Nap5 Gene Search Result

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11 records found for search term Nap5

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RGD ID	Symbol	Name	Description	Chr	Start	Stop	Species	Annotations	Match	Type
1564507	Nckap5	NCK-associated protein 5	ASSOCIATED WITH salt-sensitive hypertension; ASSOCIATED WITH proteinuria; amenorrhea (ortholog); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; 6-propyl-2-thiouracil; atrazine	13	39922576	40835849	Rat	88	old_gene_symbol	gene, protein-coding, MODEL [RefSeq]
1615726	Nckap5	NCK-associated protein 5	Predicted to be involved in microtubule bundle formation and microtubule depolymerization. Predicted to be active in microtubule plus-end. Is expressed in central nervous system; lung; and sensory organ. Orthologous to human NCKAP5 (NCK associated protein 5). [provided by Alliance of Genome Resource ... (more) s, Jul 2025]	1	125841373	126758529	Mouse	87	old_gene_symbol	gene, protein-coding, VALIDATED [RefSeq]
1625092	NCKAP5	NCK associated protein 5	Predicted to be involved in microtubule bundle formation and microtubule depolymerization. Predicted to be active in microtubule plus-end. [provided by Alliance of Genome Resources, Jul 2025]	2	132671788	133674836	Human	87	old_gene_symbol	gene, protein-coding, VALIDATED [RefSeq]
621780	Dkc1	dyskerin pseudouridine synthase 1	ENCODES a protein that exhibits box H/ACA snoRNA binding (ortholog); pseudouridine synthase activity (ortholog); RNA binding (ortholog); INVOLVED IN positive regulation of cell population proliferation; snoRNA guided rRNA pseudouridine synthesis; box H/ACA sno(s)RNA metabolic process (ortholog); PAR ... (more) TICIPATES IN ribosome biogenesis pathway; ASSOCIATED WITH anemia (ortholog); aplastic anemia (ortholog); B-Cell Chronic Lymphocytic Leukemia (ortholog); FOUND IN box H/ACA snoRNP complex; Cajal body; nucleoplasm; INTERACTS WITH (+)-schisandrin B; 2,3,7,8-tetrachlorodibenzodioxine; 2,3,7,8-Tetrachlorodibenzofuran	X	157751651	157757796	Rat	218	old_gene_name , old_gene_symbol	gene, protein-coding, PROVISIONAL [RefSeq]
1349510	DKC1	dyskerin pseudouridine synthase 1	This gene functions in two distinct complexes. It plays an active role in telomerase stabilization and maintenance, as well as recognition of snoRNAs containing H/ACA sequences which provides stability during biogenesis and assembly into H/ACA small nucleolar RNA ribonucleoproteins (snoRNPs). This g ... (more) ene is highly conserved and widely expressed, and may play additional roles in nucleo-cytoplasmic shuttling, DNA damage response, and cell adhesion. Mutations have been associated with X-linked dyskeratosis congenita. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]	X	154762864	154777689	Human	433	old_gene_name , old_gene_symbol	gene, protein-coding, REVIEWED [RefSeq]
4139859	Nckap5^em1Mcwi	NCK-associated protein 5; zinc finger nuclease induced mutant 1, Medical College of Wisconsin	This allele was made by zinc finger nuclease mutagenesis. The resulting mutation is a 10-bp frameshift deletion in exon 6 (del 1559-1568).				Rat		old_gene_symbol	gene, allele
4139862	Nckap5^em2Mcwi	NCK-associated protein 5; zinc finger nuclease induced mutant 2, Medical College of Wisconsin	This allele was made by zinc finger nuclease mutagenesis. The resulting mutation is a 4-bp frameshift deletion in exon 6 (del 1560-1563).				Rat		old_gene_symbol	gene, allele
4139861	Nckap5^em3Mcwi	NCK-associated protein 5; zinc finger nuclease induced mutant 3, Medical College of Wisconsin	This allele was made by zinc finger nuclease mutagenesis. The resulting mutation is an 11-bp frameshift deletion in exon 6 (del 1558-1568).				Rat		old_gene_symbol	gene, allele
1615626	Dkc1	dyskeratosis congenita 1, dyskerin	Predicted to enable box H/ACA snoRNA binding activity; pseudouridine synthase activity; and telomerase RNA binding activity. Predicted to contribute to telomerase activity. Acts upstream of or within RNA metabolic process; positive regulation of telomere maintenance via telomerase; and telomerase ho ... (more) loenzyme complex assembly. Located in Cajal body and nucleolus. Is expressed in several structures, including brain; epithelium; genitourinary system; skin; and surface ectoderm. Used to study dyskeratosis congenita. Human ortholog(s) of this gene implicated in X-linked dyskeratosis congenita; aplastic anemia; and dyskeratosis congenita. Orthologous to human DKC1 (dyskerin pseudouridine synthase 1). [provided by Alliance of Genome Resources, Jul 2025]	X	74139460	74153382	Mouse	310	old_gene_name	gene, protein-coding, VALIDATED [RefSeq]
1595484	Dkc1-ps2	dyskerin pseudouridine synthase 1, pseudogene 2		3	59161226	59162862	Rat		old_gene_name	gene, pseudo, MODEL [RefSeq]
1587526	Dkc1-ps3	dyskerin pseudouridine synthase 1, pseudogene 3		5	99367410	99369006	Rat		old_gene_name	gene, pseudo, MODEL [RefSeq]