ZMP
daxx
Ensembl ID:
ZFIN ID:
Description:
death domain-associated protein 6 [Source:RefSeq peptide;Acc:NP_001038414]
Human Orthologue:
DAXX
Human Description:
death-domain associated protein [Source:HGNC Symbol;Acc:2681]
Mouse Orthologue:
Daxx
Mouse Description:
Fas death domain-associated protein Gene [Source:MGI Symbol;Acc:MGI:1197015]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17864 | Nonsense | Available for shipment | Available now |
| sa29152 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa29151 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17864
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000093181 | Nonsense | 210 | 716 | 5 | 12 |
| ENSDART00000122815 | Nonsense | 210 | 715 | 5 | 12 |
| ENSDART00000123443 | Nonsense | 210 | 716 | 3 | 10 |
| ENSDART00000124094 | Nonsense | 210 | 242 | 5 | 5 |
| ENSDART00000125702 | Nonsense | 210 | 418 | 5 | 9 |
| ENSDART00000129452 | Nonsense | 210 | 419 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 19 (position 7649678)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 7108217 |
| GRCz11 | 19 | 7027142 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTCTYTNNNNCNNNNATKTTTCAGATTGCGTATCTGGAAAACCTKTTGAAAGTGTA[T/G]AATGAGGAGATCCGSCGGCTTCAGGAGGGGGATTTGAGTTTGGATGACTT
Long Flanking Sequence:
AACGGAAGGAAGATTTTTTCAACACATTATTTTAACATGATAGAAACTCATCTCTAATAACTGATTTCTTTTGTCTTCGTCATGATGACAGTACCGAACATTTGACTAGATATTTTTCAAGATACTAGTATGCAGCTTAAAGTCACATTTAAAGGTTTAATTAGGGCAAGTTAGGGTAATTAGCCAGGTCATTGTATGACTTGTTGATTGTTCTTCAGACAATCTAAAAAATATATAGCTTAAGAGGATAATAATATTGACCTTTTTAAACTGCTTTTATTCTAGCTAAAATAAAATCAGTCAGACTTTCTCCAGAAGAAAAAATATTATAGGAAATACTGTGAAAAATTCCTTGCTCTGTTAGACATCACTAGGAAAATATTTATAAAAGAAACAAAAAATCACAGGAAAACAAATAAGTGTGTCTATTTTACGGTTACAGTAATTTGTGTGTCTCTCATTTTTCAGATTGCGTATCTGGAAAACCTGTTGAAAGTGTA[T/G]AATGAGGAGATCCGCCGGCTTCAGGAGGGGGATTTGAGTTTGGATGACTTGGAGAAAGAAGATTCCAGTTATATTCAAGAGCACAAACTTAAACGCAAGGTCAGCTTGTTTATTCCTGATTTTAGTTCTTTCTGTATTTATTTAGCCGGGACAATGCTCAAAGAGAAAAACTTTAAATTAGCCAAAGTTAGTCACAAGAATTTTAGGGCGTACTCACACTATGCTATTCGAACCGTGCCCAGGGTTTCCCGGATCATTTCAGAAGTGTGAGTGCTCTGAATCGGGCTCAGGCACGGTTAAATGTCATATATATATGAGCAAAGTGCACCAGAGGCCGAAACTGAAGATGAGACGTGACTTTTACAAGACTGTTTAATATGGCATTATTATCATTCGTACTGTTCAATGAACACAAACTGTTGTAGATTTTAAAGACGCAAACCCCTCACTGCACGACAGCTGCACCTTCAGCAAACCTCCTAATTCCTGCAGCACGAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29152
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000093181 | Nonsense | 429 | 716 | 9 | 12 |
| ENSDART00000122815 | Nonsense | 429 | 715 | 9 | 12 |
| ENSDART00000123443 | Nonsense | 429 | 716 | 7 | 10 |
| ENSDART00000124094 | None | None | 242 | None | 5 |
| ENSDART00000125702 | None | None | 418 | None | 9 |
| ENSDART00000129452 | None | None | 419 | None | 9 |
Genomic Location (Zv9):
Chromosome 19 (position 7643355)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 7101894 |
| GRCz11 | 19 | 7020819 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTTTTGTACAGGCTGTTAATGGGCAACAGAGTGAAAGCAAAGAAAAA[G/T]AAAAGGAGGAGCAAGAAGAAAAAGAGAAGGAAGATGAAGAAGAAGAGGAG
Long Flanking Sequence:
CTACACCTCTGGAGCTGTAGTTAAAAAACATAGTTCTTGGCTGTTTTCTATTTCCATTTATCCCCCTATGCCCTATTAATTTAGAACATTCTAAAATTCAAAGTTGGAATGTTTAAAAATAAAAAAGTTTTACATGATTACAGTTGTGCTCCCGTTGCAGTGCACTTTAGTGTATATAAATATATATATAAATATAACTTTTATTCTCTCTATTAAAAAACAATTTTAAAAAATCTAATTCAAACTATTTACAAAGTTCTATTTCTTTGAAAAAATTAATTATTGTAATAATTTATAAGTAAAAAATATTTTTAATGAATCAACTATTTTATTATTCATTAAAAAAAAACGTAAAATATTTTACTAAATCCTGTTTCTGTATTTCCAAGACAGTCAAGCTTATTTTATTCATATGCAAGTCTGAAACCACACACTAATATAAATCTTTCCTATTTTTTGTACAGGCTGTTAATGGGCAACAGAGTGAAAGCAAAGAAAAA[G/T]AAAAGGAGGAGCAAGAAGAAAAAGAGAAGGAAGATGAAGAAGAAGAGGAGGAAGACGAAGAAGAGGACGATTCTTCAGATCCTGACATTGAAGACGAAATCCAGGCCAGCGAACAACAAGCTGGTCCAGGTAAGAAGTGAACAAATCATCTCCAAAAGCTAGAAATCACCTCATTTCACTGAGTTAACCCTGATTTCTCCCAATTTCAGAAGATGATGAAGAAGATGTGGAAGAGGAGCCTGCTAACATCAGTGACAACGATCAGCCAATCAATGAAAGCTCTCCTCTGTCAATCAAATCCTCTGTTCAGGACACAGAAGAGGATGAGGAGCAGTCTCCGCTCAGCAGCACACATGAAGGATCTGCAGAAACAAATACAAACACGAACGGACCTGCTAAACAGAGCCTCGAGTCCACAGAGATCAAGCCGGAGAGCATCAAGCCGGAGAGTATCAAGCCAGAGAGCATCAAGCCAGAGACCATCAAGCCGGAGAGCATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29151
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:
G > A
Consequence:
Essential Splice Site, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000093181 | Missense | 473 | 716 | 10 | 12 |
| ENSDART00000122815 | Essential Splice Site | 472 | 715 | 10 | 12 |
| ENSDART00000123443 | Missense | 473 | 716 | 8 | 10 |
| ENSDART00000124094 | None | None | 242 | None | 5 |
| ENSDART00000125702 | None | None | 418 | None | 9 |
| ENSDART00000129452 | None | None | 419 | None | 9 |
Genomic Location (Zv9):
Chromosome 19 (position 7643143)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 7101682 |
| GRCz11 | 19 | 7020607 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAATCACCTCATTTCACTGAGTTAACCCTGATTTCTCCCAATTTCAGAA[G/A]ATGATGAAGAAGATGTGGAAGAGGAGCCTGCTAACATCAGTGACAACGAT
Long Flanking Sequence:
TTAAAAAACAATTTTAAAAAATCTAATTCAAACTATTTACAAAGTTCTATTTCTTTGAAAAAATTAATTATTGTAATAATTTATAAGTAAAAAATATTTTTAATGAATCAACTATTTTATTATTCATTAAAAAAAAACGTAAAATATTTTACTAAATCCTGTTTCTGTATTTCCAAGACAGTCAAGCTTATTTTATTCATATGCAAGTCTGAAACCACACACTAATATAAATCTTTCCTATTTTTTGTACAGGCTGTTAATGGGCAACAGAGTGAAAGCAAAGAAAAAGAAAAGGAGGAGCAAGAAGAAAAAGAGAAGGAAGATGAAGAAGAAGAGGAGGAAGACGAAGAAGAGGACGATTCTTCAGATCCTGACATTGAAGACGAAATCCAGGCCAGCGAACAACAAGCTGGTCCAGGTAAGAAGTGAACAAATCATCTCCAAAAGCTAGAAATCACCTCATTTCACTGAGTTAACCCTGATTTCTCCCAATTTCAGAA[G/A]ATGATGAAGAAGATGTGGAAGAGGAGCCTGCTAACATCAGTGACAACGATCAGCCAATCAATGAAAGCTCTCCTCTGTCAATCAAATCCTCTGTTCAGGACACAGAAGAGGATGAGGAGCAGTCTCCGCTCAGCAGCACACATGAAGGATCTGCAGAAACAAATACAAACACGAACGGACCTGCTAAACAGAGCCTCGAGTCCACAGAGATCAAGCCGGAGAGCATCAAGCCGGAGAGTATCAAGCCAGAGAGCATCAAGCCAGAGACCATCAAGCCGGAGAGCATCAAGCCAGAGAACACAGACTCTCTAGCTGAAGTCAAGACCGAACAGGTTTCCTCCAATCACGTTGAAGCTGTGTCTGCAAGCACTGAGACTGTGTCCATTGTATCCGAGGAGTCGTCCACAGCCGTCACGAGATCCGCCAACTGCAGTCCGCTGCTCCCAACCAGCCCTTTACTAATCGACGAGACGGGCAACTACAGGAAGAGGAAACGCAGA
Associated Phenotype:
Not determined