B9d
收藏DataCite Commons2021-09-23 更新2025-04-15 收录
下载链接：
https://www.facebase.org/chaise/record/#1/isa:dataset/RID=3-JQMM
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资源简介：
This dataset is currently unpublished but is in review. **Gene(s):** [B9d1](https://www.alliancegenome.org/gene/MGI:1351471): Enables hedgehog receptor activity. Acts upstream of or within several processes, including embryonic digit morphogenesis; neuroepithelial cell differentiation; and smoothened signaling pathway. Located in ciliary transition zone and membrane. Part of MKS complex. Is expressed in embryo. Used to study Meckel syndrome. Human ortholog(s) of this gene implicated in Joubert syndrome 27 and Meckel syndrome. Orthologous to human B9D1 (B9 domain containing 1).
提供机构：
FaceBase (www.facebase.org)
创建时间：
2021-09-23
