ZMP

miox

Ensembl ID:

ENSDARG00000002764

ZFIN ID:

ZDB-GENE-050913-113

Description:

Inositol oxygenase [Source:UniProtKB/Swiss-Prot;Acc:Q4V8T0]

Human Orthologue:

MIOX

Human Description:

myo-inositol oxygenase [Source:HGNC Symbol;Acc:14522]

Mouse Orthologue:

Miox

Mouse Description:

myo-inositol oxygenase Gene [Source:MGI Symbol;Acc:MGI:1891725]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa6497	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa4738	Nonsense	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa6497

Status:

Mutation detected in F1 DNA
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
ENSDART00000019831	Essential Splice Site	2	278	2	10
ENSDART00000140752	Essential Splice Site	7	283	2	10

Genomic Location (Zv9):

Chromosome 18 (position 5828041)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	6783142
GRCz11	18	6742104

KASP Assay ID:

554-4896.1 (used for ordering genotyping assays)

KASP Sequence:

TGGAATCTATTAGCCAGTTTTCTTACACATTCATGTATTTTTTTACTCAC[A/T]GGGTCCAGACCCCTCTTTGGCATATCGACCTGAATGTCATGAGAAAGACA

Long Flanking Sequence:

CAGATCATACTACGCATTTCCCATGTCATGTAGTAACTGTTATTCAATTATTTCCTTAATAATACAAATAAAATAATAAAAAATAAAATCAAAACACAAGTCAAAATCATCTTAATCTTTAGAAAAGAAAAGTTTTTTTTTTTAATGAGCAAAATGAACTGTTCTGAAGCAGACTGCTCTATATGGGTCACAATAAGTCTGACGGACCCCTGGAATCCTGAGAAAGAAAGTAAACTGGGGAAAGTTAAAGAGTTACTAGTAATGTCGACTACAGTTCAGAGAGCTCATATAAGCACCATTGATAAACCCTGAGTGCTGACAGACACAAAACACACAACATCATCAACCACACTGAAGCACAGCTCAACATGAGGGTGGTAAACATGGTACGTACCTCACATTCACTTCATTTACATTACATGCATGTTTCACAATCCTTTTCTTCAATAATGGAATCTATTAGCCAGTTTTCTTACACATTCATGTATTTTTTTACTCAC[A/T]GGGTCCAGACCCCTCTTTGGCATATCGACCTGAATGTCATGAGAAAGACAAAACTGAATTTAGGAACTTTGAGGTCAAATTTAAATCTTTGAAATTTGCATATTCATGAATAAATCATGACTCTAATCTCATCTTTATGTGTATTTGTTTAATTCAGAATGGAGATCTGTTCGACCGAGTGTTTAACACATACAAGCTGATGCACACACACCAAACGCTGGACTTTGTCAAGCAGAAGGTTGGTACTTCAGTATATTATACACTACTGTATAATAAAGCTGCACGGTATTGGAAAAATATGATATTGCGATATATTTGTTTTCTGTGATACACATTGGGATATGAATATAATTTCACCAGGTGATCTGAACAGCCATTTGGAAAGATTGCAATCATTTAGACAGATTAGAATGATCACATCTTTATCTTTGCATAAATTATAATGAATTACAAGCATATATAAACACTAAGATAAAAGTGAAATAAACAGTGCTTGATGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa4738

Status:

F2 line generated
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
ENSDART00000019831	Nonsense	108	278	5	10
ENSDART00000140752	Nonsense	113	283	5	10

Genomic Location (Zv9):

Chromosome 18 (position 5822907)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	6778008
GRCz11	18	6736970

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGCTACTAAATTTAAAATCGTTTCTCTCATTTTCCTCTGTCTCTAGACTG[G/A]TTTCAGCTAGTTGGTCTGATCCATGATGTTGGAAAGGTCATGGCCTTGTA

Long Flanking Sequence:

CATGTTTAGAAATGTGTAGAAAAAAATCTTCTCTCTGTTAAATTGCTAAATTGCTTAAACTGCTAAATTTCCCGTAGTATATGTATGTGAATGAGAGTGTATAGGTGTTTCCCAGTGATGGGTTGCAGCTGGAAGGGCAACCGTTGCATAAAACATATGCTGGATAAGTTGTTGGTTCATTCAGCTGTGGCGACCACTGATTAATAAAGGGACTAAGCTGAAAATAAACTAAAAAAATTAATTAATATTACCTTATTTGTATTCTTTTTCTATATTATTTTAATTGGGGATGGGGTGGTTGGAAGGACTTGTCAAATGTAAAACGTTTGCTGTGTGTACATGATTGTTTAAAACTGTGTAACCTGTAATAACATGAAAAACGAAAAAATGTATTGTACTACTACTACTACTACTAATAATAATAATAATAATAATTAAAAAATCCCAAGAAGCTACTAAATTTAAAATCGTTTCTCTCATTTTCCTCTGTCTCTAGACTG[G/A]TTTCAGCTAGTTGGTCTGATCCATGATGTTGGAAAGGTCATGGCCTTGTATAGCGAGCCGCAGGTAAGACATGAATGCAGCCAATCAGTCTAATAAGCTTTGTCAGTTGACTCATGGGTTGCAGGGCTGCACAATTTGGAAAAAAAATTGACATTGAGATATCTTATTTTTCTGCAATACATATTGCAATAATTTCACCAAATGAGTTAAATGGCTTAATTTGGAAAGAGTTTACAAGTTTAGACTGATTGGGTTGGTTTGTAGACCAGTATATCTGCATAAAATATAATAAACCAATCGCAAGCACTGATAAATACAGTAGCAAAGATAATAAGTAAAGTTTTATAAACGAATTTTGAGAGAAGCACGTGCTATGATTGATCATGGCTGGTTTCTTATCTGTAATCATCGATAAACCAATCAGTTGAATTTAAGTCTACAATAAATAGCCCGTTTCGCCTTCCTTTTTCTTTGTTTTTTTAAGAATCCCCTGTCCACCC

Associated Phenotype:

Not determined