ZMP
si:ch211-206a7.2
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC566899 [Source:RefSeq peptide;Acc:NP_001128604]
Human Orthologue:
FOXO6
Human Description:
forkhead box O6 [Source:HGNC Symbol;Acc:24814]
Mouse Orthologue:
Foxo6
Mouse Description:
forkhead box O6 Gene [Source:MGI Symbol;Acc:MGI:2676586]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45665 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36803 | Nonsense | Available for shipment | Available now |
sa36804 | Nonsense | Available for shipment | Available now |
sa18163 | Nonsense | Available for shipment | Available now |
sa36805 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43248 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45665
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028957 | Nonsense | 263 | 439 | 2 | 2 |
ENSDART00000131134 | Nonsense | 263 | 714 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 19 (position 15050176)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 15713780 |
GRCz11 | 19 | 15618142 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATGGGCATTGGAAGTGAAGAGTTTGATGCCTGGACAGACCTTCACTCC[A/T]GAACAAGTTCCTCTGCATCAACGTTAAGTGGATGCTTGTCTCCTATTCTG
Long Flanking Sequence:
GATTTTGTTTATCATCCATGCTTATTATGGTTCTTCAATGTATGTATTATGGTAAATGTATAGATGTAAAGTGAATAAAAACTGTAAACAAATTAAATATGAATTTGGTACTTTGATGGCATGTTTAAAAAGACTAACACCTTATTCCTACTTTTTTTTTCTTCTGTCTACAGAACTCCATTAGACACAACCTCTCCCTGCATACCAGATTCATCCGTGTTCAAAATGAGGGAACAGGAAAAAGTTCCTGGTGGATGCTTAACCCGGAAGGTGGGAAAATGGGCAAAGGACCCCGCAGACGAGCTGTATCCATGGACAATGGCACTAAGTACCTGAAGAGCAGAGGCAGAGTCAGCAGGAAGAGAACAGCGGCTGTGGGAATGGGTAGAGAGCTTGGAGCACCTGGAATACAGGGATCGCCTGAACATGGAAGCCCAGCAGGGAAGGGAGTAATGGGCATTGGAAGTGAAGAGTTTGATGCCTGGACAGACCTTCACTCC[A/T]GAACAAGTTCCTCTGCATCAACGTTAAGTGGATGCTTGTCTCCTATTCTGGCTGAGACAGAACCTGATGAACCAGAGGAAGGAGGACTTTCTTGTTCAGCCTCCCCACGACTCTACCCTAGCCCCACCAGCACAAGATCTCCAGCACTGGGAACAGGTGGACATTGTCCATCTGTTGAGCTTCCGCATCTAGCTGATCTAACTGGAGCAATCAGCTTGGAAGAGGGCTACTCCCAGCCTCTACCACTTAAGCGCAATGGATATCACTATGGCCCTGCACCTAAAGCAGAGACCTCCTACTGTGGTACAGTCTATGGCCAACCATCCATGGGCATGCTTAGGCATCATACGCCTATGCAGACTATTCAGGAAAATAAGCCTACTAGCTTCCAGCGTGCCCTTAGGGCATACTCAGAGAACAATGCCCTTGAAAGTTTGCTTGCTGGAGGGCCACAATACTGTGGTAAGGACATGGTTGTGGGGCAAGGAGGAACATCTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36803
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028957 | Nonsense | 288 | 439 | 2 | 2 |
ENSDART00000131134 | Nonsense | 288 | 714 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 19 (position 15050251)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 15713855 |
GRCz11 | 19 | 15618217 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGTGGATGCTTGTCTCCTATTCTGGCTGAGACAGAACCTGATGAACCA[G/T]AGGAAGGAGGACTTTCTTGTTCAGCCTCCCCACGACTCTACCCTAGCCCC
Long Flanking Sequence:
TAAAAACTGTAAACAAATTAAATATGAATTTGGTACTTTGATGGCATGTTTAAAAAGACTAACACCTTATTCCTACTTTTTTTTTCTTCTGTCTACAGAACTCCATTAGACACAACCTCTCCCTGCATACCAGATTCATCCGTGTTCAAAATGAGGGAACAGGAAAAAGTTCCTGGTGGATGCTTAACCCGGAAGGTGGGAAAATGGGCAAAGGACCCCGCAGACGAGCTGTATCCATGGACAATGGCACTAAGTACCTGAAGAGCAGAGGCAGAGTCAGCAGGAAGAGAACAGCGGCTGTGGGAATGGGTAGAGAGCTTGGAGCACCTGGAATACAGGGATCGCCTGAACATGGAAGCCCAGCAGGGAAGGGAGTAATGGGCATTGGAAGTGAAGAGTTTGATGCCTGGACAGACCTTCACTCCAGAACAAGTTCCTCTGCATCAACGTTAAGTGGATGCTTGTCTCCTATTCTGGCTGAGACAGAACCTGATGAACCA[G/T]AGGAAGGAGGACTTTCTTGTTCAGCCTCCCCACGACTCTACCCTAGCCCCACCAGCACAAGATCTCCAGCACTGGGAACAGGTGGACATTGTCCATCTGTTGAGCTTCCGCATCTAGCTGATCTAACTGGAGCAATCAGCTTGGAAGAGGGCTACTCCCAGCCTCTACCACTTAAGCGCAATGGATATCACTATGGCCCTGCACCTAAAGCAGAGACCTCCTACTGTGGTACAGTCTATGGCCAACCATCCATGGGCATGCTTAGGCATCATACGCCTATGCAGACTATTCAGGAAAATAAGCCTACTAGCTTCCAGCGTGCCCTTAGGGCATACTCAGAGAACAATGCCCTTGAAAGTTTGCTTGCTGGAGGGCCACAATACTGTGGTAAGGACATGGTTGTGGGGCAAGGAGGAACATCTCATTCACTTATGTCACAATCTAATACTGCTGTGCATTCTCACGGCCACAATCAGAGCCACAATCACAGCCAGAATCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36804
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028957 | Nonsense | 418 | 439 | 2 | 2 |
ENSDART00000131134 | Nonsense | 418 | 714 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 19 (position 15050641)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 15714245 |
GRCz11 | 19 | 15618607 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAACAATGCCCTTGAAAGTTTGCTTGCTGGAGGGCCACAATACTGTGGT[A/T]AGGACATGGTTGTGGGGCAAGGAGGAACATCTCATTCACTTATGTCACAA
Long Flanking Sequence:
GTGAAGAGTTTGATGCCTGGACAGACCTTCACTCCAGAACAAGTTCCTCTGCATCAACGTTAAGTGGATGCTTGTCTCCTATTCTGGCTGAGACAGAACCTGATGAACCAGAGGAAGGAGGACTTTCTTGTTCAGCCTCCCCACGACTCTACCCTAGCCCCACCAGCACAAGATCTCCAGCACTGGGAACAGGTGGACATTGTCCATCTGTTGAGCTTCCGCATCTAGCTGATCTAACTGGAGCAATCAGCTTGGAAGAGGGCTACTCCCAGCCTCTACCACTTAAGCGCAATGGATATCACTATGGCCCTGCACCTAAAGCAGAGACCTCCTACTGTGGTACAGTCTATGGCCAACCATCCATGGGCATGCTTAGGCATCATACGCCTATGCAGACTATTCAGGAAAATAAGCCTACTAGCTTCCAGCGTGCCCTTAGGGCATACTCAGAGAACAATGCCCTTGAAAGTTTGCTTGCTGGAGGGCCACAATACTGTGGT[A/T]AGGACATGGTTGTGGGGCAAGGAGGAACATCTCATTCACTTATGTCACAATCTAATACTGCTGTGCATTCTCACGGCCACAATCAGAGCCACAATCACAGCCAGAATCACAATCATAACCCAGAGCATGGCCACAATCGCAATTCCAGTCAAAGCCTTCACAATGGTCATGGAGTAACTCATGAGCAAAACCCAAGCCATCATCACAATCCCAATCAAGCTCATAATAAGCATCACCCAAGTCTTGATTACAATCACCATAAACAACACCGTGGCCATGACTATGTTCAATCTCATGACCACAAACTCAATGCTAGTCCCAATCACATGCACAATCACCTTCAGCATAACAATTCCAGACAACCAGATCTTTCTCCTAGGGTGAGCAATGACATGTTGCAACCCTACAACCACAAATCACCCAGCCTTTATGGCCCACGTGCTCATCTTCCTTCTACTGCTCTGCCTCCTAACCCTGCCAGTGTCTTGGATGTACCCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18163
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028957 | Nonsense | 434 | 439 | 2 | 2 |
ENSDART00000131134 | Nonsense | 434 | 714 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 19 (position 15050689)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 15714293 |
GRCz11 | 19 | 15618655 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAAGGACATGGTTGTGGGGCAAGGAGGAACATCTCATTCACTTATGKCA[C/T]AATCTAATACTGCTGTGCATTCTCACGGCCACAATCAGAGCCACAATCAC
Long Flanking Sequence:
CTGCATCAACGTTAAGTGGATGCTTGTCTCCTATTCTGGCTGAGACAGAACCTGATGAACCAGAGGAAGGAGGACTTTCTTGTTCAGCCTCCCCACGACTCTACCCTAGCCCCACCAGCACAAGATCTCCAGCACTGGGAACAGGTGGACATTGTCCATCTGTTGAGCTTCCGCATCTAGCTGATCTAACTGGAGCAATCAGCTTGGAAGAGGGCTACTCCCAGCCTCTACCACTTAAGCGCAATGGATATCACTATGGCCCTGCACCTAAAGCAGAGACCTCCTACTGTGGTACAGTCTATGGCCAACCATCCATGGGCATGCTTAGGCATCATACGCCTATGCAGACTATTCAGGAAAATAAGCCTACTAGCTTCCAGCGTGCCCTTAGGGCATACTCAGAGAACAATGCCCTTGAAAGTTTGCTTGCTGGAGGGCCACAATACTGTGGTAAGGACATGGTTGTGGGGCAAGGAGGAACATCTCATTCACTTATGTCA[C/T]AATCTAATACTGCTGTGCATTCTCACGGCCACAATCAGAGCCACAATCACAGCCAGAATCACAATCATAACCCAGAGCATGGCCACAATCGCAATTCCAGTCAAAGCCTTCACAATGGTCATGGAGTAACTCATGAGCAAAACCCAAGCCATCATCACAATCCCAATCAAGCTCATAATAAGCATCACCCAAGTCTTGATTACAATCACCATAAACAACACCGTGGCCATGACTATGTTCAATCTCATGACCACAAACTCAATGCTAGTCCCAATCACATGCACAATCACCTTCAGCATAACAATTCCAGACAACCAGATCTTTCTCCTAGGGTGAGCAATGACATGTTGCAACCCTACAACCACAAATCACCCAGCCTTTATGGCCCACGTGCTCATCTTCCTTCTACTGCTCTGCCTCCTAACCCTGCCAGTGTCTTGGATGTACCCCAAGACCCATGTCGCCTGGCTTCAGCTCCCCATCCTCGCCATCAATCCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36805
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028957 | None | None | 439 | None | 2 |
ENSDART00000131134 | Nonsense | 616 | 714 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 19 (position 15051237)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 15714841 |
GRCz11 | 19 | 15619203 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCCAGGTTCCCACCTCCACCAGGGCATGACAGAACCCTGGCAGGGGTA[T/G]TACCACCACACATCACAGAATGCTAATTACCATGGAAACCACCAAGCTAG
Long Flanking Sequence:
CACAGCCAGAATCACAATCATAACCCAGAGCATGGCCACAATCGCAATTCCAGTCAAAGCCTTCACAATGGTCATGGAGTAACTCATGAGCAAAACCCAAGCCATCATCACAATCCCAATCAAGCTCATAATAAGCATCACCCAAGTCTTGATTACAATCACCATAAACAACACCGTGGCCATGACTATGTTCAATCTCATGACCACAAACTCAATGCTAGTCCCAATCACATGCACAATCACCTTCAGCATAACAATTCCAGACAACCAGATCTTTCTCCTAGGGTGAGCAATGACATGTTGCAACCCTACAACCACAAATCACCCAGCCTTTATGGCCCACGTGCTCATCTTCCTTCTACTGCTCTGCCTCCTAACCCTGCCAGTGTCTTGGATGTACCCCAAGACCCATGTCGCCTGGCTTCAGCTCCCCATCCTCGCCATCAATCCTACCCAGGTTCCCACCTCCACCAGGGCATGACAGAACCCTGGCAGGGGTA[T/G]TACCACCACACATCACAGAATGCTAATTACCATGGAAACCACCAAGCTAGCCATCACCATGATCCTCAAAATCGGTTGCAATCTGAGCTGGAAATGGATGTGCACCAGAGCAGTTTGGATTGTGATGTGGAATCCATCCTCCTGAATGACTTTATGGACTCAACAGAGGGAATGGACTTTAACTTTGACGGGTCATTATCACAGGGTGTGGGCATGGGAATGGGTTTGGGGATGGGAATGGGAGTTTTTGCAGGACCTCAACAATCACACAATAGCCAGAGTTGGGTGCCTGGGTAAACCGAGGGGACATTGAGGACCTACATATAGGCAAACATTCAACCATACAGCCTTCTGAAGGGCAGCAGGTCAAGTTGGGAATTATAAGGAACAAACTGACCAATATTCCCTTTCACTGATGTCAGATTCTGGACTCATAATTATTCCCTGAAAAATCCAACCCCACCCCACCCCATCTACTCCATTGTCCCTGCTGTGGAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43248
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028957 | None | None | 439 | None | 2 |
ENSDART00000131134 | Nonsense | 704 | 714 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 19 (position 15051499)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 15715103 |
GRCz11 | 19 | 15619465 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATGGGAATGGGTTTGGGGATGGGAATGGGAGTTTTTGCAGGACCTCAA[C/T]AATCACACAATAGCCAGAGTTGGGTGCCTGGGTAAACCGAGGGGACATTG
Long Flanking Sequence:
GACAACCAGATCTTTCTCCTAGGGTGAGCAATGACATGTTGCAACCCTACAACCACAAATCACCCAGCCTTTATGGCCCACGTGCTCATCTTCCTTCTACTGCTCTGCCTCCTAACCCTGCCAGTGTCTTGGATGTACCCCAAGACCCATGTCGCCTGGCTTCAGCTCCCCATCCTCGCCATCAATCCTACCCAGGTTCCCACCTCCACCAGGGCATGACAGAACCCTGGCAGGGGTATTACCACCACACATCACAGAATGCTAATTACCATGGAAACCACCAAGCTAGCCATCACCATGATCCTCAAAATCGGTTGCAATCTGAGCTGGAAATGGATGTGCACCAGAGCAGTTTGGATTGTGATGTGGAATCCATCCTCCTGAATGACTTTATGGACTCAACAGAGGGAATGGACTTTAACTTTGACGGGTCATTATCACAGGGTGTGGGCATGGGAATGGGTTTGGGGATGGGAATGGGAGTTTTTGCAGGACCTCAA[C/T]AATCACACAATAGCCAGAGTTGGGTGCCTGGGTAAACCGAGGGGACATTGAGGACCTACATATAGGCAAACATTCAACCATACAGCCTTCTGAAGGGCAGCAGGTCAAGTTGGGAATTATAAGGAACAAACTGACCAATATTCCCTTTCACTGATGTCAGATTCTGGACTCATAATTATTCCCTGAAAAATCCAACCCCACCCCACCCCATCTACTCCATTGTCCCTGCTGTGGAATAATGTCATAGTGCCCTAACAGTCTTTTCTGTGGTTCATGTCCTTCAGTTTGTGCTCAATTCATCACCTCCATCTCTTTCTGGGCAAAAGCTCTGAAGCACTTTACATGGCCATCCATTCTGATGCTGTAACGACCACCCCGCGACCTGGGAGGAATCACATTGTCCGCTGGCCTGGGTTTAATGTATGCAAACGACTTTGTTATCCTTGCTGAACAAAAAAAGTAAATAATTAAGCATTGGTGTTGTTTTACTAAACATGAGT
Associated Phenotype:
Not determined