اترکتین

ATRN
معین‌کننده‌ها
نام‌های دیگر	ATRN, DPPT-L, MGCA, attractin
شناسه‌های بیرونی	OMIM: 603130 MGI: 1341628 HomoloGene: 22542 GeneCards: ATRN
موقعیت ژن (موش)
کروموزوم	کروموزوم ۲ (موش)
پایان	130,872,253 bp
الگوی گسترش RNA
	; ;
	More reference expression data
هستی‌شناسی ژن
عملکرد ملکولی	• carbohydrate binding; • signaling receptor activity;
ترکیبات سلولی	• سیتوپلاسم; • integral component of membrane; • extracellular region; • پوسته یاخته; • integral component of plasma membrane; • extracellular exosome; • membrane; • extracellular space;
فرایند زیستی	• myelination; • pigmentation; • inflammatory response; • GO:0001306 پاسخ به استرس اکسیداتیو; • cerebellum development; • regulation of multicellular organism growth; • animal organ morphogenesis; • بافت زایی;
	منابع: آمیگو / کوئیک‌گو
هم‌ساخت‌شناسی
	8455
	11990
	ENSG00000088812
	ENSMUSG00000027312
	O75882
	Q9WU60
	NM_012070، NM_139321، NM_139322، NM_001323332 NM_001207047، NM_012070، NM_139321، NM_139322، NM_001323332
	XM_006498606، XM_011239259 NM_009730، XM_006498606، XM_011239259
	NP_001310261، NP_647537، NP_647538 NP_001193976، NP_001310261، NP_647537، NP_647538
	XP_006498669، XP_011237561 NP_033860، XP_006498669، XP_011237561
	ویکی‌داده
مشاهده/ویرایش انسان	مشاهده/ویرایش موش

اَترکتین (انگلیسی: Attractin) یک پروتئین است که در انسان توسط ژن «ATRN» کُدگذاری می‌شود.^[۴]^[۵]^[۶]

اَترکتین به گروه ۱۱ از لکتین نوع سی تعلق دارد.

منابع[ویرایش]

↑ ^۱٫۰ ^۱٫۱ ^۱٫۲ GRCm38: Ensembl release 89: ENSMUSG00000027312 - 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.
↑ Duke-Cohan JS, Gu J, McLaughlin DF, Xu Y, Freeman GJ, Schlossman SF (Oct 1998). "Attractin (DPPT-L), a member of the CUB family of cell adhesion and guidance proteins, is secreted by activated human T lymphocytes and modulates immune cell interactions". Proc Natl Acad Sci U S A. 95 (19): 11336–41. doi:10.1073/pnas.95.19.11336. PMC 21643. PMID 9736737.
↑ Duke-Cohan JS, Morimoto C, Rocker JA, Schlossman SF (Apr 1996). "Serum high molecular weight dipeptidyl peptidase IV (CD26) is similar to a novel antigen DPPT-L released from activated T cells". J Immunol. 156 (5): 1714–21. PMID 8596018.
↑ "Entrez Gene: ATRN attractin".

مشارکت‌کنندگان ویکی‌پدیا. «Attractin». در دانشنامهٔ ویکی‌پدیای انگلیسی، بازبینی‌شده در ۱۴ سپتامبر ۲۰۱۹.

برای مطالعهٔ بیشتر[ویرایش]

Mori M, Sakurai M, Araie M (1993). "[Topical timolol and blood-aqueous barrier permeability to protein in human eyes]". Nippon Ganka Gakkai Zasshi. 96 (11): 1418–22. PMID 1476071.
Nagase T; Ishikawa K; Miyajima N; et al. (1998). "Prediction of the coding sequences of unidentified human genes. IX. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro". DNA Res. 5 (1): 31–9. doi:10.1093/dnares/5.1.31. PMID 9628581. {{cite journal}}: Unknown parameter |name-list-format= ignored (|name-list-style= suggested) (help)
Nagle DL; McGrail SH; Vitale J; et al. (1999). "The mahogany protein is a receptor involved in suppression of obesity". Nature. 398 (6723): 148–52. doi:10.1038/18210. PMID 10086355. {{cite journal}}: Unknown parameter |name-list-format= ignored (|name-list-style= suggested) (help)
Gunn TM; Miller KA; He L; et al. (1999). "The mouse mahogany locus encodes a transmembrane form of human attractin". Nature. 398 (6723): 152–6. doi:10.1038/18217. PMID 10086356. {{cite journal}}: Unknown parameter |name-list-format= ignored (|name-list-style= suggested) (help)
Tang W; Gunn TM; McLaughlin DF; et al. (2000). "Secreted and membrane attractin result from alternative splicing of the human ATRN gene". Proc. Natl. Acad. Sci. U.S.A. 97 (11): 6025–30. doi:10.1073/pnas.110139897. PMC 18552. PMID 10811918. {{cite journal}}: Unknown parameter |name-list-format= ignored (|name-list-style= suggested) (help)
Deloukas P; Matthews LH; Ashurst J; et al. (2002). "The DNA sequence and comparative analysis of human chromosome 20". Nature. 414 (6866): 865–71. doi:10.1038/414865a. PMID 11780052. {{cite journal}}: Unknown parameter |name-list-format= ignored (|name-list-style= suggested) (help)
Strausberg RL; Feingold EA; Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932. {{cite journal}}: Unknown parameter |name-list-format= ignored (|name-list-style= suggested) (help)
Gevaert K; Goethals M; Martens L; et al. (2004). "Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides". Nat. Biotechnol. 21 (5): 566–9. doi:10.1038/nbt810. PMID 12665801. {{cite journal}}: Unknown parameter |name-list-format= ignored (|name-list-style= suggested) (help)
Friedrich D, Kühn-Wache K, Hoffmann T, Demuth HU (2003). "Isolation and characterization of attractin-2". Adv. Exp. Med. Biol. Advances in Experimental Medicine and Biology. 524: 109–13. doi:10.1007/0-306-47920-6_14. ISBN 0-306-47717-3. PMID 12675230.
Bunkenborg J, Pilch BJ, Podtelejnikov AV, Wiśniewski JR (2004). "Screening for N-glycosylated proteins by liquid chromatography mass spectrometry". Proteomics. 4 (2): 454–65. doi:10.1002/pmic.200300556. PMID 14760718.
Gerhard DS; Wagner L; Feingold EA; et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334. {{cite journal}}: Unknown parameter |name-list-format= ignored (|name-list-style= suggested) (help)
Liu T; Qian WJ; Gritsenko MA; et al. (2006). "Human Plasma N-Glycoproteome Analysis by Immunoaffinity Subtraction, Hydrazide Chemistry, and Mass Spectrometry". J. Proteome Res. 4 (6): 2070–80. doi:10.1021/pr0502065. PMC 1850943. PMID 16335952. {{cite journal}}: Unknown parameter |name-list-format= ignored (|name-list-style= suggested) (help)
Wrenger S; Faust J; Friedrich D; et al. (2007). "Attractin, a dipeptidyl peptidase IV/CD26-like enzyme, is expressed on human peripheral blood monocytes and potentially influences monocyte function". J. Leukoc. Biol. 80 (3): 621–9. doi:10.1189/jlb.1105678. PMID 16835316. {{cite journal}}: Unknown parameter |name-list-format= ignored (|name-list-style= suggested) (help)

پیوند به بیرون[ویرایش]

مکان ژنوم ATRN انسانی و صفحهٔ جزئیات ژنی ATRN در سامانه جستجوی بانک ژنی دانشگاه کالیفرنیا، سانتا کروز.

این یک مقالهٔ خرد زیست‌شناسی مولکولی است. می‌توانید با گسترش آن به ویکی‌پدیا کمک کنید.

[refGRCm38Ensembl-1] ۱٫۰ ^۱٫۱ ^۱٫۲ GRCm38: Ensembl release 89: ENSMUSG00000027312 - Ensembl, May 2017

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

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

[pmid9736737-4] Duke-Cohan JS, Gu J, McLaughlin DF, Xu Y, Freeman GJ, Schlossman SF (Oct 1998). "Attractin (DPPT-L), a member of the CUB family of cell adhesion and guidance proteins, is secreted by activated human T lymphocytes and modulates immune cell interactions". Proc Natl Acad Sci U S A. 95 (19): 11336–41. doi:10.1073/pnas.95.19.11336. PMC 21643. PMID 9736737.

[pmid8596018-5] Duke-Cohan JS, Morimoto C, Rocker JA, Schlossman SF (Apr 1996). "Serum high molecular weight dipeptidyl peptidase IV (CD26) is similar to a novel antigen DPPT-L released from activated T cells". J Immunol. 156 (5): 1714–21. PMID 8596018.

[entrez-6] "Entrez Gene: ATRN attractin".

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