This mutant was identified in an ENU screen based on its smaller size and ataxic gait. This mutation introduces a T to A substitution at nucleotide 2601 of the cDNA sequence that changes the tyrosine into a premature stop codon at position 867 of the protein sequence (Y867X) within an evolutionarily conserved spacer region 40 residues upstream of the cleavage signal between the alpha- and beta-subunits. The mutation corresponds to one identified in Mucolipidosis type II patients and leads to the production of a slightly truncated alpha-subunit retaining 95% of the wild-type equivalent and a complete lack of the beta-subunit. (J:218156)
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基础信息

模型ID
品系来源
等位基因类型
突变
遗传方式
相关基因
相关疾病
参考文献
BALB/cAnNHsd
Chemically induced
Single point
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1
4
1

表型特征

标签摘要:
hm: 纯合子
ht: 杂合子
cn: 条件基因型
cx: 复合型:涉及多基因组
tg: 转基因
ot: 其他:半合子、不确定...
(F): 雌性
(M): 雄性
观察到的表型
N: 正常表型
(#): 上标括号内为相关疾病数量
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