文章詳情
Coriell Institute|NA12878 人類(lèi)基因組DNA標(biāo)準(zhǔn)品
日期:2025-07-09 17:05
瀏覽次數(shù):2599
摘要:Coriell Institute|NA12878 人類(lèi)基因組DNA標(biāo)準(zhǔn)品
Coriell Institute|NA12878 人類(lèi)基因組DNA標(biāo)準(zhǔn)品
DNA描述:
CEPH / UTAH PEDIGREE 1463
國(guó)際HAPMAP項(xiàng)目 - CEPH(第|一欄)[來(lái)自北歐和西歐的UTAH居民]
CYTOCHROME P450,亞家族IIC,多肽19; CYP2C19
國(guó)際機(jī)會(huì)項(xiàng)目 - CEPH [來(lái)自北歐和西歐的UTAH居民]
NA CUSTOM SERVICE PLATE 01
受影響:
沒(méi)有數(shù)據(jù)
性別:
女
年齡:
沒(méi)有數(shù)據(jù)
知識(shí)庫(kù) | NIGMS人類(lèi)遺傳細(xì)胞庫(kù) |
子集合 |
CEPH Repository Linkage Families Pharmacogenetics PIGI同意樣本 |
數(shù)量 | 50微克 |
定量方法 | 請(qǐng)參閱我們的常見(jiàn)問(wèn)題 |
活檢來(lái)源 | 外周靜脈 |
細(xì)胞類(lèi)型 | B淋|巴細(xì)胞 |
組織類(lèi)型 | 血液 |
轉(zhuǎn)化 | 愛(ài)潑斯坦 - 巴爾病毒 |
種族 | 高加索 |
種族 | 猶他州/ MORMON |
出生國(guó)家 | 美國(guó) |
家庭成員 | 2 |
與Proband的關(guān)系 | 母親 |
確認(rèn) | 臨床總結(jié)/病史 |
ISCN | 46,XX [23] .arr [hg19] 9p13.1(38,787,480-40,911,212)x3 |
種類(lèi) | Homo sapiens |
通用名稱 | 人的 |
備注 | 母親; 供體受試者在CYP2C19基因(CYP2C19 * 2)的外顯子5中的核苷酸681處具有單個(gè)bp(G至A)轉(zhuǎn)變,其產(chǎn)生異常剪接位點(diǎn)。該變化改變了mRNA的閱讀框架,從氨基酸215開(kāi)始,并在下游產(chǎn)生20個(gè)氨基酸的過(guò)早終止密碼子,產(chǎn)生截短的無(wú)功能蛋白質(zhì)。由于異常剪接位點(diǎn),在外顯子5開(kāi)始時(shí)(從bp 643到bp 682)發(fā)生40bp的缺失,導(dǎo)致氨基酸215到227的缺失。截短的蛋白質(zhì)具有234個(gè)氨基酸并且將是催化失活的因?yàn)樗狈ρt素結(jié)合區(qū)域。 |
原產(chǎn)地物種的鑒定 | 核苷磷酸化酶,葡萄糖-6-磷酸脫氫酶和乳酸脫氫酶同工酶電泳確認(rèn)的原產(chǎn)地種類(lèi) |
備注 | 母親; 供體受試者在CYP2C19基因(CYP2C19 * 2)的外顯子5中的核苷酸681處具有單個(gè)bp(G至A)轉(zhuǎn)變,其產(chǎn)生異常剪接位點(diǎn)。該變化改變了mRNA的閱讀框架,從氨基酸215開(kāi)始,并在下游產(chǎn)生20個(gè)氨基酸的過(guò)早終止密碼子,產(chǎn)生截短的無(wú)功能蛋白質(zhì)。由于異常剪接位點(diǎn),在外顯子5開(kāi)始時(shí)(從bp 643到bp 682)發(fā)生40bp的缺失,導(dǎo)致氨基酸215到227的缺失。截短的蛋白質(zhì)具有234個(gè)氨基酸并且將是催化失活的因?yàn)樗狈ρt素結(jié)合區(qū)域。 |
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