ZMP
dido1
Ensembl ID:
Description:
death inducer-obliterator 1 [Source:RefSeq peptide;Acc:NP_001073424]
Human Orthologue:
DIDO1
Human Description:
death inducer-obliterator 1 [Source:HGNC Symbol;Acc:2680]
Mouse Orthologue:
Dido1
Mouse Description:
death inducer-obliterator 1 Gene [Source:MGI Symbol;Acc:MGI:1344352]
Alleles
There are 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14468 | Nonsense | Available for shipment | Available now |
| sa10169 | Nonsense | Available for shipment | Available now |
| sa16666 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14468
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 |
|---|---|---|---|---|---|
| ENSDART00000103950 | Nonsense | 80 | 530 | 3 | 6 |
| ENSDART00000110882 | Nonsense | 161 | 2779 | 2 | 15 |
| ENSDART00000122078 | Nonsense | 161 | 598 | 4 | 8 |
| ENSDART00000125453 | Nonsense | 161 | 282 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 18971828)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 18389142 |
| GRCz11 | 11 | 18551484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCTTCCGAGGCCAGCTTTGAWGGAAATGCAGAAGCCAAAATAGAGGAA[C/T]AAAAAGTAGCTTCAYCAGAGAAAAAGAAAAGGGGCAGAGGAAGGGCAAAG
Long Flanking Sequence:
TAGAATTCACATCATAATTTTGTGATCCACATTTTATATCTGCTGCGTTCTGATAATTAAACATTTGTTGTCAACTGTAATTATGCTACGTCTCACACACAGAACCAACATCAGTATCAGAAGAAGTCAAAGATCAGGAGCAAGGTGATGTTAGTGAAGACAAAGTAGAAGACCCTGACAAATCCTTAAAGCCTGCATGTGGTTTTAAGAAGACTTGGGGCTTTCGTCGGACCACCATTGCTAAGAGAGAAATCCCTGGAGAAATGGCAGCAGAGACCCCAGAAAGCAAAGGTGCACCTGTCCGTCGCAGTGGCCGGCAGGCGAAGCGCACGGACAAACTGGAAGAGTTTCTGGTCACAGTGAAGAGAGGAAGAGGAGCGGGTAGGAGAAGTTGCCCTTCACGAATTGAGGGAGGGGATCCTCCATCCCAGACCCCAACCGATGCTGAAACTGCTTCCGAGGCCAGCTTTGATGGAAATGCAGAAGCCAAAATAGAGGAA[C/T]AAAAAGTAGCTTCACCAGAGAAAAAGAAAAGGGGCAGAGGAAGGGCAAAGAGGCCAGTGAAGCCCAAAACAGGTGGAGGCTCGGTGAGTGATGATGGCAGCTCTGAAAATGAAGAGGAGACTGGCGAAGAGGTAGCTAAAGACACTCAAGAACATGTTGAGACTGTGGCCTGTGCTGAAGATGCAAAGAATGTGGAAGCAAAAGAGGAGCAACCGATGGATGTTGTAACAAAAGAAGAAGAGGTTTTGGAGGAGGGTAGTAAGAATGATGAGAAGTCCTTAAACGAGTCTGTAAATAGACGTCTTACCAGAGCTTGTAAAGACTCTAAACGTGACACTAAACCCAAAGTAGGAGTGAAACTCCGCAAAGAGAAAAAAGAGGAGAAAGATGATGACGATGATGATGACGACGATGATGATGATAATGATGAGTCATCGTCAGCCAGTGAGTCCGACAGTGATGGGTATGACCCGAATGCACTTTACTGCATCTGCAGGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10169
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 |
|---|---|---|---|---|---|
| ENSDART00000103950 | Nonsense | 242 | 530 | 3 | 6 |
| ENSDART00000110882 | Nonsense | 323 | 2779 | 2 | 15 |
| ENSDART00000122078 | Nonsense | 323 | 598 | 4 | 8 |
| ENSDART00000125453 | None | None | 282 | None | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 18971340)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 18388654 |
| GRCz11 | 11 | 18550996 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGCCAGTGAGTCCGACAGTGATGGGTATGACCCKAATGCACTTTACTG[C/A]ATCTGCAGGCAGAAACACAACAAAAGGTATGTTTCTTTGTGTGCCAGTAT
Long Flanking Sequence:
AAAATAGAGGAACAAAAAGTAGCTTCACCAGAGAAAAAGAAAAGGGGCAGAGGAAGGGCAAAGAGGCCAGTGAAGCCCAAAACAGGTGGAGGCTCGGTGAGTGATGATGGCAGCTCTGAAAATGAAGAGGAGACTGGCGAAGAGGTAGCTAAAGACACTCAAGAACATGTTGAGACTGTGGCCTGTGCTGAAGATGCAAAGAATGTGGAAGCAAAAGAGGAGCAACCGATGGATGTTGTAACAAAAGAAGAAGAGGTTTTGGAGGAGGGTAGTAAGAATGATGAGAAGTCCTTAAACGAGTCTGTAAATAGACGTCTTACCAGAGCTTGTAAAGACTCTAAACGTGACACTAAACCCAAAGTAGGAGTGAAACTCCGCAAAGAGAAAAAAGAGGAGAAAGATGATGACGATGATGATGACGACGATGATGATGATAATGATGAGTCATCGTCAGCCAGTGAGTCCGACAGTGATGGGTATGACCCGAATGCACTTTACTG[C/A]ATCTGCAGGCAGAAACACAACAAAAGGTATGTTTCTTTGTGTGCCAGTATTTGTGGCCAATAATATTACTTAAATTTGAAATTGTAAAATGTGTGACTTTAAAATCTAAATGTTTAATAATGACACACTTGTAGTTTGGTTAACTTGGCTTATTTGGTTGGATCAAAAAAAGAAAGTGAGCCATTCAGTCCTGGTTTGCTTAGCCTTCACACTTATTTTTAAAACTGGTGTCCTGACATTTTATACCTGTCAGATTATGCTACCAACACTGCATTTGAATGGTTATGAGGTTGGGTTAGGAATTACGTATGTCAGGGCTATATTACAGCTTCATATTACAATAATCCACATTAAAATTTACACTGGTAGCAACATTTGATGGGTGCAAATTGCATCATCAAGATTTGCTACCTACTTTTTGAATTAGAGGTAGCTCAATCTGACAAGGAAGGACAAAAATAAATCTAACACAGGATCAAGATAAATAATCCAAACAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16666
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000103950 | None | None | 530 | None | 6 |
| ENSDART00000110882 | Nonsense | 2539 | 2779 | 15 | 15 |
| ENSDART00000122078 | None | None | 598 | None | 8 |
| ENSDART00000125453 | None | None | 282 | None | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 18956527)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 18373841 |
| GRCz11 | 11 | 18536183 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGCAGAGAGTCMGATCGGGGCAAGGAGTCCGATCGGGGCAAGGAGTCC[G/T]AWCGGGGCAAGGAGTCCGAACGGGGCAAGGAGTCCGAACGGGGCAAGGAG
Long Flanking Sequence:
GAGATATTAGACCTATTCGTGGACCTCTGCTACCAACACCTCCTGAAGGTCCTATACCAATACTGGCTCGTATAGGTGGACACAGCCCCGACACCCACCGTGATGACCCCTGGAGAAGGCACTCCCCTGAAATGCGAAGACGAAGCTGTTCCAGCAGAGATGGTTCAGAGTCACATACCCGCCCAAGTAGATTTGAGGGTGGTCCACGTGACAGAGATGCCCCCTCAAGATTGTCAGAGGAGAGGCAGCGTGAAATGTCTGAAGACAGGAGAAGAGACAGAGACAGAGAAGGTGGTCATGGTGGACGGTCTTGGGCCTGGAACAGAGAACATGAGTATGACCGAAGCAAAGAAAGGGATCGGGAAAGAGACCGGAGCAGAGAAAGAGATAGGGAGCAAGGTCACAGCAGGGAAAAGGAGAGAGAACACAGCAAAGAGAGGGATCGCAGTAGAGGCAGAGAGTCCGATCGGGGCAAGGAGTCCGATCGGGGCAAGGAGTCC[G/T]AACGGGGCAAGGAGTCCGAACGGGGCAAGGAGTCCGAACGGGGCAAGGAGTCCGAACGGGGCAAGGAGTTCGATCGGGGCAAGGAGTCCGATCGGGGCAAGGAGTCCGATCGGGGCAAGGAGTCCGATCGGGGCAAGGAGTCGGAACGGGGCAAGGAGTCGGAACGGGGCAAGGAGTCCGATCGGGGCAAGGAGTCCGATCGGGGCAAGGAGTCCGATCGGGGCAAGGAGTCCGATCGGGGCAAGGAGTCCGATCGGGGCAAGGAGTCCGATCGGGGCAAGGAGTCCGACCGAGGCAAGGAGTCCGACCGAGGCAAGGAGTCCGACCGAGGCAAGGAGTCCGACCGAGGCAAGGAGTCCGACAAATATGGAGATGGAGACAAAAGAAGAGACCGGGATCGAGACAGAGAGCGAGAGCGTGGCAGAGAGAGAGAGGACAGAAAGGACCATGATCGAGATAGAGCGAAAAACAGAGAGAGAGAAAAAGACCGTGACAGAGAC
Associated Phenotype:
Not determined