ZMP

LOC797147

Ensembl ID:

ENSDARG00000075774

Human Orthologue:

FOXJ3

Human Description:

forkhead box J3 [Source:HGNC Symbol;Acc:29178]

Mouse Orthologue:

Foxj3

Mouse Description:

forkhead box J3 Gene [Source:MGI Symbol;Acc:MGI:2443432]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35095	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa41847	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa35095

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115037	Essential Splice Site	425	593	7	11

Genomic Location (Zv9):

Chromosome 11 (position 27175849)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	26004674
GRCz11	11	26242290

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGCAGCACCAGAATCTCTCCCACCAGCAACAGATGCAGTGCAATACTGG[T/C]AAGAGTTCACCATTATGTCTACATTACAACACATTGTTTTTTCTAATACC

Long Flanking Sequence:

AAAAAAGTCTAGATGTGAAAGCACCCTAAAATGCTAATCATCAGGTACTTTAATATGACTACAAACTTCTTAGGCTTTGCTTAAAATGATGTTCTCTGTCTGCTCCTGCCAGGTCTGATGGGTTTGCCCTCGGAGTCATCCCAGCAGACCCACACCTCCTGCTCCTACCAACACTCCCCCAGCAGCCACCCTCACAACAACCAGAACAGCATCACTAACTCGCACCCCAACAACATCCCCAACAATGGCAGTCAGGTGCCCCTCTCCCACCCGCCCCACTCGGCCCACAACTCGCCACACGGACAGCACCTCTCCCAGCATGGCCCTCACAGCCAACACCCGCACACGGCGCACAGCCAGCACCCGCAGCACAGCCAACATCCCCAGCACAGCCAACACAGCCAGCATGGGCACCAGGCCCACGGGCAGCACACGGCACAGCAACAACAGCAGCAGCACCAGAATCTCTCCCACCAGCAACAGATGCAGTGCAATACTGG[T/C]AAGAGTTCACCATTATGTCTACATTACAACACATTGTTTTTTCTAATACCTGATTCTGGCTATGTTTCTGCTAAACTGCCAAGCCATACTTGTAAACATGCTTCCATTCAGATTCTGGCTGAAATTAATGTTAGTAGACAGAATTTGTTTTTCCACAATTTAGAGCTGGGTGATATGACAAAATCACATATCCCCGTAAATGTCATCTTTAGGTGTGTGACAAGATCTTGCAAGACTAAATCGCTATGTGATTTCTCTCCCATGTCCTTACTTGCATCCAGTTGTGAGTGGAGTTTGTCCAGTCAGTAGAGTTTAGCAAAATATTTTGCAGTGTTTGCATGTTCTTTATGGAAAATTTCATTTAAATAGAATTAAAATAACATTCATTACACGATTATTTGAGAAAGCAAAAAAACATTTGTTGAATAAAAATCTATTTTCCATTCATGTTACAAAGTATTTTGCTAATAATTAAACACTATTTTCCTTTTACATATTAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41847

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115037	Essential Splice Site	458	593	8	11

Genomic Location (Zv9):

Chromosome 11 (position 27172556)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	26001381
GRCz11	11	26238997

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CATCGCATCCAACTGCAACTGGTCTGATGTGGATTTGTCTCCCTTCCAAG[G/A]TTATAATTATTCATTTTGAACTAGGTCCACAGAACATAATAAGGGCCCAT

Long Flanking Sequence:

ACAGACTGCCTGTTAAGGTTAATAATTAAAAAAATAATTGAATGTTTAAGTAACTGATGATCAATTTTGGGAATTTGTATAAATTGACATCCATATTCTGAACCTCCTGTCTCGAGGTTTCAGCTCCAGCATTGCCTTGACACGCCGATTTATTCAGGCCGCTTCTAACAATCATTTATTTTGCATTAAGAAATTTATGGCAACTTTGGAGCATTCAGCAGTAAATCACAGGGTGATTTATACAGCTGCTTCTAATGAGAACAAAGCACAGGCAGCACACTTCAGAGAGCTGGCCTGAAGCGGAGGGTTGTGGCGCCCCCTGCTGCTTCAAACAGCAAGTGCACAGATTCGCATGTCTGCTGTGGCCTTCATTGCTGTCTGGTTTTGCCTTGTTGCAGGTCTTCTTAGTGACTGGTACCCCAACCTGGATGCGCTAAAAGAAAGCTGCCGCATCGCATCCAACTGCAACTGGTCTGATGTGGATTTGTCTCCCTTCCAAG[G/A]TTATAATTATTCATTTTGAACTAGGTCCACAGAACATAATAAGGGCCCATAGTAGACGATAATAATATTGCAATAATAATGATAAATGCATTGAAATTATTTTTAATTAAGATCATGTAAATATAAATCTTTAATTGCATTTTTTTATTCATTATTATTATTATTATTATTATTTTCAAATTGACATTTCAGCCTTTGTAAATATTAAACGTAGTAATTAATTCATGCACTTATTTAAATATTTATTTAAATATAGGGTATATGTTTGTTTAAATATTATTATCTAAAAGGTTAAAAAATATTTAGTGATAGACCTGGTGAAGCTTGTTAAATGCAATTACCTTTTTAAATATGAATGATAACTTTTTATGTTGTTTTTATTTTGTTAGTGTAATTAATCAGTAATTATGAATAATTTTCTTGAAACTATGTTTTAAAATAAAGAACATTGCTTAGTCTATAATTACCAACTGTTAAAAAATGGTTTTGATTATCTCAGG

Associated Phenotype:

Not determined