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Gene ENSMUSG00000033898 (BC026782)
Chromosomal location
Chr 1: 141701945 - 141915487 (-)
Description
complement factor H-related protein B  [Source:RefSeq peptide;Acc:NP_001020746]
RefSeq_dna
NM_001025575 
RefSeq_peptide
NP_001020746.1 
UniGene
Mm.400770 
MGI
MGI:3611575 
Uniprot/SPTREMBL
Q4LDF6 Q61407 Q8R0I8 Q61405 
Human Ortholog
ENSG00000116785 (CFHR3)
Omim 126700 - BASAL LAMINAR DRUSEN  235400 - HEMOLYTIC UREMIC SYNDROME, ATYPICAL  609814 - COMPLEMENT FACTOR H DEFICIENCY  610698 - MACULAR DEGENERATION, AGE-RELATED, 4  
UniTrap UNI31983
Vector Insertion
Chr 1: 141820584 - 141827475
Public Clones IST11400D2 (tigm)
Private Clones not available
Severity of mutation (?) Insertion after 0% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

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