WB:tbx-9

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Annotations

Qualifier	GO ID	GO term name	Reference	Evidence Code	with/from	Aspect	Notes
	GO:0002119	nematode larval development	WB_REF:WBPaper00006477 PMID:15066124^[1]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00063136 WB:WBPhenotype:0000059	P	From WB
	GO:0002119	nematode larval development	WB_REF:WBPaper00024194 PMID:15102704^[2]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00063247 WB:WBPhenotype:0000054	P	From WB
	GO:0002119	nematode larval development	WB_REF:WBPaper00024194 PMID:15102704^[2]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00063248 WB:WBPhenotype:0000054	P	From WB
	GO:0003700	sequence-specific DNA binding transcription factor activity	PMID:12520011^[3] PMID:12654719^[4]	IEA: Inferred from Electronic Annotation	INTERPRO:IPR001699	F	From WB
	GO:0003700	sequence-specific DNA binding transcription factor activity	PMID:12520011^[3] PMID:12654719^[4]	IEA: Inferred from Electronic Annotation	INTERPRO:IPR018186	F	From WB
	GO:0003705	RNA polymerase II distal enhancer sequence-specific DNA binding transcription factor activity	WB_REF:WBPaper00002132 PMID:7774921^[5]	ISS: Inferred from Sequence or Structural Similarity	UniProtKB:P20293	F	From WB
	GO:0005634	nucleus	PMID:12520011^[3] PMID:12654719^[4]	IEA: Inferred from Electronic Annotation	INTERPRO:IPR001699	C	From WB
	GO:0005634	nucleus	PMID:12520011^[3] PMID:12654719^[4]	IEA: Inferred from Electronic Annotation	INTERPRO:IPR018186	C	From WB
	GO:0005634	nucleus	WB_REF:WBPaper00002132 PMID:7774921^[5]	ISS: Inferred from Sequence or Structural Similarity	UniProtKB:P20293	C	From WB
	GO:0005667	transcription factor complex	WB_REF:WBPaper00002132 PMID:7774921^[5]	ISS: Inferred from Sequence or Structural Similarity	UniProtKB:Q60707	C	From WB
	GO:0006355	regulation of transcription, DNA-dependent	PMID:12520011^[3] PMID:12654719^[4]	IEA: Inferred from Electronic Annotation	INTERPRO:IPR001699	P	From WB
	GO:0006355	regulation of transcription, DNA-dependent	PMID:12520011^[3] PMID:12654719^[4]	IEA: Inferred from Electronic Annotation	INTERPRO:IPR018186	P	From WB
	GO:0006357	regulation of transcription from RNA polymerase II promoter	WB_REF:WBPaper00002132 PMID:7774921^[5]	ISS: Inferred from Sequence or Structural Similarity	UniProtKB:P20293	P	From WB
	GO:0007413	axonal fasciculation	WB_REF:WBPaper00028984 PMID:17213328^[6]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00066065 WB:WBPhenotype:0000632	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00006477 PMID:15066124^[1]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00063136 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00024194 PMID:15102704^[2]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00063247 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00024194 PMID:15102704^[2]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00063248 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00025190 PMID:15892873^[7]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00069646 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00025190 PMID:15892873^[7]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00069647 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00025190 PMID:15892873^[7]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00069648 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00025190 PMID:15892873^[7]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00069649 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00025190 PMID:15892873^[7]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00069650 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00025190 PMID:15892873^[7]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00069651 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00025190 PMID:15892873^[7]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00069653 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00025190 PMID:15892873^[7]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00069654 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00025190 PMID:15892873^[7]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00069655 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00025190 PMID:15892873^[7]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00069656 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00025190 PMID:15892873^[7]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00069657 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00025190 PMID:15892873^[7]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00069658 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00028381 PMID:16884526^[8]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00086361 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB_REF:WBPaper00028381 PMID:16884526^[8]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00086365 WB:WBPhenotype:0000050	P	From WB
	GO:0010171	body morphogenesis	WB_REF:WBPaper00006395 PMID:14551910^[9]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00026226 WB:WBPhenotype:0000535	P	From WB
	GO:0010171	body morphogenesis	WB_REF:WBPaper00006395 PMID:14551910^[9]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00027463 WB:WBPhenotype:0000535	P	From WB
	GO:0010171	body morphogenesis	WB_REF:WBPaper00006477 PMID:15066124^[1]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00063136 WB:WBPhenotype:0000535	P	From WB
	GO:0010171	body morphogenesis	WB_REF:WBPaper00006477 PMID:15066124^[1]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00063137 WB:WBPhenotype:0000535	P	From WB
	GO:0010171	body morphogenesis	WB_REF:WBPaper00024194 PMID:15102704^[2]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00063244 WB:WBPhenotype:0000535	P	From WB
	GO:0010171	body morphogenesis	WB_REF:WBPaper00024194 PMID:15102704^[2]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00063252 WB:WBPhenotype:0000535	P	From WB
	GO:0040007	growth	WB_REF:WBPaper00006477 PMID:15066124^[1]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00063136 WB:WBPhenotype:0000059	P	From WB
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Notes

References

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

↑ ^1.0 ^1.1 ^1.2 ^1.3 ^1.4 Andachi Y (2004) Caenorhabditis elegans T-box genes tbx-9 and tbx-8 are required for formation of hypodermis and body-wall muscle in embryogenesis. Genes Cells 9: 331-44 PubMed GONUTS page
↑ ^2.0 ^2.1 ^2.2 ^2.3 ^2.4 ^2.5 Pocock R et al. (2004) A regulatory network of T-box genes and the even-skipped homologue vab-7 controls patterning and morphogenesis in C. elegans. Development 131: 2373-85 PubMed GONUTS page
↑ ^3.0 ^3.1 ^3.2 ^3.3 ^3.4 ^3.5 Mulder NJ et al. (2003) The InterPro Database, 2003 brings increased coverage and new features. Nucleic Acids Res 31: 315-8 PubMed GONUTS page
↑ ^4.0 ^4.1 ^4.2 ^4.3 ^4.4 ^4.5 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
↑ ^5.0 ^5.1 ^5.2 ^5.3 Agulnik SI et al. (1995) Conservation of the T-box gene family from Mus musculus to Caenorhabditis elegans. Genomics 25: 214-9 PubMed GONUTS page
↑ Schmitz C et al. (2007) Axon guidance genes identified in a large-scale RNAi screen using the RNAi-hypersensitive Caenorhabditis elegans strain nre-1(hd20) lin-15b(hd126). Proc Natl Acad Sci U S A 104: 834-9 PubMed GONUTS page
↑ ^7.00 ^7.01 ^7.02 ^7.03 ^7.04 ^7.05 ^7.06 ^7.07 ^7.08 ^7.09 ^7.10 ^7.11 Baugh LR et al. (2005) Synthetic lethal analysis of Caenorhabditis elegans posterior embryonic patterning genes identifies conserved genetic interactions. Genome Biol 6: R45 PubMed GONUTS page
↑ ^8.0 ^8.1 Tischler J et al. (2006) Combinatorial RNA interference in Caenorhabditis elegans reveals that redundancy between gene duplicates can be maintained for more than 80 million years of evolution. Genome Biol 7: R69 PubMed GONUTS page
↑ ^9.0 ^9.1 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

[PMID:15066124-0] 1.0 ^1.1 ^1.2 ^1.3 ^1.4 Andachi Y (2004) Caenorhabditis elegans T-box genes tbx-9 and tbx-8 are required for formation of hypodermis and body-wall muscle in embryogenesis. Genes Cells 9: 331-44 PubMed GONUTS page

[PMID:15102704-1] 2.0 ^2.1 ^2.2 ^2.3 ^2.4 ^2.5 Pocock R et al. (2004) A regulatory network of T-box genes and the even-skipped homologue vab-7 controls patterning and morphogenesis in C. elegans. Development 131: 2373-85 PubMed GONUTS page

[PMID:12520011-2] 3.0 ^3.1 ^3.2 ^3.3 ^3.4 ^3.5 Mulder NJ et al. (2003) The InterPro Database, 2003 brings increased coverage and new features. Nucleic Acids Res 31: 315-8 PubMed GONUTS page

[PMID:12654719-3] 4.0 ^4.1 ^4.2 ^4.3 ^4.4 ^4.5 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

[PMID:7774921-4] 5.0 ^5.1 ^5.2 ^5.3 Agulnik SI et al. (1995) Conservation of the T-box gene family from Mus musculus to Caenorhabditis elegans. Genomics 25: 214-9 PubMed GONUTS page

[PMID:17213328-5] Schmitz C et al. (2007) Axon guidance genes identified in a large-scale RNAi screen using the RNAi-hypersensitive Caenorhabditis elegans strain nre-1(hd20) lin-15b(hd126). Proc Natl Acad Sci U S A 104: 834-9 PubMed GONUTS page

[PMID:15892873-6] 7.00 ^7.01 ^7.02 ^7.03 ^7.04 ^7.05 ^7.06 ^7.07 ^7.08 ^7.09 ^7.10 ^7.11 Baugh LR et al. (2005) Synthetic lethal analysis of Caenorhabditis elegans posterior embryonic patterning genes identifies conserved genetic interactions. Genome Biol 6: R45 PubMed GONUTS page

[PMID:16884526-7] 8.0 ^8.1 Tischler J et al. (2006) Combinatorial RNA interference in Caenorhabditis elegans reveals that redundancy between gene duplicates can be maintained for more than 80 million years of evolution. Genome Biol 7: R69 PubMed GONUTS page

[PMID:14551910-8] 9.0 ^9.1 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

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Species (Taxon ID)	Caenorhabditis elegans (nematode) (taxon:6239)
Gene Name(s)	tbx-9 ( synonyms: T07C4.6 )
Protein Name(s)	No Information Provided.
External Links
WB	WBGene00006546

WB:tbx-9

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