🧬 基因注释：ZMYM3
📝 官方信息
官方名称：zinc finger MYM-type containing 3
功能摘要：This gene is located on the X chromosome and is subject to X inactivation. It is highly conserved in vertebrates and most abundantly expressed in the brain. The encoded protein is a component of histone deacetylase-containing multiprotein complexes that function through modifying chromatin structure to keep genes silent. A chromosomal translocation (X;13) involving this gene is associated with X-linked cognitive disability. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2010].
🎯 作为靶基因的剪接因子
- CELF2 置信度: 2.0
- CPSF6 置信度: 2.0
- CPSF7 置信度: 2.0
- CSTF2T 置信度: 2.0
- EIF4A3 置信度: 2.0
- EWSR1 置信度: 2.0
- GRSF1 置信度: 2.0
- HNRNPA2B1 置信度: 2.0
- HNRNPH1 置信度: 2.0
- HNRNPK 置信度: 2.0
- KHSRP 置信度: 2.0
- MBNL1 置信度: 2.0
- NOVA1 置信度: 2.0
- PTBP1 置信度: 2.0
- RBFOX2 置信度: 2.0
- RBM15 置信度: 2.0
- AQR 置信度: 1.0
- CPSF1 置信度: 1.0
- CPSF2 置信度: 1.0
- ELAVL3 置信度: 1.0
🏥 关联疾病
intellectual developmental disorder, X-linked 112
(0.630)
prostate adenocarcinoma
(0.562)
neurodegenerative disease
(0.336)
medulloblastoma
(0.275)
chronic lymphocytic leukemia
(0.245)