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中文人类
FANCG - FA Complementation Group G
Alias:
FAG
XRCC9
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范科尼贫血补充分组（FANC）目前包括FANCA、FANCB、FANCC、FANCD1（也称为BRCA2）、FANCD2、FANCE、FANCF、FANCG、FANCI、FANCJ（也称为BRIP1）、FANCL、FANCM和FANCN（也称为PALB2）。之前定义的FANCH组与FANCA相同。范科尼贫血是一种遗传异质性隐性障碍，特点是细胞遗传不稳定、对DNA交叉链接剂的超敏感性、染色体破裂增加和DNA修复缺陷。范科尼贫血补充分组的成员之间没有共享的序列相似性；它们通过组装成共同的核蛋白复合物而相关。此基因编码补充分组G的蛋白质。[由RefSeq，2008年7月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
FANCG Genetics information (-)
GRCh38
Sequence Homology
Related Diseases and Mutations
#
Disease
Anatomical Category
Score
Mutations
Transcripts & Proteins
Table View
Tile View
#
Transcript
Length(nt)
Exon Count
CDS(bp)
Protein
Length(aa)
* This data comes from NCBI.
Gene Expression
Tissue-specific RNA expression
Organ
Abundance
Alphabetical
Cell-specific RNA expression
Organ
Abundance
Alphabetical
Interactions
Acting
Regulation
Detail
Mechanism
Target
Residues
Reference
Score
Related Mouse Models
Type
Name
MGI
Strain of Origin
Publications
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Link
References Literature
Title
PMID
Journal
Year
IF
