mao

Ensembl ID:
ENSDARG00000023712
ZFIN ID:
ZDB-GENE-040329-3
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]
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]

Alleles

There are 4 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa21528 Essential Splice Site Available for shipment Available now
sa34685 Nonsense Mutation detected in F1 DNA During 2016
sa31732 Nonsense Available for shipment Available now
sa21527 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa21528
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Essential Splice Site
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
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TTTGTGGCTTGTCTGAGTTTCACTAACAACTTTATCACCTGTGTAATTTC[A/T]GAATAAGGAGACCAAATGGGTGGATCTGGGAGGAGCGTACATTGGACCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34685
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
G > A
Consequence:
Nonsense
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
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TTCCCTCCCATGTGGAACCCTTTTGCCTACATGGACTACAACAACCTCTG[G/A]AGGACAATGGATAAGATGGGAATGGAGGTAAAGGATATTTTTATTTAGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31732
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
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
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CTGGCGGTGCCAATCAGATCAGTGAGGGGATGGCAAGAGAGCTGGGTGAT[C/T]GAGTGAAGCTAAGCAGAGCTGTGTGCAGTATTGACCAGACTGGAGACCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21527
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > A
Consequence:
Essential Splice Site
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
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ATTCTGGCACGAAAATCACGGAAGCTGGCAAATCTGACGAGGGATGAAAG[G/A]TAGATTTTTATTTCTTCACATATTATTAAATGTCACTATACTGTGATGTT
Associated Phenotype:
Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

(GWAS data comes from http://www.genome.gov/gwastudies/.)

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