ZMP
dcaf11
Ensembl ID:
ZFIN ID:
Description:
DDB1- and CUL4-associated factor 11 [Source:RefSeq peptide;Acc:NP_001026845]
Human Orthologue:
DCAF11
Human Description:
DDB1 and CUL4 associated factor 11 [Source:HGNC Symbol;Acc:20258]
Mouse Orthologue:
Dcaf11
Mouse Description:
DDB1 and CUL4 associated factor 11 Gene [Source:MGI Symbol;Acc:MGI:90168]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa12275 | Essential Splice Site | Available for shipment | Available now |
| sa12157 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12275
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000002992 | Essential Splice Site | 163 | 541 | 5 | 15 |
| ENSDART00000131370 | Essential Splice Site | 155 | 218 | 5 | 7 |
| ENSDART00000133166 | Essential Splice Site | 155 | 255 | 5 | 8 |
| ENSDART00000133324 | Essential Splice Site | 163 | 230 | 6 | 8 |
| ENSDART00000002992 | Essential Splice Site | 163 | 541 | 5 | 15 |
| ENSDART00000131370 | Essential Splice Site | 155 | 218 | 5 | 7 |
| ENSDART00000133166 | Essential Splice Site | 155 | 255 | 5 | 8 |
| ENSDART00000133324 | Essential Splice Site | 163 | 230 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 24 (position 12881084)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 12832532 |
| GRCz11 | 24 | 12976951 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCGTGGGTCAAGTTTCTCTCATGGAGAGTGCAGCCGTATTCGTTCACAG[T/A]AAGTTATGATRCATGCAATGCAACATTGCAATATTTAAATATTTMAATGC
Long Flanking Sequence:
GCACATTCTTAGGTGTACCTGTGATATTTTTAGCATCTGACAATTTAATTGAGATGTTGCTCTGAAAGTCTCTTTACCAAAATGTCAGTGTTTTATTTTATTTTATTAAGATTTATTTATTTGAAGAGATTGTAATTGTTTCATACCTTTAGGTTTCCTAAAAAAGACTAGAAAGTTAAATAGAAAAATATTGTTAATAAAAAAAAAGTGCATTTGAGAAAAAGATTACATAGGTACTAGATAATTTTAATAACAATATAGAGTCTGAGCAGTTCATTGAGTTATCATACAGCAAGTTGTGTTTTTTTATTAGCTTTTTTTGTGATCACATAACCAGGAAATTTATGCCAAAGTAGCTATGATTTTTAAAAAAAGTTGCTCTATAAAATACACAATTGTGCAACTTTATATAAATTGTGCTTTTCTTTCTGAAGCGGGAACAGGGGCGATGTCGTGGGTCAAGTTTCTCTCATGGAGAGTGCAGCCGTATTCGTTCACAG[T/A]AAGTTATGATGCATGCAATGCAACATTGCAATATTTAAATATTTAAATGCTAGATAGATACTCACAGGTACACACAGGCTCAGCTGTCTAGTTTGTTGTTGCAATACAGTACATGTAATCATTCATATTTGTTTCTTCATAGTTTTTTGCCCAATCATGTGGTTTACAAGGACACTTATCAGCAGAAAGTATTTTGTGGAGTCTACAGTGATGAGGGAAATATGTTCCTGTCTGCATGCCAAGGTGAAACTGTAATTCAAGACTTCAAGTTAGCATAGCTGTTATTAGCTTAGTTCTTTCATAATCCACATAGCAGAAATGTTCAAATTGATAACCCATCCTTATTTAAGTCATTTAGTGCTAATGTTTAAGTTTTTTTACATTAATTTATGTACACTGTTGTTTAAAGGTGCCCTAGAATGAAAATCTGGATATAAGTAGGCAGAGTTCATTATATGGAAATGACATACTGTGAGCCTCAAACACCATTGCTTTTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12157
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000002992 | Nonsense | 294 | 541 | 10 | 15 |
| ENSDART00000131370 | None | None | 218 | None | 7 |
| ENSDART00000133166 | None | None | 255 | None | 8 |
| ENSDART00000133324 | None | None | 230 | None | 8 |
Genomic Location (Zv9):
Chromosome 24 (position 12875457)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 12826905 |
| GRCz11 | 24 | 12971324 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGATGTGCTTTTCATTTTGATTAAACAGTGCAAACGATGGCTGCCTTTA[T/A]GTGTTTGATCGAGAGCAAAACAAAAGAACACTAAAGGTATGGTAAAACYT
Long Flanking Sequence:
ATTTATTTAGTGGGGGTAGAATGGTACACATAAATAAGGATTTGGAACATACTTTGGCTTTTAATAAAGCAGAGGGAAAACAAAATACAATTTTTTGGGAGGGGTGGTGGGATTATTAAACAGTGGTTTACTAAACGTGTTTAATTTTTCTTCAAATAAATTAAATAATAATTAAATTAAAAAAATTTTATAGATAAAAAACTAAATAATACTGTAGACTAAATATGTGGCACTGTTACTGTACTGTTAAATATTACTGTAACATTAAAGGTCATGGTTTACAACAGCTTAAACTATTCAATTCAATGATCAATTATTTATTTTAACATATAATAACACTCAATTTGAATCTTAATAACTGGTTTTCATTAATCATGTACCGTTACACCTCTACCACATCTAAAAGATTCATGTGAGAATAGTGTTTGTTTAAAATGAGCTTATTTGTTAATGATGTGCTTTTCATTTTGATTAAACAGTGCAAACGATGGCTGCCTTTA[T/A]GTGTTTGATCGAGAGCAAAACAAAAGAACACTAAAGGTATGGTAAAACTTTTTAATCCAAGGATATTTTATTATTTATTTTTGTATGTACTTTTATTTTAGTATGTATATAAAATTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATTTATCATTTTAGATAGGTAAATATTTTAATTTTAAATATGCAATATTTATTTATTTATGCAATATTTAATATACTTTTGGGCTTTTCATTGTTACTTGTTATTGTTATTTCTCAAACTCCACACTTGACCTAAAAAACACCCTTATGACAACCTGTTATAAATGTCAGACAATCTGTTGCACAACCTTTACAGTTCAATGTACTTATTAGTATCAATGCACCAAAGGTCTATTGCTCTGAAATAATTGTGATTTAGTGAGAACTCTATCAAGACATTGTCATCATCTATTCAATCACATTTTCTCTTCGTCTTTTA
Associated Phenotype:
Not determined