Busch Lab

ZMP

dcaf11

Ensembl ID:
ENSDARG00000009868
ZFIN ID:
ZDB-GENE-050809-116
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
sa30059 Essential Splice Site Mutation detected in F1 DNA Not yet available
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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:
sa30059
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
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:
None
Flanking Sequence:
GTCGTGGGTCAAGTTTCTCTCATGGAGAGTGCAGCCGTATTCGTTCACAG[T/C]AAGTTATGATGCATGCAATGCAACATTGCAATATTTAAATATTTAAATGC
Long Flanking Sequence:
GCACATTCTTAGGTGTACCTGTGATATTTTTAGCATCTGACAATTTAATTGAGATGTTGCTCTGAAAGTCTCTTTACCAAAATGTCAGTGTTTTATTTTATTTTATTAAGATTTATTTATTTGAAGAGATTGTAATTGTTTCATACCTTTAGGTTTCCTAAAAAAGACTAGAAAGTTAAATAGAAAAATATTGTTAATAAAAAAAAAGTGCATTTGAGAAAAAGATTACATAGGTACTAGATAATTTTAATAACAATATAGAGTCTGAGCAGTTCATTGAGTTATCATACAGCAAGTTGTGTTTTTTTATTAGCTTTTTTTGTGATCACATAACCAGGAAATTTATGCCAAAGTAGCTATGATTTTTAAAAAAAGTTGCTCTATAAAATACACAATTGTGCAACTTTATATAAATTGTGCTTTTCTTTCTGAAGCGGGAACAGGGGCGATGTCGTGGGTCAAGTTTCTCTCATGGAGAGTGCAGCCGTATTCGTTCACAG[T/C]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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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