ZMP
dcaf6
Ensembl ID:
ZFIN ID:
Description:
DDB1- and CUL4-associated factor 6 [Source:RefSeq peptide;Acc:NP_001138562]
Human Orthologue:
DCAF6
Human Description:
DDB1 and CUL4 associated factor 6 [Source:HGNC Symbol;Acc:30002]
Mouse Orthologue:
Dcaf6
Mouse Description:
DDB1 and CUL4 associated factor 6 Gene [Source:MGI Symbol;Acc:MGI:1921356]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41468 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2525 | Nonsense | F2 line generated | Not yet available |
sa21532 | Nonsense | Available for shipment | Available now |
sa25430 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41468
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111027 | Nonsense | 131 | 988 | 4 | 21 |
ENSDART00000113194 | Nonsense | 131 | 907 | 4 | 19 |
ENSDART00000142664 | None | None | 271 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 35175688)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 34395199 |
GRCz11 | 9 | 34204384 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGCATCATTTTCTACACACACACAGAGAAGAGCCAAGAAATCAACAGA[C/T]AGTGCCAGTTCACCTGCCACTATGGCACTGCTTATGAGGTACGAGCGTCA
Long Flanking Sequence:
AAATATATTTCAGAACATGCAATAAAGCTGTAAACATAGTAGTAAAGTATCTATATAATATTGGCTAGTAATCCAAATCTAAATGATTCATATTTTATATTCTTTTCATTAAGAGAACATGACATTTTCTAACTGATCCAGTGTGTAGTGTATAAGATGATCATAACATGAAAATAATTATCATCTGGAGTTTTCAGCTAGAATTTTCTAAAAATGTTCTAAACGTTGAAGCACTGAATTAGGATAATTAAAAGTTAATTTTCAAAGCTTGATTCAATCAAACCTATGCTAATGAGTGGCTTATTTAAAAATTCTCTCCACTGATTTTAAAACGATCATGCTTTTGTCCTCAGGTCAAAACGACTATTCGTTCAGGACATCGGGCCAACATCTTTAGCGCAAAGTTCATGCCCCACACTAACGATCAACAGATTGTGTCCTGCTCAGGAGATGGCATCATTTTCTACACACACACAGAGAAGAGCCAAGAAATCAACAGA[C/T]AGTGCCAGTTCACCTGCCACTATGGCACTGCTTATGAGGTACGAGCGTCATTTAAAGGGATAGTTCACCCAGAAATGAACATTCTGTCATTTACTCATCCTCCACATGCTCCAAACCTGTTTGAGTTTCTTTCTTCTGTTGAACTTTAAGTTTTTCTAAAGAATGTTGAAAGCAGCAGGGATAAACTTCCATTGTGTGTTTTGTTTATACTATGGACGTTTTATAATGGCTGTTATTGATTATTAAAACTGATATTTAGCAAAAGAGATTGTGTGATATTCAGCAAAATATGTTTCATATTTTCAGTAAATGAAAGCAGGCAGTAATGTTATAGGCTTCCGTTTTGTTATAGTTATGCATACAGTGAAGATGATGGTCATATAAATATGTAGCTACATGACGCCTCAACATTTTTTGCGTCTGTTAAGTTAATATCAAAATGAAAATAGCAGTTTTTTTATATCATGTTTTCATTTTATTGTCAAGATAGCGAAACAACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2525
Status:
F2 line generated
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111027 | Nonsense | 348 | 988 | 9 | 21 |
ENSDART00000113194 | Nonsense | 348 | 907 | 9 | 19 |
ENSDART00000142664 | Nonsense | 51 | 271 | 2 | 5 |
ENSDART00000111027 | Nonsense | 348 | 988 | 9 | 21 |
ENSDART00000113194 | Nonsense | 348 | 907 | 9 | 19 |
ENSDART00000142664 | Nonsense | 51 | 271 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 35161134)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 34380645 |
GRCz11 | 9 | 34189830 |
KASP Assay ID:
554-3430.1 (used for ordering genotyping assays)
KASP Sequence:
AGTCCGAATGTTTCACTCATGCAGAGGATGTCGGACATGTTATCTCGATG[G/A]TTTGAGGAGGCCAGCGAGGCTCAGAGCAGCAGAGCTCGTCCACAAACTCG
Long Flanking Sequence:
TATTTTCATTGCTTCATTGCTGAAGAATATCTCCAAGGACTATTACAGCTCCTCCGCTCTTCCTGATTTACCATAACTCATGTGTTCCTCCACTTCATCTCCAGCTGTCTCCTTCATGAGCAGAACTGTTGTCTGCGCATCTTTTCTCCTCCATGTTTTTAATGATCTGAGTCTCCAGTGCCTCTCAGTGCATCTTTAATCTCTCTCAGTACCTCCAGCCATGAATATCAACAGCACTCAGCCTGTCTAAGGGGAGCTTGTTAGCTTTTCACAGGGATTTAATCTGCAGATTGCTTCACTTCACTGCTTTTCAGTGTGTTTCATGGAGCTCTAGAAGTAGAAGAACGGCAGGGTCTTAGTGCTGCTGCTTTTTTTTAGAGAAAACATTTGAGGGTCTGATCTGGTTTGAGATTGATTATGAAGAGGTTTGTTGTCTTTGCAGGAGAGCAGAGTCCGAATGTTTCACTCATGCAGAGGATGTCGGACATGTTATCTCGATG[G/A]TTTGAGGAGGCCAGCGAGGCTCAGAGCAGCAGAGCTCGTCCACAAACTCGACCCAGAGGTACAAGATTTACATTTATTACAATTATGCATTTGGCTTTGAGCTTTTATCCAAAGCAACTTACTTGGTTACTCAGCTTTTTTTGTATGTAAGTGAATGCTAAAAATTAAGCTTATGAATTGAAGCTTTGCCTCCAGGTACAGCAGCTCAAGCAGAAGGCACGAGCTCAGAGACAACCGCTCAGGCACAGGTGTCCTCTGGCGTGGCAGCTGAAGGAGTGATGGAGCTGGAGACGCCAACCATAAATCCTCTCCCTACACCTCCTGCTCCTGCTCCACCATCAGAGCCTCTCCCGAAGTCGGTCTCCTCATCCTCTTCAGGCTCCTCCTCCACTGTGACAGCTCCTCCCCCTTCGAGCTCCTCGTCCATGGAAAGCGCCACCTCTTCCTCTCTGCTCTCATCTCCAGACACTGAGCAGAAGAGCCAGGGTGAAGTCACGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21532
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111027 | Nonsense | 478 | 988 | 10 | 21 |
ENSDART00000113194 | Nonsense | 478 | 907 | 10 | 19 |
ENSDART00000142664 | Nonsense | 185 | 271 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 35160608)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 34380119 |
GRCz11 | 9 | 34189304 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGAGCCAGGGTGAAGTCACGCCCACTCCCTCAGCCACGCCCACTCCCT[C/A]AGCCACACCCACTGCATCTAGAGAGGCAGCTTTGTCTGGTAAGATAACAG
Long Flanking Sequence:
GCAGCAGAGCTCGTCCACAAACTCGACCCAGAGGTACAAGATTTACATTTATTACAATTATGCATTTGGCTTTGAGCTTTTATCCAAAGCAACTTACTTGGTTACTCAGCTTTTTTTGTATGTAAGTGAATGCTAAAAATTAAGCTTATGAATTGAAGCTTTGCCTCCAGGTACAGCAGCTCAAGCAGAAGGCACGAGCTCAGAGACAACCGCTCAGGCACAGGTGTCCTCTGGCGTGGCAGCTGAAGGAGTGATGGAGCTGGAGACGCCAACCATAAATCCTCTCCCTACACCTCCTGCTCCTGCTCCACCATCAGAGCCTCTCCCGAAGTCGGTCTCCTCATCCTCTTCAGGCTCCTCCTCCACTGTGACAGCTCCTCCCCCTTCGAGCTCCTCGTCCATGGAAAGCGCCACCTCTTCCTCTCTGCTCTCATCTCCAGACACTGAGCAGAAGAGCCAGGGTGAAGTCACGCCCACTCCCTCAGCCACGCCCACTCCCT[C/A]AGCCACACCCACTGCATCTAGAGAGGCAGCTTTGTCTGGTAAGATAACAGACTCGATAAAACTTGTTGTTGGTTATATGAGACAATGAGTTGGTTTACTTGCACATAAGGGTCTAAATGTTGTTAAGTTATCTAAACTTTGCACGGCTCCACAAAGCAAGCCAGACCCGTAACAATAAATTAAATTAGATAGGCCACTTCTAAAATAATGTAGGAGCCCGGAATCTCATCTCCCGTTCAAAAGAAAACAACAACAAAGACGATTGACCAAAGAAATAAAATATAGTCAAATTTATTTGACATTTTCCTTTAAGGCGGAGGTAAAGACAAAATAACAAACAAAAAAACTCAACAACTAACGAAGTTTTAAACCCTCTTACCTGCACATAAATAAAAACAAAATAAACATTTACTTACCTCCCAACTAACCACAAAACATGAGAAAACTTAATAAAACAAAAAGGCACCCTCCTCATCACATGCGTCTCCCTGTTGATCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25430
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111027 | Nonsense | 601 | 988 | 13 | 21 |
ENSDART00000113194 | Nonsense | 528 | 907 | 11 | 19 |
ENSDART00000142664 | None | None | 271 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 35151057)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 34370568 |
GRCz11 | 9 | 34179753 |
KASP Assay ID:
554-7568.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGCTTCTCCAGAGACTACGGAAAGTGTGCCATCCACATCAGCGCCTT[C/A]GCTTGGCACCAGCCCTGGCAACATCAGCGTCAGCACTCCTTCGGGATCTG
Long Flanking Sequence:
ATATAGTCGTAATAATATAGTAAACTGTGAGAATAATAATTTTCAACATCAAAAGTTGACAAAGTAGAAATCGAGGTCCCATAATGCAATTCACAGCTATAAATAAATGGAAAACACTTGTGAATCACAAAATATGAAAACTTTTAATTAACAGATATACTTTACAGTGTATCCTAATAACAGACAGGTAATAATGCATTAGTTAATAGTGAGAATTGTTGCTTAAAGTATAGTGTTACCTCAATTAATCATTCTTGCCTTTCACAATAATAATCACATGCTAATATTTCAGAAAAGCTGCTTATGATTAACCCAGTGTTTCTGAGGAAGGCACTTTTTTCTGTAAGCTTAGTTTTACATCCCGCTTGTTTGCTTTGTTGTCTCTCCAGGTGTGAAATCTTCAGGAGAAGCAGCGGTGCGTGTAATCGGTGATCAGAGTACAGGCGTCACTGAAGCTTCTCCAGAGACTACGGAAAGTGTGCCATCCACATCAGCGCCTT[C/A]GCTTGGCACCAGCCCTGGCAACATCAGCGTCAGCACTCCTTCGGGATCTGGCCGGTCCGGGACGGCAGAACCTGTGCTTAGTCTGCACTACAGCACTGAGGGCACCACCACTAGCACCATCAAGCTGGACTTCACAGATGAGTGGTGAGCAACCACACTCAATCAGTCTTGACTTAAATATGTACAGGAATATGAGATGTACAGTGCACAATATAAATGAGTACACCCCCTTTTGGATTGAATAATCTGTTTCTCTGTGAATGTAGATAATATAGTTTGGTGCATTTAAACAAAATAGTTGTATAAATAGTTGTATATTCATTAAAATAAGAGTTTGGTCACCTAACAAGATTAGGAATGGAAAGATGATGCATTTAAATTCAAATGGTGGATTGCACACACACACAAAAAAAAATTCCAACTACAAAAGTTCAACAAGAACAAATGACGAAAGAATTGGATATTCCTAAATCACATTTCTTCAGATATCTAAAGGTAAA
Associated Phenotype:
Not determined