ZMP
fmo5
Ensembl ID:
ZFIN ID:
Description:
flavin containing monooxygenase 5 [Source:RefSeq peptide;Acc:NP_944592]
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 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17238 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17238
Status:
Available for shipment
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Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034011 | Essential Splice Site | 395 | 560 | 7 | 9 |
The following transcripts of ENSDARG00000016357 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 15102331)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 15196967 |
GRCz11 | 20 | 15096470 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGCCCATCTCTGAGATGCAAGCRCGYTGGGCCACACGTGTTTTTAAAG[G/A]TATCAAACATGATGYTGATACACAGAAAAATACAGAAMGTTTTTAATACR
Long Flanking Sequence:
AGGTACTGTGAATACTGAAGAACAATATTTACATCCCATTGGTTAGTCTCAGTATTTGTACTTTTTCATGATGTTATCTTTTTTATGTTTTATTATCTGCCCTATTCAACATGTATTATATTACGTCTGTTGCTAATTTATCAGGTTTTTCAGCCAACATCCCATGGTCAATGATGATTTGCCAAACCGGATCCTCTCTGGTACTGTCTCAGTCAAGCCCAATGTGCAGGAGTTTCGTGGATCTAGTGTGGTGTTTGAGGATGGCACTGTTGAAGATAACATTGATCTGGTGGTGTTTGCCACAGGCTACACTTTCTCATTCCCCTTCCTTTCCTCACATGTGATCCCTGTTTCAAACAACAAGGTATCCCTGTACAAATTTGTATATCCTCCAGGATTGGAGCGCTCAACTTTAGCAGTGATTGGTCTGATCCAGCCTCTTGGAGCCATTATGCCCATCTCTGAGATGCAAGCGCGCTGGGCCACACGTGTTTTTAAAG[G/A]TATCAAACATGATGTTGATACACAGAAAAATACAGAAAGTTTTTAATACGTTATATGATATATTTCAAGCATATTTAAAATCCTCTACTTGATTTCTGGTTCATAAAAAGCCACTGCTTTAGAAAAATCAGGCCATACCAACTAAGGGAATGCTGAACCAAGAGCCAGCAATAAAATCCTTTGTGCTAGGTTCACACCAAATGCAGAATTAAGTATTCACATGAGTAAGGTTCAAACAAAATCAATGCAACACATGGAATTCAGCTCAATCACGTCACAAGTAAAGGCCAATCATGTTGGCCAATCAGAAAGGAGCATTGGTGTACACACTGACCAAGCGGCAACCTCCCGCTTTCCCTCAGGAAGCCAATACGGAAGTAACTAAAACTGCAATTCATCCAAAATTCCGCTAGTCCTGGCCGCTCTTGGCTTGAGCAAATTTCAATTGAGCCCACTGTTAGAATGGCCAACTTTACAGCAGAAAAAAAGGTGTTTACAGC
Associated Phenotype:
Not determined