ZMP
fryb
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 21 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21770 | Essential Splice Site | Available for shipment | Available now |
sa10244 | Nonsense | Available for shipment | Available now |
sa21771 | Nonsense | Available for shipment | Available now |
sa12198 | Nonsense | Available for shipment | Available now |
sa13238 | Splice Site, Nonsense | Available for shipment | Available now |
sa31789 | Essential Splice Site, Missense | Available for shipment | Available now |
sa12244 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21770
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 |
---|---|---|---|---|---|
ENSDART00000044294 | Essential Splice Site | 659 | 2973 | 18 | 62 |
ENSDART00000138547 | None | None | 162 | None | 4 |
ENSDART00000142881 | Essential Splice Site | 717 | 3080 | 19 | 61 |
Genomic Location (Zv9):
Chromosome 10 (position 34956594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33984452 |
GRCz11 | 10 | 33928312 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATGGGAGCTGTGTACCCAATCACCTGTTTTTGTATGTTTGTTGAGCTC[A/T]GATGGGATCCCAGAGCAGCGGAAGCTCCAGGCTGGCGCCTGATCGCAGTC
Long Flanking Sequence:
TTGCTCTGTTAAACATCACTTAGGAAATATTAAAAAAATTGAATAAACATTTCTCAGAAGGGCTAATAATTATGTCTTCAACTGTGCATATATAGTTTTTAAAGCTCATTGGTCTTTTGCACTTTGAAATAAAAGCATAAAACTTTGTCATTGATTTGTTTATGTTTCATATTTAGGCTGACGGTCCACATGGACGATGAACTCAGACTCATTGCTCAGAATTCCCTGCAGAGTTTGCTGCTGGACTTCTCTGATTGGCGAGAGGATGTGTTGTTCGGGTACACAAACTTCTTACTGCGTGAGGTGCAGGACACACAGCAGGGCCTGCAAGACTCTTCCGTTAAACTGCTGCTGCATTTCCTGACACAGTGGAGGCTGGCAATTCAAGCGCCTGGAAAACGCTCAGCGGAGGTATCAGCGGGATCATTTTCTTTACCGGTTATACAATGTAAATGGGAGCTGTGTACCCAATCACCTGTTTTTGTATGTTTGTTGAGCTC[A/T]GATGGGATCCCAGAGCAGCGGAAGCTCCAGGCTGGCGCCTGATCGCAGTCCTCACTCTACTGTCCTGCACGCTGTGGAGGGTCTGGCCCTGCTGCTGCTGTGTTCCTGCCAGACCAGCACCCGAAAACTGGCCGTTTCAGTCCTCAGAGAGATACGCTTGCTGTTTACAGCCATCGGACAAGCCGAGGTGAGAAACATAACTAAAACTGAATTCCATAAAAAGACAATATAATGGAATACGATGTATTAAGTGTAGTTTCATAAACTAATTTTGAGAGGAGCACTTGATATGATTACGGCTGGTCTCTCATCCATAATCAGCAGTAATCAGATTGATCCAAGCCTACAATAAATAGACTGATTTCTCCTTACTGCCTAATCTTCATATCGGAAAAATCCCCCCTTCCACCCCATCTCCTCCTTTTTCTTCTTTACCAGGGGAAGCTCTCGTGACCTACCTGATTTCAGACCCCTTACATGCTAATTGACTAGGCGGGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10244
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044294 | Nonsense | 819 | 2973 | 20 | 62 |
ENSDART00000138547 | None | None | 162 | None | 4 |
ENSDART00000142881 | Nonsense | 891 | 3080 | 21 | 61 |
Genomic Location (Zv9):
Chromosome 10 (position 34959031)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33986889 |
GRCz11 | 10 | 33930749 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGGCCAGAGCATCTACCCAAACACTGTCCTACAGCGCKCAGCTATGCCT[G/A]GCCCTACGCCTTTACTCGCCTACAGCTGCTKATGCCAYTTGTAGACCCAA
Long Flanking Sequence:
ATACTGATCAGTATGAGATCTGTTAGTGCAGCATAAACATTCAGCAACCCTTCTGCTGTCATGTTTCTGCTTACAGGATGACGACAAGTCCATGATTGAGGTTATGGATCAGCTTGCCCCCAGTGTGCTGGACAGTTTTGTTCATGTGGCCGTCTCTGACTCGGTAAGAATTTCCCAATGGATGTGTTTCTGTCTTTTTATCCATATTTTTATGCGTTTATGCCACAAGACACCAAATGTCTGCCTGTAGAGTCATGATCCTCATTTTAACCTGTTGAAATCTTCTGTGAAGGCCACTCTTCCCCTGAGTCATCACGTGGACCTGCAGTGGCTGGTAGAGTGGAACGCCCGTCTGGTTAACAGCCACTACGACGTAAAGAGCCCTTCTCACGTGTGGATCTTCGCCCAGTCTGTGAAGGACCCATGGGTGCTGTGTCTGTATAGCTTCCTTAGGCCAGAGCATCTACCCAAACACTGTCCTACAGCGCTCAGCTATGCCT[G/A]GCCCTACGCCTTTACTCGCCTACAGCTGCTTATGCCACTTGTAGACCCAAAGTGAGTACTCCTAAAAGATGATTATCATGAGTCTCTTTTAAAGGGATAGTTTACCCAAAACTGAAAATTCTGCCATCTTTACTCGCTCCTTTACTTCTTCTGAACCTGTTGGACATTCTGTCTTCTGTTGAGCACAAAAGAAGATATTTTGAAAAATGCTGCAAACCTGTAATCAATGACGTTTATAGTATTTGTTTATCCTACTTACTGGTACTACTTACTTACTTACTTACAGGTTACTGGTTTCCAGTTTTATTCAAAATATTTTCTTTTGTATTCAACAGAATAAAGAAGCTACTATAGCTTGGTAACCCCCTGAAAGCATGTAAACAGGGAAAACATTTTCATTTTTGGGAGAACTAATTTTTAATCTGAAGCAAGTCTTACACAAGGTGCATGGAAACAAATAACATGTAAAAATATTGGGGGGAATGGGGAAAATTTAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21771
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044294 | Nonsense | 884 | 2973 | 21 | 62 |
ENSDART00000138547 | None | None | 162 | None | 4 |
ENSDART00000142881 | Nonsense | 956 | 3080 | 22 | 61 |
Genomic Location (Zv9):
Chromosome 10 (position 34961169)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33989027 |
GRCz11 | 10 | 33932887 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCCAAGCCCAGCATCATGAGCCCAGGTCACCTGAGAGCCTCTACACCT[G/T]AAATAATGGCTACCACCCCTGATGGCAGTGTCACGTACGATAACAAGGTC
Long Flanking Sequence:
TTAAAGAGCAGACGCGAATGGCACTCGAGAGAAATTTGAGATCTCAAAAAGCTTACACAGTGAGCTATGGTGGATTTGCAAAAACAAAAACGCAAAAAATGTAGCTCTTGGAATGTATTTGGCGCTCTCCAGAATCAATATTATAGATGTGGTGGGAATAATTTTTTAACAATTTTAAACTACATATTTATTAATATATTTATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTGCACTTTTGATATCTGAGTCACTTTCTCTGGTACGCCCTTGCAGCAGTCCTGTTTATGCCAAAAAGACCAGCACGCCAGGCTCAGCTGATGGCTATGTGACGCTCTGGAGGAACTATTTGATAATGTGCCTCGGTGTTGCCAAGCCCAGCATCATGAGCCCAGGTCACCTGAGAGCCTCTACACCT[G/T]AAATAATGGCTACCACCCCTGATGGCAGTGTCACGTACGATAACAAGGTCAGTTACACACATATTCTGATATCTATGATTCAGAAAATGAAAGAAATTGTGGCGTAATGAGTGCATTTGTGTGTTTATAACCAGGTGATAGGCACACCATCAGTGGCGTGGCTTCTGAAACAGCTGGTTCCCCTCATGAGATCAGAGAGTTTAGAGATCACAGAGTCTCTAGTCCTCGGTTTTGGACGAACTAATTCCCTGGTGTTCAGGTATTTTTTTATTTTCACCAAACATGCTCCTTTCTCATCGTAAATGACTGGATTTCATAGTTTTAATTAAGTTATTTTCTAAATCAGGGCACATTTACAGCATATACACAGTCCCAATGTACTCTGGCATCCACATTGGTCACATTGGGTTTTTGACTATGGCGAATGAAAAAAGCATTAAGTAATGTGTTTGCCAAACTAAATAGCAGAGATTAGTGTCATTCCATTCTGACGTGTGCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12198
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 |
---|---|---|---|---|---|
ENSDART00000044294 | Nonsense | 1178 | 2973 | 28 | 62 |
ENSDART00000138547 | None | None | 162 | None | 4 |
ENSDART00000142881 | Nonsense | 1250 | 3080 | 29 | 61 |
Genomic Location (Zv9):
Chromosome 10 (position 34970497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33998355 |
GRCz11 | 10 | 33942215 |
KASP Assay ID:
2260-3456.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTAACTGGGCTGTGGATCGCTGTTTCACTGGATCATACCAGCTYGCTT[C/A]AGGATGTTTCAAAGCTATCGCTACTGTGTGCGGTAGCAGGTAATCAGAGC
Long Flanking Sequence:
GTGGGCCTTTCTACAGACGGATACCTGTACAAGTGGCTGGACAATATCTTAGCCTGCCATGATCTCCGAGTAAGCACACTTGCTCTTTTTTTATTGCTGGAAGGATCAGCTTTAGTCCTTGTTATAACCTGCTGATGCTGAACAGACTTCCTGTTTAAATCTTTTGTCAGATTTAATAACCATCATTAAAACTAAACCAGCAAGCCTGACAGGATTAGCTTGAGAGGGATATTTGTATTATTAGCTTTATGAGTAATCTTGTTTGTTTAGGTCTGCCGTTAAACTATAATGACTAGTGTAATGTTGACGTTTGGATTGTCAGTTTTGATTGAAGGAAAAGCACCCATTTAAATACTCATGTTTATATCACCGCCTTGGGATACAGGTGCATCGGCTTGGCTGTGAGGTTGTCATTTTGCTCCTGGAGCTCAACCCAGATCAGGTGAATCTGTTTAACTGGGCTGTGGATCGCTGTTTCACTGGATCATACCAGCTCGCTT[C/A]AGGATGTTTCAAAGCTATCGCTACTGTGTGCGGTAGCAGGTAATCAGAGCTCATGTCATCATTGCCATGGTGTTACTTAATGAAGTTTGAAGGTTTTTATTATCAGACAAAACCTATTTATTTTTCTCTCTTCTTTTTAGGAATTATCCATGTGACATTGTGACTCTTTTGAATCTGGTGCTGTTCAAGTCATCTGACACAAGCAGAGAGATTTATGAGATATCCATGCAGCTCATGCAGGTACGTTTAGTTGCAGTTTTAAGAAAAGGAATCTACAGTGCTCAGCCTATATAAGTACACCCCTCACAAATCTCTCTTTTTAATTCATCCCAGCAGGCACACAACATTATTAGACGTTAATATTAGGTTAGATATAGGTCATGACTTCAGGTGACCAAAATTCAATGTCTAGCGTTTAAGGACAACATTATTTTGACGTCCAATAACGACGCCAAATTATGTTGATATTTGGTTGATTTTAGGTTGTGTTGGAGAGTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13238
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044294 | Splice Site, Nonsense | 1416 | 2973 | 32 | 62 |
ENSDART00000138547 | None | None | 162 | None | 4 |
ENSDART00000142881 | Splice Site, Nonsense | 1522 | 3080 | 33 | 61 |
Genomic Location (Zv9):
Chromosome 10 (position 34973004)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 34000862 |
GRCz11 | 10 | 33944722 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCTCATTAGCCTGTGCGGAGTCAGCAGCGACACCACACTGCTGCCATA[T/G]GTGAGCCWTACAGACACACTYAGCCCACATTCAATTTATTAGCTCTRTAT
Long Flanking Sequence:
GTGATAAATATTGTGTAATATTCTTACATTTTAAATCATTTAACAATATGCTAAAATTTACTAGCAATGTGCTAAATAGTACTAGAGCAAAAGTGAGCATGCTAGACACAGCAGGCTAAAACATGCTAGCAATATTCAAAATCATAAGCCTTCAAACTGTATGCTTTTATGAAGTTATTTTAAGCTTCAACAGTTATTTATAATCAAACTTTACTTGTGTACATGACATTAAAGCAAGATGTGTTGTTATAGGTGGACTATGGAAAAACACAATGCTATGAACGTATTAGAAATCACCCCTTTAAAATTTCATCAAACGACTCGGACATCATTTTCTGTATGGTTTCTCTACAGTATGGGGATGAAGTCCCTGGTCCTGAGATGGAGAACGCCTGGAATGCTCTTGTGTCCAATGACAAGTGGAGTAACAACCTGAGAATAACACTGCAGTTCCTCATTAGCCTGTGCGGAGTCAGCAGCGACACCACACTGCTGCCATA[T/G]GTGAGCCATACAGACACACTTAGCCCACATTCAATTTATTAGCTCTGTATAATAGACTAAACTTGTATCTGACTGTTTTTAGATTAAGAAAGTGGTGATATATCTGTGTCGGAACAACACCATTCAGACCATGGAGGAGCTGCTTTTTGAGCTTCAGCAGACAGACCCAGTAAACCCAGTTGTCCTACACTGCGACAACCCACCATTCTACCGCTTCGCTGCCAGCAACAAGACCTCTGTTGTGGCTTCAGGTAAATCAAATAATAATGTTTGACGCAAGGTATTAGGAGAAACTGTAACACTTTATTTTAAGTACCAATTCTCACTATGAACTAGTGGCTTATTACATGCCTAATATTAGGATTATTAGACCGTTTATTAGTAATTAAAAAGTAGTACATATTCTGCATGATCATATTCAGTACTCCTAATTCTAAACATATAAGCGTAAGCATTAATGAGAAGCTAATTAGGAGTTTATTGAGGCAAAAGTCATAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31789
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044294 | Essential Splice Site | 1745 | 2973 | None | 62 |
ENSDART00000138547 | None | None | 162 | None | 4 |
ENSDART00000142881 | Missense | 1861 | 3080 | 41 | 61 |
Genomic Location (Zv9):
Chromosome 10 (position 34985985)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 34013843 |
GRCz11 | 10 | 33957703 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGGTGGTGGTGGTGGTACAGTGCATGGAGTACTGTCCTGTCCTTACTC[A/T]GGGCTTTCGGACCGCTTTGGTGCCATGAAGACATCACTCCGAAGAATCTC
Long Flanking Sequence:
AAATTTCCATTTATTTCAAGCTCCAAATGTTTATATCGTATCTCAAAAGAAGAACAATATATGTAAATAAAAATAAAAAGATATGTGAACAAACAAGTTTTGTTAATTTATGATCCTTATTATACAACATGTATTGCCCTTTGCAGGAAATGTATGCAGATGCATGTATGCAGAATTATAAAATGGAACACTTAGCAGTTTAGCATATTGCATTCATACTCTAGCTGAATCTGATCACCTGTAAATAGTTAGCATGAGATGAAAACTGAATTTGATTGTTTAATATCACTTTCTTACCACAATAATACATAGTACAAACCTGATGAAAAAATTAAATGGTGTTATTGGAGGAAAATCTCGAGTGTGATGTCACGTGGAAACTATGAATCAGGCCATTTCCCGCATCATTAGGTCAAGTTAGTGAGCAGTAGTTGATGTATTTGTGATTCTGGTGGTGGTGGTGGTGGTACAGTGCATGGAGTACTGTCCTGTCCTTACTC[A/T]GGGCTTTCGGACCGCTTTGGTGCCATGAAGACATCACTCCGAAGAATCTCAACTCTAAGAGTGCTGAGCAGCTCACCAATTTCCTGCGACATGTCGTCTCTGTATTCAAAGAATCCAAATCAGGTAATAATCATTTATGTGTCATCCTCAATACAAAAACATATCCATCTTTTTCTGCATGTGATGACTGAGTTTTAAATTTTGAGTTGAGCTTTTACAACTTTCTTTCACAATATTAAAGTTATGTGCTATGAATTTTCCACATATATATATACACACATACATATATATGAAAGTTAGGGAGAGGTACATCTAGTTCTGTGCTGTATATTTTTTATCCATCATGAAAATTGTGTTACATTTGATATTTTAACTTGAATTTTATATCACACATTTATATGTGTCCAAAACTATTTTGAGTTATTTATATACTGTATATTATTTATAGTGTTTATATTTATTTTGATTTGTTTATAGTAGTTATTTATGGTATATTATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12244
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044294 | Splice Site, Nonsense | 2784 | 2973 | 60 | 62 |
ENSDART00000138547 | Splice Site, Nonsense | 9 | 162 | 2 | 4 |
ENSDART00000142881 | Splice Site, Nonsense | 2891 | 3080 | 59 | 61 |
Genomic Location (Zv9):
Chromosome 10 (position 35019150)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 34047008 |
GRCz11 | 10 | 33990868 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTGATTCCTTTATTGTCATGTGACTAAACTATTCATATCTTCCACAG[C/T]AATTGGAGTTGTGTCAGCGACTATACAAACTTCACTTCCAGCTCCTTCTG
Long Flanking Sequence:
TTACACCTGATTTTCTTGTGCACTTTCACCTGTTCTGCATGATTTATACGGGTTGCTTCTTGGGTTGAATCTGACTGGCACTAATCCTCTAATTATGTTAATGGGATTTCTGAGCTGACATTCGGTCTCACAGATTGCATGCTGGGAATTAATGCTGTCTATTTCTCCCTTGTCAACTCTTTTCTGTTTTATGACATGCTTGCTCTGCAGCAAATGGAAACTCTGGCTGTAAGTTTGAAACTAAAGAACCGTTCTCTTTCTTTGTCTTCTGCTAGAGCGAGTGTTTTATAGTTTAGTACATGCATTCAATTCAGAGCGTTTATATGCACATTCCTACACAACCTTAACCACTTCTATTATTGAAATTTATATTTTAATTGTTTTTGTGCATATAAACACCCTCATTGATGTATATTTGAGTTGTGTATTTACTGTTTGTGGCTGTGCATATGTGTGATTCCTTTATTGTCATGTGACTAAACTATTCATATCTTCCACAG[C/T]AATTGGAGTTGTGTCAGCGACTATACAAACTTCACTTCCAGCTCCTTCTGCTGTTTCAGTCCTATTGTAAACTTATCGGACAAGTGAACACCATCAGCTCTGTGCCGGAGGTATACTCTTTTGAATGGTTTTTAAATTTGAATCAAAATTAATGGTCACACTTTATTTTGATGGTGTGTTTGTTGAATTTAAGTTACATTGCATCTACATGACTAATTCTCATTAGATTATAAGTAGACTGTTAGGTTGGGGTTGGGGTTAGGGTTAGTGTAAATTGAAATGTACTTGCAAAGTTTTCTGCAAAGTCAGTTAATTGTCTGTTGAAGGAGCAGTACCAACAGATATTAAGCAGACAGTCTACTAATACTCAAGTGGACCATCAAAATAATGTGTTACAAAGCAAATTTTTCAATGTGAGCAGATTTGGAAAACAATTATTTGACCACCAGTTTCTTTAGATTGATTAGGTATGGTTAATGTATAGTGTGTGTCTTTTTTCT
Associated Phenotype:
Not determined