ZMP
zgc:77439
Ensembl ID:
ZFIN ID:
Description:
dimethylanaline monooxygenase-like [Source:RefSeq peptide;Acc:NP_001184218]
Human Orthologues:
FMO1, FMO2, FMO3, FMO4, FMO5, FMO6P
Human Descriptions:
flavin containing monooxygenase 1 [Source:HGNC Symbol;Acc:3769]
flavin containing monooxygenase 2 (non-functional) [Source:HGNC Symbol;Acc:3770]
flavin containing monooxygenase 3 [Source:HGNC Symbol;Acc:3771]
flavin containing monooxygenase 4 [Source:HGNC Symbol;Acc:3772]
flavin containing monooxygenase 5 [Source:HGNC Symbol;Acc:3773]
flavin containing monooxygenase 6 pseudogene [Source:HGNC Symbol;Acc:24024]
flavin containing monooxygenase 2 (non-functional) [Source:HGNC Symbol;Acc:3770]
flavin containing monooxygenase 3 [Source:HGNC Symbol;Acc:3771]
flavin containing monooxygenase 4 [Source:HGNC Symbol;Acc:3772]
flavin containing monooxygenase 5 [Source:HGNC Symbol;Acc:3773]
flavin containing monooxygenase 6 pseudogene [Source:HGNC Symbol;Acc:24024]
Mouse Orthologues:
Fmo1, Fmo2, Fmo3, Fmo4, Fmo5, Fmo9, Gm4846, Gm4847
Mouse Descriptions:
flavin containing monooxygenase 1 Gene [Source:MGI Symbol;Acc:MGI:1310002]
flavin containing monooxygenase 2 Gene [Source:MGI Symbol;Acc:MGI:1916776]
flavin containing monooxygenase 3 Gene [Source:MGI Symbol;Acc:MGI:1100496]
flavin containing monooxygenase 4 Gene [Source:MGI Symbol;Acc:MGI:2429497]
flavin containing monooxygenase 5 Gene [Source:MGI Symbol;Acc:MGI:1310004]
flavin containing monooxygenase 9 Gene [Source:MGI Symbol;Acc:MGI:3606068]
predicted gene 4846 Gene [Source:MGI Symbol;Acc:MGI:3643319]
predicted gene 4847 Gene [Source:MGI Symbol;Acc:MGI:3643320]
flavin containing monooxygenase 2 Gene [Source:MGI Symbol;Acc:MGI:1916776]
flavin containing monooxygenase 3 Gene [Source:MGI Symbol;Acc:MGI:1100496]
flavin containing monooxygenase 4 Gene [Source:MGI Symbol;Acc:MGI:2429497]
flavin containing monooxygenase 5 Gene [Source:MGI Symbol;Acc:MGI:1310004]
flavin containing monooxygenase 9 Gene [Source:MGI Symbol;Acc:MGI:3606068]
predicted gene 4846 Gene [Source:MGI Symbol;Acc:MGI:3643319]
predicted gene 4847 Gene [Source:MGI Symbol;Acc:MGI:3643320]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20942 | Nonsense | Available for shipment | Available now |
sa20941 | Nonsense | Available for shipment | Available now |
sa40892 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10179 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20942
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 |
---|---|---|---|---|---|
ENSDART00000057288 | Nonsense | 38 | 449 | 2 | 8 |
ENSDART00000140817 | Nonsense | 42 | 229 | 2 | 6 |
ENSDART00000146440 | Nonsense | 38 | 225 | 2 | 6 |
ENSDART00000146935 | Nonsense | 38 | 225 | 2 | 6 |
The following transcripts of ENSDARG00000039211 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 27432096)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26035035 |
GRCz11 | 7 | 26306228 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCGTCACCTGCTCTCCCGCCCGGACACCTTCGCGGCGCCGGTGGTCTA[C/A]GAGCTCACCAAGAACATCGGAGGAACCTGGGTCTATGAGGAAAAAGTGGG
Long Flanking Sequence:
ACATTTCTCTCTAAATAGGTACAAAAAAACAAACAGTTTTAAATTAGTATTAATTTATTTATTATTATTTTTTTTTTTTGCAATGAAAAAGAAGTGCCATCAAAGCACAAAGGGTTAACATGATTGAGCTGCCGGTGAGCTGGACAGATTCCAGCGCGCACTCGATAAAATTAGCGGAGTATTGAGTCTCGTCCGCTTTGAGAGACTGACGGATCCCGGTGCTGGTGGTCGTCCGAGGACAGCTGTAGAGACCAGCTTCATATCCTACAGTATGCGGGATTTAAAATCACTGTGATCTGCCTCCACCCAGACTGGTTTAACCAAAGTGTTTTTCGTCTGTTTTGACAGGTGTCAACTTTCCGTTTCACACCCGTAGTGTGCTGTACAATGCCTGGCGTAAGGAAGCTGCGTGTGGCTGTTATCGGCGCCGGTGCTGCGGGACTCTGCGCTGCCCGTCACCTGCTCTCCCGCCCGGACACCTTCGCGGCGCCGGTGGTCTA[C/A]GAGCTCACCAAGAACATCGGAGGAACCTGGGTCTATGAGGAAAAAGTGGGACACTATGAAGATGGCTCACCGATTCACAGCAGCATGTACAGAGACCTCAGGTGAAATGTTCAGGGCCAGCATTTATCTCTTTATATGGTGGTTGTAAGTGAAATAGTTAGTTTTATTGCACAGTAATAAACACACTGCATGATATATGGATATAAAAAATGTAAGTTATGAATAAAACATTAAGTATGTGTAAATGATTATGGTTGTATACAGTTGAAGTCAAAATTATTAGCCCGCTTTGATTTTTTTAAAAATTATTTTTAAATATTTCCTAAATTATGTTTAACAGAGCAAGGAACTTTTTACAGTATGTCTGATACTATTGTTTCATCTGGAGAAAGTCTTGTTTGTTTTTATTTTGGCTAGAATAAAAGCTGTGTTTATTAAAAAAAAAAAAAACATTTAAAGGGCAATATTATTGGCCCCTTTAAGATATATTTTTTGATTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20941
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057288 | Nonsense | 148 | 449 | 4 | 8 |
ENSDART00000140817 | Nonsense | 152 | 229 | 4 | 6 |
ENSDART00000146440 | Nonsense | 148 | 225 | 4 | 6 |
ENSDART00000146935 | Nonsense | 148 | 225 | 4 | 6 |
The following transcripts of ENSDARG00000039211 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 27430598)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26033537 |
GRCz11 | 7 | 26304730 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGGATGGGTGGAATGGTTTGGCATGGAACGTCACCTCAAATAATGGCT[T/A]AGACCACAGCAAATCCACTACAGAGCGCTTTGATGCTGTCATGGTGTGTA
Long Flanking Sequence:
TTTGTTTTTCTCGCTTTACAGAACCAATATTCCCAAAGAGGTGATGTCTTTCCCTGACTTTCCTTTTGCAAAACACCTCTCTTCTTTCGTCCATCACACCGAGGTACGAAAGTACCTTGAGCAGTACTGTGATCATTTTCGCCTTCGGGACTACATACAAGTGAGAAACAACACATTTCTCATTTCTCTCTCTCTCTCTTTTTAATCTCACCTGGTTGTTCATGTTCATGCTATTTTCCAAAGTTTTGATAGATAATCATTAATTGTGCTGTTTATGACCAGTCAGAAATCACACACCTTATCTTTATGGTATATTCACTGATGGTCTACGGGAATTGTGGAAAATTACTAGAGAGTTAGTGGATACTTGTATACAAGAGTATTAATTTGTGTAATTCTTTCTGCCACCAAGTTTGGGACCTCAGTGGCCTCAGTGAACCCAGTCTCTGTGAAGGATGGGTGGAATGGTTTGGCATGGAACGTCACCTCAAATAATGGCT[T/A]AGACCACAGCAAATCCACTACAGAGCGCTTTGATGCTGTCATGGTGTGTAACGGGTAAGTGCTCAGCAACAGGCAGAAAAGCTTCCTACATTGCACTATAGTTAAAATGTACATGCCTGGATCAATAAGGACATCGGGTACAGGAGATTAAACAGTAACTAATGATGCAATGAAACTATACTGCACTTTCACTCAAATACTGTGCCAGCTGTCCTGGGTATGATTCTATTATATAATAAAAGGAGATCATTTTTTACAAATTGAGTTTTACAAATGACTTTTGTGTGTTTATTGCAGACATTTCTATGACCCTTACATCCCTGCAATACCTGGACTGGAGAAATTCAAAGGTTTTTGCTTTCATGTATTGCGTAATAGGCTCTTGCTGTTCCAGAGTCAATCAAAAGAATCTGATGTCTTGCGAACCAAGTATCTGTGTGCTTAGCGGCAAAACAACTTCGATATGTGCTGAGACTTGCAGATTCCTAAAGCTGTAATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40892
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057288 | Nonsense | 169 | 449 | 5 | 8 |
ENSDART00000140817 | Nonsense | 173 | 229 | 5 | 6 |
ENSDART00000146440 | Nonsense | 169 | 225 | 5 | 6 |
ENSDART00000146935 | Nonsense | 169 | 225 | 5 | 6 |
The following transcripts of ENSDARG00000039211 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 27430291)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26033230 |
GRCz11 | 7 | 26304423 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAATTGAGTTTTACAAATGACTTTTGTGTGTTTATTGCAGACATTTCTA[T/G]GACCCTTACATCCCTGCAATACCTGGACTGGAGAAATTCAAAGGTTTTTG
Long Flanking Sequence:
TGGTATATTCACTGATGGTCTACGGGAATTGTGGAAAATTACTAGAGAGTTAGTGGATACTTGTATACAAGAGTATTAATTTGTGTAATTCTTTCTGCCACCAAGTTTGGGACCTCAGTGGCCTCAGTGAACCCAGTCTCTGTGAAGGATGGGTGGAATGGTTTGGCATGGAACGTCACCTCAAATAATGGCTTAGACCACAGCAAATCCACTACAGAGCGCTTTGATGCTGTCATGGTGTGTAACGGGTAAGTGCTCAGCAACAGGCAGAAAAGCTTCCTACATTGCACTATAGTTAAAATGTACATGCCTGGATCAATAAGGACATCGGGTACAGGAGATTAAACAGTAACTAATGATGCAATGAAACTATACTGCACTTTCACTCAAATACTGTGCCAGCTGTCCTGGGTATGATTCTATTATATAATAAAAGGAGATCATTTTTTACAAATTGAGTTTTACAAATGACTTTTGTGTGTTTATTGCAGACATTTCTA[T/G]GACCCTTACATCCCTGCAATACCTGGACTGGAGAAATTCAAAGGTTTTTGCTTTCATGTATTGCGTAATAGGCTCTTGCTGTTCCAGAGTCAATCAAAAGAATCTGATGTCTTGCGAACCAAGTATCTGTGTGCTTAGCGGCAAAACAACTTCGATATGTGCTGAGACTTGCAGATTCCTAAAGCTGTAATTCTGTTACTGTTGCAACATGTTATCAGTCTATCAGATCGGTGGTCTACTGAGAAATGCTTTTGAAAGAAGCTTAGCTCTGGTTGGGAGTAGACCCAATTTTGGTTAATCATTATTATATTACTTCACATTTAACAGTGAGCTAATTGTGTTTATATACAGGTTAAGTCAGAATTATTAGCCCCCCTTTGAATTTTTTTCCTTTTTTAAATATTTCCCAAATAATGTTGAACAGAGCAAAGAAATGTTCACAGTATGTCTGATAATATATTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTCCGACTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10179
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 |
---|---|---|---|---|---|
ENSDART00000057288 | Nonsense | 298 | 449 | 7 | 8 |
ENSDART00000140817 | None | None | 229 | None | 6 |
ENSDART00000146440 | None | None | 225 | None | 6 |
ENSDART00000146935 | None | None | 225 | None | 6 |
The following transcripts of ENSDARG00000039211 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 27426637)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26029576 |
GRCz11 | 7 | 26300769 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATTCCTAGATGAGAAAGTGGGTGTAAAAGTGCAGGAGCACCTTGTCTG[G/A]CCCCTCTATAAGTTCCTAATTCCTCCAGCCTACCCGTCCCTCTTTATTGT
Long Flanking Sequence:
TTTTGGAAATATTTAAAAAAGAAAAAAACTCAAAGGGGGCTAATAATTCTGACATCAACTGTATGTATAATAGCAGTGTTTCTCAACCACATTCCTGGAGGACCACCAGCTCTGCATGTTTTGGATCTCTCCTTTGTCAGTCACATACATTACAGGTCTTTCAGTCTCTGCTAATGAGCTGATGATCTGAATCAGGCACAGAGCTGGTGGTCCTCCAGAAACATGGTTGAAAACAATATTATAGTACACTAATAATAGAGATGAATCATTATTTGTCTCCAGGTGATTTTGAGTCATGGACAGAAGCCTTTGACATGTCCTCTTCCTCCTGGAGTCCAGCAGGCTCCTCCGGTCACCTCTGTGCTGGACGATGGCACTCTGGAGTTCAAAGATGGCAAGAAGGCCAATCCAGAAGTGTTCATGTTTTGCACTGGCTACAACTTCACCTTCCCATTCCTAGATGAGAAAGTGGGTGTAAAAGTGCAGGAGCACCTTGTCTG[G/A]CCCCTCTATAAGTTCCTAATTCCTCCAGCCTACCCGTCCCTCTTTATTGTGGGCATCTGCAGAGCCATATGCCCTTTCCCACATTTCCACATTCAGGTTAGTTAACTGAGTTCACCAACAATTTATTATTTTGCTTTAAGTTGCTTTAATTTTGCTTTAAGTAGCTTTAAATAAAACAAAATCCTGACTTTTTCCCCCAGTCTCAGTTTGTCCTGTCAGTGTTGGATGGTTCTTTCCGTCTGCCATCACGTGAAGATATGGAGAAGGATATCGAGCTGGACATTGCTGCCCGTCGGGCCCGTGGAATCGCCACCCGTCATATTCTTAAACTGGATTCAGAGCAGTGGGCCTACAATGACGAGCTCGCCCATCTCGGGGGGTTCAAGCCCCTGCCCCGCTACTGGAGCAATTTGTACGAATCCAACAAGGTGTTTCGTGCCCGAGACATGCTCAATTACAAGACCCACAACTTCACTGTCCTCGATAACATGGAGTGGAAG
Associated Phenotype:
Not determined