WB:C41G7.1b

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Annotations

Qualifier	GO ID	GO term name	Reference(s)	Evidence Code	with/from	Aspect	Notes
	GO:0000003	reproduction	WB:WBPaper00004402 PMID:11099033^[1]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00003132 WB:WBPhenotype:0001037	P	From WB
	GO:0000003	reproduction	WB:WBPaper00004651 PMID:11231151^[2]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00002092 WB:WBPhenotype:0001037	P	From WB
	GO:0000003	reproduction	WB:WBPaper00032235 PMID:18829666^[3]	IMP: Inferred from Mutant Phenotype	WB:WBVar00091652 WB:WBPhenotype:0000688	P	From WB
	GO:0002119	nematode larval development	WB:WBPaper00004651 PMID:11231151^[2]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00002092 WB:WBPhenotype:0000059	P	From WB
	GO:0002119	nematode larval development	WB:WBPaper00006395 PMID:14551910^[4]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00024793 WB:WBPhenotype:0000059	P	From WB
	GO:0002119	nematode larval development	WB:WBPaper00006395 PMID:14551910^[4]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00024794 WB:WBPhenotype:0000059	P	From WB
	GO:0002119	nematode larval development	WB:WBPaper00024497 PMID:15489339^[5]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00030287 WB:WBPhenotype:0000054	P	From WB
	GO:0002119	nematode larval development	WB:WBPaper00024497 PMID:15489339^[5]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00030287 WB:WBPhenotype:0000059	P	From WB
	GO:0002119	nematode larval development	WB:WBPaper00032235 PMID:18829666^[3]	IMP: Inferred from Mutant Phenotype	WB:WBVar00091652	P	From WB
	GO:0003676	nucleic acid binding	PMID:12520011^[6] PMID:12654719^[7]	IEA: Inferred from Electronic Annotation	INTERPRO:IPR002999	F	From WB
	GO:0003723	RNA binding	PMID:12520011^[6] PMID:12654719^[7]	IEA: Inferred from Electronic Annotation	INTERPRO:IPR010304	F	From WB
	GO:0005634	nucleus	PMID:12520011^[6] PMID:12654719^[7]	IEA: Inferred from Electronic Annotation	INTERPRO:IPR010304	C	From WB
	GO:0005634	nucleus	WB:WBPaper00003775 PMID:10545592^[8]	IDA: Inferred from Direct Assay		C	From WB
	GO:0005737	cytoplasm	PMID:12520011^[6] PMID:12654719^[7]	IEA: Inferred from Electronic Annotation	INTERPRO:IPR010304	C	From WB
	GO:0006397	mRNA processing	PMID:12520011^[6] PMID:12654719^[7]	IEA: Inferred from Electronic Annotation	INTERPRO:IPR010304	P	From WB
	GO:0007281	germ cell development	WB:WBPaper00003775 PMID:10545592^[8]	IMP: Inferred from Mutant Phenotype		P	From WB
	GO:0007281	germ cell development	WB:WBPaper00032235 PMID:18829666^[3]	IMP: Inferred from Mutant Phenotype	WB:WBVar00091652 WB:WBPhenotype:0000812	P	From WB
	GO:0008340	determination of adult lifespan	WB:WBPaper00031212 PMID:18006689^[9]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00070473 WB:WBPhenotype:0001171	P	From WB
	GO:0008340	determination of adult lifespan	WB:WBPaper00031212 PMID:18006689^[9]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00070474 WB:WBPhenotype:0001171	P	From WB
	GO:0008340	determination of adult lifespan	WB:WBPaper00031212 PMID:18006689^[9]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00070475 WB:WBPhenotype:0001171	P	From WB
	GO:0008340	determination of adult lifespan	WB:WBPaper00032235 PMID:18829666^[3]	IMP: Inferred from Mutant Phenotype	WB:WBVar00091652	P	From WB
	GO:0008340	determination of adult lifespan	WB:WBPaper00032235 PMID:18829666^[3]	IMP: Inferred from Mutant Phenotype	WB:WBVar00091652 WB:WBPhenotype:0001171	P	From WB
	GO:0008406	gonad development	WB:WBPaper00032235 PMID:18829666^[3]	IMP: Inferred from Mutant Phenotype	WB:WBVar00091652 WB:WBPhenotype:0000691	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB:WBPaper00003775 PMID:10545592^[8]	IMP: Inferred from Mutant Phenotype		P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB:WBPaper00004402 PMID:11099033^[1]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00003132 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB:WBPaper00004651 PMID:11231151^[2]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00002092 WB:WBPhenotype:0000050	P	From WB
	GO:0009792	embryo development ending in birth or egg hatching	WB:WBPaper00025054 PMID:15791247^[10]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00042315 WB:WBPhenotype:0000050	P	From WB
	GO:0040007	growth	WB:WBPaper00004651 PMID:11231151^[2]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00002092 WB:WBPhenotype:0000059	P	From WB
	GO:0040007	growth	WB:WBPaper00006395 PMID:14551910^[4]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00024793 WB:WBPhenotype:0000059	P	From WB
	GO:0040007	growth	WB:WBPaper00006395 PMID:14551910^[4]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00024794 WB:WBPhenotype:0000059	P	From WB
	GO:0040007	growth	WB:WBPaper00024497 PMID:15489339^[5]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00030287 WB:WBPhenotype:0000059	P	From WB
	GO:0040010	positive regulation of growth rate	WB:WBPaper00004402 PMID:11099033^[1]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00003132 WB:WBPhenotype:0000031	P	From WB
	GO:0040011	locomotion	WB:WBPaper00003775 PMID:10545592^[8]	IMP: Inferred from Mutant Phenotype		P	From WB
	GO:0040011	locomotion	WB:WBPaper00006395 PMID:14551910^[4]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00024793 WB:WBPhenotype:0000643	P	From WB
	GO:0040011	locomotion	WB:WBPaper00006395 PMID:14551910^[4]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00024794 WB:WBPhenotype:0000643	P	From WB
	GO:0040011	locomotion	WB:WBPaper00024497 PMID:15489339^[5]	IMP: Inferred from Mutant Phenotype	WB:WBRNAi00030287 WB:WBPhenotype:0000643	P	From WB
	GO:0040011	locomotion	WB:WBPaper00032235 PMID:18829666^[3]	IMP: Inferred from Mutant Phenotype	WB:WBVar00091652 WB:WBPhenotype:0000643	P	From WB
	GO:0040025	vulval development	WB:WBPaper00003775 PMID:10545592^[8]	IMP: Inferred from Mutant Phenotype		P	From WB
	GO:0043050	pharyngeal pumping	WB:WBPaper00032235 PMID:18829666^[3]	IMP: Inferred from Mutant Phenotype	WB:WBVar00091652	P	From WB
	GO:0043050	pharyngeal pumping	WB:WBPaper00032235 PMID:18829666^[3]	IMP: Inferred from Mutant Phenotype	WB:WBVar00091652 WB:WBPhenotype:0000634	P	From WB
	GO:0043621	protein self-association	WB:WBPaper00003775 PMID:10545592^[8]	IPI: Inferred from Physical Interaction		F	From WB
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Notes

References

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

↑ ^1.0 ^1.1 ^1.2 Fraser AG et al. (2000) Functional genomic analysis of C. elegans chromosome I by systematic RNA interference. Nature 408: 325-30 PubMed GONUTS page
↑ ^2.0 ^2.1 ^2.2 ^2.3 Maeda I et al. (2001) Large-scale analysis of gene function in Caenorhabditis elegans by high-throughput RNAi. Curr Biol 11: 171-6 PubMed GONUTS page
↑ ^3.0 ^3.1 ^3.2 ^3.3 ^3.4 ^3.5 ^3.6 ^3.7 ^3.8 Briese M et al. (2009) Deletion of smn-1, the Caenorhabditis elegans ortholog of the spinal muscular atrophy gene, results in locomotor dysfunction and reduced lifespan. Hum Mol Genet 18: 97-104 PubMed GONUTS page
↑ ^4.0 ^4.1 ^4.2 ^4.3 ^4.4 ^4.5 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
↑ ^5.0 ^5.1 ^5.2 ^5.3 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
↑ ^6.0 ^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
↑ ^7.0 ^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
↑ ^8.0 ^8.1 ^8.2 ^8.3 ^8.4 ^8.5 Miguel-Aliaga I et al. (1999) The Caenorhabditis elegans orthologue of the human gene responsible for spinal muscular atrophy is a maternal product critical for germline maturation and embryonic viability. Hum Mol Genet 8: 2133-43 PubMed GONUTS page
↑ ^9.0 ^9.1 ^9.2 Samuelson AV et al. (2007) Gene activities that mediate increased life span of C. elegans insulin-like signaling mutants. Genes Dev 21: 2976-94 PubMed GONUTS page
↑ Sönnichsen B et al. (2005) Full-genome RNAi profiling of early embryogenesis in Caenorhabditis elegans. Nature 434: 462-9 PubMed GONUTS page

{{{LINEAGE}}}

[PMID:11099033-0] 1.0 ^1.1 ^1.2 Fraser AG et al. (2000) Functional genomic analysis of C. elegans chromosome I by systematic RNA interference. Nature 408: 325-30 PubMed GONUTS page

[PMID:11231151-1] 2.0 ^2.1 ^2.2 ^2.3 Maeda I et al. (2001) Large-scale analysis of gene function in Caenorhabditis elegans by high-throughput RNAi. Curr Biol 11: 171-6 PubMed GONUTS page

[PMID:18829666-2] 3.0 ^3.1 ^3.2 ^3.3 ^3.4 ^3.5 ^3.6 ^3.7 ^3.8 Briese M et al. (2009) Deletion of smn-1, the Caenorhabditis elegans ortholog of the spinal muscular atrophy gene, results in locomotor dysfunction and reduced lifespan. Hum Mol Genet 18: 97-104 PubMed GONUTS page

[PMID:14551910-3] 4.0 ^4.1 ^4.2 ^4.3 ^4.4 ^4.5 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:15489339-4] 5.0 ^5.1 ^5.2 ^5.3 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

[PMID:12520011-5] 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

[PMID:12654719-6] 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

[PMID:10545592-7] 8.0 ^8.1 ^8.2 ^8.3 ^8.4 ^8.5 Miguel-Aliaga I et al. (1999) The Caenorhabditis elegans orthologue of the human gene responsible for spinal muscular atrophy is a maternal product critical for germline maturation and embryonic viability. Hum Mol Genet 8: 2133-43 PubMed GONUTS page

[PMID:18006689-8] 9.0 ^9.1 ^9.2 Samuelson AV et al. (2007) Gene activities that mediate increased life span of C. elegans insulin-like signaling mutants. Genes Dev 21: 2976-94 PubMed GONUTS page

[PMID:15791247-9] Sönnichsen B et al. (2005) Full-genome RNAi profiling of early embryogenesis in Caenorhabditis elegans. Nature 434: 462-9 PubMed GONUTS page

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Species (Taxon ID)	Caenorhabditis elegans (nematode) (taxon:6239)
Gene Name(s)	C41G7.1b ( synonyms: C41G7.1, SMN )
Protein Name(s)	No Information Provided.
External Links
WB	WBGene00004887

WB:C41G7.1b

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