ZMP
cby1
Ensembl ID:
ZFIN ID:
Description:
protein chibby homolog 1 [Source:RefSeq peptide;Acc:NP_001003838]
Human Orthologues:
CBY1, CBY3
Human Descriptions:
chibby homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:1307]
chibby homolog 3 (Drosophila) [Source:HGNC Symbol;Acc:33278]
chibby homolog 3 (Drosophila) [Source:HGNC Symbol;Acc:33278]
Mouse Orthologues:
Cby1, Cby3
Mouse Descriptions:
chibby homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1920989]
chibby homolog 3 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1923903]
chibby homolog 3 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1923903]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa12790 | Essential Splice Site | Available for shipment | Available now |
| sa22078 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12790
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 |
|---|---|---|---|---|---|
| ENSDART00000109541 | None | None | 125 | 1 | 4 |
| ENSDART00000134726 | Essential Splice Site | None | 85 | None | 4 |
| ENSDART00000148011 | Essential Splice Site | None | 125 | None | 5 |
Genomic Location (Zv9):
Chromosome 12 (position 20285047)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 19066891 |
| GRCz11 | 12 | 19188765 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAGTTAGCGCGAATCTCGAAGCTAACGGTAGTCTCACCTCCACGTTTGG[T/C]GAGTCACTTTGAGATCAAGATGAACNNNNNTGTCTTTTGTTCAACTTTAGTTGAC
Long Flanking Sequence:
CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTATATATATATATATATATATATATATATATATATATATATATAATGATATAATGTATACATTTCAAATTATATATGTTTTTTGTCCTTATATTTTCACGAATCCCCTAGCTCACCAGAAAATCTTTAAGATCAGTGTAATCTATGAATGTAACCTCTGGATCCAGTGAAAATGTTTAACAACGCCTCAGAATTTTTGCAGGCGTTGGATATTTTTGAAAGGGTACTTTTATCTAACAAATATTAACTTCCGGCGTTGCTAGGCTCCCCCCGGAATTAGCCGTTTGTTTACACATGTCTCTTATGGTTTCAGGAGCATCTAAGAAGCTGTCGTGAGGAAAATGCGTTTGTTTTATAAAAGCAGTTTCACTCCATCAATAAATTGAATACTATGTGTTAATAACGTGCATGTAAGTTACTAGTAAGTTAGCGCGAATCTCGAAGCTAACGGTAGTCTCACCTCCACGTTTGG[T/C]GAGTCACTTTGAGATCAAGATGAACTGTCTTTTGTTCAACTTTAGTTGACTGTAATCAAAGCCGAACTCGAACACTATCACGTTGTAAAATGTTGTCGATTTACGCTTGTGTTATTGATGCAGGTTAAGAAGTCAGACTATCTACTTCAAAATGCCCCTCTTTGGCAATATTTTCAGTCCCAAGAAAACCCCACCTCGAAAGTCTGCATCGCTTTCCAATCTACATACAGTAAGTACACGTTTCTGTTAATTAAACCAATAACGTTATCCCTATAAAAAATTGACCATGTTTTAACCGCAAAAAAGGGGAAAAAAACTGTGGTTGTTGTAGGAAACAATAGTACAGTGCTTACATCCCATTTTGAAATTGAAAAAAAATAAATAAATTTCTCCGTGAATATGAGCAATATATATATTGAGGCATTTTAACAAAACAAATTTATCAAACAGATATATTTATTCAAATTATATTTAAGTCACAGAACATCTTTAAAAATGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22078
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 |
|---|---|---|---|---|---|
| ENSDART00000109541 | Nonsense | 81 | 125 | 3 | 4 |
| ENSDART00000134726 | None | None | 85 | None | 4 |
| ENSDART00000148011 | Nonsense | 81 | 125 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 12 (position 20286180)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 19068024 |
| GRCz11 | 12 | 19189898 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGAAATGTGTCAGGAAAAGAAGTTCAGCGACTGAAGAAGAGGAATCTA[C/T]AGTTAGAGGAGGAGAATAATCTGCTCAGGCTGAAGATTGAAGTTCTTCTT
Long Flanking Sequence:
TATTATTTCTATATTTTCCCCTAACATATAAATTTGTACTACTAATTTTTGAACATCCTATAGAAATATCAATTTAAATGAAAGATTTGTGGGGAGTATAGTCATAAATTGCTGAGTACTGTAACCACAAACTCACTTAACGTTAGCATTATCCATACAGTATCCTATACTAAAATTTCAGATAATCATCATATATCATTGTATCATATAATGACTGAAATAAAAAATTTGTATCCATTGTATGTTCTTTTGAAAGTTGGATCGGTCGACCCGTGAGATTGAATTGGGTCTGGAATATGGATCTCCTGTGATGAACATTGGTGGTCAGAGCCTCAAATTCGAAGACGGACAGTGGATTTCAGGTATGGCCTTGCATGCTGCAACAGTACCCCCAATACATATAATGACAATTAGCCGTAATAAATAAATTTGTCAACACCTCAGAATCAGGTGGAAATGTGTCAGGAAAAGAAGTTCAGCGACTGAAGAAGAGGAATCTA[C/T]AGTTAGAGGAGGAGAATAATCTGCTCAGGCTGAAGATTGAAGTTCTTCTTGATATGGTGAGAGTTAAAGGATTCTCATTTCAAAAGCTGCCACATCTTGAAAACATAACAATATTCTTTATAATTATGTGGTGTCAAATTTGATGGATTGTTATTCATCCTTTCTAGCTTTCAGAATCGACAGCAGAAACACATCTAGTACAGAAGGAGCTTGAAGATATGAAGAGCAGTTCTAGGAGAAAGAAATAAAGGGAGGACACCTTTTATATTACTTTGTATATTTAGCTTTTTTACATTTCATTTGATATTTTTATTGGCAATTATGTTAGGAGTCAATGAAGAAAAGTTTTTTAAGGATATGCATAACCGGTCAAAAGTTTGGGGTCAGTTTTAAATTGTTGAATATTTATTACATTTGAAATAACTGCTTTCTTATTGTATGAAGTTTTAAATGAAATCTATACTCCAGTGATTATTGCTTTTATTACTATTACCATTAAT
Associated Phenotype:
Not determined