HBS1L Gene - GeneCards | HBS1L Protein | HBS1L Antibody
2024年12月25日 · HBS1L (HBS1 Like Translational GTPase) is a Protein Coding gene. Diseases associated with HBS1L include Bladder Diverticulum and Beta-Thalassemia. Among its related …
HBS1L HBS1 like translational GTPase [ (human)] - National Center …
2025年2月8日 · HBS1L-related genetic variants play a key role in control of fetal hemoglobin levels. This gene encodes a member of the GTP-binding elongation factor family. It is …
HBS1 样翻译 GTPase（HBS1L）基因 | MCE - MCE-生物活性分子大师
该基因与 MYB 基因的基因间区域已被鉴定为控制胎儿血红蛋白水平的数量性状位点 (QTL) ，该区域影响红细胞、血小板和单核细胞计数以及红细胞体积和血红蛋白含量。 该区域的 DNA 多态 …
Mammalian Hbs1L deficiency causes congenital anomalies and ...
We recently reported a novel human phenotype resulting from a mutation in the critical coding region of the HBS1L gene characterized by facial dysmorphism, severe growth restriction, …
hbs1l 又名erfs、ef-1a，是酿酒酵母和原核 细胞hbs1 基因的人类同源物，进化上与真核细胞 终止因子erf3 相近，但是未发现erf3 活性[4]。酵 母hbs1 参与了mrna 上停滞的核糖体的识别和释 …
HBS1L protein expression summary - The Human Protein Atlas
HBS1L is a prognostic marker in Breast invasive carcinoma, Kidney renal clear cell carcinoma
HBS1L HBS1 like translational GTPase [ Homo sapiens (human) ]
2025年2月8日 · Title: A short splicing isoform of HBS1L links the cytoplasmic exosome and SKI complexes in humans. genome-wide association analyses identified a new genome-wide …
HBS1L人源基因|HBS1L基因突变_致病性_靶点-RDDC官网
这个基因和MYB基因的基因间区已经被鉴定为控制胎儿血红蛋白水平的数量性状位点（QTL），这个区域影响红细胞、血小板和单核细胞计数以及红细胞体积和血红蛋白含量。 这个区域 …
HBS1L-MYB intergenic variants modulate fetal hemoglobin via
Genetic studies have identified common variants within the intergenic region (HBS1L-MYB) between GTP-binding elongation factor HBS1L and myeloblastosis oncogene MYB on …
Human Gene HBS1L (ENST00000367837.10) from GENCODE V44
Description: Homo sapiens HBS1 like translational GTPase (HBS1L), transcript variant 1, mRNA. (from RefSeq NM_006620) RefSeq Summary (NM_006620): This gene encodes a member of …
- 某些结果已被删除