Homo Sapiens
FANCB - FA Complementation Group B
Alias:
FA2
FAB
FACB
FAAP90
FAAP95
This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Models
Reference
FANCB Genetics information (-)
GRCh38
Chr : -
Sequence Homology
Selected Gene:
Human：FANCB
Disease & Mutation
#
Disease
Anatomical category
Score
Count
Transcripts & Proteins
Table View
Tile View
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Transcript
Length(nt)
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CDS(bp)
Protein
Length(aa)
* This data comes from NCBI.
Gene Expression
Tissue-specific RNA expression
Organ
Expression
Alphabetical
Cell-specific RNA expression
Organ
Expression
Alphabetical
Protein Interaction
Acting
Regulation
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Mechanism
Target
Residues
Reference
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Related Models
Type
Name
MGI
Strain of Origin
Publications
Drugs
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Phase
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References
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PMID
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Year
IF
