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 is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14769 | Nonsense | Available for shipment | Available now |
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