RNAiDB Tree View

Gene: R166.3

R166.3	SMap	S_parent	Sequence	R166
	Chromosome	II
	Identity (5)
	Gene_info	Contained_in_operon	CEOP2492
		Structured_description	Provisional_description	The R166.3 gene encodes an unfamiliar protein, with homologs in yeast and archaea, that is orthologous to the human gene ALPORT SYNDROME, MENTAL RETARDATION, MIDFACE HYPOPLASIA, AND ELLIPTOCYTOSIS CHROMOSOMAL REGION GENE 1 (AMMECR1; OMIM:300195); AMMECR1, when mutated, may be at least partially responsible for mental retardation, midface hypoplasia, or elliptocytosis.	Paper_evidence	WBPaper00012753
					Person_evidence	WBPerson567
					Curator_confirmed	WBPerson567
					Date_last_updated	17 Jun 2004 00:00:00
			Concise_description	The R166.3 gene encodes an unfamiliar protein, with homologs in yeast and archaea, that is orthologous to the human gene ALPORT SYNDROME, MENTAL RETARDATION, MIDFACE HYPOPLASIA, AND ELLIPTOCYTOSIS CHROMOSOMAL REGION GENE 1 (AMMECR1; OMIM:300195); AMMECR1, when mutated, may be at least partially responsible for mental retardation, midface hypoplasia, or elliptocytosis.
	Molecular_info (5)
	Experimental_info	RNAi_result	Cenix:112-e4
			JA:R166.3
		WB_RNAi_result	JA:R166.3
			MV_SV:mv_R166.3
			Cenix:112-e4
	Method	Gene