ZMP
ches1
Ensembl ID:
ZFIN ID:
Description:
checkpoint suppressor 1 [Source:RefSeq peptide;Acc:NP_001116217]
Human Orthologue:
FOXN2
Human Description:
forkhead box N2 [Source:HGNC Symbol;Acc:5281]
Mouse Orthologue:
Foxn2
Mouse Description:
forkhead box N2 Gene [Source:MGI Symbol;Acc:MGI:1347478]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23660 | Nonsense | Available for shipment | Available now |
| sa25132 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23660
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000104137 | Nonsense | 41 | 443 | 1 | 6 |
| ENSDART00000137601 | Nonsense | 41 | 263 | 1 | 3 |
| ENSDART00000104137 | Nonsense | 41 | 443 | 1 | 6 |
| ENSDART00000137601 | Nonsense | 41 | 263 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 16539334)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 16599287 |
| GRCz11 | 20 | 16498870 |
KASP Assay ID:
2261-4088.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTCCGCTCTACCAGGACACAGATGCAGCCGATCTTTCGCTGGCACTGT[C/A]GACCTCTCTCAGCCGGGCCGAGGATGAGGAGCTCACCAGCCTCAGCTGGC
Long Flanking Sequence:
AACACATGAAGATAGAATAAAATTTAATTTTAGTTTAATTAGTTTAATTTTAGTTTAGGCTTGGTTCTTTGTTTTTATATTCAGTATAATCATGGTTTCAAAGGACAAAATATTCAGCGGGCCTTCAGATTTAGGTGAAAATTATATTTAAAAAAAATTGGTGGTAGTAGCTGGCAACTTAAAAAAAAAAAAAAGTCAGAGTTGGTTTTAACTATAATTCCTGCCAGAGTTTTATTATTATTTTTAAACATGGGAGACTAATATGTACTTTATAAATAATAAGTAAATAAATGAATGAATGACAAAAGTGTCGTCATATAAAAACCTGCAGTCGCAATAATCCTGTCATCACTTTTTGTGTGCAGGAGCCGGGGGCCGCATGGGTCCGGTGGTCATGCCTCCAGGTAAGAAGGCCGAGGGTCCCAGCAGTGGCAGTGTGGCGCGGGGTCTCAGTCCGCTCTACCAGGACACAGATGCAGCCGATCTTTCGCTGGCACTGT[C/A]GACCTCTCTCAGCCGGGCCGAGGATGAGGAGCTCACCAGCCTCAGCTGGCTGCATGAGAGCACTGACCTGCTGACCAGCCTGGGCCAGTCTGGCCTGCGCAGTGTCAGCCCTGTCCAGGATGCCAACGGAGCCCACGAGCCCTCGCCCTCGTCTTCCCCGGAACCCAACGAGCCGCCCTACCACCTGTCTACAGGACCCAGCCGCAAACCACCATACTCCTTCAGCTGCCTCATATTCATGGCCATTGAGGACGCCCCGTCGAAAAGACTGCCCGTAAAAGACATCTACGGCTGGATACTGGAACACTTCCCCTACTTCTCCAGTGCCCCGACTGGCTGGAAGAACTCAGTGCGACACAACCTGTCTCTCAATAAATGCTTCAAAAAGGTGGATAAGGATCGCAGTCAGGTGAGGATTCCCTGGATTTTAGACTGGTGTGGCTTTTAGTCCCATATATTGTGACCTTGTCTTTTTTTTGTCTTGAAGTTGTGTTGCTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25132
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 |
|---|---|---|---|---|---|
| ENSDART00000104137 | Nonsense | 41 | 443 | 1 | 6 |
| ENSDART00000137601 | Nonsense | 41 | 263 | 1 | 3 |
| ENSDART00000104137 | Nonsense | 41 | 443 | 1 | 6 |
| ENSDART00000137601 | Nonsense | 41 | 263 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 16539334)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 16599287 |
| GRCz11 | 20 | 16498870 |
KASP Assay ID:
2261-4088.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTCCGCTCTACCAGGACACAGATGCAGCCGATCTTTCGCTGGCACTGT[C/A]GACCTCTCTCAGCCGGGCCGAGGATGAGGAGCTCACCAGCCTCAGCTGGC
Long Flanking Sequence:
AACACATGAAGATAGAATAAAATTTAATTTTAGTTTAATTAGTTTAATTTTAGTTTAGGCTTGGTTCTTTGTTTTTATATTCAGTATAATCATGGTTTCAAAGGACAAAATATTCAGCGGGCCTTCAGATTTAGGTGAAAATTATATTTAAAAAAAATTGGTGGTAGTAGCTGGCAACTTAAAAAAAAAAAAAAGTCAGAGTTGGTTTTAACTATAATTCCTGCCAGAGTTTTATTATTATTTTTAAACATGGGAGACTAATATGTACTTTATAAATAATAAGTAAATAAATGAATGAATGACAAAAGTGTCGTCATATAAAAACCTGCAGTCGCAATAATCCTGTCATCACTTTTTGTGTGCAGGAGCCGGGGGCCGCATGGGTCCGGTGGTCATGCCTCCAGGTAAGAAGGCCGAGGGTCCCAGCAGTGGCAGTGTGGCGCGGGGTCTCAGTCCGCTCTACCAGGACACAGATGCAGCCGATCTTTCGCTGGCACTGT[C/A]GACCTCTCTCAGCCGGGCCGAGGATGAGGAGCTCACCAGCCTCAGCTGGCTGCATGAGAGCACTGACCTGCTGACCAGCCTGGGCCAGTCTGGCCTGCGCAGTGTCAGCCCTGTCCAGGATGCCAACGGAGCCCACGAGCCCTCGCCCTCGTCTTCCCCGGAACCCAACGAGCCGCCCTACCACCTGTCTACAGGACCCAGCCGCAAACCACCATACTCCTTCAGCTGCCTCATATTCATGGCCATTGAGGACGCCCCGTCGAAAAGACTGCCCGTAAAAGACATCTACGGCTGGATACTGGAACACTTCCCCTACTTCTCCAGTGCCCCGACTGGCTGGAAGAACTCAGTGCGACACAACCTGTCTCTCAATAAATGCTTCAAAAAGGTGGATAAGGATCGCAGTCAGGTGAGGATTCCCTGGATTTTAGACTGGTGTGGCTTTTAGTCCCATATATTGTGACCTTGTCTTTTTTTTGTCTTGAAGTTGTGTTGCTGTT
Associated Phenotype:
Not determined