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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
罕见病
Immunodeficiency 55 (IMD55)
Alias:
Combined Immunodeficiency Due to Gins1 Deficiency
Imd55
Combined Immunodeficiency with Intrauterine Growth Retardation-Natural Killer Cell Deficiency-Neutropenia
Combined Immunodeficiency with Intrauterine Growth Retardation-Nk Cell Deficiency-Neutropenia
Cid Due to Gins1 Deficiency
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基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
免疫缺陷55,又称由于GINS1缺乏导致的联合免疫缺陷,与免疫缺陷54和家族性噬血性淋巴细胞增生症2有关。与免疫缺陷55有关的重要基因是GINS1(GINS复合物亚基1),其相关通路/超级通路包括II型干扰素信号通路和胰腺癌中自然杀伤细胞的相互作用。附属组织包括骨髓和自然杀伤细胞,相关表型为异常面部形状和矮小。
Related ID:
MALACARDS:IMM190
OMIM:617827
MESH:D007153
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
胎儿期
<1/1000000
17
119
3
IMM190
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
#
Gene
Function
Score
Mutations
No data available
Related Drugs
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available
References Literature
Title
PMID
Journal
Year
IF
No Data Found!
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