ZMP
mao
Ensembl ID:
ZFIN ID:
Description:
Amine oxidase [flavin-containing] [Source:UniProtKB/Swiss-Prot;Acc:Q6NSN2]
Human Orthologues:
MAOA, MAOB
Human Descriptions:
monoamine oxidase A [Source:HGNC Symbol;Acc:6833]
monoamine oxidase B [Source:HGNC Symbol;Acc:6834]
monoamine oxidase B [Source:HGNC Symbol;Acc:6834]
Mouse Orthologues:
Maoa, Maob
Mouse Descriptions:
monoamine oxidase A Gene [Source:MGI Symbol;Acc:MGI:96915]
monoamine oxidase B Gene [Source:MGI Symbol;Acc:MGI:96916]
monoamine oxidase B Gene [Source:MGI Symbol;Acc:MGI:96916]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21528 | Essential Splice Site | Available for shipment | Available now |
sa34685 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31732 | Nonsense | Available for shipment | Available now |
sa21527 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21528
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028225 | Essential Splice Site | 49 | 522 | 3 | 15 |
Genomic Location (Zv9):
Chromosome 9 (position 34656001)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 33889029 |
GRCz11 | 9 | 33698214 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTGGCTTGTCTGAGTTTCACTAACAACTTTATCACCTGTGTAATTTC[A/T]GAATAAGGAGACCAAATGGGTGGATCTGGGAGGAGCGTACATTGGACCAA
Long Flanking Sequence:
AGATCAGAACAAGTGGAACCGGAGAACACTGAACTCACAAGCTTGAGCCATCTATACTTTCATTAATTAGCACTTTAGATGAAGCTTTTATAAAAACATTAAACTTTTTTGGGGGGAGTCAGCTCACTATTTTAATCTTAAATCAGCAGTACCAGCACAAAACGCCTAGCAAGATGTCTTATAATTATCAAGAAAATACTTTTTGTCAATTTCACACAAACTGACATCCCTCAGACTATTTATATTTTCCTGATTTTGAGTCATGAGTTACAGACCTCTGACAGATAGGTAAACTATGGATTCATGTTGCCAAGACAGGAATAGCCTTTAATATTATTATTGTGACCATGCAAAATCAAGTTTCAAGTTGTATAGTGGTAGCTGGTAGGCTACCTATAAGTAGAAGGGAATCTGCTGTCTATTATTCTGACACTTTCTTTATTTGGTCATTTTGTGGCTTGTCTGAGTTTCACTAACAACTTTATCACCTGTGTAATTTC[A/T]GAATAAGGAGACCAAATGGGTGGATCTGGGAGGAGCGTACATTGGACCAACTCAAAACCGCATTCTAAGAATAGCCAAACAGTATGGGGTGAAAACATACAAAGTCAATGAAGAGGAGTCTCTTGTTCATTATGTGAAGGTAAACCTCAGTAGAGATACACACACATTATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTGTATTGTATTGTATTATATTATATTATATTATATTACATTACATTACATTACATTACATTACATTACATTATATTATATTATATTATATTAGTTGAAGTCAGATTTATTAGCCCCCTCTGAATTATTAGCCTCCCTATTTATTTTTTCCCCAATTTTTGTTAACGGAGAGAGGATTTTTTAAACACAATTCTAAACATAATATTTTTAATAACTCATTTCTAATAACTGATTCATTTTATCTTTGCCATGATGACAGTAAATAATATTTTTCTAGAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34685
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 |
---|---|---|---|---|---|
ENSDART00000028225 | Nonsense | 120 | 522 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 9 (position 34637376)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 33870404 |
GRCz11 | 9 | 33679589 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCCTCCCATGTGGAACCCTTTTGCCTACATGGACTACAACAACCTCTG[G/A]AGGACAATGGATAAGATGGGAATGGAGGTAAAGGATATTTTTATTTAGCT
Long Flanking Sequence:
TGCTGTTTGCCAAAGACCAATATTGTCATTATCTGTGATTATGAATTTCCTTTTTATTGCATTAGCCGTTATCGGTTACGTCTATTTATAGGGTCTCTATTATCGTTCTTGTATAGTATATTCTACCCCAAATGAGCATATATCCAAAGATAATTGTCAGTTTTTTTAATAAGGTCAAGTTGTTTCTGATCTTCTATTAATGCAAACAGTAAAGGCCTTCCATTAACTGCAAGCCAGGCGAAAATGCAGTTACGTATATTTTAGGCAGTAAAAACTGTTTTCCATTCCAGACTGGTTACACGTCTAATGATAATGAGGTCATGGTGGCTATGATAAAGACATTACGTCAACAATGACAAAATAATCCTTTTCATTATTTGCTGATAAGCTGGTAGCTTTCTTACATTGTTTCTTGTTTCCCAGGGAAAGTCATACCCATTCAAAGGGCCTTTCCCTCCCATGTGGAACCCTTTTGCCTACATGGACTACAACAACCTCTG[G/A]AGGACAATGGATAAGATGGGAATGGAGGTAAAGGATATTTTTATTTAGCTCCGTTTAAAAATGTAATCAACTGTTGCCCTGCATACATCAGATTCCTTGGCAATGTTTATTGAATAAGTTGCTTTTGATTTGAAATATTCACCGGATGTTGGGAACAACAACCAAATAAACCCATACTATATGCAAGGAAAATAAACTGATTAGTTTAGAAATGAAGTTATGTGTAATAAAATGAAATGATGAAGGGAAAATAATATTGAACACATGAAGAAAGGGAGGTGTAAAAAGGCAGTGAAAGCCCAGACAGTAGCTGAAATCTCTCAGACGTTATTCAGCAACCCTCTGCCCTTCGTCACTGTAAATGAAAATTATCTGCTTCAGTCCAACATCTACATTAGATGATGAAGATAAAATACATCATATTACCTGGCAATGTTTATTGAACAATAGTTCTGACCAAGAATGAATGGTGTCAATCCTAGTAGTGACAACAAGTGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31732
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 |
---|---|---|---|---|---|
ENSDART00000028225 | Nonsense | 229 | 522 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 9 (position 34633206)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 33866234 |
GRCz11 | 9 | 33675419 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCGGTGCCAATCAGATCAGTGAGGGGATGGCAAGAGAGCTGGGTGAT[C/T]GAGTGAAGCTAAGCAGAGCTGTGTGCAGTATTGACCAGACTGGAGACCTG
Long Flanking Sequence:
TGATTATGTAACATACTAAAATAGTGGCCACTGTATCTGGGTCACATTTATAGCAGGAGTCTCCTAGCAAATGTGGCATTTGAGGGTGCACAAAAAACAGTTTTGTATAAGCTGGTGATAAACTGTTGCTTCTTTTATGATGGGCTTCCTATATGATTAATGTCATAAATTCTCAGAGCCTGTTTGTCTTCCTTAACTTGCTTTATATTCTTAACTTGTGTGATAAAGGCATGTGCATAGTGGCCAATATTATACAACTGTGTCAAAAAGCTCTTTTTTTAATAAACAGAGACCCCTCATGGTGAATTAAAGAACTGCAGTCCTTATCAAAGTGTAAATATCTGTTTAAATGAGTGTGAAACTGATCAAACCTTTTACATTCAATGTAGTTTTACACATAACCCTGAAAAACGTCTTATCTCTCAAAAAAATGACAGGAGCGCAAGTTTGCTGGCGGTGCCAATCAGATCAGTGAGGGGATGGCAAGAGAGCTGGGTGAT[C/T]GAGTGAAGCTAAGCAGAGCTGTGTGCAGTATTGACCAGACTGGAGACCTGGTGGAGGTCAGGACGGTGAATGAGGAGGTTTACAAGGTGAGAAGACGCATATAAACTCATATATGGCTGACTACTACTGCTTAATGTATTTTTTGCACTACAAAACTTGTCAGGAAGGCTGTATTTAGAACAAGAACTAATTCTTGACATATTAAATGACTTAACTTAACTCTCTCTCAGAGTTAAACAGTTTTATTGTGCCATTTTTGAACCCATTCAGCCAGTCGCTGTGTCTGGCGGGAGCCCACTTAGCTTAGCATAGATCATTGCATTGGATTGTACCATTAGCATCTTGTTCATAAATTATGAAACAAAGAGTGTGAAGAATGACTCTTCTTTATAGTTAAATAGCAATTGACAGAAATTGCTATTTTCTACAGCAATATGGCTAGGAACTATACTATCATTTTGCCGTAATAATTAAGAAACTTTGCTGCTGTGCCATGGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21527
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 |
---|---|---|---|---|---|
ENSDART00000028225 | Essential Splice Site | 361 | 522 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 9 (position 34626783)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 33859811 |
GRCz11 | 9 | 33668996 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCTGGCACGAAAATCACGGAAGCTGGCAAATCTGACGAGGGATGAAAG[G/A]TAGATTTTTATTTCTTCACATATTATTAAATGTCACTATACTGTGATGTT
Long Flanking Sequence:
GCATGCTAAGCTGGGCTGTTTTGCTGTTTTTTTCAGGATACTGTGGCAGCATGGTGATCGAGGAGGAAGATGCACCTATTGGTCTCACACTAGACGACACTAAGCCTGATGGGTCTGTGCCTGCTATAATGGGGTAAATAAATTGCGTTTTTATTGCAGAATAAATGTAAGCCACTAACAAAATGATAGACACAAAAGTAATGCTCGGTTTAGGCAACACAATATATTAGTTTATGATAGTCACATTGTCTATTCATAAATTACTGTCATTTTAAGGCCCTGAAATGCATGATGTCATCGAGGAGGTGGAACTAACAAGGACTGACTAAAGCATCAAATAATGACTAAAGAAGCAGTGTATTTTGTATTTTAAAAAAGACTCAGCAGGCTCTGACATTAAAATGGTGTGGTCTGAATCTGACATAAGCTGCTTCTTTCTGTTTTAGTTTTATTCTGGCACGAAAATCACGGAAGCTGGCAAATCTGACGAGGGATGAAAG[G/A]TAGATTTTTATTTCTTCACATATTATTAAATGTCACTATACTGTGATGTTATGCTTACCTGAATGTTATTTCTGCCAGAAAGAGAAGGATCTGTGAGATTTATGCTCGTGTCCTGGGATCAGAGGAGGCGTTATATGTGAGTCTCGATTTCCAGAAATCTTCATTTAGTCTTGAAATGTTTCATTCTTTATTTTCATGGCTGTCTCCTTCTCAGCCTGTGCACTATGAGGAGAAAAACTGGTGTGAGGAGGAATATTCTGGTGGCTGCTATACCGCCTACTTCCCTCCCGGTATCATGACACAGTTTGGCAGGTTAGTGCAGCATCTCTTGTTCGGTATTGTTTTCTCTATCCTGCTTTTGCTGAGTAACCTAGAGCATGAGTTGATACGAGGACTCACTGTTATCTGGATTTCAGGGTCTTGCGGGAGCCGGTGGGCAGGCTGTACTTTGCAGGAACTGAAACGGCCACAGAGTGGAGTGGTTACATGGAGGGGGCCGT
Associated Phenotype:
Not determined