UBIAD1

UBIAD1
Identifiers
Aliases	UBIAD1, SCCD, TERE1, UbiA prenyltransferase domain containing 1
External IDs	OMIM: 611632; MGI: 1918957; HomoloGene: 8336; GeneCards: UBIAD1; OMA:UBIAD1 - orthologs
Gene location (Human)
Chr.	Chromosome 1 (human)
End	11,296,049 bp
Gene location (Mouse)
Chr.	Chromosome 4 (mouse)
End	148,529,228 bp
RNA expression pattern
	Top expressed in
	gastrocnemius muscle; ; muscle of thigh; ; gonad; ; secondary oocyte; ; skin of thigh; ; ganglionic eminence; ; islet of Langerhans; ; nipple; ; granulocyte; ; ventricular zone;
	Top expressed in
	zygote; ; proximal tubule; ; right kidney; ; secondary oocyte; ; primary oocyte; ; human kidney; ; interventricular septum; ; yolk sac; ; muscle of thigh; ; Rostral migratory stream;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	transferase activity; antioxidant activity; protein binding; prenyltransferase activity; transferase activity, transferring alkyl or aryl (other than methyl) groups;
Cellular component	cytoplasm; integral component of membrane; integral component of Golgi membrane; Golgi apparatus; endoplasmic reticulum membrane; membrane; mitochondrial membranes; Golgi membrane; endoplasmic reticulum; mitochondrion; nucleus;
Biological process	menaquinone biosynthetic process; ubiquinone biosynthetic process; vitamin K biosynthetic process; vitamin K metabolic process; cellular oxidant detoxification; ubiquinone biosynthetic process via 3,4-dihydroxy-5-polyprenylbenzoate;
	Sources:Amigo / QuickGO
Orthologs
	29914
	71707
	ENSG00000120942
	ENSMUSG00000047719
	Q9Y5Z9
	Q9DC60
	NM_013319; NM_001330349; NM_001330350
	NM_027873
	NP_001317278; NP_001317279; NP_037451
	NP_082149
	Wikidata
View/Edit Human	View/Edit Mouse

UbiA prenyltransferase domain-containing protein 1 (UBIAD1) also known as transitional epithelial response protein 1 (TERE1) is a protein that in humans is encoded by the UBIAD1 gene.^[5]^[6]^[7]

Recent evidence suggests that ubiad1 has enzymatic activity in the vitamin K pathway, a role in blood vessel development, and may be involved in oxidative stress pathways.^[8]^[9]^[10]

Clinical significance

Mutations of the UBIAD1 gene cause Schnyder crystalline corneal dystrophy.^[11]^[12]^[13]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000120942 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000047719 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ McGarvey TW, Nguyen T, Puthiyaveettil R, Tomaszewski JE, Malkowicz SB (Dec 2002). "TERE1, a novel gene affecting growth regulation in prostate carcinoma". Prostate. 54 (2): 144–55. doi:10.1002/pros.10174. PMID 12497587.
^ McGarvey TW, Nguyen T, Tomaszewski JE, Monson FC, Malkowicz SB (Apr 2001). "Isolation and characterization of the TERE1 gene, a gene down-regulated in transitional cell carcinoma of the bladder". Oncogene. 20 (9): 1042–51. doi:10.1038/sj.onc.1204143. PMID 11314041.
^ "Entrez Gene: UBIAD1 UbiA prenyltransferase domain containing 1".
^ Nakagawa, K; Hirota, Y; Sawada, N; Yuge, N; Watanabe, M; Uchino, Y; Okuda, N; Shimomura, Y; Suhara, Y; Okano, T (Nov 2010). "Identification of UBIAD1 as a novel human menaquinone-4 biosynthetic enzyme". Nature. 468 (7320): 117–21. doi:10.1038/nature09464.
^ Fredericks, WJ; McGarvey, T; Wang, H; Lal, P; Puthiyaveettil, R; Tomaszewski, J; Sepulveda, J; Labelle, E; Weiss, JS; Nickerson, ML; Kruth, HS; Brandt, W; Wessjohann, LA; Malkowicz, SB (Nov 2011). "The Bladder Tumor Suppressor Protein TERE1 (UBIAD1)Modulates Cell Cholesterol: Implications for Tumor Progression". DNA Cell Biol. 30 (11): 851–64. doi:10.1089/dna.2011.1315.
^ R Postel, Identification and Characterization of Novel Genes by Reverse and Forward Genetics in Zebrafish, igitur-archive.library.uu.nl/dissertations/2008-0522.../UUindex.html, 2008.
^ Weiss JS, Kruth HS, Kuivaniemi H, Tromp G, White PS, Winters RS, Lisch W, Henn W, Denninger E, Krause M, Wasson P, Ebenezer N, Mahurkar S, Nickerson ML (November 2007). "Mutations in the UBIAD1 gene on chromosome short arm 1, region 36, cause Schnyder crystalline corneal dystrophy". Invest. Ophthalmol. Vis. Sci. 48 (11): 5007–12. doi:10.1167/iovs.07-0845. PMID 17962451.
^ Orr A, Dubé MP, Marcadier J, Jiang H, Federico A, George S, Seamone C, Andrews D, Dubord P, Holland S, Provost S, Mongrain V, Evans S, Higgins B, Bowman S, Guernsey D, Samuels M (2007). Kronenberg, Florian (ed.). "Mutations in the UBIAD1 Gene, Encoding a Potential Prenyltransferase, Are Causal for Schnyder Crystalline Corneal Dystrophy". PLoS ONE. 2 (1): e685. doi:10.1371/journal.pone.0000685. PMC 1925147. PMID 17668063.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link)
^ Weiss JS, Kruth HS, Kuivaniemi H, Tromp G, Karkera J, Mahurkar S, Lisch W, Dupps WJ, White PS, Winters RS, Kim C, Rapuano CJ, Sutphin J, Reidy J, Hu FR, Lu da W, Ebenezer N, Nickerson ML (February 2008). "Genetic analysis of 14 families with Schnyder crystalline corneal dystrophy reveals clues to UBIAD1 protein function". Am. J. Med. Genet. A. 146 (3): 271–83. doi:10.1002/ajmg.a.32201. PMID 18176953.

Clinical significance

References

Further reading