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WB:T05C12.6c

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Contents

Species (Taxon ID) Caenorhabditis elegans (nematode) (taxon:6239)
Gene Name(s) T05C12.6c ( synonyms: T05C12.6 )
Protein Name(s) No Information Provided.
External Links
WB WBGene00003241

Annotations

Qualifier GO ID GO term name Reference(s) Evidence Code with/from Aspect Notes Status
GO:0000132

establishment of mitotic spindle orientation

WB:WBPaper00005375
PMID:12110172[1]

IGI: Inferred from Genetic Interaction

WB:WBGene00001102
WB:WBGene00005077

P

From WB

GO:0000132

establishment of mitotic spindle orientation

WB:WBPaper00028396
PMID:16899238[2]

IMP: Inferred from Mutant Phenotype

WB:WBVar00241539
WB:WBVar00241555

P

From WB

GO:0001709

cell fate determination

WB:WBPaper00028396
PMID:16899238[2]

IMP: Inferred from Mutant Phenotype

WB:WBVar00241539
WB:WBVar00241555

P

From WB

GO:0001714

endodermal cell fate specification

WB:WBPaper00005375
PMID:12110172[1]

IGI: Inferred from Genetic Interaction

WB:WBGene00001102
WB:WBGene00005077

P

From WB

GO:0001764

neuron migration

WB:WBPaper00028396
PMID:16899238[2]

IMP: Inferred from Mutant Phenotype

WB:WBVar00241539
WB:WBVar00241555

P

From WB

GO:0002009

morphogenesis of an epithelium

WB:WBPaper00005654
PMID:12529635[3]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00009114
WB:WBPhenotype:0000038

P

From WB

GO:0004871

signal transducer activity

PMID:12520011[4]
PMID:12654719[5]

IEA: Inferred from Electronic Annotation

INTERPRO:IPR001158

F

From WB

GO:0005515

protein binding

PMID:12520011[4]
PMID:12654719[5]

IEA: Inferred from Electronic Annotation

INTERPRO:IPR001478

F

From WB

GO:0005622

intracellular

PMID:12520011[4]
PMID:12654719[5]

IEA: Inferred from Electronic Annotation

INTERPRO:IPR001158

C

From WB

GO:0005737

cytoplasm

WB:WBPaper00028396
PMID:16899238[2]

IDA: Inferred from Direct Assay

C

From WB

GO:0005938

cell cortex

WB:WBPaper00028396
PMID:16899238[2]

IDA: Inferred from Direct Assay

C

From WB

GO:0007052

mitotic spindle organization

WB:WBPaper00024624
PMID:15572126[6]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00062593
WB:WBPhenotype:0001102

P

From WB

GO:0007052

mitotic spindle organization

WB:WBPaper00024624
PMID:15572126[6]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00062595
WB:WBPhenotype:0001102

P

From WB

GO:0007052

mitotic spindle organization

WB:WBPaper00024624
PMID:15572126[6]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00062596
WB:WBPhenotype:0001102

P

From WB

GO:0007052

mitotic spindle organization

WB:WBPaper00024624
PMID:15572126[6]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00062597
WB:WBPhenotype:0001102

P

From WB

GO:0007052

mitotic spindle organization

WB:WBPaper00024624
PMID:15572126[6]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00062603
WB:WBPhenotype:0001102

P

From WB

GO:0007052

mitotic spindle organization

WB:WBPaper00024624
PMID:15572126[6]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00062607
WB:WBPhenotype:0001102

P

From WB

GO:0007052

mitotic spindle organization

WB:WBPaper00024624
PMID:15572126[6]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00062609
WB:WBPhenotype:0001102

P

From WB

GO:0007052

mitotic spindle organization

WB:WBPaper00024624
PMID:15572126[6]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00062610
WB:WBPhenotype:0001102

P

From WB

GO:0007052

mitotic spindle organization

WB:WBPaper00024624
PMID:15572126[6]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00062611
WB:WBPhenotype:0001102

P

From WB

GO:0007052

mitotic spindle organization

WB:WBPaper00024624
PMID:15572126[6]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00062620
WB:WBPhenotype:0001102

P

From WB

GO:0007052

mitotic spindle organization

WB:WBPaper00024624
PMID:15572126[6]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00062621
WB:WBPhenotype:0001102

P

From WB

GO:0007052

mitotic spindle organization

WB:WBPaper00024624
PMID:15572126[6]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00062626
WB:WBPhenotype:0001102

P

From WB

GO:0007275

multicellular organismal development

PMID:12520011[4]
PMID:12654719[5]

IEA: Inferred from Electronic Annotation

INTERPRO:IPR001158

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00005599
PMID:12445391[7]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00007682
WB:WBPhenotype:0000050

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00005654
PMID:12529635[3]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00009114
WB:WBPhenotype:0000050

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00024497
PMID:15489339[8]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00035194
WB:WBPhenotype:0000050

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00026633
PMID:15990090[9]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00063744
WB:WBPhenotype:0000050

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00026633
PMID:15990090[9]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00063745
WB:WBPhenotype:0000050

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00029082
PMID:17276345[10]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00077092
WB:WBPhenotype:0000050

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00033015
PMID:19298786[11]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00078112
WB:WBPhenotype:0000050

P

From WB

GO:0009792

embryo development ending in birth or egg hatching

WB:WBPaper00033015
PMID:19298786[11]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00078113
WB:WBPhenotype:0000050

P

From WB

GO:0016477

cell migration

WB:WBPaper00005278
PMID:12023307[12]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00022935
WB:WBPhenotype:0000594

P

From WB

GO:0016477

cell migration

WB:WBPaper00005278
PMID:12023307[12]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00022936
WB:WBPhenotype:0000594

P

From WB

GO:0016477

cell migration

WB:WBPaper00028396
PMID:16899238[2]

IMP: Inferred from Mutant Phenotype

WB:WBVar00241539
WB:WBVar00241555

P

From WB

GO:0018991

oviposition

WB:WBPaper00005654
PMID:12529635[3]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00009114
WB:WBPhenotype:0000640

P

From WB

GO:0023019

regulation of gene expression as a consequence of signal transmission

WB:WBPaper00033015
PMID:19298786[11]

IGI: Inferred from Genetic Interaction

WB:WBGene00001102

P

From WB

GO:0023034

intracellular signaling pathway

PMID:12520011[4]
PMID:12654719[5]

IEA: Inferred from Electronic Annotation

INTERPRO:IPR000591

P

From WB

GO:0032878

regulation of establishment or maintenance of cell polarity

WB:WBPaper00027345
PMID:16631156[13]

IGI: Inferred from Genetic Interaction

WB:WBGene00003029

P

From WB

GO:0032878

regulation of establishment or maintenance of cell polarity

WB:WBPaper00027345
PMID:16631156[13]

IMP: Inferred from Mutant Phenotype

WB:WBVar00091579

P

From WB

GO:0040010

positive regulation of growth rate

WB:WBPaper00031036
PMID:17897480[14]

IMP: Inferred from Mutant Phenotype

WB:WBRNAi00068155
WB:WBPhenotype:0000031

P

From WB

GO:0040039

inductive cell migration

WB:WBPaper00028396
PMID:16899238[2]

IMP: Inferred from Mutant Phenotype

WB:WBVar00241539
WB:WBVar00241555

P

From WB

GO:0048598

embryonic morphogenesis

WB:WBPaper00028396
PMID:16899238[2]

IMP: Inferred from Mutant Phenotype

WB:WBVar00241555

P

From WB

GO:0048598

embryonic morphogenesis

WB:WBPaper00033015
PMID:19298786[11]

IGI: Inferred from Genetic Interaction

WB:WBGene00001102

P

From WB

GO:0048730

epidermis morphogenesis

WB:WBPaper00028396
PMID:16899238[2]

IMP: Inferred from Mutant Phenotype

WB:WBVar00241555

P

From WB

GO:0060069

Wnt receptor signaling pathway, regulating spindle positioning

WB:WBPaper00024624
PMID:15572126[6]

IGI: Inferred from Genetic Interaction

WB:WBGene00001102

P

From WB

GO:0060071

Wnt receptor signaling pathway, planar cell polarity pathway

WB:WBPaper00027345
PMID:16631156[13]

IGI: Inferred from Genetic Interaction

WB:WBGene00003029

P

From WB

GO:0060573

cell fate specification involved in pattern specification

WB:WBPaper00033015
PMID:19298786[11]

IGI: Inferred from Genetic Interaction

WB:WBGene00001102

P

From WB


Notes

References

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

  1. 1.0 1.1 Bei Y et al. (2002) SRC-1 and Wnt signaling act together to specify endoderm and to control cleavage orientation in early C. elegans embryos. Dev Cell 3: 113-25 PubMed GONUTS page
  2. 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 2.8 Walston T et al. (2006) mig-5/Dsh controls cell fate determination and cell migration in C. elegans. Dev Biol 298: 485-97 PubMed GONUTS page
  3. 3.0 3.1 3.2 Kamath RS et al. (2003) Systematic functional analysis of the Caenorhabditis elegans genome using RNAi. Nature 421: 231-7 PubMed GONUTS page
  4. 4.0 4.1 4.2 4.3 4.4 Mulder NJ et al. (2003) The InterPro Database, 2003 brings increased coverage and new features. Nucleic Acids Res 31: 315-8 PubMed GONUTS page
  5. 5.0 5.1 5.2 5.3 5.4 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
  6. 6.00 6.01 6.02 6.03 6.04 6.05 6.06 6.07 6.08 6.09 6.10 6.11 6.12 Walston T et al. (2004) Multiple Wnt signaling pathways converge to orient the mitotic spindle in early C. elegans embryos. Dev Cell 7: 831-41 PubMed GONUTS page
  7. Piano F et al. (2002) Gene clustering based on RNAi phenotypes of ovary-enriched genes in C. elegans. Curr Biol 12: 1959-64 PubMed GONUTS page
  8. 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
  9. 9.0 9.1 Hawkins NC et al. (2005) MOM-5 frizzled regulates the distribution of DSH-2 to control C. elegans asymmetric neuroblast divisions. Dev Biol 284: 246-59 PubMed GONUTS page
  10. Mizumoto K & Sawa H (2007) Cortical beta-catenin and APC regulate asymmetric nuclear beta-catenin localization during asymmetric cell division in C. elegans. Dev Cell 12: 287-99 PubMed GONUTS page
  11. 11.0 11.1 11.2 11.3 11.4 King RS et al. (2009) The N- or C-terminal domains of DSH-2 can activate the C. elegans Wnt/beta-catenin asymmetry pathway. Dev Biol 328: 234-44 PubMed GONUTS page
  12. 12.0 12.1 Korswagen HC et al. (2002) The Axin-like protein PRY-1 is a negative regulator of a canonical Wnt pathway in C. elegans. Genes Dev 16: 1291-302 PubMed GONUTS page
  13. 13.0 13.1 13.2 Wu M & Herman MA (2006) A novel noncanonical Wnt pathway is involved in the regulation of the asymmetric B cell division in C. elegans. Dev Biol 293: 316-29 PubMed GONUTS page
  14. Byrne AB et al. (2007) A global analysis of genetic interactions in Caenorhabditis elegans. J Biol 6: 8 PubMed GONUTS page


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