ZMP
LOC799091
Ensembl ID:
Human Orthologue:
FBXO38
Human Description:
F-box protein 38 [Source:HGNC Symbol;Acc:28844]
Mouse Orthologue:
Fbxo38
Mouse Description:
F-box protein 38 Gene [Source:MGI Symbol;Acc:MGI:2444639]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19091 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa39010 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13849 | Nonsense | Available for shipment | Available now |
sa35737 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35738 | Essential Splice Site | Available for shipment | Available now |
sa11788 | Nonsense | Available for shipment | Available now |
sa16333 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19091
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020625 | Essential Splice Site | 322 | 1120 | 6 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 40055532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 38325137 |
GRCz11 | 14 | 38665451 |
KASP Assay ID:
2260-7811.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCACTTGAAGTGGATCTGGGTTACCTCATCATTACTGCTGCTCGCAGG[T/C]AAGTCAGTTTAAAGAACATTATAAACGAAACATTTAGTTTGTTCAGATGT
Long Flanking Sequence:
CATCTCAGTTTGCACCGTGCCTCTGCATTTGGTGTAGACTTGATGTAAATCACCTTTGGAAAGTAACTTTAAGTCATCAGCAATTAAACAATTGTTATGAGTGGCCTATTGAAATCATTCACTTAAACCAGTTTTTTAATAACCGTCAAATTATTTTAATTCTTTAAAATGGACTGAAGTGATTATATTTTTATTATCTAATTCTAGACGATTTTATGTCTTTTTAGAGTGGGAAGCCATGTGTTAGAGAAACAAATAATTGTCAATTTATCCAGAATCCTACAGATCTTCTTTAATGTTGCTTTTTCAATTCCTTTTTTTTCATACATTTAAATATTGTTTTGTCTTTAAATATTTCAAACAAGAAAAGTGTGTGTTCAGTCTGAGACACTTTTGCTCTTCTAGGGGGTTTTCGCAATTTGCACACAATTGTATTTGGTGCCTGTAAAAATGCACTTGAAGTGGATCTGGGTTACCTCATCATTACTGCTGCTCGCAGG[T/C]AAGTCAGTTTAAAGAACATTATAAACGAAACATTTAGTTTGTTCAGATGTTGACAGAATTTACTTTGGTTGTCCAGGTTGCATGAAGTTCGCATCCAGCCTTCCTTAACCAAAGATGGGGTTTTCTCCGCACTGAAGATGGCTGAACTGGAGTTCCCCCAGTTCGAGACTTTGCACCTTGGATATGTTGATGAGTTTCTGTTGCAATGTAAGTCATTTTTATTGTATGTTTGAAAGATCACATTTTATCTTGAGACGCTTTCCCTCGCAGTACCAAAAATTATATTGAATATCAATACTTTTCTTGCTATAAAATCGAAGTTAGAAATTCCACTATGGTGACAGCACTAGTGGGTCTTCAGGTGAATTGTATGAAAGTGTGGAAGATCACATTTTATCTTGTGATAGTTTTTTTTTTTTCGCAGTATCGAAATCGGTATCGAATATTGTTATTTTGCTTGGAACCGTATCGAAGTTACAAATTCAAGATTCTTGACAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39010
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020625 | Essential Splice Site | 365 | 1120 | 7 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 40055740)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 38325345 |
GRCz11 | 14 | 38665659 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGTTCGAGACTTTGCACCTTGGATATGTTGATGAGTTTCTGTTGCAAT[G/T]TAAGTCATTTTTATTGTATGTTTGAAAGATCACATTTTATCTTGAGACGC
Long Flanking Sequence:
CGATTTTATGTCTTTTTAGAGTGGGAAGCCATGTGTTAGAGAAACAAATAATTGTCAATTTATCCAGAATCCTACAGATCTTCTTTAATGTTGCTTTTTCAATTCCTTTTTTTTCATACATTTAAATATTGTTTTGTCTTTAAATATTTCAAACAAGAAAAGTGTGTGTTCAGTCTGAGACACTTTTGCTCTTCTAGGGGGTTTTCGCAATTTGCACACAATTGTATTTGGTGCCTGTAAAAATGCACTTGAAGTGGATCTGGGTTACCTCATCATTACTGCTGCTCGCAGGTAAGTCAGTTTAAAGAACATTATAAACGAAACATTTAGTTTGTTCAGATGTTGACAGAATTTACTTTGGTTGTCCAGGTTGCATGAAGTTCGCATCCAGCCTTCCTTAACCAAAGATGGGGTTTTCTCCGCACTGAAGATGGCTGAACTGGAGTTCCCCCAGTTCGAGACTTTGCACCTTGGATATGTTGATGAGTTTCTGTTGCAAT[G/T]TAAGTCATTTTTATTGTATGTTTGAAAGATCACATTTTATCTTGAGACGCTTTCCCTCGCAGTACCAAAAATTATATTGAATATCAATACTTTTCTTGCTATAAAATCGAAGTTAGAAATTCCACTATGGTGACAGCACTAGTGGGTCTTCAGGTGAATTGTATGAAAGTGTGGAAGATCACATTTTATCTTGTGATAGTTTTTTTTTTTTCGCAGTATCGAAATCGGTATCGAATATTGTTATTTTGCTTGGAACCGTATCGAAGTTACAAATTCAAGATTCTTGACAACACTAGTGGGTCTTTAGATAAATTGTATGAAAGTGTGGAAGATCACATTTTATCTTGTTATACTTTTCCGTACAGTATCGAAAATGGTATCGAATATCGATATTTTTCCTGGAATTTTATTGAAGTTACAAATTCCAGTATCTTGACAACACTAGGGGGTCTTCAGATGAGTTGTATGAAAGATCACGTTTTATCTTGTGATATTTTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13849
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020625 | Nonsense | 582 | 1120 | 11 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 40059662)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 38329267 |
GRCz11 | 14 | 38669581 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCAGAGTTCCAGTCAGACTCCAAAYCCTTCKCTTGAACAGGATGAAGAA[C/T]AAGCTGGTCTGAAGAAATCAWATAAACACTCAAAAARTRACNNNNNNNNN
Long Flanking Sequence:
ATAAAGTCACATTTCTAACATTTTTAAATGAATTAAAACACGTTACGGATGAGTTATGTGACATTTAAAACTGTATAAATGGTTGCAGAAAATTCTGCTTTATCATCACAGGAATAAATAGCAATTTTAAATATATTCAAATTGATAACAGTTGATTTTAAATTGTAATAATTATTACAAATATTGCAGTGTTTCTCTATATTTTATTATACACATGCAGCCCTTGTTATTATAGGAGACTGATCAAATAACCAATTAAAATGTTCCACCTGCATGTTTTTTATAATGTATGTATTTAATGTATGTCTAGTCTTTGATAATTATTTGGTTGCTTAAAGATATGAATTGACTTCTCGTGCCTTCCAGCAGAGATTCCAGTTGTGGAGGGCATGGTGGCAGAAAACATAGAGCCCGAGCCAGTTCTTGTGGCTGCCAATCCACAGGAGGAGAACCAGAGTTCCAGTCAGACTCCAAACCCTTCGCTTGAACAGGATGAAGAA[C/T]AAGCTGGTCTGAAGAAATCATATAAACACTCAAAAAATGACATTTACTATTAGTTAAAACAGATTTTAAACTGAGCTTAAACAACACAATCCTTAGGGTTTAATTGTTTTATGTCCAATCCACTTAAATTTGTAACAATTAAGTAGTTAACTTAATTCCATCATGTTGTCGCATCACAAATCGATTATGTGGAACCCAGCATTTTTTTCAGTGAATAATGCGAACAGGCAGGGTGTGTTTGTGATTTAAACCATTTACATCTGTCTTCTACAACTTCACTCAGGGCCTAGTGGCGTTCAGACATCAGTAAAGAAGCCGTCTGTGGTGGTGTCGGACTCTGACAGTGAGGATGAGTACAGTCCAGTCAGAACTCCGGCTGCTGCACGCTCTCAAGGCCAGTACCCTGAGACAGAGGCCCAGGGCAAGAGCAGCACCGCTGGGACTCCACATGGTAATGAATGTTTAAAATCCTCATAATCAGAAATGGTTATTGCATACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35737
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020625 | Essential Splice Site | 640 | 1120 | 12 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 40060115)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 38329720 |
GRCz11 | 14 | 38670034 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGAGACAGAGGCCCAGGGCAAGAGCAGCACCGCTGGGACTCCACATGG[T/A]AATGAATGTTTAAAATCCTCATAATCAGAAATGGTTATTGCATACAGGCA
Long Flanking Sequence:
AGAGTTCCAGTCAGACTCCAAACCCTTCGCTTGAACAGGATGAAGAACAAGCTGGTCTGAAGAAATCATATAAACACTCAAAAAATGACATTTACTATTAGTTAAAACAGATTTTAAACTGAGCTTAAACAACACAATCCTTAGGGTTTAATTGTTTTATGTCCAATCCACTTAAATTTGTAACAATTAAGTAGTTAACTTAATTCCATCATGTTGTCGCATCACAAATCGATTATGTGGAACCCAGCATTTTTTTCAGTGAATAATGCGAACAGGCAGGGTGTGTTTGTGATTTAAACCATTTACATCTGTCTTCTACAACTTCACTCAGGGCCTAGTGGCGTTCAGACATCAGTAAAGAAGCCGTCTGTGGTGGTGTCGGACTCTGACAGTGAGGATGAGTACAGTCCAGTCAGAACTCCGGCTGCTGCACGCTCTCAAGGCCAGTACCCTGAGACAGAGGCCCAGGGCAAGAGCAGCACCGCTGGGACTCCACATGG[T/A]AATGAATGTTTAAAATCCTCATAATCAGAAATGGTTATTGCATACAGGCAACTCGGGGTTCTAGAATAACTTTTTGCACTGGTAGCACTTGTGCTCCACACTTTTTTTTTCTTTTTTTAGATGTACCAGCACAAAAGTTTATTGCAGCCAAAATTTTGACCACATTGCATTTTTCATAGTGCCCTTCACTATCTCTGATTTTTTTAAACAACAACATGGGCCTAACGTGTGTCTGTTCTTCAACTTCAGTCACTGATACATTTTTTTATTTATTGCTCTCAAATGGCTTGTCGCACCGGTGCAACCTCAAAATTTTTTAGTTGCACCATTGAGAGATAGTGCTTACATGCAACCTAATTAGTCACACTCTAGAGTCATGGATAGTGTATAAGTAACAATGGAATGTTTTGCAATGAGCCATGTTTCTTGTTTCCCTATGTACAATATGTGAGGTATTTACAGAGCGTTATAGCCGCTATACCATGTATAGTTTTTGTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35738
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020625 | Essential Splice Site | 850 | 1120 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 40068228)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 38337833 |
GRCz11 | 14 | 38678147 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAATCCACCAGTACCAGTGACCCGGTGACTGAAGATGATCACGTGCAGG[T/C]GGGTTTGTAGTCTTCTCTCACTTATCTTGATGTTTCTTTAAAGGTTCGTC
Long Flanking Sequence:
GGGGATTGCATCTGGATAAAATGTCTTCTGCCTAAACTCGCTTAAAATGCTGACAGTCAAATAGAAGTGCAAATGACGAACATCAGCTTTATTTTAATTAAACTTTGCCGTACCCCCCAAAAAACATGTGTTTTGAAATGTTTCAAAAGTTTTAATCCCCACTATTGTGGATATGCATATTGTGATCTTGAGGCTGAAACAATGTATTATTAGCCTTAGTTTTAATTATGCTCAAAATAGTTTGCACTCATTATCATACCATTGGAAATAGTATTACTTTTGCGGAAACCATTATCTTATATTTACAAATACAGAGCTTTTTAATTGATTTTTGGTTCAGATTTTTTGAAGTTCTAGTTTGTTTATATTATTCCTCATCACCTTTTTGATTTGTCCAGAACTGCCCAAAGCAAAGCCTCGGACCGCAGTGAAAAGGAAACGTATGGCAGACAAATCCACCAGTACCAGTGACCCGGTGACTGAAGATGATCACGTGCAGG[T/C]GGGTTTGTAGTCTTCTCTCACTTATCTTGATGTTTCTTTAAAGGTTCGTCACAGCATTATCATTCTGTCATTTTTTTACTCACTCTCATTTTGTCTCAGAATCATTTTTAAAATGTCTTTCTCTCTATTTAATGCTTATTCAGCCCAAAAATGTTGCACCTTACAATAATGTATTAAATATATTAACTAGCATGAATGAACTTTACATTTGTTGGTTCTCTATTGTAAGTTTATGTTGTCAACTCGCATTGCATTGCAACTAAATTTAACAATCATAAATTTGGATTTTATTTAAGCATCAATAAATGTTGAACAATGATTAATACATTTGGTATTGGTAATGTTAGTAATTATATTAACTAACATTAACTAATGAAACCCTATTGTAAAGTGTGACCAATAAGTTAGTAAACCTAAATTAGAGATTTAAATATATGTATATACACTACTTGACAAAAGTCTCGTCGCCTATCCAAGTTTTAGGAACAACAAATAATAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11788
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020625 | Nonsense | 994 | 1120 | 18 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 40072198)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 38341803 |
GRCz11 | 14 | 38682117 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCACCAAGCTGCTTTTTGTTTATCCTTTCACAAGAGAACTCATCAAGTA[T/A]GAATTCTTTCCGGAGGCCACACGAACGGAAGAGGATGTGAAGAAGTATCC
Long Flanking Sequence:
CTGTTTTTGTTTGTAATAAAATAATAATAAAAAAAGTTCTTCTTTATGTCTTTTAACTCATTATTTGTATTTGAAATTTGTAGGAAATGTTATCAGATTTGTTAATTAATTATAGAATTAAAACGTTATGATTTTTTACACAAGCCATACTCAATAAATCCAGTGAATTTGTCATTTAAGTTGTCTTTAAATTTTTATTTTTCATAGTTTTCATATGAAAAGCTTACATATTTTATTTCATCTTGTTGCATAGATTTAAAAATATATTTGTTTAGTGTTTAAGATGCATATTACAATCTCTATAAAGCTGTATTTTTGCAAAGTTGTAATAATTTCTAGTTTTTCAGTAGCCTACTTCTTTAGACTTATAATAATTCACAAAAAATGTACCTTTCCAAATCTGCTTCCTGCTTTGTCCACCAGATGGCACTGTTTTCTTTCCATGGTTAACTCACCAAGCTGCTTTTTGTTTATCCTTTCACAAGAGAACTCATCAAGTA[T/A]GAATTCTTTCCGGAGGCCACACGAACGGAAGAGGATGTGAAGAAGTATCCCAGCTATCCCTGGGGCAGAGACATCTACACATTAGAGGGTGAGAGGAAACAGAGCCCTTAGAGACCAGATCCAAACCCCCTCATTCATTTCCTCTGGAAACATGGTCATACTGGAGAGTGTGAGAGAGAGCGAGAAATTTACAGTCATATTTACATTGCCCAAATCCCTTACATGGGGTTATTTATCTAAAAGGGATAGTTCACCCAAAACTTAATATTCTTTCATCATTTACTCACCCTTTACTTGTTCTAAACTTATTTAAGTTTCTTTCTTCAGGTGGCATGGTGGCTCAGTGGTTAGCAATGTTGTATCCCAGCAAAAAGGTTACTGGTTCGAGCCCAGCTGGGCCAGTTGTTGTTTCTGTGTGGAGTTTGCATGCTCTCCCAGTGTTGGCGTGGGCTTCCTCTGGGTGCTCCTGTTTCCTCCACAGTCCAAAAACATGCGCTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16333
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020625 | Nonsense | 1043 | 1120 | 19 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 40074812)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 38344417 |
GRCz11 | 14 | 38684731 |
KASP Assay ID:
2260-7815.1 (used for ordering genotyping assays)
KASP Sequence:
GGATGGGGCGCCGTATTCGATGATCACTGATTTCCCATGGCTTCGCTCTT[T/A]ACGCACAGCAGAGCCCAACACTTACGCTCGATACGACTTTGAAGATGATG
Long Flanking Sequence:
AAGGGGGCGGGGCATGTCAGATACTAGAAAGCATTTGATTGGTCATGATTTGATGAGAAACTGAAGTATGAGGTGACGTGAAAAAAAAAAAAGTTGATCCATTTTGGCGTAATTGAAAAACTACAAGCTTTACATGTTTATATCAGTTTTATATCTTCTAAATGTGAATTTTGTCACTGTTTTAGAGTGCACTAGCTTATAGATATCTTAAAAATGAACAATACTGATGCTAAAAATATATATATATTTAAATTTTATGGGACCTTGAAACTCAAAAAAACAGAAAATCTGTTTTTACCTGCTGTGTCTTGCTTTAATGGATGAGAAAAGTTGCAGGCTCCATAATGTCAAATCGGCCTGTAAGGATGTGCAGGATGCTTTTCAGTCTAATGGAATAAAAATAGTAATAACATTCAACCTTTCCCACACTCCCTGTGCTTTAGGGGTCGTGGATGGGGCGCCGTATTCGATGATCACTGATTTCCCATGGCTTCGCTCTT[T/A]ACGCACAGCAGAGCCCAACACTTACGCTCGATACGACTTTGAAGATGATGAAAGCAGTAAGTGATGCAATGTCTGTCAGGAAATAATAATGGTCAGGTGTTAATCTTTAACACATTGATGTTAAATGATGGATGAAGTCTTGCTCAGTAGTTTAGCATGAATCTTTGTTATTAACAGTTTAACACTGATCTTCATTATAGTTAAGCTGAAATGTAAAGTTATCATTGTTTGCTTCTTAAAAAAAAAATATGTACATAAAAAGAGCTTAATCTATTTTATTTTCAACTTTATGCTTGGAATTTTTTTAGTTAGTCAACAAAAATCTAATTATAATAATAATAATAATAATAATTCGTTACATTTATATAGCGCTTTTCTGGGCACTCAAAGCGCTTTACACAATGGGGGGGATCTCCTCATCCACCACCAGTGTGCAGCATCCACCTGGATGACGCGACGGCAGCCATTTTGCGCCAGACCGCACACCACACACCAGCTGA
Associated Phenotype:
Not determined