ZMP
si:dkey-38o19.8
Ensembl ID:
ZFIN ID:
Human Orthologues:
FOXJ2, FOXJ3
Human Descriptions:
forkhead box J2 [Source:HGNC Symbol;Acc:24818]
forkhead box J3 [Source:HGNC Symbol;Acc:29178]
forkhead box J3 [Source:HGNC Symbol;Acc:29178]
Mouse Orthologues:
Foxj2, Foxj3
Mouse Descriptions:
forkhead box J2 Gene [Source:MGI Symbol;Acc:MGI:1926805]
forkhead box J3 Gene [Source:MGI Symbol;Acc:MGI:2443432]
forkhead box J3 Gene [Source:MGI Symbol;Acc:MGI:2443432]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39083 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32077 | Essential Splice Site | Available for shipment | Available now |
sa22778 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39083
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 |
---|---|---|---|---|---|
ENSDART00000080396 | Nonsense | 168 | 516 | 4 | 9 |
ENSDART00000139916 | Nonsense | 168 | 448 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 16 (position 14528112)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12886571 |
GRCz11 | 16 | 12776691 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATACTTTTGTTTCAGACTCCTTTCCCAGAGACACAACTGCCTGCCAAT[C/T]AACCGGAGCCCCTCCCCCCTCAGCCAGACACCAAGAGCACATTCCCTCCT
Long Flanking Sequence:
GGCATGAACTGGTCTGAAAGGAACAGTTCACCCAAAAAATTATTATTTACTTTAAGAGTTTCTTTCTACTGTTAAACACAAAAGAAAATATTTTGAAAAATGTTGGAACCATTGACATCCACAGTAGGAATAAAATTCCATGAAAGTCAATGGCTACCAGTTTCCAAAGTTTTTCTAAATATCTTCTATAGTGTTTAACAGAAGAAAGAAACTCAAACATGTTTGGAACTAGCGAAGGCTGAGTAAATGGTGAAAATTTTAAGTTTTGAGTGAAATGTGTCTGATGTGTGACAATAAAATGAGTTGATCATATATTCACATAATAATATGATCACAATAATTAAATCACAATGACAATATTTCACGCAAGAAAAATTATTTGTCGAGACAGGCCAAGAAATAATCACATGAAGGATTTCATCACATCTGTGAGATCAATATTTCACTCACTAATACTTTTGTTTCAGACTCCTTTCCCAGAGACACAACTGCCTGCCAAT[C/T]AACCGGAGCCCCTCCCCCCTCAGCCAGACACCAAGAGCACATTCCCTCCTCCTCCATGCAAGGTTCGAAGTCATTTCTTCTGCTTTCTGTTTCCATTAAGATCCTCTTAACCCAGAGCTTGAGGCTTAAAACTAAGGAAATGAGAGTGAGATGAACAAAATAGAACGGTTCTGTCACTTCCACTTATAATGAATCTAAATGCATGCATAGTTCAGACATATAAGTTTAGGGGCATTTACAGGACGCTAGGTGTGCAGGTGCAGAGTTTTCAGCCTTTTTAGACATTTTCAAAGAACCAAAAGACAAAAAACAAACTTTTAGGAACATTTAAAATATGTTTATATGAAGCAAAATTCATATTTCATATTTGTCAGAATTTTCTCACCCTTACGTTTAATTACTTATCCATGCAATGCAAAAACGTTTGTCAAGCTTCAATAAGAATTAAAATCATTATGAAAATAGCCGGTATGACTTGTGTGCTATTTTACAAGCTGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32077
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080396 | Essential Splice Site | 240 | 516 | 5 | 9 |
ENSDART00000139916 | Essential Splice Site | 240 | 448 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 16 (position 14524807)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12883266 |
GRCz11 | 16 | 12773386 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTTCAGTCGCTCTGTCGCTCCATGAGAGAGAAGGTCACTTCCCAATG[T/C]AAGTAAAACTGCTTTTTCATTTAAGCTCATTAATTAAGATTCACAATTAT
Long Flanking Sequence:
TCTGTCTGTCTGTCTGTCTGTCTGTCTATATAATCTATCTATAATCTATATATATATATATAAATGTATATGTGTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTATGTGTGTATGTATGTGTGTATGTATGTATGTATGTATGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTATATGTGTGTGTATATATAAATAAGTTTATTGTGTGAGTAAATCATGACATAATTTTGTTATATTTTGGCTAAACTGTTATAATAAATAAAAAATATATAATATCATTTATCCAAAGTAAGTTTATCCCTCATTGTTTTTGCAGCAACGTCCAGCCATCCCAGTTCCCTCATCTCTTCCATCAAACCCTCATGCTGATCCTCCTCTTCGCTTCTCCTTTGCTGATTTGAACCTTCCAGATCTGTACAACTCCTTTCAGTCGCTCTGTCGCTCCATGAGAGAGAAGGTCACTTCCCAATG[T/C]AAGTAAAACTGCTTTTTCATTTAAGCTCATTAATTAAGATTCACAATTATTAAATAAATCTTTCTCTTTCTCATAGCGGACGTTTCCACTTTACTTGGACTCACCCATGATAGTACACCCCTTCACACCCCAACCCTGCCTCCTCTCTCCCCCTGTCCAAACCCCAATATTAACCAGTTTATCAACCCAAACTCAACTCATATTCCAAACCTCAATACCAACGGTAACTTCAATCCAAATGCACCCCATAGCTTTATCCCCACCCTAAACCCAAACCAGAACTCTAGCATTCATCCAAACTCGAGCACTGAACCTGACAAGGTGCTTCCCAACGGTGAGTAAAACTGCTCAGTAGTGATCTGTTGGTGGAATATGAGTGTCCAGATGAACTGATCTTCTTTTTTATCTCTTAAAGTTGTTCCTGCGGACTGGTTCAGTAACCCGGACTCTTTGAGAGAAAGTTTCAGAATCGCCAGTAGTCTGGATTGGGCAAACATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22778
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080396 | Essential Splice Site | 483 | 516 | None | 9 |
ENSDART00000139916 | None | 449 | 448 | None | 8 |
Genomic Location (Zv9):
Chromosome 16 (position 14515514)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12873973 |
GRCz11 | 16 | 12764093 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCCAGGGGGACTGCAGCCCACCACCAGCCAGCCCATGACTCCCAACGG[T/G]ATGTCCAGAGATCACTTACATCCATATAGGAACAGTGCATATTTAGACTA
Long Flanking Sequence:
TCAATACAATTTTACAGACTTTACAGACAAAAAAACAATACATGTGTAATCATGACTGCATCCAATATTCTAAACTGCCCAGCATCACTAAGGTTTAAGATGTGTCTCTATCTGTTTTGTTTTCATGCAGACCTGTTAGAAAGCATGCGTCAGGCCGAACTGCGAGATTGGGCTCTGGATCCAGCACTCTTCACCTCGCTCTGTGATTCGCTCAACCGTTTCTTCACTCACAAGGGTCTCATTGGCTCGTCTTCTGGTGGTCCATCTTCTTTCGGACACATGGCACCACCTTCTGTCAATATGCCCCCCACTAACCCTCCCACACTGTCAAGTTTAACTCAACCATCTCCACTCATTTACCCCTCCCAGCTCCCTCCTGGCAGCGGTGAAGCTCCTCTACAGGGTCCCAGGAGGAACCTGACCCCTCTTGCCCAGAACCAGACCACACAGACCCCAGGGGGACTGCAGCCCACCACCAGCCAGCCCATGACTCCCAACGG[T/G]ATGTCCAGAGATCACTTACATCCATATAGGAACAGTGCATATTTAGACTATATTAGTGGTGTAACTGATCCCAAATCTCACGGTTCGGATCACGTTTTGTTTTTGTAGTCACAGATCGAATCATTTTTCGAATCAGCCAAAAAGGGAGGGATGCTTTCCATTTTTACAAAAACAGCACTTCAAGAAACTTTTGGCTTTAACAAACAGAACTTAGAACCTGTACATTTATTCAAAATAAAATGAAGAAATAATCAGCTCAATCAAAATAAATCGTAAAATATTCTGTGAAAAATTCACTGTTACTACTACTGTTGCTAATGACGCTAAATGTAGAAATCTTACATTATAATTTGTACAATTCAGAATTATTTTTAGTCTCATTTTCAAGAAATGATTCAGTTATTCACTCATAAAACTTCCTGTTCATGTTTTGATGGCTGGTTGTCGCCACCTATTGGTTAAATAATGTAATTGCTGTCGGAGAAATATCCAGCTGCAGA
Associated Phenotype:
Not determined