ZMP
dao.3
Ensembl ID:
ZFIN ID:
Description:
D-amino acid oxidase [Source:RefSeq peptide;Acc:NP_991257]
Human Orthologue:
DAO
Human Description:
D-amino-acid oxidase [Source:HGNC Symbol;Acc:2671]
Mouse Orthologue:
Dao
Mouse Description:
D-amino acid oxidase Gene [Source:MGI Symbol;Acc:MGI:94859]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38457 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa6967 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16754 | Essential Splice Site | Available for shipment | Available now |
| sa26442 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa20379 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38457
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051611 | Essential Splice Site | None | 353 | None | 11 |
| ENSDART00000122587 | Essential Splice Site | None | 224 | None | 12 |
Genomic Location (Zv9):
Chromosome 5 (position 21986624)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 19699496 |
| GRCz11 | 5 | 20203296 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTATTATATGCAGCAAATATGCTCACTTTTAAGGCACTCTTCTGTCTGC[A/T]GTCATGAAGGTGTGCATCATTGGCGCAGGGGTCATCGGTCTCTCCACTGC
Long Flanking Sequence:
CTGATTCAGGCTCAAACTAATACAGCTACACTGACTGACAGTATTTACAAAGCAGAGGCAAAGCGCGTACTTATCGGGGTGTGACGCTTTTGGTGACGTGGAGCCAGTCTGTGAATCACAGCACATTATGTTAGCTGAGCAATCAGAGCCTCTGGAGGGCGGCCTTTCGGAGGACCTTGGAAATATGACAGTGGTTTTCATGTTAGCTGAGTAGCTGTATATATTTAATGTAAGAAATATGAAAAAATATGTGATTTTTTTTTTTTATAAATGAAGGATGAGCACACATTACTTTGCACCCCATAAACACAACCAAGTCTTAAAAATAGACTCTTGACCCCCCCTTTAAGTCAGCTGCAAGGTTAATCATATGGCAGCATTGAGCTCAAAGAATGAGCTAAATTCACTTGCACATCAGATAAATTAGAAGTTTAGTCCTTTAACAAATTACCTATTATATGCAGCAAATATGCTCACTTTTAAGGCACTCTTCTGTCTGC[A/T]GTCATGAAGGTGTGCATCATTGGCGCAGGGGTCATCGGTCTCTCCACTGCTCAGAGCATCTACCAGCACTTCCACAGCAGAGTCTCTCCTCTCACCATAGAGGTTTATGCTGATTTCTTCACTCCTCTGACCACCAGCGATGGGGCAGCTGGACTCTGGCAGCCCTATCTCTACGACAAGGGAATTGTCAAAGAAACGTGAGCCTTTTATCTGTCCATAGGCTGTTTCTGAGATATCCTGAAGAACCCTGCTAATAAAATGTTTTCTTTTCTATTCTCAGTCAATGGAACAAAGAGACCTTTGACTATCTACTGAGTTTCATCAACTCTCCAGATTCAATCAAAATGGGTATCTTCCTTCAGTCTGGCTACAATCTGTGCGCTGAAACTGCAGCAGTGAGAACACTGACATTTCCCATTTTAAAGGGACAGTTCACCCAAAAATTACAATTTACTCACTACTTACTCTGCCTCAAGTGGTTCCAAAGCCTTTATGACTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6967
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051611 | Nonsense | 151 | 353 | 6 | 11 |
| ENSDART00000122587 | Nonsense | 28 | 224 | 6 | 12 |
Genomic Location (Zv9):
Chromosome 5 (position 21984502)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 19697374 |
| GRCz11 | 5 | 20201174 |
KASP Assay ID:
554-5156.1 (used for ordering genotyping assays)
KASP Sequence:
AAACTTAAGANNNNNNACACATATGAATCATTTTCTTGTTTTCTTAACAG[G/A]TTAAAAGAAAGAAATGTCAAGTTTTATCAAAGAAAGATTGATTCATTTAA
Long Flanking Sequence:
GTTTTGTCTAAAAATAATGTAAACATGGCACCTTTTTGGTTGAAAAACTGGGCTCTAAATACATACTGTACACTGTATTTTATTTCCAATAGGGTATAGTGAGTATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATAGCTATTACTTTATATTTTGAAAAAGCCGCTGGTGCTTGTGTTTATCGACAACTTTGACTTTCCATTTAAATTAAATGAAACTGTTCTCAGGGTCATCCTTTCATTTTGCATTACCATCTATTCTCAGCTTTGGCTGGTTCAACACTTCTATCATGATTGAAGGAAAAACATATCTGCCCTGGCTGATGGACTGGTGAGAGATACACAAATTGTACACAATACATGTATATTTTTAAAACTTAAGATCTAGAACACATATGAATCATTTTCTTGTTTTCTTAACAG[G/A]TTAAAAGAAAGAAATGTCAAGTTTTATCAAAGAAAGATTGATTCATTTAAAGAGGTTTGGATGTGTTTTTGCCCTATTTTGAGTAAATATAAAGCTCTAGATTAAGATACTTTATTCAGAAAAACATCACCCTGTGAAAATACAGTATATTTTTCTTCATATATTTTGTCTGAAAAGTAATTTAGTCTGAGATGGCTTTTAGCTATATTTAAAAAGGCATTTAATAACAAACAGCATATTTGAAAGAAATATAATTACTTTGCAAAAAAGACTGTCAAACCATGTAATGTTTTAAATTAATGATTAATTTCTTAATAGCTTTTTTCCTTAAGCATGTACAATCTTTTTTAGTTAAACAAATGAAATAAAATTACAAAATGCACCAAAATGTTATATTCAAAATCATATAATTTCTCTGATTCTCTAAATTTATTTACACAGAACTGCAAGTGCATTAGATTACCTAAAAAGTTGTCCCTTTCATTTTTCTAGTCAATAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16754
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051611 | Essential Splice Site | 204 | 353 | 7 | 11 |
| ENSDART00000122587 | Essential Splice Site | 81 | 224 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 5 (position 21983542)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 19696414 |
| GRCz11 | 5 | 20200214 |
KASP Assay ID:
2259-5639.1 (used for ordering genotyping assays)
KASP Sequence:
ARCTGCAGCCTGATCCTGAGCTCCAGCCAGCCAGAGGACAGATCATTAAG[G/A]TGACTTTTAATGGWTTAATTGCCTAATTCCCTCTGTCTTCACTGGATTGT
Long Flanking Sequence:
TTACCTAAAAAGTTGTCCCTTTCATTTTTCTAGTCAATAAGTACTTTAATTACAGTAACTAAACAATTTACAAAATGTGTATTCAAAGATTCAGTAGCAGTTTAAATCGTAGGTCTCAAACTCAATTCCTGGAGAGCTGCAGCTCTGCACAGTTTTGCTCCAACCCTAATCAAACATAGTTGCAGAAACAAATCAAGGTGTTTAAGATTCGTTTGAACACTTGATTATTTGGATCAGCTGTGTTTAAATAGGGTTGGAACAAAACTATGCAGAGCTGTGGCCCTCCAGGAATCGAGTTTGAGACCTTTGACTTAAGCATAGCAGCATTATAATTCATTTGAGTTACTCTAAGAATATAGAGTCACACTAGAAATATACTGTATGATGTTTTCCAGTTGTCAGCCTGTGGTGCTGATGTGATAATCAACTGCTCGGGTGTTCGCTCAGGAGAGCTGCAGCCTGATCCTGAGCTCCAGCCAGCCAGAGGACAGATCATTAAG[G/A]TGACTTTTAATGGTTTAATTGCCTAATTCCCTCTGTCTTCACTGGATTGTGTGAAAGGTGCCAAATATATTAGATCAATTCCAATGGCAGTTCTAGTTTAAATGGCACCCTGGGCAAAACCACTCCAAACATACCCCCTCCCCCAAGAAATAAAGGCACTATGTGGTTGACTTTTTATATTTTAAATATTTAATTATATATTTCAAATATATACATTTAAATAATTATTATAAATACATTTAAATATACTTATTTATTTTCAATAAATATAACAATTTGTGTATTATTATTATCATTATTATTATACAAGTAATTTTCTAAATAAATAAGAGAAGTCGATCCTAAATGTAACTGAAAAACAATGTAAAGACACGACTTTTGCATGAATAAGTTCTTTATGGGTTCTTTAGAATACAAAAAATATGTTTTATAGAATTACCTGTTGTCTTAGACCTGGCTTATGGCAGAGAATTAATGTTATAAAGTCTTAGTTGCCTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26442
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
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051611 | Essential Splice Site | 231 | 353 | 8 | 11 |
| ENSDART00000122587 | Essential Splice Site | 108 | 224 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 5 (position 21981376)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 19694248 |
| GRCz11 | 5 | 20198048 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCACACATAATTTCTCGTCTAGGGGTAATTCAGCTTACATCATACCTGG[G/A]TGAGCATCTTCATGATCAAAATCAAATCCTATTCACAAAATATTAAAGTC
Long Flanking Sequence:
ATGTGCAGAATAATCATACTTCTCATACTATTCAAGTGAGAGGTTTATTGTGTAGCTTGTGAATGAGATATCTAATAAAATCCAGAGCAGGGGTGTTGTTATAGGACCCTATTTACTAGGGCATGTGCTCCAGTAAAAACCTGCTGTGCCCCAGTAAATGCTTTGAGTTTCAATTTACTTTACATGTCCTTGTATTTATCACGATTGGTAATCTCAGAATAAAGATATTCCAAATATCGGCTTTTTTTTTCAACAGAACAAAAAAAAGAATCGCAGACTGGTTTGGAACAAGTGAACGTTCCCTCAATACTAACAATGTGTGCTAGTAAAACAAACATTACAAATTTTGATTTATAAAAAAACAACAAAAATCAATAGGGGTGAAAACATCCCCTCAAACTGTGTGCTGTATGTGAACAGGTAGACGCTCCCTGGATAAAACACTGGATCTCCACACATAATTTCTCGTCTAGGGGTAATTCAGCTTACATCATACCTGG[G/A]TGAGCATCTTCATGATCAAAATCAAATCCTATTCACAAAATATTAAAGTCAGAGTTTTGTTTTTAAAAGCAAAATGTGATCTTAGCAGTGTTTCAGACCTGTTTGTTTCCGCAGGAGTCGTTTGGTCACTGTTGGTGGAGTTTTCCAAGTGGGAAACTGGAATCGGCTGAACAGTTCTGTTGACCATAAACAAATCTGGGAAGCCGCCTGCAAACTTGAGCCCAGTCTACAGGTAGAAGATCAGATGGTTTTATTATTGGTTAAGTATTGAATTTCCTAACAAAACATCTTTTCTGTCTAGCATGCGCGGATAGTAGAAGACTGGACTGGTCTCAGACCTGCACGCAGTAAAGTCAGACTAGAGAGAGAATCCATACGATGTGGAGGACACTCATTTGAGGTGAGCTCATCTAGTGAAAAGAGCAGCATTTCATTTCATTACATCTCTTTTTTTCATACGTCATGCTGTTTTTATTGCCTCAGGTCATCCATAACTATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20379
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051611 | Nonsense | 246 | 353 | 9 | 11 |
| ENSDART00000122587 | Nonsense | 123 | 224 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 5 (position 21981216)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 19694088 |
| GRCz11 | 5 | 20197888 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCAGGAGTCGTTTGGTCACTGTTGGTGGAGTTTTCCAAGTGGGAAACTG[G/A]AATCGGCTGAACAGTTCTGTTGACCATAAACAAATCTGGGAAGCCGCCTG
Long Flanking Sequence:
CTTTGAGTTTCAATTTACTTTACATGTCCTTGTATTTATCACGATTGGTAATCTCAGAATAAAGATATTCCAAATATCGGCTTTTTTTTTCAACAGAACAAAAAAAAGAATCGCAGACTGGTTTGGAACAAGTGAACGTTCCCTCAATACTAACAATGTGTGCTAGTAAAACAAACATTACAAATTTTGATTTATAAAAAAACAACAAAAATCAATAGGGGTGAAAACATCCCCTCAAACTGTGTGCTGTATGTGAACAGGTAGACGCTCCCTGGATAAAACACTGGATCTCCACACATAATTTCTCGTCTAGGGGTAATTCAGCTTACATCATACCTGGGTGAGCATCTTCATGATCAAAATCAAATCCTATTCACAAAATATTAAAGTCAGAGTTTTGTTTTTAAAAGCAAAATGTGATCTTAGCAGTGTTTCAGACCTGTTTGTTTCCGCAGGAGTCGTTTGGTCACTGTTGGTGGAGTTTTCCAAGTGGGAAACTG[G/A]AATCGGCTGAACAGTTCTGTTGACCATAAACAAATCTGGGAAGCCGCCTGCAAACTTGAGCCCAGTCTACAGGTAGAAGATCAGATGGTTTTATTATTGGTTAAGTATTGAATTTCCTAACAAAACATCTTTTCTGTCTAGCATGCGCGGATAGTAGAAGACTGGACTGGTCTCAGACCTGCACGCAGTAAAGTCAGACTAGAGAGAGAATCCATACGATGTGGAGGACACTCATTTGAGGTGAGCTCATCTAGTGAAAAGAGCAGCATTTCATTTCATTACATCTCTTTTTTTCATACGTCATGCTGTTTTTATTGCCTCAGGTCATCCATAACTATGGACATGGAGGTTTTGGGCTGACCATCCATCGTGGATGTGCTGAGGAAGCTGCTCGGCTCTTTGGACAGTTCCTGGAGCAGAAAGGCTTGCTTGTTCAATCTAAATCACAAGCAGCACAAGCTAAATCACGTCTCTGAAAAAATGTGAGCCTCTTTGAACAG
Associated Phenotype:
Not determined