Help:References for how to manage references in GONUTS.

  1. 1.0 1.1 1.2 1.3 1.4 Clark SG et al. (1997) A dynamin GTPase mutation causes a rapid and reversible temperature-inducible locomotion defect in C. elegans. Proc Natl Acad Sci U S A 94: 10438-43 PubMed GONUTS page
  2. Sönnichsen B et al. (2005) Full-genome RNAi profiling of early embryogenesis in Caenorhabditis elegans. Nature 434: 462-9 PubMed GONUTS page
  3. 3.0 3.1 Kinchen JM et al. (2008) A pathway for phagosome maturation during engulfment of apoptotic cells. Nat Cell Biol 10: 556-66 PubMed GONUTS page
  4. 4.0 4.1 4.2 4.3 Simmer F et al. (2003) Genome-wide RNAi of C. elegans using the hypersensitive rrf-3 strain reveals novel gene functions. PLoS Biol 1: E12 PubMed GONUTS page
  5. 5.0 5.1 5.2 Rual JF et al. (2004) Toward improving Caenorhabditis elegans phenome mapping with an ORFeome-based RNAi library. Genome Res 14: 2162-8 PubMed GONUTS page
  6. 6.0 6.1 6.2 6.3 6.4 Mulder NJ et al. (2003) The InterPro Database, 2003 brings increased coverage and new features. Nucleic Acids Res 31: 315-8 PubMed GONUTS page
  7. 7.0 7.1 7.2 7.3 7.4 Camon E et al. (2003) The Gene Ontology Annotation (GOA) project: implementation of GO in SWISS-PROT, TrEMBL, and InterPro. Genome Res 13: 662-72 PubMed GONUTS page
  8. 8.0 8.1 8.2 8.3 8.4 Thompson HM et al. (2002) The large GTPase dynamin associates with the spindle midzone and is required for cytokinesis. Curr Biol 12: 2111-7 PubMed GONUTS page
  9. 9.0 9.1 9.2 Grant B & Hirsh D (1999) Receptor-mediated endocytosis in the Caenorhabditis elegans oocyte. Mol Biol Cell 10: 4311-26 PubMed GONUTS page
  10. 10.0 10.1 10.2 10.3 10.4 Yu X et al. (2006) C. elegans Dynamin mediates the signaling of phagocytic receptor CED-1 for the engulfment and degradation of apoptotic cells. Dev Cell 10: 743-57 PubMed GONUTS page
  11. Balklava Z et al. (2007) Genome-wide analysis identifies a general requirement for polarity proteins in endocytic traffic. Nat Cell Biol 9: 1066-73 PubMed GONUTS page
  12. 12.0 12.1 Salcini AE et al. (2001) The Eps15 C. elegans homologue EHS-1 is implicated in synaptic vesicle recycling. Nat Cell Biol 3: 755-60 PubMed GONUTS page
  13. Tsuboi D et al. (2002) Isolation of the interacting molecules with GEX-3 by a novel functional screening. Biochem Biophys Res Commun 292: 697-701 PubMed GONUTS page
  14. 14.0 14.1 14.2 Kamath RS et al. (2003) Systematic functional analysis of the Caenorhabditis elegans genome using RNAi. Nature 421: 231-7 PubMed GONUTS page
  15. 15.0 15.1 Skop AR et al. (2004) Dissection of the mammalian midbody proteome reveals conserved cytokinesis mechanisms. Science 305: 61-6 PubMed GONUTS page
  16. Nakayama Y et al. (2009) Dynamin participates in the maintenance of anterior polarity in the Caenorhabditis elegans embryo. Dev Cell 16: 889-900 PubMed GONUTS page
  17. Frand AR et al. (2005) Functional genomic analysis of C. elegans molting. PLoS Biol 3: e312 PubMed GONUTS page
  18. Parker S et al. (2007) Muscular dystrophy associated mutations in caveolin-1 induce neurotransmission and locomotion defects in Caenorhabditis elegans. Invert Neurosci 7: 157-64 PubMed GONUTS page
  19. Cram EJ et al. (2006) A systematic RNA interference screen reveals a cell migration gene network in C. elegans. J Cell Sci 119: 4811-8 PubMed GONUTS page


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