【佳學(xué)基因檢測(cè)】微陣列疾病篩查FLII突變的結(jié)果高效嗎?
基因檢測(cè)的序列名稱:
FLII
人體基因序列變化與疾病表征數(shù)據(jù)庫(kù)中的基因代碼:
2314
人體基因序列數(shù)據(jù)庫(kù)中國(guó)際交流名稱全稱
FLII actin remodeling protein
中國(guó)數(shù)據(jù)庫(kù)中基因全稱:
FLII肌動(dòng)蛋白重塑蛋白
基因檢測(cè)報(bào)告英文版基因簡(jiǎn)介
This gene encodes a protein with a gelsolin-like actin binding domain and an N-terminal leucine-rich repeat-protein protein interaction domain. The protein is similar to a Drosophila protein involved in early embryogenesis and the structural organization of indirect flight muscle. The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]
基因突變所影響的基因信息
該基因編碼具有凝溶膠蛋白樣肌動(dòng)蛋白結(jié)合結(jié)構(gòu)域和N末端富含亮氨酸的重復(fù)蛋白蛋白質(zhì)相互作用域的蛋白質(zhì)。該蛋白類似于果蠅蛋白,它參與早期胚胎發(fā)生和間接飛行肌肉的結(jié)構(gòu)組織。該基因位于第17號(hào)染色??體的Smith-Magenis綜合征區(qū)域內(nèi)。[由RefSeq提供,2008年7月]
國(guó)際國(guó)內(nèi)該堿基基因序列的其他英語(yǔ)文字母簡(jiǎn)稱:
FLI, FLIL, Fli1
基因解碼對(duì)該基因序列在細(xì)胞核中的染色體所給予的編號(hào):
該基因序列位于人類第17號(hào)染色體上。
基因解碼對(duì)基因序列的正確定位
該基因序列在GRCh37版本中的起始位置坐標(biāo)為:18148129;結(jié)束位置坐標(biāo)為:18162230。該基因序列在GRCh38版本中的起始位置坐標(biāo)為:18244815;結(jié)束位置坐標(biāo)為:18258916。正確的基因信息定位是基因檢測(cè)和對(duì)檢測(cè)結(jié)果進(jìn)行正確解讀的關(guān)鍵。
佳學(xué)基因解碼對(duì)該基因的功能分類:國(guó)際版
正在通過(guò)基因解碼技術(shù)進(jìn)行收集、查證并編輯,請(qǐng)關(guān)注佳學(xué)基因,獲得及時(shí)更新的人類基因序列變化與疾病表征數(shù)據(jù)庫(kù)的更新內(nèi)容
基因解碼對(duì)該基因的功能分類:中文版
正在通過(guò)基因解碼技術(shù)進(jìn)行收集、查證并編輯,請(qǐng)關(guān)注佳學(xué)基因,獲得及時(shí)更新的人類基因序列變化與疾病表征數(shù)據(jù)庫(kù)的更新內(nèi)容
結(jié)構(gòu)與功能基因解碼所揭示的該基因在細(xì)胞內(nèi)發(fā)揮作用的場(chǎng)所(國(guó)際版):
Cytosol;Microtubule organizing center;Nucleoplasm
結(jié)構(gòu)與功能基因解碼所揭示的該基因發(fā)揮作用的細(xì)胞內(nèi)位置(中文版):
胞質(zhì)溶膠;微管組織中心;核質(zhì)
該基因序列變化后增加的疾病風(fēng)險(xiǎn)(國(guó)際版):
Abnormality of the tracheobronchial system; Smith-Magenis syndrome; Corticospinal tract hypoplasia; Large face; Delayed eruption of primary teeth; Hyperacusis; Self-Injurious Behavior; Large elongated pulp chamber; Taurodontism; Inverted V-shaped upper lip; Tented mouth; Tented upper lip; Decreased pain sensation; Serum cholesterol raised; Hypoplasia or absence of the corpus callosum; Abnormality of cardiovascular system morphology; Abnormally-shaped vertebrae; Hoarseness; Failure to thrive in infancy; Hypertriglyceridemia result; Sleep disturbances; Stereotyped Behavior; Hypercholesterolemia; Stereotypic Movement Disorder; Synophrys; Open mouth; Syndactyly of the toes; Corneal diameter decreased; Microcornea; Chronic otitis media; ear infection chronic; Short philtrum; Reduced fetal movement; Speech Disorders; Broad forehead; Enophthalmos; Sunken eyes; Acquired flat foot; Flatfoot; Upward slant of palpebral fissure; Heartburn; Class III malocclusion; Hypertrophy of lower jaw; Increased size of mandible; Mandibular hyperplasia; mandibular excess (physical finding); Gastroesophageal reflux disease; Brachycephaly; Broad cranium shape; Wide skull shape; Electroencephalogram abnormal; Decreased projection of midface; Hypotrophic midface; Midface retrusion; Small midface; Bilateral fifth finger clinodactyly; Curvature of little finger; Attention deficit hyperactivity disorder; Delayed speech and language development; Language Delay; Speech Delay; Speech impairment; Myopia; Anxiety; Anxiety disease; Conductive hearing loss; Decreased tendon reflex; Dilated ventricles (finding); Brachydactyly; Short nose; Small nose; Gait abnormality; Dyschezia; Constipation; Frontal bossing; Feeding difficulties in infancy; Anteverted nostril; Concave bridge of nose; Depressed nasal bridge; Depressed nasal root/bridge; Broad flat nasal bridge; Nasal bridge wide; Orbital separation excessive; Strabismus; Obesity; Hypoplastic mandible condyle; Mandibular hypoplasia; Micrognathism; Acquired scoliosis; Curvature of spine; Short stature; Muscle hypotonia; Cognitive delay; Global developmental delay; Mental and motor retardation; Dull intelligence; Low intelligence; Mental Retardation; Mental deficiency; Poor school performance; Intellectual Disability
如果該基因突變后,風(fēng)險(xiǎn)可能增加的疾病類型(中文版):
氣管支氣管系統(tǒng)異常; Smith-Magenis 綜合征;皮質(zhì)脊髓束發(fā)育不全;大臉;乳牙延遲萌出;聽覺過(guò)敏;自殘行為;大而細(xì)長(zhǎng)的牙髓室;牛牙癥;倒V型上唇;帳篷的嘴巴;帳篷狀的上唇;痛覺減弱;血清膽固醇升高;胼胝體發(fā)育不全或缺失;心血管系統(tǒng)形態(tài)異常;異常形狀的椎骨;嘶啞;未能在嬰兒期茁壯成長(zhǎng);高甘油三酯血癥結(jié)果;睡眠障礙;刻板行為;高膽固醇血癥;刻板運(yùn)動(dòng)障礙;同義詞;張開嘴;腳趾并趾;角膜直徑減?。恍〗悄?;慢性中耳炎;耳部感染慢性;短人中;胎動(dòng)減少;言語(yǔ)障礙;額頭寬闊;眼球內(nèi)陷;凹陷的眼睛;后天性扁平足;扁平足;瞼裂向上傾斜;胃灼熱; III 類咬合不正;下頜肥大;下頜骨增大;下頜骨增生;下頜過(guò)長(zhǎng)(物理發(fā)現(xiàn));胃食管反流病;短頭畸形;寬顱骨形狀;寬顱骨形狀;腦電圖異常;面部中部突出減少;中面部營(yíng)養(yǎng)不良;面中部后縮;中臉?。浑p側(cè)小指彎曲;小指彎曲;注意力缺陷多動(dòng)障礙;言語(yǔ)和語(yǔ)言發(fā)育遲緩;語(yǔ)言延遲;語(yǔ)音延遲;言語(yǔ)障礙;近視;焦慮;焦慮癥;傳導(dǎo)性聽力損失;肌腱反射減弱;擴(kuò)張的心室(發(fā)現(xiàn));短指;鼻子短;小鼻子;步態(tài)異常;排便困難;便秘;正面凸起;嬰兒喂養(yǎng)困難;鼻孔前傾;鼻梁凹陷;鼻梁凹陷;鼻根/鼻梁凹陷;寬扁的鼻梁;鼻梁寬;軌道分離過(guò)度;斜視;肥胖;發(fā)育不全的下頜骨髁;下頜發(fā)育不全;小頜畸形;后天性脊柱側(cè)凸;脊柱彎曲;身材矮??;肌肉張力減退;認(rèn)知延遲;整體發(fā)育遲緩;智力和運(yùn)動(dòng)遲緩;智力遲鈍;智力低下;智力低下;精神缺陷;學(xué)習(xí)成績(jī)差;智力殘疾
GWAS基因檢測(cè)所建立的與該基因的疾病關(guān)聯(lián)(國(guó)際版):
正在通過(guò)基因解碼技術(shù)進(jìn)行收集、查證并編輯,請(qǐng)關(guān)注佳學(xué)基因,獲得及時(shí)更新的人類基因序列變化與疾病表征數(shù)據(jù)庫(kù)的更新內(nèi)容
GWAS基因檢測(cè)所解碼的該基因突變會(huì)增加風(fēng)險(xiǎn)的疾病種類(中文版):
正在通過(guò)基因解碼技術(shù)進(jìn)行收集、查證并編輯,請(qǐng)關(guān)注佳學(xué)基因,獲得及時(shí)更新的人類基因序列變化與疾病表征數(shù)據(jù)庫(kù)的更新內(nèi)容
以該基因做靶點(diǎn)的藥物(國(guó)際版):
正在通過(guò)基因解碼技術(shù)進(jìn)行收集、查證并編輯,請(qǐng)關(guān)注佳學(xué)基因,獲得及時(shí)更新的人類基因序列變化與疾病表征數(shù)據(jù)庫(kù)的更新內(nèi)容
針對(duì)該基因所產(chǎn)生的突變,可能有正確效果的藥物(中文版):
正在通過(guò)基因解碼技術(shù)進(jìn)行收集、查證并編輯,請(qǐng)關(guān)注佳學(xué)基因,獲得及時(shí)更新的人類基因序列變化與疾病表征數(shù)據(jù)庫(kù)的更新內(nèi)容
(責(zé)任編輯:佳學(xué)基因)