ZMP

fbxo25

Ensembl ID:

ENSDARG00000075172

ZFIN ID:

ZDB-GENE-040801-19

Description:

F-box only protein 25 [Source:RefSeq peptide;Acc:NP_991287]

Human Orthologue:

FBXO25

Human Description:

F-box protein 25 [Source:HGNC Symbol;Acc:13596]

Mouse Orthologue:

Fbxo25

Mouse Description:

F-box protein 25 Gene [Source:MGI Symbol;Acc:MGI:1914072]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa11687	Essential Splice Site	Available for shipment	Available now
sa37763	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa11687

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
Order Allele From EZRC

Mutation:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000113643	Essential Splice Site	157	356	6	10
ENSDART00000138660	None	None	150	None	6

Genomic Location (Zv9):

Chromosome 23 (position 35531389)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	35380981
GRCz11	23	35479895

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCTGCTCAGAAGAACTACTTTAACGTTCTGGAGAAGATTGTGAGGAAAGG[T/G]GAATGAACAGGTGTTACTCGCATACAGTTGAAATCAGAATTATTAGCCCT

Long Flanking Sequence:

ATTATTCCTTTAATAGTATAATATATATGGATTAATTATATTTTATCTTTTTTTTTTATTCAGTTTTGTTCCAGGAGAGGTGGATCTATGTTCAAAAAGAGAGTACAAGAGAGGTGAGAAAAAATATATCATAGCATAACAAGTACAAAAAGCAGCTAAAAATACAACACGAGTTAACCAGTTTTGAATGTGAACCATGTGTTTGTTTTTGCAGAGACATGGGTATTGTACGCTTGGTGAGGCCTTTAATCGTCTGGACTTTTCCAGCGCCATTCAGGATGTGCGGCGATTCAACTATGTAGTTAAAGTAAGAAGTTGTCATCTCTGCTGAACAACTGCATTTCAATAACTTTCTTTTCTTTCCATAATAATTTTTTCTCACTTTACCTTCTGTTTCCAACTCAGCTTCTGCAGCTGATTGCCAAATCCCAGCTGACGTCTTTGAGTGGAGCTGCTCAGAAGAACTACTTTAACGTTCTGGAGAAGATTGTGAGGAAAGG[T/G]GAATGAACAGGTGTTACTCGCATACAGTTGAAATCAGAATTATTAGCCCTCTTGTGGTTTTGTAATTTCTAAATTATGTTTAAATTAAAGGAAATTTTCACAGTATGTTCTATGATATTTTTACAAAGTCTTATTTGTTTTATTTTCGGCTAGAATAAAAGCAGTTTTACATTTTTTAAAAACCGTTTAAGGTCAATATTATTAGCCCTTTAAAGCAATACCGTTTTTCGATTGTCCACAGAACATACCATAATTATACAAATAACCTAACTTGCCTAATTAACCTAGTTAAGCCTTTAAATGTCACTAAGCTGAATACTTGTATCTTGAAAAGTATCTAATAAAATATTATTTACTGTCATCATGGCAAAGATAAAAGAAATCAGTTATTAGAAATTTGTTATTACACCTACTGTATTATGTTTACAAATGTGTTGAAAACATGTGTTCTTCTTTTCGTAATCAGAAATTGGGGAAAAACATTTACAGGGGGCTAATGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37763

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000113643	Nonsense	231	356	8	10
ENSDART00000138660	None	None	150	None	6

Genomic Location (Zv9):

Chromosome 23 (position 35528288)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	35377880
GRCz11	23	35476794

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTTTGTGTGCAGCAAGTTTCAAACGGGATGACACTGAGCGACCTCCCTT[T/A]GCACATGCAAACCAACATCCTTTACCAGTTTACCGATGCCTATGACATCA

Long Flanking Sequence:

TGCATAATTACCCTAAGCTGCCTAGTTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGTGTCTTGAAAAATATCTAGTCAAATATTATTTACTGTCGTCATGGCAAAATATGGGCGAAGCAGTGGTGCAGTAGGTAGTGCTGTTGCCTCACAGCAAGAAGGTTGCTGGGTCGCTGGTTCGAGCCTCGGCTCAGTTGGCGTGTCTGTGTGGAGTTTGCATGTTCTCCCTGCGTTCGCGTGGGAGAACCAACTCACAAAATCTCAAAAATATTTGCATAGAGGTAGCTAACACATGTTACTATGAGCTATTAGATATGCCTGTGTTATTTACATGCACACACACACATGCTATCTCTTGCACATTTTCTTTTCTTAAACTGATATAATTTCACATCATGAATTCATTTTGTATTCATCTTCAGTTTATATTTACATACCTCATGCTGAATCTGTTTGTGTGCAGCAAGTTTCAAACGGGATGACACTGAGCGACCTCCCTT[T/A]GCACATGCAAACCAACATCCTTTACCAGTTTACCGATGCCTATGACATCATCAATCTGGGACAAGCCACGCCAACGCTGCAAATGCTCAGCGAGGACCGACATCTGTGGAAGAAACTGTGCCAGTTTCACTTTGCTGAAAAACAGGTGAGGACTAAGTATCCTGTTAATTACTAATTGTACTGATTTTTTAATTAGAAAACACTGTTATAATTACCATCAAACACAATATCACATGTCCACGCAGGCAGTATCAGTGGTTTCTATATTTTTCAAGATTTTAAATTGTAGCATTGTCAAATAAAAGTATTTATATTTGATAGCTTGAAGCACTTTGTTTTGGTGATATGGCTTCACCAGTCTGCCACGCTATAGTTGCACTTTGTTAAATGAGCCGCTGTAAACTGGATAAATTAACACTTTCATGCATAAATGAACAGTTAAATGTTTCAGGTTTTATCTGATTAAAGATGCGGCAAGTCAGAACAGAGAATTCAGCACT

Associated Phenotype:

Not determined