ZFIN ID: ZDB-ALT-150218-7
Genomic Feature: st89
Synonyms:
Affected Genomic Regions: xpr1b (1)
Type: Small Deletion (1)
Protocol: embryos treated with TALEN1-xpr1b
Lab Of Origin: Talbot Lab
Location: Chr 2: 6999690 - 6999699 (GRCz11) (1) Details
Sequence:
Current Sources:
MUTATION DETAILS
DNA/cDNA Change: 10 bp deleted (1)
Transcript Consequence: Frameshift, Premature Stop (1)
Protein Consequence: at position 146 (1)
FLANKING SEQUENCENo data available
NOTES
Comment Citation
mutation in XPR1B is a 10 bp deletion causing a frameshift resulting in a stop  ... ZFIN Staff
OTHER st89 PAGESNo links to external sites
GENOTYPES
Zygosity Genotype (Background) Affected Genomic Regions Parental Zygosity
Homozygous xpr1bst89/st89 xpr1b ♀+/- ♂+/-
Heterozygous xpr1bst89/+ xpr1b Unknown
Complex xpr1bst87/+; xpr1bst89/+ xpr1b

CITATIONS  (3)