ZMP
ENSDARG00000088879
Ensembl ID:
Human Orthologues:
FOXO1, FOXO3, FOXO4, FOXO6
Human Descriptions:
forkhead box O1 [Source:HGNC Symbol;Acc:3819]
forkhead box O3 [Source:HGNC Symbol;Acc:3821]
forkhead box O4 [Source:HGNC Symbol;Acc:7139]
forkhead box O6 [Source:HGNC Symbol;Acc:24814]
forkhead box O3 [Source:HGNC Symbol;Acc:3821]
forkhead box O4 [Source:HGNC Symbol;Acc:7139]
forkhead box O6 [Source:HGNC Symbol;Acc:24814]
Mouse Orthologues:
Foxo1, Foxo3, Foxo4, Foxo6
Mouse Descriptions:
forkhead box O1 Gene [Source:MGI Symbol;Acc:MGI:1890077]
forkhead box O3 Gene [Source:MGI Symbol;Acc:MGI:1890081]
forkhead box O4 Gene [Source:MGI Symbol;Acc:MGI:1891915]
forkhead box O6 Gene [Source:MGI Symbol;Acc:MGI:2676586]
forkhead box O3 Gene [Source:MGI Symbol;Acc:MGI:1890081]
forkhead box O4 Gene [Source:MGI Symbol;Acc:MGI:1891915]
forkhead box O6 Gene [Source:MGI Symbol;Acc:MGI:2676586]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42473 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14769 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42473
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124932 | Nonsense | 111 | 139 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 3394401)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 3297660 |
GRCz11 | 15 | 3285166 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGCCATCGAGAGCTCCCCAGAAAAGCGGCTCACCTTGTCTCAGATATA[C/A]GACTGGATGGTGAAAAGCGTCCCGTATTTTAAAGACAAGGGGGATAGTAA
Long Flanking Sequence:
GACAGTATTGCTGGTACCATGGCTGACGCAGCCCAAAACCAGATGGTGGAGATCGACCCGGACTTCGAGCCGCTGTCCCGGCCCCGCTCCTGCACTTGGCCGCTGCCGCGACCCGAGTTCCCAAACCCCGCCGCCGCGGACTCCAACACTTCATCCCCGGCTCCGTCCGTCAAACAGGAGCCTTCCAGCACCGCGGACTTCATCAACAACCTCAGTCTGCTAGAGGAGAATGAGGACTACCCGGACCAGAAGCCTCTCATGCTCTGCAGCGAGTTCCAGTGCCAGGAGAACTGCATCCACCAGCAGCAGATCCCGAGTCAGCAGCAACAGGTGCCCGTGCTGTCCTCTCCGGTGGCCGCCGCCGCCGCAGCCGCAGCAGCCGCGCAACGCAAAAGCAGCTCGTCTCGGCGCAACGCCTGGGGAAATATGTCGTACGCGGACCTGATCACCAAAGCCATCGAGAGCTCCCCAGAAAAGCGGCTCACCTTGTCTCAGATATA[C/A]GACTGGATGGTGAAAAGCGTCCCGTATTTTAAAGACAAGGGGGATAGTAACAGCTCCGCGGGCTGGAAGGTATTTATCATTTCATATCTTGAGTTTTGCGGTTTAAAACTGTTAGATGCTCCTCGAAAAGTGGCTCACATTGTCTTAGATCTACGAATGGTTGGTGAAAGCGTGCCTTATTTTACAGACAGTGTTGATAGTAACAGCTCCGCAGGTTTGGATAGTATTTATATTGTTCTCGTATTCTGAGTTTTGGGGGTTTTAAACTTTTATAGGCGCGTCTGGGTTACCATGGTTGCCGTTTAGCGGATGCGCGCGCCCCTCCAGCTGTTCTGTAAACAAACAAAAGCGCGCCCCTCTTGTCGTGCCAACACTTGGTGTCAATTTGTGCTGCCCCGTGTGGCATAATTTCTGCTCAGATCTACGACTGAATAGTGAAAAGCGTCCCTTATTTTAAAGAGAATTGGAGGATAGTAGCTCCAGGGACGGAAGGTATTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14769
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124932 | Nonsense | 120 | 139 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 3394428)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 3297687 |
GRCz11 | 15 | 3285193 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGCTCACCTTGTCTCAGATATACGACTGGATGGTGAAAAGCGTCCCGTA[T/A]TTTAAAGACAAGGGGGATAGTAACAGCWCCGCGGGCTGGAAGGTAYTTAT
Long Flanking Sequence:
GCAGCCCAAAACCAGATGGTGGAGATCGACCCGGACTTCGAGCCGCTGTCCCGGCCCCGCTCCTGCACTTGGCCGCTGCCGCGACCCGAGTTCCCAAACCCCGCCGCCGCGGACTCCAACACTTCATCCCCGGCTCCGTCCGTCAAACAGGAGCCTTCCAGCACCGCGGACTTCATCAACAACCTCAGTCTGCTAGAGGAGAATGAGGACTACCCGGACCAGAAGCCTCTCATGCTCTGCAGCGAGTTCCAGTGCCAGGAGAACTGCATCCACCAGCAGCAGATCCCGAGTCAGCAGCAACAGGTGCCCGTGCTGTCCTCTCCGGTGGCCGCCGCCGCCGCAGCCGCAGCAGCCGCGCAACGCAAAAGCAGCTCGTCTCGGCGCAACGCCTGGGGAAATATGTCGTACGCGGACCTGATCACCAAAGCCATCGAGAGCTCCCCAGAAAAGCGGCTCACCTTGTCTCAGATATACGACTGGATGGTGAAAAGCGTCCCGTA[T/A]TTTAAAGACAAGGGGGATAGTAACAGCTCCGCGGGCTGGAAGGTATTTATCATTTCATATCTTGAGTTTTGCGGTTTAAAACTGTTAGATGCTCCTCGAAAAGTGGCTCACATTGTCTTAGATCTACGAATGGTTGGTGAAAGCGTGCCTTATTTTACAGACAGTGTTGATAGTAACAGCTCCGCAGGTTTGGATAGTATTTATATTGTTCTCGTATTCTGAGTTTTGGGGGTTTTAAACTTTTATAGGCGCGTCTGGGTTACCATGGTTGCCGTTTAGCGGATGCGCGCGCCCCTCCAGCTGTTCTGTAAACAAACAAAAGCGCGCCCCTCTTGTCGTGCCAACACTTGGTGTCAATTTGTGCTGCCCCGTGTGGCATAATTTCTGCTCAGATCTACGACTGAATAGTGAAAAGCGTCCCTTATTTTAAAGAGAATTGGAGGATAGTAGCTCCAGGGACGGAAGGTATTTATCTCTTTCATATTTTGAGTTTTGTGGGT
Associated Phenotype:
Not determined