ZMP
si:dkey-8f21.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens FBXO41, F-box protein 41 (FBXO41) [Source:UniProtKB/TrEMBL;Acc:B8
Human Orthologue:
FBXO41
Human Description:
F-box protein 41 [Source:HGNC Symbol;Acc:29409]
Mouse Orthologue:
Fbxo41
Mouse Description:
F-box protein 41 Gene [Source:MGI Symbol;Acc:MGI:1261912]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19548 | Nonsense | Available for shipment | Available now |
| sa39662 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31221 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19548
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113650 | Nonsense | 169 | 805 | 1 | 12 |
| ENSDART00000140945 | None | None | 323 | None | 8 |
| ENSDART00000145789 | Nonsense | 169 | 387 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 42073427)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40989743 |
| GRCz11 | 1 | 41690907 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGACGAGAGGCTGGAGAAGCTGTCAGAAGAGGTGGAGCAAAAGATTT[C/A]AGCAAGAGTCAGTCGTCTGCAGGCCGAGTTGGAGAGGAAAAGCTCAGAGC
Long Flanking Sequence:
CTCTTTGGACCTGCCATACCGTTGTCCTCGCTGTGGGGAACACAAGCGCTTTCGAAGCCTGTCCTCTCTACGCGCCCATCTGGAGTACAATCATACCTACGAGACCCTGTATGTGCTGTCCAAGTCCAACAGCGTATGCGATGCCGCAGCGCTGCTCCCCCTAGTGGCTGACGGAGCCCTCACTGCAGAATCTCGTTTTCCGTACCGCGAGCTGCCCTGCTCTGGTGAAGAGCTTGGCCTTGCACCCTCGTCAACTGCTTGCTACCTGCCCAATGTGGAGTTTCCCCTGGGGGAGATTCTGGTGAAGACAGCCATGAGCTCCAGCGACGCCTTGTCCTCTGCAGGGAACAATGCCGTGGCAGTGGCCGCTAATGTGGCCGCTAGTGCGGTGGAGGCAGCTTACGAGGAAGGGCTGGCTCGGTTGAAAGCCCGAGCTTTTGAAAGACTTGAGCTGGACGAGAGGCTGGAGAAGCTGTCAGAAGAGGTGGAGCAAAAGATTT[C/A]AGCAAGAGTCAGTCGTCTGCAGGCCGAGTTGGAGAGGAAAAGCTCAGAGCTGGAAAAGGCAAAGTTGGAGAGCGAGAGGCTCAGTCAGGAGAAGCAAGACCTGGAGGACAAAGCCACAGAGCTTTCACGGCAAGTGGACGTGTCCGTGGAGATGCTGGCCAGCCTTAAGCAGGATCTGGTTAACAAAGAGCAGGAGCTTTCACACAAACAACAGTGAGTTCTTTTTTTCATGATAAACCTCCTACACCTAAATGCTTCACATTTTATCACCGCAATAGTATTGTGTGCATGCTGACCGAATTTTGTAACTATGCATACTTTGTACCATCCAGTTACAAAATGTAACTTAACCATGCAATCATTCATTTTCCTTCGGTTTAGTCCCTTAATTTATAAGGGGTTGCGACAGCGGAATGAATCGCCAACTTATCCCGCACATGTTTCACAAAGCGGATGCCTTTTAAGCTGCAACTCAGTACTGGGAAACATCAATACACACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39662
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113650 | Nonsense | 239 | 805 | 1 | 12 |
| ENSDART00000140945 | None | None | 323 | None | 8 |
| ENSDART00000145789 | Nonsense | 239 | 387 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 42073636)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40989952 |
| GRCz11 | 1 | 41691116 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGCCTTAAGCAGGATCTGGTTAACAAAGAGCAGGAGCTTTCACACAAA[C/T]AACAGTGAGTTCTTTTTTTCATGATAAACCTCCTACACCTAAATGCTTCA
Long Flanking Sequence:
AGCTGCCCTGCTCTGGTGAAGAGCTTGGCCTTGCACCCTCGTCAACTGCTTGCTACCTGCCCAATGTGGAGTTTCCCCTGGGGGAGATTCTGGTGAAGACAGCCATGAGCTCCAGCGACGCCTTGTCCTCTGCAGGGAACAATGCCGTGGCAGTGGCCGCTAATGTGGCCGCTAGTGCGGTGGAGGCAGCTTACGAGGAAGGGCTGGCTCGGTTGAAAGCCCGAGCTTTTGAAAGACTTGAGCTGGACGAGAGGCTGGAGAAGCTGTCAGAAGAGGTGGAGCAAAAGATTTCAGCAAGAGTCAGTCGTCTGCAGGCCGAGTTGGAGAGGAAAAGCTCAGAGCTGGAAAAGGCAAAGTTGGAGAGCGAGAGGCTCAGTCAGGAGAAGCAAGACCTGGAGGACAAAGCCACAGAGCTTTCACGGCAAGTGGACGTGTCCGTGGAGATGCTGGCCAGCCTTAAGCAGGATCTGGTTAACAAAGAGCAGGAGCTTTCACACAAA[C/T]AACAGTGAGTTCTTTTTTTCATGATAAACCTCCTACACCTAAATGCTTCACATTTTATCACCGCAATAGTATTGTGTGCATGCTGACCGAATTTTGTAACTATGCATACTTTGTACCATCCAGTTACAAAATGTAACTTAACCATGCAATCATTCATTTTCCTTCGGTTTAGTCCCTTAATTTATAAGGGGTTGCGACAGCGGAATGAATCGCCAACTTATCCCGCACATGTTTCACAAAGCGGATGCCTTTTAAGCTGCAACTCAGTACTGGGAAACATCAATACACACTTATTCGCACTCATACACTACGGCCAATTTAGTTTATTCAATTCACCCATAGCACATGTCTTTGGACTGTGGGGGAAACCGGAGCACCTAGAGGAAACCCACATCAACACGGGGAGAAAATGCAAACTCCACACAGAAATGTCAACTGGTCCAACCGGGACTCAAACCAGTAACCTTCTTGCTGTGAGGCACCAGTGCTAACCACTGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31221
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 |
|---|---|---|---|---|---|
| ENSDART00000113650 | Nonsense | 617 | 805 | 7 | 12 |
| ENSDART00000140945 | Nonsense | 135 | 323 | 3 | 8 |
| ENSDART00000145789 | None | None | 387 | None | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 42130001)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 41046317 |
| GRCz11 | 1 | 41747481 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTGACAGATCGCTCTCTGTGGTTGGCCAGCTGTTACTGCAGGGCACTA[C/T]AAGCTGTCACATACAGGTGAGTCCCTGTGTGCTTTTATCACTCTATGGTC
Long Flanking Sequence:
ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACTTTACCCAATAATGTAAATTCTGTCATCAATTACTCACCTTTGACCTGCTTTGTTTGTTCTGTTGAACACGAAAGAAGATGTTTTGAAGAATCCTGAAAACCTGTAACCACTGACTTCCATAGTAGGACAAACAAATACTTTGGAGATTAATGGTTTCCAGCTTACTTCAGAAAATTGTCCTTTTTGTTCAACAGGAAGAACTCTAATCGTTCAAGTCAAGGTTGAGTAAATGATTTTTATTTTTTGGTTGAACTATCCTTTTAATGTATTCTCTTGGTTTTGTGTGTAGCGGGTGTCTGGAGGAGGGTCTGGAGGCTTTATTGAAAGGCACCGGCAGTAATCTGCTCATCCTGAAGGTGTCACATTGTCCAAATCTACTGACAGATCGCTCTCTGTGGTTGGCCAGCTGTTACTGCAGGGCACTA[C/T]AAGCTGTCACATACAGGTGAGTCCCTGTGTGCTTTTATCACTCTATGGTCTGGTACAGTACACTGGATTCTGATTGGTCAATTTCAGTATTTTACATGTATATTCTTACTGTACCCAAAGAATACAAAGTCAGTAAATAGATGTTATGACTATATTATCAACTGTTGTTAATTTTACAAGTTTATTTAATAATTTAAAAATAGATGTAATGTCATTTTTTCTATTAAATTTAATTCTTGATCAAATTATTTCATGATATAAAAAATAATTGAGAGACAGAAGATTTTATTGTATTGAAGTGCCCATGATAATATTGTGCACATTCATTACCACAATATATTGTATTAATGAATACTGGCACAAGTTTTCTCAGATATTGATTATATGTCAGGAGTGCGACAGACCCGGTTGGACAGGAGGTTATCTGGGCTCTCGGAGCTGGTTGCAGAGACATCATTTCACTACAGGTGGCACCTTTACATCCATGGTAAGATCTAAAA
Associated Phenotype:
Not determined