Ung Gene Search Result

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Genes search result for Homo sapiens
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15 records found for search term Ung

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RGD ID	Symbol	Name	Description	Chr	Start	Stop	Species	Annotations	Match	Type
1316252	UNG	uracil DNA glycosylase	This 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 dea ... (more) mination or misincorporation of dUMP residues. Alternative promoter usage and splicing of this gene leads to two different isoforms: the mitochondrial UNG1 and the nuclear UNG2. The UNG2 term was used as a previous symbol for the CCNO gene (GeneID 10309), which has been confused with this gene, in the literature and some databases. [provided by RefSeq, Nov 2010]	12	109097597	109110992	Human	288	symbol , COSMIC , description , Human Proteome Map , old_gene_symbol	gene, protein-coding, REVIEWED [RefSeq]
16560067	AC025437.6	uracil-DNA glycosylase (UNG) pseudogene		5	158188980	158189911	Human		name	gene, pseudo, INFERRED [RefSeq]
16558074	AC092658.1	uracil-DNA glycosylase (UNG) pseudogene		4	87166846	87167931	Human		name	gene, pseudo, INFERRED [RefSeq]
16563068	AC137527.1	uracil-DNA glycosylase (UNG) pseudogene					Human		name	gene, processed_pseudogene
1349423	UNGP1	uracil-DNA glycosylase pseudogene 1		16	51278043	51280029	Human		symbol , COSMIC , Human Proteome Map	gene, pseudo, INFERRED [RefSeq]
1349949	UNGP2	uracil-DNA glycosylase pseudogene 2		14	26925466	26926253	Human		symbol , GTEx , COSMIC , Human Proteome Map	gene, pseudo, INFERRED [RefSeq]
1351551	UNGP3	uracil-DNA glycosylase pseudogene 3		14	81258328	81260234	Human		symbol , COSMIC , Human Proteome Map	gene, pseudo, INFERRED [RefSeq]
1346890	CCNO	cyclin O	This 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 symbol ... (more) of UNG2, was erroneously identified as a uracil DNA glycosylase in PubMed ID: 2001396. A later publication, PubMed ID: 8419333, identified this gene's product as a cyclin protein family member. The UNG2 symbol is also used as a specific protein isoform name for the UNG gene (GeneID 7374), so confusion exists in the scientific literature and in some databases for these two genes. [provided by RefSeq, Jul 2014]	5	55231152	55233608	Human	185	description , old_gene_symbol	gene, protein-coding, REVIEWED [RefSeq]
1606814	SMUG1	single-strand-selective monofunctional uracil-DNA glycosylase 1	This 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]	12	54158235	54188985	Human	99	old_gene_symbol	gene, protein-coding, REVIEWED [RefSeq]
1343236	AFF2	ALF transcription elongation factor 2	This 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. Fra ... (more) gile X E syndrome is a form of nonsyndromic X-linked cognitive disability. In addition, this gene contains 6-25 GCC repeats that are expanded to >200 repeats in the disease state. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jul 2016]	X	148500617	149000663	Human	134	GenBank Protein	gene, protein-coding, REVIEWED [RefSeq]
69093	HNF4A	hepatocyte nuclear factor 4 alpha	The 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 ... (more) play a role in development of the liver, kidney, and intestines. Mutations in this gene have been associated with monogenic autosomal dominant non-insulin-dependent diabetes mellitus type I. Alternative splicing of this gene results in multiple transcript variants encoding several different isoforms. [provided by RefSeq, Apr 2012]	20	44355699	44434596	Human	922	GenBank Protein	gene, protein-coding, REVIEWED [RefSeq]
736831	SELE	selectin E	The 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 lec ... (more) tin- and EGF-like domains followed by short consensus repeat (SCR) domains that contain 6 conserved cysteine residues. These proteins are part of the selectin family of cell adhesion molecules. Adhesion molecules participate in the interaction between leukocytes and the endothelium and appear to be involved in the pathogenesis of atherosclerosis. [provided by RefSeq, Jul 2008]	1	169722640	169734079	Human	335	GenBank Protein	gene, protein-coding, REVIEWED [RefSeq]
1316692	PIP4P1	phosphatidylinositol-4,5-bisphosphate 4-phosphatase 1	TMEM55B 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]	14	20457681	20461434	Human	98	description	gene, protein-coding, VALIDATED [RefSeq]
1602110	PIP4P2	phosphatidylinositol-4,5-bisphosphate 4-phosphatase 2	TMEM55A 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]	8	90993802	91040859	Human	109	description	gene, protein-coding, VALIDATED [RefSeq]
1604844	TP63	tumor protein p63	This 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 result ... (more) s in multiple transcript variants encoding different isoforms that vary in their functional properties. These isoforms function during skin development and maintenance, adult stem/progenitor cell regulation, heart development and premature aging. Some isoforms have been found to protect the germline by eliminating oocytes or testicular germ cells that have suffered DNA damage. Mutations in this gene are associated with ectodermal dysplasia, and cleft lip/palate syndrome 3 (EEC3); split-hand/foot malformation 4 (SHFM4); ankyloblepharon-ectodermal defects-cleft lip/palate; ADULT syndrome (acro-dermato-ungual-lacrimal-tooth); limb-mammary syndrome; Rap-Hodgkin syndrome (RHS); and orofacial cleft 8. [provided by RefSeq, Aug 2016]	3	189596746	189897276	Human	862	description	gene, protein-coding, REVIEWED [RefSeq]