Busch Lab

ZMP

foxo3a

Ensembl ID:
ENSDARG00000023058
ZFIN ID:
ZDB-GENE-050116-1
Description:
forkhead box O3A [Source:RefSeq peptide;Acc:NP_001009988]
Human Orthologue:
FOXO3
Human Description:
forkhead box O3 [Source:HGNC Symbol;Acc:3821]
Mouse Orthologue:
Foxo3
Mouse Description:
forkhead box O3 Gene [Source:MGI Symbol;Acc:MGI:1890081]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa15218 Essential Splice Site Available for shipment Available now
sa22992 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa15218
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000030773 Essential Splice Site 190 643 1 2
Genomic Location (Zv9):
Chromosome 17 (position 6557981)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 6636917
GRCz11 17 6794147
KASP Assay ID:
2261-0574.1 (used for ordering genotyping assays)
KASP Sequence:
GCCATACTTCAAGGACAAAGGTGACAGCAACAGCTCTGCAGGATGGAAGG[T/C]ACGTCAGGTCAAATRTTTTAACCTTGGCTTCCTTTTAACCCTTTATCAGA
Long Flanking Sequence:
GCCCAGGTCTTGCACATGGCCTCTGCCCAGACCCGAGTCCAATTCGGGCAAAGCAGAACCTTCAGATGTGGGGATCATTCCTGAAGAAGAGGTAGATGAAAATGGCACTGATGATGCTTGTGCATCTGGTGACATTACAGGCGCATCAAAGCCTGCCAGTGTCACAGAAGGAGACCCGAGTTCTGCTGCTGCTCTTCCTGCCATAGAAACGAACGCTTCTGCCAATGATAAAGACATCTATGGCTCTCCTGGATCTTCCCAACACGCTCTAGCAGCATGCAGCGACTCCAGCATCAATGGTCTGATTCCTCAGCAGCCCAGAAAATCCTCTGCCCGCAGGAACGCCTGGGGAAACTATTCCTACGCCGACCTCATCACCCAAGCCATCGAGAGCTCGCCAGAGAAGAGGCTGACACTGGCCCAGATTTATGATTGGATGGTCCGAAATGTGCCATACTTCAAGGACAAAGGTGACAGCAACAGCTCTGCAGGATGGAAGG[T/C]ACGTCAGGTCAAATGTTTTAACCTTGGCTTCCTTTTAACCCTTTATCAGACAGAAAACTCCTTTGATATCATATTGATTGCAAGTAACTGAAGTCCAAATTAATTTTTGAAATATTTAATTCCTTTAGAATTTCATGAGATGTATCTCCCCAGGATATCTTGACTGTTTAAGGCAGTGTTTCTCAACCATGTTCCTGGAGGACCACCAGCTCTGCCTATTTTCCCTGTCTCCTTAACCAAACACACCTGATTTAGATCATCAGTTTATTAGCAGAGACTGAAAGACCTGTAATGGGTGTGACAAGGGAGACCTCCAAAACATGCAGTGTTGGTGGTCCTCCAGGAACATGGTTGAGGGTGTTAAAAGAGGGACTAAGTCATTATTATTATTGCTTTTCTTTTCTTAAAAATGAGATTCTGACTTCCCAGCTTATTTTAAAAGCTGCCAAGCATATTTAATTAATAATTTTAAACAGATTTCCTTCAAAGTATTAATTATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22992
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000030773 Nonsense 245 643 2 2
Genomic Location (Zv9):
Chromosome 17 (position 6570278)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 6649214
GRCz11 17 6806444
KASP Assay ID:
2261-0575.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCTCCACGCAGGCGTGCAGTATCAATGGACAACAGTAATAAGCTCATC[A/T]AGAGCGCCCGTGGCCGTGCCGCAAAGAAGAAAGCCGCTCTGCAGGCATCC
Long Flanking Sequence:
TTTTTGGGTGAACTATCCATTTTAGGTAACCCCCTAATTCTAAGAAATGTTAAAATTCTAAACATGTATAAAAGGGAGACAGAAAGCATATTTTTTTAAGCTATACACATGAACTCTATTGGTCAAAGGGACCACATGACTCTTCAATCTCTGGATAAAGCAATCAAGTCATAGTGGCATTGTCCCTCACTGCACATTGTGCTTCACTGAGTCAGAGACTATTGAGGCTTGAACATTTGACCATTATTTTGCTCCTTAATGGTCAGATAGTTAATGTTAAGTGTTTCAGGCATGTCCAATGATGCATGGGCTAACCTTCTACTCCTCTCTTTTCACAGAACTCAATACGACATAACCTGTCGCTCCATAGTCGCTTTGTCAGAGTCCAAAATGAAGGAACAGGAAAGAGTTCATGGTGGATGGTCAACCCTGATGGTGGAAAAGGGGGCAAAGCTCCACGCAGGCGTGCAGTATCAATGGACAACAGTAATAAGCTCATC[A/T]AGAGCGCCCGTGGCCGTGCCGCAAAGAAGAAAGCCGCTCTGCAGGCATCCCAGGACGGAAGCTCTGAGAGTTCCTCCAGTCTGTCCAAATGGACCGGCAGCCCCACGTCCCGTAGTAGTGACGAGCTAGATGCTTGGACAGATTTTCGTTCTCGCACTAATTCTAATGCCAGCACCCTCAGTGGACGTCTTTCCCCAATTCTAGCCAACCTGGAGGTGGATGAAGTTCCCGATGATGACTCTCCCCTGTCACCCATGCTGTACTCCAGCCCCAGCAGTATGTCTCCGTCCACTGGGCTCACCGAACTGCCACGTCTAGCTGACCTTGCAGGAACTATGAACCTCAACGATGGCCTCTCTGACAACCTAATGGATGACCTTCTGGACAACATCAGCTTGACGGCTTCACAGTCTCCGGGCCATGATGAGAGTGGAGCCAACCTACAGGGAAGCCCTGTGTTTACCTTCAGCTGCTCTGGGAGCAGTCTGGCAATTCCCTCC
Associated Phenotype:
Not determined