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Allele : Zbtb7b<hd> zinc finger and BTB domain containing 7B; helper deficient

Primary Identifier  MGI:3530739 Allele Type  Spontaneous
Gene  Zbtb7b Inheritance Mode  Recessive
Strain of Origin  mixed Is Recombinase  false
Is Wild Type  false
description  Mutation arose from mixed C57BL/6, BALB/c, C3H, and 129/Sv parentage.
molecularNote  An A-to-G mutation at coding nucleotide 1165 resulted in an arginine to glycine substitution at amino acid position 389 (p.R389G). This mutation is within the second of four zinc finger domains and affects a residue predicted to interact directly with DNA.
  • mutations:
  • Single point mutation
  • synonyms:
  • HD<->,
  • Th-POK<->,
  • Zbtb7b<->,
  • ThPOK<hd>,
  • HD<->,
  • ThPOK<hd>,
  • Zbtb7b<->,
  • Th-POK<->
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

15 Publication categories

Trail: Allele