ZMP
mybbp1a
Ensembl ID:
ZFIN ID:
Description:
Myb-binding protein 1A-like protein [Source:UniProtKB/Swiss-Prot;Acc:Q6DRL5]
Human Orthologue:
MYBBP1A
Human Description:
MYB binding protein (P160) 1a [Source:HGNC Symbol;Acc:7546]
Mouse Orthologue:
Mybbp1a
Mouse Description:
MYB binding protein (P160) 1a Gene [Source:MGI Symbol;Acc:MGI:106181]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa44599 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa14338 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44599
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 |
|---|---|---|---|---|---|
| ENSDART00000038767 | Essential Splice Site | 533 | 1141 | 12 | 25 |
| ENSDART00000097189 | Essential Splice Site | 533 | 625 | 12 | 15 |
| ENSDART00000136619 | Essential Splice Site | 532 | 1140 | 11 | 24 |
Genomic Location (Zv9):
Chromosome 5 (position 8987582)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 8230901 |
| GRCz11 | 5 | 8735539 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGCATGGAGAAAGCTCAGGCTAAGAAATCCAAAAAGAAGAAAGCAAG[T/A]GAGTTTAAGCCATTCTCTGCAGTTAAAGACTGCTGTTTTAGATTTGTGAT
Long Flanking Sequence:
TAAGCATTGAACATGGAAGAGATTCTTATAATGTCAATCAGAAAATTAGCATCTAACTAAATCTATAAATGTGAATGTAGGTTGTCACGCTTTTACACAATAAAATAAATAAAAAGAAATGTGTACTAACTAATTAATACAATGAAATAACTCCAACTCAAATATATACATTAAATTGAATGGGGGATGAATATATTGGATTGAATGGGGGATGAATATATTGGATTGAATGGGGGATGAATATATTGGATTGAATGGGGGATGAATATATTGGATTGAATGGGGGATGAATATATTGGATTGAATGGGGGATGAATATATTGGATTGTATGTGGGGTGATTTTTAGAAAGTCTTGAAGGCTGTTTGTTGTGATCAAGTCAGAAATGTTCATGTTTTTGTCTTCACTTCAGTCTCCAGAAGAAAGTTTGGACCTGTTGAAGGATTTGCAGACCTGCATGGAGAAAGCTCAGGCTAAGAAATCCAAAAAGAAGAAAGCAAG[T/A]GAGTTTAAGCCATTCTCTGCAGTTAAAGACTGCTGTTTTAGATTTGTGATTAAAAAAAAGGTTTTTGCCACATGTAAAACAGCTAAGCTTTTTATATACTATTTTTGTTATTATTTTTTTTTCTTTTCCATTTTTTTTCTTGCTTTGGGAAAAAATCCACTCATTAAAAATGGAAAAATACATATAATAAATATATATATATTTTTTGTTTAATTTGTGTAATTTAATTAAGGATTTTTCTCTGTAGCAAATTTTTCCCCATAACATTCAATTATCCCATTGTTGCTTTTCTTTTAACTTAATTAAATTAATGCATTAAAAATGGCCAAATACTTGTAACAAATATACATAAATGTTGTGTATTTTATTTTGAATTGTGTAATTTAATTGTGGATTTTATTTTTCTATGGCAATTAAAAAATATATATAATTCATTGTTAAATATTATGGAAAACTTATCAAAATTAAATTAAATGAGAATAAAAAAATACAATTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14338
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 |
|---|---|---|---|---|---|
| ENSDART00000038767 | Nonsense | 818 | 1141 | 18 | 25 |
| ENSDART00000097189 | None | None | 625 | None | 15 |
| ENSDART00000136619 | Nonsense | 817 | 1140 | 17 | 24 |
Genomic Location (Zv9):
Chromosome 5 (position 8998647)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 8219836 |
| GRCz11 | 5 | 8724474 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGACGGCCGAGAGGCRGAACTTCATGAAATGCTGGAGCGTCTGATTGGC[C/T]GAGCCCAGAAACTGACAGACTCATCTGTGGCTTTGTACTACTTTAGGTGA
Long Flanking Sequence:
GGAAAATATGTCTCAACGAAATCCCTTTATCACAAGGAAAATGCATTTTATAACATAACTGAGTTACCAAAAAGCCATGGAGCGCTCACCGGCCCTGCCCGCACTGCTTGACATGGATGAATCTGTTAACGATATAACTGTGCTGTTCTCACGGGTGGTGTGTGATATTGCGCTGATGCTTTTGACATCTTTTGTACTGTACTTTATTATATGCATACGCAAGATTAATAACAATACCGGCCTTTACATGAGTAGCGATATTAGTTTACATATAGCTGCCACTCCGATGGCAGACAGCATCTAGTAACTAACGTTTTGTGAAATATCGCAAGAAACATGCTTTTTATTTTCCCCAATTGGAAGATATTTCTATTTATTTAATTAAACGTGTACCTCTGTCTCTGATTGGCAGGAATCGGCTCTGTCGTGGGAAGTTTTACTGCAAGGAAATTGACGGCCGAGAGGCGGAACTTCATGAAATGCTGGAGCGTCTGATTGGC[C/T]GAGCCCAGAAACTGACAGACTCATCTGTGGCTTTGTACTACTTTAGGTGAGGACTCAATGATATTGATTTATTATTCAACTGCATTTAGTATTGATTAATATTAATATTGATTTATTAATTAACTGTATTTAATATTTATTAATAGTAATATTAATATTGATTTATTAATTAACTGTATTTAATTTTGTATTGTGCAAACTCTTAATTTGTCTATTGTAATTGTCTAAAAGCATCTTCTAAATGACTGAACGAGTGTGTTGGTCTTCTGCTTTTGCAGTGCTGCTCTCTATGTGCTGAAGGTGTTAAGAGGGTCTGTGGTCGATCAGGAGGTAAAATACAATCTCATATTGACTATGTTAATAATCTGCAAGCACTGAGGCTGATGTAATCTATTTATTGTATTGAGTGCAGTTAAGTACTATGGGTAAAGTGGAGGTTGAGAGAGCGACGACATGCTTAAAGAATGCTTTGACGTCTTTTATGACAAAGAGAAAAAGTC
Associated Phenotype:
Not determined