ZMP
si:ch211-55i2.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
BBX
Human Description:
bobby sox homolog (Drosophila) [Source:HGNC Symbol;Acc:14422]
Mouse Orthologue:
Bbx
Mouse Description:
bobby sox homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1917758]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa8933 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| hu7857 | Nonsense | Available for shipment | Available now |
| sa6137 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8933
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000018788 | Essential Splice Site | 139 | 906 | None | 24 |
| ENSDART00000137008 | None | None | 129 | None | 2 |
| ENSDART00000137964 | None | 139 | 139 | None | 3 |
| ENSDART00000139994 | None | None | 317 | None | 4 |
| ENSDART00000142476 | Essential Splice Site | 139 | 229 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 29184078)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 28615672 |
| GRCz11 | 10 | 28502297 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YGTAYTGGACCCCAAAGAAAAGCAGAAATACACAGACATGGCCAAGGAGG[T/A]AARAACTAACCAACACACACGACTCAATTGAAYGATTAGCTAACATAAAG
Long Flanking Sequence:
TTTTATATATGTAAAATTCAAATATTAACTGTCATTTATGTAACTTGCACATATTTCTAGATTTCTACAAGGGAAACAGCCATTGACTAATTCTGGCAAATTGTATATTCTGTATTATTAATGTGCATAGTCTTTGTCAAATACACCTGAACATTTTTATTTTGATCTAAAGTGGGCTTATTCCACTGACTATATCTCCATATTTCTCTGTCCACCTTTTCTGCACTCGTCTTCCCCTCAGGAGCCGGTGTTATGTGCGGAGAGCAGTGTTCAGGAGGGAGAGTGTGGCGGGATGGAGGATGACAGTGAAGAATACTCCTCTGAACAGCGGGCTCGGCGGCCCATGAACGCCTTTCTGCTATTCTGCAAACGCCATCGCTCGCTGGTCCGTCAGGAGCATCCACGATTAGACAACCGAGGAGCCACTAAAATCCTGGCCGACTGGTGGGCCGTATTGGACCCCAAAGAAAAGCAGAAATACACAGACATGGCCAAGGAGG[T/A]AAGAACTAACCAACACACACGACTCAATTGAATGATTAGCTAACATAAAGCCAAACTAAAAATTGTTCTGACGCCATTTTCACATTATTACAGTTCTTTTGCTGGAGATTACAAAATGGTAATAAAATATGACGAGCTCATTTTCTTTGCAGTAAACTGTCAGAACAATTGATAATGTAAGATAACTTTGATTGAAAGGTACAGTATGTAATAGGGGTTAAACGACTTTACGATTTTTAAAGTCGACTTTTATTTTATTAAAGTCTAGTCAACGTTGACTAGTCAAAGAAAAGTTGCCTATAGCTGGAACAAACAGAAACTTGACAGCTCTGCTGCTTAAGAAATATGACTGAAAACTGAGGCTGCGTCCGAAACCGCATACTTCCATACTATATAGTACGCTAAAATCAGTATGTGAGCCAAGTAGTATGTCCAAATTCATAGACTTCGAAAATCAGTATGCGAGAAGTATCCAGATGACTTACTACTCCCAGCGAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu7857
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 |
|---|---|---|---|---|---|
| ENSDART00000018788 | Nonsense | 313 | 906 | 9 | 24 |
| ENSDART00000137008 | None | None | 129 | None | 2 |
| ENSDART00000137964 | None | None | 139 | None | 3 |
| ENSDART00000139994 | None | None | 317 | None | 4 |
| ENSDART00000142476 | None | None | 229 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 29174558)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 28606152 |
| GRCz11 | 10 | 28492777 |
KASP Assay ID:
554-2411.1 (used for ordering genotyping assays)
KASP Sequence:
AGCACACTGGGAAATCAGCCCTTTTCCAGCTGGCTGAGGTGAGATTACCT[A/T]AAAAACTTGTCTGTCAGACCCATAAWACCCTACTTAGSSNCKRRRACGTYT
Long Flanking Sequence:
CTATAATATATATAATATTATATATATTTTTAATCTGAATATTATTAAAGCTATAATTATGTTTATTTGAAATACTACTAAAATAGCCTAAGTCAGTGGATTTCATTAAACAAAATGTTGACATAATCATTTGTATGTTTTTCCATTGCTGATGCTTAGTTTTCAAGCACAGCTCATCTCCAGTCACGTTATCTGTCACTTCCTGTTTAGACAGCGTAATTGATGGCTATATATATTTTTTATTTTATTGACTCTACCTGTGGCTTTTCCATCAAACTGTCAACAGAGGGAGGTGTTGAGTTGTAAATGCCAGCGGTCGCTTCAAGGCGAATGTTGATTTAAGATTGTTTGTTTATGGCTTGTTCTACTCCACTGATTTCATTTCTTTATTTTTTGAATGCTTTCAGATTTCCTCCAGCTCTTCCCAGACTGGATGCACAGATGTTGCTAAGCACACTGGGAAATCAGCCCTTTTCCAGCTGGCTGAGGTGAGATTACCT[A/T]AAAAACTTGTCTGTCAGACCCATAAAACCCTACTTAGCGCTGAGACGTCTCAGATACGGATGGTTGCCTGTGAACGTGTAAATGATTTGCTTAATGATCTGAACGTGTTTTGTTGGACTTCTTCTCAGATTTCTTCCAGTCCAGCACAGTCAGCTGGAGGAAGTAAGAATGCAGAGGACACAAGCTCACTTACACATGTAGAGGTGAGGGACAGTCAAAGCTTTTATAGTGAGTTCTTTAAATTACATCTGAACACTGATTATGTTTACTTTTATGACCTCCTTAGGCTTCTGGACCGTCTCAGCCAAGCTCACCAGACCTGCCCAAGAGTTGTGTTAAATCACCCCTGTTTCAGCTGGCTGAGGTACAGTACTAAACTAATTTAACATGAGTTTTTGTGATCCAATCCAAAGGGTCAGCTGTAGTTAAGGTTTAAGGTTATGACGGTATAATAACAATATCACGGTTTCATGATATTGTGATCACTGCTTTAAAATATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6137
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000018788 | Essential Splice Site | 381 | 906 | 10 | 24 |
| ENSDART00000137008 | None | None | 129 | None | 2 |
| ENSDART00000137964 | None | None | 139 | None | 3 |
| ENSDART00000139994 | None | None | 317 | None | 4 |
| ENSDART00000142476 | None | None | 229 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 29172982)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 28604576 |
| GRCz11 | 10 | 28491201 |
KASP Assay ID:
554-3767.1 (used for ordering genotyping assays)
KASP Sequence:
ATTTCTTGTGTTGAAAAGGCATCTYTGGATACCTTTCTTTTCTTTGGATA[T/A]AAAGTAAGCAACTNNNNTGTTCAGGTCTATAACATTACAAATGTCTGCTS
Long Flanking Sequence:
AAGCCTGGTATTTAGTGCGATATGGTGCTATACAGTGCTAAAGTCTAATATCTCCAGATTGGCTTTAGTCTTGACTAGTGCGGTTGAATGACATTTGTTCTGGGAGCACTGTATAAATGTGGCGGCGCTATTGACGCATACTCAGGGTCCGTATGCGATATCTAGTGTATATATCTATGAAAAGCAACAACAAAACACTACATATTTTAATTTAAGAAACATTTAAGATATTTCCCAGTACTGGGTTGCGGCTGGAAGTGCATCCGCTGTGTAAAACATGCACCGGAATAGTTGGCGGTTTATTCCGCTGCGGCAACCTCTAAATAAATAAGGGACTATGCTGTAAGAAAATAATAAAATGAACATTTAAAACATTTACAGTAAACATGTCAGGCTAAATAATTCATGCAAATCCTTGACTTCTGCTGTCTTTGTTAGTTTCAACAACAGATTTCTTGTGTTGAAAAGGCATCTCTGGATACCTTTCTTTTCTTTGGATA[T/A]AAAGTAAGCAACTGCACTGTTCAGGTCTATAACATTACAAATGTCTGCTCAATCGCTGAATTTAATGATCAATATTTTAATAAAAATATATACTACATACATGAGTATAAAAATATATACAAACAGATGCCATGAAAAAATATATATATTGTATAAAAATAGAACAAAAAATCAGATATGCTGTATATGATAGGAATGTCAGCTTTTAATCTTGTCCAGCAACATCACAGCAATTTTGGTCTGAATAGTGTTGTCTTTTGCACCGTTAAGCCCGACCAGTAGCTTTTAATATGGATGGTCCTTTTCTGCTGGAGATACTGTTGCCCTAAAAAAGGTCTTTGACAACATAAAAAAGTTACATATACCATAGTAACATTATGACAGAAGATGGTAATGGTTTTAAAACCTTGACTTTTCCTAACCGTGGTAAACCTTGAAACCAGTTATCATCCCATGCCTAGGTGTGATCATTACCGTTTCCACCTAGTATCAAAGAAACA
Associated Phenotype:
Not determined