- accession:NM_172058
- 基因别名:EYA1
- 基因描述:Homo sapiens eyes absent homolog 1 (Drosophila) (EYA1), transcript variant 2, mRNA.
- 载体: 现货载体
- CDS区长度:1779
- 翻译后氨基酸长度:592
- TranscriptVariant:This variant (2), also known as EYA1B, encodes the longest isoform b.
- 基因简介:This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may play a role in the developing kidney, branchial arches, eye, and ear. Mutations of this gene have been associated with branchiootorenal dysplasia syndrome, branchiootic syndrome, and sporadic cases of congenital cataracts and ocular anterior segment anomalies. A similar protein in mice can act as a transcriptional activator. Four transcript variants encoding three distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
- 载体信息:自有图片地址
- 规格:10ul 质粒
CDS区参考序列: 点击查看序列翻译后氨基酸参数序列: 点击查看序列