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33 records found for search term Ung
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1307200Unguracil-DNA glycosylaseENCODES a protein that exhibits uracil DNA N-glycosylase activity; damaged DNA binding (ortholog); ribosomal small subunit binding (ortholog); INVOLVED IN base-excision repair; negative regulation of apoptotic process; base-excision repair, AP site formation via deaminated base removal (ortholog); P124814583848154789Rat263symbol , PhenoGengene, protein-coding, PROVISIONAL [RefSeq]
1316252UNGuracil DNA glycosylaseThis gene encodes one of several uracil-DNA glycosylases. One important function of uracil-DNA glycosylases is to prevent mutagenesis by eliminating uracil from DNA molecules by cleaving the N-glycosylic bond and initiating the base-excision repair (BER) pathway. Uracil bases occur from cytosine dea12109097597109110992Human288symbol , COSMIC , description , Human Proteome Map , old_gene_symbolgene, protein-coding, REVIEWED [RefSeq]
1316253Unguracil DNA glycosylaseEnables uracil DNA N-glycosylase activity. Acts upstream of or within isotype switching and somatic hypermutation of immunoglobulin genes. Located in mitochondrion and nucleus. Is expressed in several structures, including alimentary system; brain; genitourinary system; lung5114268427114277382Mouse292symbol , PhenoGen , description , old_gene_symbolgene, protein-coding, VALIDATED [RefSeq]
8932125Unguracil DNA glycosylaseENCODES a protein that exhibits damaged DNA binding (ortholog); ribosomal small subunit binding (ortholog); uracil DNA N-glycosylase activity (ortholog); INVOLVED IN base-excision repair (ortholog); base-excision repair, AP site formation via deaminated base removal (ortholog); isotype switching (orNW_0049554551026698910282196Chinchilla31symbolgene, protein-coding, MODEL [RefSeq]
11866356UNGuracil DNA glycosylaseENCODES a protein that exhibits uracil DNA N-glycosylase activity (ortholog); INVOLVED IN base-excision repair (ortholog); isotype switching (ortholog); negative regulation of apoptotic process (ortholog); ASSOCIATED WITH Bloom syndrome (ortholog); Colorectal Neoplasms (ortholog); dysgammaglobulinem12106674073106687054Bonobo49symbolgene, protein-coding, MODEL [RefSeq]
12325467UNGuracil DNA glycosylaseENCODES a protein that exhibits damaged DNA binding (ortholog); ribosomal small subunit binding (ortholog); uracil DNA N-glycosylase activity (ortholog); INVOLVED IN base-excision repair (ortholog); isotype switching (ortholog); negative regulation of apoptotic process (ortholog); ASSOCIATED WITH Bl261790035417911126Dog43symbolgene, protein-coding, MODEL [RefSeq]
12664996Unguracil DNA glycosylaseENCODES a protein that exhibits uracil DNA N-glycosylase activity (ortholog); INVOLVED IN base-excision repair (ortholog); isotype switching (ortholog); negative regulation of apoptotic process (ortholog); ASSOCIATED WITH Bloom syndrome (ortholog); Colorectal Neoplasms (ortholog); dysgammaglobulinemNW_004936769911296922770Squirrel48symbolgene, protein-coding, MODEL [RefSeq]
14161097UNGuracil DNA glycosylaseENCODES a protein that exhibits uracil DNA N-glycosylase activity (ortholog); INVOLVED IN base-excision repair (ortholog); isotype switching (ortholog); negative regulation of apoptotic process (ortholog); ASSOCIATED WITH Bloom syndrome (ortholog); Colorectal Neoplasms (ortholog); dysgammaglobulinemPig48symbolgene, protein-coding, MODEL [RefSeq]
18383985UNGuracil DNA glycosylaseENCODES a protein that exhibits uracil DNA N-glycosylase activity (ortholog); INVOLVED IN base-excision repair (ortholog); isotype switching (ortholog); negative regulation of apoptotic process (ortholog); ASSOCIATED WITH Bloom syndrome (ortholog); Colorectal Neoplasms (ortholog); dysgammaglobulinemGreen Monkey48symbolgene, protein-coding, MODEL [RefSeq]
18909406Unguracil DNA glycosylaseENCODES a protein that exhibits damaged DNA binding (ortholog); ribosomal small subunit binding (ortholog); uracil DNA N-glycosylase activity (ortholog); INVOLVED IN base-excision repair (ortholog); isotype switching (ortholog); negative regulation of apoptotic process (ortholog); ASSOCIATED WITH BlNaked Mole-Rat43symbol , old_gene_namegene, protein-coding, MODEL [RefSeq]
20865874UNGuracil DNA glycosylaseGreen Monkeysymbolgene, protein-coding
155256693ungTropical Clawed Frogsymbolgene, null
626038063Unguracil DNA glycosylaseENCODES a protein that exhibits damaged DNA binding (ortholog); ribosomal small subunit binding (ortholog); uracil DNA N-glycosylase activity (ortholog); INVOLVED IN base-excision repair (ortholog); base-excision repair, AP site formation via deaminated base removal (ortholog); isotype switching (orBlack Rat31symbolgene, protein-coding, MODEL [RefSeq]
14389130ung-1Roundwormsymbolgene, null
155260243ung.LAfrican Clawed Frogsymbolgene, null
9366689Ung-ps1uracil-DNA glycosylase, pseudogene 1174740184247402913Ratsymbol , PhenoGengene, pseudo, MODEL [RefSeq]
41009085Ung-ps2uracil-DNA glycosylase, pseudogene 2X2619526826197680Ratsymbol , PhenoGengene, pseudo, MODEL [RefSeq]
1622097Ccnocyclin OPredicted to enable cyclin-dependent protein serine/threonine kinase regulator activity. Acts upstream of or within several processes, including cilium assembly; seminiferous tubule development; and spermatogenesis. Located in cytoplasm. Is expressed in brain; nasal epithelium; reproductive system; 13113124363113127313Mouse122old_gene_symbolgene, protein-coding, VALIDATED [RefSeq]
16560067AC025437.6uracil-DNA glycosylase (UNG) pseudogene5158188980158189911Humannamegene, pseudo, INFERRED [RefSeq]
16558074AC092658.1uracil-DNA glycosylase (UNG) pseudogene48716684687167931Humannamegene, pseudo, INFERRED [RefSeq]
16563068AC137527.1uracil-DNA glycosylase (UNG) pseudogeneHumannamegene, processed_pseudogene
14389129UNG1Yeastsymbolgene, null
1349423UNGP1uracil-DNA glycosylase pseudogene 1165127804351280029Humansymbol , COSMIC , Human Proteome Mapgene, pseudo, INFERRED [RefSeq]
1349949UNGP2uracil-DNA glycosylase pseudogene 2142692546626926253Humansymbol , GTEx , COSMIC , Human Proteome Mapgene, pseudo, INFERRED [RefSeq]
1351551UNGP3uracil-DNA glycosylase pseudogene 3148125832881260234Humansymbol , COSMIC , Human Proteome Mapgene, pseudo, INFERRED [RefSeq]
1346890CCNOcyclin OThis gene encodes a member of the cyclin protein family, and the encoded protein is involved in regulation of the cell cycle. Disruption of this gene is associated with primary ciliary dyskinesia-19. Alternative splicing results in multiple transcript variants. This gene, which has a previous symbol55523115255233608Human185description , old_gene_symbolgene, protein-coding, REVIEWED [RefSeq]
1606814SMUG1single-strand-selective monofunctional uracil-DNA glycosylase 1This gene encodes a protein that participates in base excision repair by removing uracil from single- and double-stranded DNA. Many alternatively spliced transcript variants exist for this gene; the full-length nature is known for some but not all of the variants. [provided by RefSeq, Aug 2011]125415823554188985Human99old_gene_symbolgene, protein-coding, REVIEWED [RefSeq]
1343236AFF2ALF transcription elongation factor 2This gene encodes a putative transcriptional activator that is a member of the AF4\FMR2 gene family. This gene is associated with the folate-sensitive fragile X E locus on chromosome X. A repeat polymorphism in the fragile X E locus results in silencing of this gene causing Fragile X E syndrome. FraX148500617149000663Human134GenBank Proteingene, protein-coding, REVIEWED [RefSeq]
69093HNF4Ahepatocyte nuclear factor 4 alphaThe protein encoded by this gene is a nuclear transcription factor which binds DNA as a homodimer. The encoded protein controls the expression of several genes, including hepatocyte nuclear factor 1 alpha, a transcription factor which regulates the expression of several hepatic genes. This gene may 204435569944434596Human922GenBank Proteingene, protein-coding, REVIEWED [RefSeq]
736831SELEselectin EThe protein encoded by this gene is found in cytokine-stimulated endothelial cells and is thought to be responsible for the accumulation of blood leukocytes at sites of inflammation by mediating the adhesion of cells to the vascular lining. It exhibits structural features such as the presence of lec1169722640169734079Human335GenBank Proteingene, protein-coding, REVIEWED [RefSeq]
1316692PIP4P1phosphatidylinositol-4,5-bisphosphate 4-phosphatase 1TMEM55B catalyzes the degradation of phosphatidylinositol 4,5-bisphosphate (PtdIns-4,5-P2) by removing the 4-phosphate (Ungewickell et al., 2005 [PubMed 16365287]).[supplied by OMIM, Mar 2008]142045768120461434Human98descriptiongene, protein-coding, VALIDATED [RefSeq]
1602110PIP4P2phosphatidylinositol-4,5-bisphosphate 4-phosphatase 2TMEM55A catalyzes the degradation of phosphatidylinositol 4,5-bisphosphate (PtdIns-4,5-P2) by removing the 4-phosphate (Ungewickell et al., 2005 [PubMed 16365287]).[supplied by OMIM, Mar 2008]89099380291040859Human109descriptiongene, protein-coding, VALIDATED [RefSeq]
1604844TP63tumor protein p63This gene encodes a member of the p53 family of transcription factors. The functional domains of p53 family proteins include an N-terminal transactivation domain, a central DNA-binding domain and an oligomerization domain. Alternative splicing of this gene and the use of alternative promoters result3189596746189897276Human862descriptiongene, protein-coding, REVIEWED [RefSeq]