The protein encoded by this gene belongs to the KHDC1 family, members of which contain an atypical KH domain that may not bind RNA like canonical KH domains. This gene is specifically expressed in the oocytes, and recent studies suggest that it may function as a regulator of genomic imprinting in the oocyte. Mutations in this gene are associated with recurrent biparental complete hydatidiform mole. [provided by RefSeq, Dec 2011]
人 KHDC3L (NM_001017361) cDNA克隆
| Accession: | NM_001017361 |
|---|---|
| 基因名称: | KHDC3L |
| 基因别名: | ECAT1; HYDM2; C6orf221 |
| 基因描述: | Homo sapiens KH domain containing 3-like, subcortical maternal complex member (KHDC3L), mRNA. |
| 种属: | Human |
| CDS区长度: | 654 (查看编码区序列) |
| 翻译后氨基酸长度: | 217 (查看氨基酸序列) |
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