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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
小鼠
Mcph1 - microcephaly, primary autosomal recessive 1
Alias:
MCT
BRIT1
5430437K10Rik
D030046N04Rik
Tg(HLA-A2.1)1Enge
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Basic Information
Sequence Homology
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
References Literature
预测能够实现相同的蛋白质结合活性。在几个过程的上游或内部发挥作用,包括有丝分裂纺锤体定位的建立;神经元干细胞群体的维持;以及蛋白质定位到中心体。预测位于细胞质和细胞骨架中。在大脑中表达。用于研究小头畸形。这个基因的人类同源物与乳腺癌;子宫内膜癌;小头畸形;原发性常染色体隐性小头畸形;以及原发性常染色体隐性小头畸形1有关。与人类MCPH1(小头蛋白1)正交。[由基因组资源联盟,2022年4月提供]
Related ID:
NCBI:244329
ENSEMBL:ENSMUSG00000039842
UNIPROT:Q7TT79
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
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Reference
244329
22
14
212974 bp
90.37
9
4
Mcph1 Genetics information (+)
GRCm39
Sequence Homology
Transcripts & Proteins
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* This data comes from NCBI.
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