ZMP
frya
Ensembl ID:
ZFIN ID:
Human Orthologue:
FRY
Human Description:
furry homolog (Drosophila) [Source:HGNC Symbol;Acc:20367]
Mouse Orthologue:
Fry
Mouse Description:
furry homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2443895]
Alleles
There are 12 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22679 | Essential Splice Site | Available for shipment | Available now |
| sa12657 | Essential Splice Site | Available for shipment | Available now |
| sa13092 | Essential Splice Site | Available for shipment | Available now |
| sa22680 | Nonsense | Available for shipment | Available now |
| sa15169 | Essential Splice Site | Available for shipment | Available now |
| sa22681 | Essential Splice Site | Available for shipment | Available now |
| sa14402 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22679
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045921 | Essential Splice Site | 236 | 3024 | 8 | 62 |
Genomic Location (Zv9):
Chromosome 15 (position 31078646)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 31974298 |
| GRCz11 | 15 | 31832277 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCTGTGCTTCATCCCACACTCTTATTTTATTTGTTGTTTTCTTTTTGT[A/T]GATTTCCTGCTGTTAAAAAGAGGTTCACGAGTGAGTTGAAGGAGCTTCGT
Long Flanking Sequence:
GCAAGGCCGAGGTCATGGATCTTGGACTGTGGTTGGTGACCACTGTTTTAGACTTTCAGAACTGCATAACATTCAAATTGTCTGGATTCTTAGCATCCTTTGTACATAAGTGTCATTCTTAAAATCTGTGTGGTCCTCTACACTCCAGGACAGTTGCTTTTGTGCATCTGTTTTATTTAGATCTGAATGAAACATTGTGGGAAACTTTGTTTTGTTTAATAATTCAAAAAACACTGCTATTAGTCATATTTTAATTGAATACTAATACTTTAACCCATAATTATACTATTTTGTTCATTTCATTTTGCTGTTAAAATTATTGTTTTATTTATCTGTTATTAATTATTACTAATTGTTTAAGGTGTAACAAGCTGAAGTAATTTTTAAAAAATCCTCAATATGTTTTTTCACAGTGTCATTTATATTATTGTCAGCATACTTTGGTTCACATATCTGTGCTTCATCCCACACTCTTATTTTATTTGTTGTTTTCTTTTTGT[A/T]GATTTCCTGCTGTTAAAAAGAGGTTCACGAGTGAGTTGAAGGAGCTTCGTCAGAAGGAACAGAGCCCTTATGTTGTCCAGAGCACCATCAGCCTCATCATGGGTGTGAAGTTCTTCCGAGTAAAGATGTATCCTGTAGAGGAGTTTGAAGCCTCCTTTCAGTTCATGCAGGTAAAAGTACAATATCAAAATGTTTGGATAATCTTCTCTCCTATTGGCTTGTTTGCATTATTTATTTATTTATTTATTAGGCATTACATTACAGTATTGATTTTGCTGAATTTAGAGACTGCAGTGACATTAGCTTAGGAATGTGAAAAGTGAAAAGCTAATTCTCTTTTTCATGATGCTGTGCTCTTTTCAACAGGAGTGTGCTCAGTATTTCCTGGAAGTGAAGGACAAAGACATCAAACATGCTTTGGCTGGACTCTTTGTGGAAATTCTTGTTCCTGTAGCAGCGGTAAAGAGACATTTTTTAAAAAGATCTGTCAACACTCTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12657
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 |
|---|---|---|---|---|---|
| ENSDART00000045921 | Essential Splice Site | 390 | 3024 | 11 | 62 |
| ENSDART00000045921 | Essential Splice Site | 390 | 3024 | 11 | 62 |
Genomic Location (Zv9):
Chromosome 15 (position 31079583)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 31975235 |
| GRCz11 | 15 | 31833214 |
KASP Assay ID:
2260-8723.1 (used for ordering genotyping assays)
KASP Sequence:
CCTYAATAGATGGCATGTCTTCCTCAACAACTGCCTCTCCAATCTAAAGG[T/C]ATGTGGTTTCACTGGTTATCTTTATTCATATGTGATTCTWCAAGAAGCTA
Long Flanking Sequence:
AAATTCTTGTTCCTGTAGCAGCGGTAAAGAGACATTTTTTAAAAAGATCTGTCAACACTCTACAAATTGAATGTCTTATTTACATGTGCTTTGCACATTAATCAGCACTTTGTTGGTTCTATAATTGTTTAAATAACATAAATAGCCTGTATACCACCCTTTTAAAAACTTATTTTGCTGGAAATGTCTGTTTCTGTTCCTTAACAGGCTGTCAAGAATGAGGTGAATGTCCCATGTTTGAGGAACTTTGTAGAGAGCTTGTATGATACCACCTTGGACCTTTCATCGAGAAAGAAACATTCTCTGGTCAGTTGGGTTTTCATTATATATATATATATATATATATATATTATTTTAAACTATAAGTAAATTTTAAATGGTTTTTCTGGTCTTTCAGGCTCTCTACCCAATGGTCACATGTCTACTATGTGTTAGCCAAAAGCAGTTCTTCCTCAATAGATGGCATGTCTTCCTCAACAACTGCCTCTCCAATCTAAAGG[T/C]ATGTGGTTTCACTGGTTATCTTTATTCATATGTGATTCTTCAAGAAGCTAAATGTGATAGCATACATTTGATCTGTTGTTACAGAGTAAGGACCCTAAAATGGCACGGGTAGCGCTAGAGTCCCTCTACAGACTTTTATGGGTCTACATGATCCGCATCAAATGCGAAAGCAACACTGCAACTCAAGGGTAAGCATGTTCCTGTTACAGTGCTCTCCACTTATATCAGCACTCTTGATAAATATAAACAAATAAACTAATATAACCTAAATAATAAAATAAAAACAGATGATGTTTCCTTTTGGGTGAGACTAGAGGCTTTTTTGCGAAAAACTTTTAAACAGTTTGTGCTGATGTTGAAGATGTTGGAGATTTTAAGACCCTACTGACTTCTACTATTTCTTCAGCTGTGATCCTTGGAGATTTTTGACCACTCCAACCTTCCTCCTTACAGTGTTTTAGGACTTACACAAGGATAGACACACAAATACCTCCAGATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13092
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 |
|---|---|---|---|---|---|
| ENSDART00000045921 | Essential Splice Site | 390 | 3024 | 11 | 62 |
| ENSDART00000045921 | Essential Splice Site | 390 | 3024 | 11 | 62 |
Genomic Location (Zv9):
Chromosome 15 (position 31079583)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 31975235 |
| GRCz11 | 15 | 31833214 |
KASP Assay ID:
2260-8723.1 (used for ordering genotyping assays)
KASP Sequence:
CCTYAATAGATGGCATGTCTTCCTCAACAACTGCCTCTCCAATCTAAAGG[T/C]ATGTGGTTTCACTGGTTATCTTTATTCATATGTGATTCTWCAAGAAGCTA
Long Flanking Sequence:
AAATTCTTGTTCCTGTAGCAGCGGTAAAGAGACATTTTTTAAAAAGATCTGTCAACACTCTACAAATTGAATGTCTTATTTACATGTGCTTTGCACATTAATCAGCACTTTGTTGGTTCTATAATTGTTTAAATAACATAAATAGCCTGTATACCACCCTTTTAAAAACTTATTTTGCTGGAAATGTCTGTTTCTGTTCCTTAACAGGCTGTCAAGAATGAGGTGAATGTCCCATGTTTGAGGAACTTTGTAGAGAGCTTGTATGATACCACCTTGGACCTTTCATCGAGAAAGAAACATTCTCTGGTCAGTTGGGTTTTCATTATATATATATATATATATATATATATTATTTTAAACTATAAGTAAATTTTAAATGGTTTTTCTGGTCTTTCAGGCTCTCTACCCAATGGTCACATGTCTACTATGTGTTAGCCAAAAGCAGTTCTTCCTCAATAGATGGCATGTCTTCCTCAACAACTGCCTCTCCAATCTAAAGG[T/C]ATGTGGTTTCACTGGTTATCTTTATTCATATGTGATTCTTCAAGAAGCTAAATGTGATAGCATACATTTGATCTGTTGTTACAGAGTAAGGACCCTAAAATGGCACGGGTAGCGCTAGAGTCCCTCTACAGACTTTTATGGGTCTACATGATCCGCATCAAATGCGAAAGCAACACTGCAACTCAAGGGTAAGCATGTTCCTGTTACAGTGCTCTCCACTTATATCAGCACTCTTGATAAATATAAACAAATAAACTAATATAACCTAAATAATAAAATAAAAACAGATGATGTTTCCTTTTGGGTGAGACTAGAGGCTTTTTTGCGAAAAACTTTTAAACAGTTTGTGCTGATGTTGAAGATGTTGGAGATTTTAAGACCCTACTGACTTCTACTATTTCTTCAGCTGTGATCCTTGGAGATTTTTGACCACTCCAACCTTCCTCCTTACAGTGTTTTAGGACTTACACAAGGATAGACACACAAATACCTCCAGATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22680
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 |
|---|---|---|---|---|---|
| ENSDART00000045921 | Nonsense | 933 | 3024 | 22 | 62 |
Genomic Location (Zv9):
Chromosome 15 (position 31098433)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 31994085 |
| GRCz11 | 15 | 31852064 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTGTGTTTTGGTGTGGCCAAACCAAGCATCATGAGCCCGGGTCATCTT[C/T]GAGCATCCACCCCTGAGATCATCACTCCCAGCCCAGACAGCAACAGCAGC
Long Flanking Sequence:
CTTACTCTAATCTAGGCTCTTAAACATTCAACTTTAATTAATTAGTTTAATTATTAATCATAAAGACATAAGAAAAGCTAATTGTTACTTCATTCTGGAGCGGACATCCATCAGAAAGTCCACGTCATCAAAACATAAGAAATTGGAAGGATCATGTAATTGTTACTTAAAAATTACTTTCAAAACTTCTAACAAATTATTCAAATATAGTAAAATAGAAATCTGTTTTAAATTGCAGTAATATTTTGCATAATTATGTGGATTAATGTTTTTTTTAAGGTGATTTTTCCAGAAAAGGGCTCCATCCACAATTTTATACATTTATTTGTATTTCATTAGTCAGTTAATTCATTTGAATGTTTGAATCTTTTAGCAATCCAGTCAACGCCAAGAAGACGAGTTCGGCTGGTTCAGCAGACACTTATGTGTCTCTATGGAGAAACTATTTGATTCTGTGTTTTGGTGTGGCCAAACCAAGCATCATGAGCCCGGGTCATCTT[C/T]GAGCATCCACCCCTGAGATCATCACTCCCAGCCCAGACAGCAACAGCAGCTATGACAACAAGGTGGGTGGGTCTTTTAGCATCACACACCAAGTCATGCGCCTCAGTCAGTCATTTAATAACTTGATGGAATCACTGATTAACATCTTGTTCATTAGATCCTGGGCACGCCATCTGTGGCTTGGCTGCTGAAGCAGTTGGTCCCTCTGATGCGTTCAGAAAGCATTGAGATCACAGAGTCTTTGGTGCTAGGATTCGGCCGTACAAACTCACTTGTTTTCAGGTATTTGGAAGCACAAATATAAACATTTTTTAAAAAATGAGGTAGCTTGACTGTTTCACAAATGGCAAACATTGTACTAAATGGTCAAGTTTTTACAAGATTCATAGTCTTACAGGGCAATGACATTATTTAACCATATTGAAATTAGGCTCACTCATTGTCGTTTTTGTTTATTACAGTATATACAGCGTGGGATATAAGTATTGAACACATAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15169
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045921 | Essential Splice Site | 1045 | 3024 | 26 | 62 |
Genomic Location (Zv9):
Chromosome 15 (position 31102213)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 31997865 |
| GRCz11 | 15 | 31855844 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAACTCACAGCCTGAGAARCAAGACATAACTCCGGTCTCTGTGTCTCTC[A/T]GCACAAATGGAGCCCTGGAACGYRATACACTGGCCCTGGGCGCKCTCTTT
Long Flanking Sequence:
TTGAATCAGATTGCCATTTTCTTACCCTTAGAAAAACTGACTTGTGTCTTGTGTCAGAAATCTGGTGATTTCAGACATATCTGGAAATGTCTATGTGAGTTTTGTAGAATTTTTAATGAAAGATTTTTCCTTTCACTAAAGACTTGAATTACTAGCCAATGAAAGATTGTAAAATAGATGGTCGTGTTATTGTATATGATGACATGAGACACCTATACCACTGTTATGTCATTACAAATCTTTAAATAAATGTTTAAAAAATCTTCATAACAGTCATTTCTTTGCAAAATCTTTCATCTAGAATAAAAAACGGCGAGAGAGGAGAGATCTTCTGAGACTCCAGCTCCTCAGGATCTTTGAGCTGCTGGCAGATGCTGGTGTCATCAGTGACAGGTGAGAAAGATGTTGTTATTATTTTTAATGGATTCTGTCCTTCTTTGCACCTCATTGTGAACTCACAGCCTGAGAAACAAGACATAACTCCGGTCTCTGTGTCTCTC[A/T]GCACAAATGGAGCCCTGGAACGTGATACACTGGCCCTGGGCGCTCTCTTTCTTGAGTATGTCGACCTGACACGGATGCTTCTGGAAGCGGAGAGTGACAAAGACATGGAGATTCTCAAAGACATCCGAGCTCACTTCAGCGCCATGGTGGCCAACCTCATACAGTCGGTCCCAGGTGAAGATCAAGCTTAATGCTTTTCACAAGCTCTCATGTCAAAATAAAATCCAGATTCAGCCCATTTGCTGCATTAGCAGACATTCTTGTTTGTGAACAGTTTATTGGTACACATTTTAATTCATAAGTAGTCATAATATTGTTTTCCTACTTTAAATATTTGTTCCCCATTTTACGTCATGACATCATATGGATGGCTGTGAAGTTGTATCTCACTCTGGGAAGCACTCCACATTTTCTTTGTTTAGGAAAGGGAATTCATTGCTAGGTGACGGCGGATTCAGTCACAGGACTCCTGACGTCAGTCTTGATTTAGACTCCCTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22681
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045921 | Essential Splice Site | 1527 | 3024 | 34 | 62 |
Genomic Location (Zv9):
Chromosome 15 (position 31113171)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32008823 |
| GRCz11 | 15 | 31866802 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATTCTACCGATTTTCAGCCACAAGTAAAATTGTCACCACCTCTTCTGG[T/A]ATGCAAAGCCTTACTCAACATAAAGAAAAGTTGTGTGCGCGTTTAAAACA
Long Flanking Sequence:
TGATGTCCCTGGTGCTGAAATGGAGAATGCGTGGAACGCTCTAGTCAGTAATGAACGATGGACTAATAACCTACGAACCGTGCTGCAGTTCCTCATCAGCTTATGTGGGGTCAGCAGTGACACCTCTCTCCTGCCTCATGTAAGCCAGATTTATGTTATGTTATGTTACAATATGTTATGTTATGTTATGTTATGTTTTGTTATGTTATGTTATGTTATGTTATGTTATGTTGTGTTTAATAAGCAGGTCATTTGTTTTAAGATGGTAAATTGCCAAAGGTAAATTGCCAGATTTGAGTATATGGATTGTTGGTTTATTCCTATGCTCAGATTAAGAAGGTGGTGATCTACCTGTGTCGCAACAACACCATGCAAACCATGGAGGAGCTGCTTTATGAACTTCAGCAGACGGATCCTGTGAATCCTGTAGTGGTGCACTGTGACAATCCTCCATTCTACCGATTTTCAGCCACAAGTAAAATTGTCACCACCTCTTCTGG[T/A]ATGCAAAGCCTTACTCAACATAAAGAAAAGTTGTGTGCGCGTTTAAAACATTGTGCTCAGTTCTTATTTAAAAGCATTGATCATTTGATTTCAGTAAAAAATAACAGCGAAATTAATACTGGCTCATGAACCTGAGATAGTGAGTAAATAAACCAGACACAGGTGAACATAGTCAGCAAGCCAATGTGTATCTATAGAAACAAGGGAAATAATATTAAAAATAACAAAATGAAGCTGCACAACTTTTTTTTACATTGATAAATAATAATAATATAATTAATAATAATAATAATAATAATAATAATACATTAATATAATATGAAACATTACATAACATTACTTAGCATCAAATCAGCATATTACAATGCTTTCTGAAAGATCATGTGACAGACTGGAACAATGGCTGCTTTATTATCACAGAAATAATTAACATTTTAAAATACATTAAACTAGAAAATAAAGATTGACAGGAATATTATTTGACATTATTACTGTTACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14402
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 |
|---|---|---|---|---|---|
| ENSDART00000045921 | Nonsense | 2346 | 3024 | 49 | 62 |
Genomic Location (Zv9):
Chromosome 15 (position 31135366)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32031018 |
| GRCz11 | 15 | 31888997 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACGCCGGTGATTGGTCGACGGTATGATGAGCTTCACGGTTCTCCAAGA[C/T]AAGATGGKAAGAATCAAGGAGTGGTTACGGTGACACGCAGYACCTCCTCT
Long Flanking Sequence:
GAAATGATGTCACTCCGGCTGCGGCGCTTTGCATCCAGAGCCTCCAGTCTTAAAAAGCAGACTCCTCTGCCCGCTGTCAAATACCTCAGGGACGTATTTAGCCTCTAGCAAGTGGGTGAGACAGTAGGGGAAAAAAACTCAAAACTGACAAGAAACTCAAAACAAGCTCCAATACATCCCAGCAGAAAGGATTTTACAGGAATTAAGGGCAGGTGAACTCAATAAGGGAAATCCTGACATCCCCTCAAGCTTATTTGGCTTGTTTTATTAAAGTTTCTGTTTCCAAATATTCACTACAAGGAACTGGACCATCGAAAAAAGGCGGCAGCTTGATGCTAGCAAAGGAAATGTGCTGGAATGAAGACTCCTGGGCGAGGAGCTCATGACATGAAAGGCAAAGAGCAGACGTGAAATCCCTGAGCTTAAATGGTGCGTGACTTTGTGTGTTTCAGACGCCGGTGATTGGTCGACGGTATGATGAGCTTCACGGTTCTCCAAGA[C/T]AAGATGGTAAGAATCAAGGAGTGGTTACGGTGACACGCAGCACCTCCTCTACGTCCTCAGGCTCCTACCAAAGCAACCACGTGCTGGTACCTGTCAGCTGGAAACGACCACAGTCCTCACAGGTATCAACTGATAAATCATGCCTGTTTCTGATACAATTCCTTGATTTGATATTTTATTTCTTTTTATGTTATTTTATCTGAATTGTTTATATTTGACTTTAATTTGAATGTTGTTTTACGTTTTATTTTTGTGTCGTTTGCCTCACTATTTAGAAGCGAACTCGTGAGAAGTTGGTGAATGTATTAACCTTGTGTGGCCAAGAAGTTGGACTCACCAAAAACCCATCTGTAAGTGACACAGAAAACGTCATCCACTCAGTATTACAGCTTTGTCATTTTGTAGTTTTTGAAGTATTTGTACTTCTGTACCAGTTTTAAAAACCCAACATTTCCAGTTCTTCTCTGAATACTTTACTAATGAAATCCTGTTTCCACCAT
Associated Phenotype:
Not determined