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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
人类
SHH - Sonic Hedgehog Signaling Molecule
Alias:
TPT
HHG1
HLP3
HPE3
SMMCI
ShhNC
TPTPS
MCOPCB5
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码的蛋白质在胚胎早期模式形成中起着关键作用。它被认为是腹侧神经管模式形成、前后肢轴和腹侧体节模式形成的关键诱导信号。在显示与果蝇sonic hedgehog蛋白序列和功能相似性的三种人类蛋白质中,这种蛋白质最相似。该蛋白质作为前体产生,通过自催化切割;N端部分可溶并含有信号活性,而C端部分参与前体加工。更重要的是,C端产物将胆固醇部分共价连接到N端产物上,限制N端产物位于细胞表面,防止其在发育中的胚胎中自由扩散。该蛋白质或其信号通路中的缺陷是导致全前脑畸形(HPE)的原因,这是一种发育中的前脑不能正确分离成左右半球的病症。HPE表现为面部畸形。还认为,该基因或其信号通路中的突变可能是VACTERL综合征的原因,其特征是椎骨缺陷、肛门闭锁、气管食管瘘合并食管闭锁、桡骨和肾发育异常、心脏异常和四肢畸形。此外,位于该基因上游约1兆碱基处的远距离增强子的突变会破坏四肢模式,并可能导致前轴多指症。[由RefSeq,2008年7月提供]
Related ID:
NCBI:6469
ENSEMBL:ENSG00000164690
HGNC:10848
UNIPROT:Q15465
OMIM:600725
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
6469
5
3
12484 bp
49.61
336
18
27
39
SHH Genetics information (-)
GRCh38
Sequence Homology
Related Diseases and Mutations
#
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No data available
Transcripts & Proteins
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Transcript
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* This data comes from NCBI.
Gene Expression
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Status
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Link
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