SNTB2

SNTB2
التراكيب المتوفرة
بنك بيانات البروتين	Ortholog search: PDBe RCSB
قائمة رموز معهدات بنك بيانات البروتين
	2VRF
المعهدات
الأسماء المستعارة	SNTB2, D16S2531E, EST25263, SNT2B2, SNT3, SNTL, syntrophin beta 2
معهدات خارجية	الوراثة المندلية البشرية عبر الإنترنت 600027 MGI: MGI:101771 HomoloGene: 4911 GeneCards: 6645
أورثولوج
	Q13425; A0A0G2JM75; A0A024R732
	Q61235
	‏NM_006750 NM_130845، ‏NM_006750
	‏NM_001368316 NM_009229، ‏NM_001368316
	NP_006741; NP_006741.1
	‏NP_001355245 NP_033255، ‏NP_001355245
	ويكي بيانات
اعرض/عدّل إنسان	اعرض/عدّل فأر

SNTB2‏ (Syntrophin beta 2) هوَ بروتين يُشَفر بواسطة جين SNTB2 في الإنسان.

الوظيفة

هذا القسم فارغ أوغير مكتمل، ساهم بتحريره.

الأهمية السريرية

هذا القسم فارغ أوغير مكتمل، ساهم بتحريره.

المراجع

^ Ahn AH, Yoshida M, Anderson MS, Feener CA, Selig S, Hagiwara Y, Ozawa E, Kunkel LM (June 1994). "Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24". Proc Natl Acad Sci U S A. 91 (10): 4446–50. doi:10.1073/pnas.91.10.4446. PMC 43802. PMID 8183929.
^ "Entrez Gene: SNTB2 syntrophin, beta 2 (dystrophin-associated protein A1, 59kDa, basic component 2)". مؤرشف من الأصل في 05 ديسمبر 2010.
^ Ahn AH, Freener CA, Gussoni E, Yoshida M, Ozawa E, Kunkel LM (March 1996). "The three human syntrophin genes are expressed in diverse tissues, have distinct chromosomal locations, and each bind to dystrophin and its relatives". J Biol Chem. 271 (5): 2724–30. doi:10.1074/jbc.271.5.2724. PMID 8576247.

قراءة متعمقة

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Jones KJ, Compton AG, Yang N, Mills MA, Peters MF, Mowat D, Kunkel LM, Froehner SC, North KN (2003). "Deficiency of the syntrophins and alpha-dystrobrevin in patients with inherited myopathy". Neuromuscul. Disord. 13 (6): 456–67. doi:10.1016/S0960-8966(03)00066-X. PMID 12899872.
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