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Gene ENSMUSG00000020679 (Hnf1b)
Chromosomal location
Chr 11: 83664371 - 83719419 (+)
Description
HNF1 homeobox B Gene [Source:MGI (curated);Acc:Hnf1b-001]
RefSeq_dna
NM_009330 
RefSeq_peptide
NP_033356.2 
UniGene
Mm.7226 
MGI
MGI:98505 
Uniprot/SWISSPROT
P27889 
Uniprot/SPTREMBL
B0QZT3 Q2M4H2 Q5NC37 Q5SS49 Q5NC38 Q5SS48 
Human Ortholog
ENSG00000108753 (HNF1B)
Omim 125853 - DIABETES MELLITUS, NONINSULIN-DEPENDENT  137920 - RENAL CYSTS AND DIABETES SYNDROME  158330 - MULLERIAN APLASIA AND HYPERANDROGENISM  604284 -  606391 - MATURITY-ONSET DIABETES OF THE YOUNG  611955 - PROSTATE CANCER, HEREDITARY, 11  
UniTrap UNI27119
Vector Insertion
Chr 11: 83677681 - 83696154
Public Clones not available
Private Clones OST69675 (lexicon)
Severity of mutation (?) Insertion after 62% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

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