mutations in the human homolog are associated with Joubert syndrome, an autosomal recessive disorder resulting in severe mental retardation [RGD, Feb 2006]
Accession: | NM_001002277 |
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基因名称: | Ahi1 |
基因别名: | Ahi-1 |
基因描述: | Rattus norvegicus Abelson helper integration site 1 (Ahi1), mRNA. |
种属: | Rat |
CDS区长度: | 3144 (查看编码区序列) |
翻译后氨基酸长度: | 1047 (查看氨基酸序列) |
mutations in the human homolog are associated with Joubert syndrome, an autosomal recessive disorder resulting in severe mental retardation [RGD, Feb 2006]