FUT1

FUT1
식별자
별칭	FUT1, HH, HSC, fucosyl transferase 1 (H 혈액 그룹), H
외부 ID	OMIM: 211100 MGI: 109375 HomoloGene: 120 GeneCard: FUT1
유전자 위치(인간)
쳇.	19번 염색체(인간)
끝	48,755,190 bp
유전자 위치(마우스)
쳇.	7번 염색체(쥐)
끝	45,195,483 bp
RNA 표현 패턴
	표현된 상단
	질질 끌다; ; 췌장체; ; 췌장; ; 펀두스; ; 오른쪽 폐; ; 뱃속; ; 좌측 폐 상부엽; ; 난소의; ; 위체; ; 편평한 상피;
	추가 참조 표현식 데이터
	추가 참조 표현식 데이터
유전자 온톨로지
분자함수	전이효소 활동; 갈락토사이드 2-알파-L-푸코실전달효소 활성; 후코실전달효소 활동; 글리코실전달효소 활성;
셀룰러 컴포넌트	막의 적분 성분; 골지 시스테나 막; 골지 기구; 플라스마 막의 적분 성분; 막으로 막다;
생물학적 과정	단백질 당화; L-푸코오스 카타볼라 공정; 푸코실화; 탄수화물 대사 과정;
	출처:아미고 / 퀵고
직교체
	2523
	14343
	ENSG00000174951
	ENSMUSG00000008461
	P19526
	O09160
	NM_000148; NM_001329877; NM_001384359
	NM_001271981; NM_008051
	NP_000139; NP_001316806
	NP_001258910; NP_032077
	위키다타
인간 보기/편집	마우스 보기/편집

갈락토사이드 2-알파-L-푸코실전달효소 1은 인간에서 FUT1 유전자에 의해 인코딩되는 효소다.^[5]

효소는 H항원 합성에 관여한다.

참조

^ ^a ^b ^c GRCh38: 앙상블 릴리스 89: ENSG00000174951 - 앙상블, 2017년 5월
^ ^a ^b ^c GRCm38: 앙상블 릴리스 89: ENSMUSG00000008461 - 앙상블, 2017년 5월
^ "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.
^ "Entrez Gene: FUT1 fucosyltransferase 1 (galactoside 2-alpha-L-fucosyltransferase, H blood group)".

추가 읽기

Ball SP, Tongue N, Gibaud A, Le Pendu J, Mollicone R, Gérard G, Oriol R (July 1991). "The human chromosome 19 linkage group FUT1 (H), FUT2 (SE), LE, LU, PEPD, C3, APOC2, D19S7 and D19S9". Annals of Human Genetics. 55 (Pt 3): 225–33. doi:10.1111/j.1469-1809.1991.tb00417.x. PMID 1763885. S2CID 30777695.
Larsen RD, Ernst LK, Nair RP, Lowe JB (September 1990). "Molecular cloning, sequence, and expression of a human GDP-L-fucose:beta-D-galactoside 2-alpha-L-fucosyltransferase cDNA that can form the H blood group antigen". Proceedings of the National Academy of Sciences of the United States of America. 87 (17): 6674–8. Bibcode:1990PNAS...87.6674L. doi:10.1073/pnas.87.17.6674. PMC 54599. PMID 2118655.
Reguigne-Arnould I, Couillin P, Mollicone R, Fauré S, Fletcher A, Kelly RJ, Lowe JB, Oriol R (1995). "Relative positions of two clusters of human alpha-L-fucosyltransferases in 19q (FUT1-FUT2) and 19p (FUT6-FUT3-FUT5) within the microsatellite genetic map of chromosome 19". Cytogenetics and Cell Genetics. 71 (2): 158–62. doi:10.1159/000134098. PMID 7656588.
Bruneau N, Lombardo D (June 1995). "Chaperone function of a Grp 94-related protein for folding and transport of the pancreatic bile salt-dependent lipase". The Journal of Biological Chemistry. 270 (22): 13524–33. doi:10.1074/jbc.270.22.13524. PMID 7768954.
Kelly RJ, Ernst LK, Larsen RD, Bryant JG, Robinson JS, Lowe JB (June 1994). "Molecular basis for H blood group deficiency in Bombay (Oh) and para-Bombay individuals". Proceedings of the National Academy of Sciences of the United States of America. 91 (13): 5843–7. Bibcode:1994PNAS...91.5843K. doi:10.1073/pnas.91.13.5843. PMC 44093. PMID 7912436.
Koda Y, Soejima M, Kimura H (March 1997). "Structure and expression of H-type GDP-L-fucose:beta-D-galactoside 2-alpha-L-fucosyltransferase gene (FUT1). Two transcription start sites and alternative splicing generate several forms of FUT1 mRNA". The Journal of Biological Chemistry. 272 (11): 7501–5. doi:10.1074/jbc.272.11.7501. PMID 9054453.
Wagner FF, Flegel WA (March 1997). "Polymorphism of the h allele and the population frequency of sporadic nonfunctional alleles". Transfusion. 37 (3): 284–90. doi:10.1046/j.1537-2995.1997.37397240210.x. PMID 9122901. S2CID 25273202.
Kaneko M, Nishihara S, Shinya N, Kudo T, Iwasaki H, Seno T, Okubo Y, Narimatsu H (July 1997). "Wide variety of point mutations in the H gene of Bombay and para-Bombay individuals that inactivate H enzyme". Blood. 90 (2): 839–49. doi:10.1182/blood.V90.2.839. PMID 9226185.
Koda Y, Soejima M, Johnson PH, Smart E, Kimura H (September 1997). "Missense mutation of FUT1 and deletion of FUT2 are responsible for Indian Bombay phenotype of ABO blood group system". Biochemical and Biophysical Research Communications. 238 (1): 21–5. doi:10.1006/bbrc.1997.7232. PMID 9299444.
Koda Y, Soejima M, Kimura H (September 1998). "Changing transcription start sites in H-type alpha(1,2)fucosyltransferase gene (FUT1) during differentiation of the human erythroid lineage". European Journal of Biochemistry. 256 (2): 379–87. doi:10.1046/j.1432-1327.1998.2560379.x. PMID 9760178.
Roos C, Kolmer M, Mattila P, Renkonen R (February 2002). "Composition of Drosophila melanogaster proteome involved in fucosylated glycan metabolism". The Journal of Biological Chemistry. 277 (5): 3168–75. doi:10.1074/jbc.M107927200. PMID 11698403.
Yip SP, Chee KY, Chan PY, Chow EY, Wong HF (October 2002). "Molecular genetic analysis of para-Bombay phenotypes in Chinese: a novel non-functional FUT1 allele is identified". Vox Sanguinis. 83 (3): 258–62. doi:10.1046/j.1423-0410.2002.00184.x. hdl:10397/32501. PMID 12366770. S2CID 37005881.
López-Ferrer A, de Bolós C (January 2002). "The expression of human FUT1 in HT-29/M3 colon cancer cells instructs the glycosylation of MUC1 and MUC5AC apomucins". Glycoconjugate Journal. 19 (1): 13–21. doi:10.1023/A:1022576712961. PMID 12652076. S2CID 13065601.
Shi S, Stanley P (April 2003). "Protein O-fucosyltransferase 1 is an essential component of Notch signaling pathways". Proceedings of the National Academy of Sciences of the United States of America. 100 (9): 5234–9. Bibcode:2003PNAS..100.5234S. doi:10.1073/pnas.0831126100. PMC 154328. PMID 12697902.
Brandenberger R, Wei H, Zhang S, Lei S, Murage J, Fisk GJ, Li Y, Xu C, Fang R, Guegler K, Rao MS, Mandalam R, Lebkowski J, Stanton LW (June 2004). "Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation". Nature Biotechnology. 22 (6): 707–16. doi:10.1038/nbt971. PMID 15146197. S2CID 27764390.
Guo ZH, Xiang D, Zhu ZY, Wang JL, Zhang JM, Liu X, Shen W, Chen HP (October 2004). "[Analysis on FUT1 and FUT2 gene of 10 para-Bombay individuals in China]". Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 21 (5): 417–21. PMID 15476160.
Yan L, Zhu F, Xu X, Hong X, Lv Q (May 2005). "Molecular basis for para-Bombay phenotypes in Chinese persons, including a novel nonfunctional FUT1 allele". Transfusion. 45 (5): 725–30. doi:10.1111/j.1537-2995.2005.04305.x. PMID 15847661. S2CID 21841537.
Mejías-Luque R, López-Ferrer A, Garrido M, Fabra A, de Bolós C (July 2007). "Changes in the invasive and metastatic capacities of HT-29/M3 cells induced by the expression of fucosyltransferase 1". Cancer Science. 98 (7): 1000–5. doi:10.1111/j.1349-7006.2007.00484.x. PMID 17459061. S2CID 24079329.

19번 염색체의 유전자에 관한 이 기사는 단조롭다.위키피디아를 확장하여 도울 수 있다.

[refGRCh38Ensembl-1] GRCh38: 앙상블 릴리스 89: ENSG00000174951 - 앙상블, 2017년 5월

[refGRCm38Ensembl-2] GRCm38: 앙상블 릴리스 89: ENSMUSG00000008461 - 앙상블, 2017년 5월

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-5] "Entrez Gene: FUT1 fucosyltransferase 1 (galactoside 2-alpha-L-fucosyltransferase, H blood group)".

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FUT1

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