ZMP
fbxo25
Ensembl ID:
ZFIN ID:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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