ZMP
fryl
Ensembl ID:
ZFIN ID:
Description:
furry homolog-like [Source:RefSeq peptide;Acc:NP_001153139]
Human Orthologue:
FRYL
Human Description:
FRY-like [Source:HGNC Symbol;Acc:29127]
Mouse Orthologue:
Fryl
Mouse Description:
furry homolog-like (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1919563]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23688 | Nonsense | Available for shipment | Available now |
sa23689 | Essential Splice Site | Available for shipment | Available now |
sa23690 | Nonsense | Available for shipment | Available now |
sa12460 | Nonsense | Available for shipment | Available now |
sa43429 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18085 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23688
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 |
---|---|---|---|---|---|
ENSDART00000058522 | Nonsense | 73 | 3079 | 3 | 59 |
ENSDART00000132248 | Nonsense | 129 | 3142 | 4 | 60 |
ENSDART00000136922 | None | None | 148 | None | 5 |
ENSDART00000144261 | None | None | 182 | None | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 23330902)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 23444289 |
GRCz11 | 20 | 23343389 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTACAGTTAATAAGCTCTATGAGCTCCATAGCAGAACACTGTTTGCCTT[C/A]GCTGCTGCGGACACTGTTTGACTGGTACAGACGACAGAGCGGGACAGAAG
Long Flanking Sequence:
CTATAAACTACTGATTTTTGTCTCTCAAATAAATAAAAGTCATTTGAGTCAGTTTATTTTCATTAAATATTTAAAATGTTAATGTTTTGAGACTTGTTTATATTAATTTTAGACACCACTATCTTCAAAAGAGATTGGTGAAATAACCCTGATTTCCACACAAAAAATAAACATGTTTTTTCTTTCTAATTGTAATTTTCTGATGAAAATTAAATGCTCTAAAAAATTATATTTATATGAAATTTTAAACGAGTATCAGGCCTTTATAGATATTGCTATCAAAATCTAGCTGTTTTTAATTTTGCTTACTTGAAGTTAGTTGCATTATACCAGTCATGTTGAAATGTCACAATATATTCTAAATGACTAAATAATATTGTAAAATAATTATATTGAGGTTTTTACCCCTCATGAAAGGTTAGTTGTTGAGCTTCATTATTGTCTTTGTGTGTTACAGTTAATAAGCTCTATGAGCTCCATAGCAGAACACTGTTTGCCTT[C/A]GCTGCTGCGGACACTGTTTGACTGGTACAGACGACAGAGCGGGACAGAAGACGAGTCGTACGAGTACAGACCTCGCTCCAGCACCAAATCCAAAGGGTGAGGAGACCTGATACCAAACATACATCTTACAAAAATACAAAACAGAAGAAAGTTTCAGTTTTATCTTCTATTCAGCCAGTTCTGCCACAGCTCCAGATGCTTTTTTTCTTGTGACTATTTGGAGTTCATAAAATACGATTATATTCTAACTTCTGAATCTTTCTTTTTAGAGATGAGCAACATCGGGATAAAGACTACCTAGTGGAGCGAAGGGACTTAGCCATAGACTTCATGTTTTGTTTAGTTTCTGTGGAAGTTTTGAAACAGGTAAGGTGTTGTGCGTTTCATTGCTTAGGTGTGGTGTTTTTCTGAACTCAGAGATAGGTGTGTTGTGGTATTAGCATGCATAGACTTGCTAATGGTATATCAAGGATTCTGCTGTAAAATAGTGACCCTTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23689
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058522 | Essential Splice Site | 717 | 3079 | 18 | 59 |
ENSDART00000132248 | Essential Splice Site | 780 | 3142 | 19 | 60 |
ENSDART00000136922 | None | None | 148 | None | 5 |
ENSDART00000144261 | None | None | 182 | None | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 23353551)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 23466938 |
GRCz11 | 20 | 23366038 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTTCTCAAAGAGGTCCGATCGCTGCACACGGCCCTCGGCATTGCCAAG[G/T]TAACCATCCTCCCTGCATAACTTCCTGTTATTCTCCCACATCGCATGACC
Long Flanking Sequence:
TTCCTCACTGTAAACTATAAATGCTTTGAGCACAATTATGAGCATATTTAAGTGATTACTAAATAGAATCATTTAATTCTGAAGATTGGAGTAATGATTTGTTTTTACCATAAATAATTTCAAGTTTATTAAAAAAAGAAAACATTTTAAATGGTAATAATATTATTGGACTTTTCATGAAAACAACAAAAACAAAATTGTACTCTTTTAAAAACGTCTAAAAGACTTGCTGACCTTAAACTTTTGAATGCTTTGTGTTTTTCTTATTTTAAGTTTTTCTTGTAGCATATCATACATTTTAGCTTGTGTTTTACCTTTGTTTGTTTCTGTTTTAGAGCCCGTCTCTCCCTCTGGAGCGATCTCCTCTCTGGACAGTTCTGCATGTGGTGGAGGGTCTGGCTCTGGTGGTGCTGTGCAGCTGTCGACCTGCAACACGCAGACTCGCTGTCAACGTTCTCAAAGAGGTCCGATCGCTGCACACGGCCCTCGGCATTGCCAAG[G/T]TAACCATCCTCCCTGCATAACTTCCTGTTATTCTCCCACATCGCATGACCTCCTTTGTTTGCTCTTCAAATTTATTGCTTCGTCTTTATCTTTGTTTTTCCTCTTTCTCAGGGAGATGAAGAGCTGGCTATAGACGTGATGGACAGATTGAGTGCTTCAGTCCTTGAGAGCTTTATTCATCTTACTGGGGCTGATCAGGTAGGGAAATGTGAAACAGTATGTATTTTCAATGTTTGTGTACAATTCAAACAAAAAAATAATAATAAAAATGGCACATTGTTTTAAAATTAACATATTTTTGCCCCTTTTTGCTGTAGACAAGTCTGCTGTATTGTCCCAGTGGAATAGACTTACAGACTCTGGCAGAGTGGAGTTCGTCTCCTATCAGCCATCAGTTTGATGTCGTAAGCCCCTCCCACATCTGGGTGTTTGCCCATGTGACGCAAGGTCAGGACCCCTGGGTCATCAGTCTGTCTAGTTACCTGCGGCAAGAGAACCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23690
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058522 | Nonsense | 1225 | 3079 | 29 | 59 |
ENSDART00000132248 | Nonsense | 1288 | 3142 | 30 | 60 |
ENSDART00000136922 | None | None | 148 | None | 5 |
ENSDART00000144261 | None | None | 182 | None | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 23359784)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 23473171 |
GRCz11 | 20 | 23372271 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTGAATCTCATCTTGTTTAAGGCTGCAGACTCTTCCAGAGACATCTA[T/G]GAGGTTGCAATGCAGCTATTGCAGGTCCGTGGAAATTATTATTATTATTA
Long Flanking Sequence:
TGTTGTGGTCCAGTGGCTGATAACGTCGGCCTGTCCTCTGATGGGTATCTGTATAAGTGGCTGGACAACATTCTAGATTCTCAAGACCGGAAGGTATAACTTTATTCCAGTCAGATTAGTATCACTAACCGGTCGACTGTTATTAACTGTGATGAGTCTGTCTTTGTGCTCAGGTGCATCAGTTGGGTTGTGAGGCGGTGATGTTGTTATTAGAACTGAACCCAGATCAGAGTAATCTGATGTTCTGGGCAGTGGATCGCTGCTATACTGGCACGCGAAGGGTTGCTGCAGGGTGCTTCAGAGCCATTGCAAATGTCTTTCACAACAGGTATATACTACAAGGTTTACAATATTAACTGTGACTGAATTCGTGACAGTAAAAAGGTTGGTTTATTGAACAATGTGTGCATGTTTTTGTCTTGCAGGGATTATCAGTTTGACACTGTGGTTTTGCTGAATCTCATCTTGTTTAAGGCTGCAGACTCTTCCAGAGACATCTA[T/G]GAGGTTGCAATGCAGCTATTGCAGGTCCGTGGAAATTATTATTATTATTATTTTCAGTCAAAGGAAGCCATAACAGCACAATTGGGTTAAAAAAATAATAATAAATAAAAATGTTTTTTTTGGTTTTGTATTCCTATATTTTCAGTGTTACATCCCTGATGTTAAGTGTCTAGGAGTGAGAGGAATAGTGAAAAGTTGGTTGGAGTTAGTGTGGATCAGTGTCCTGCCTTTACCACAACACACAAAATTCAGTTAAAGAATTGGTTAACAAAAATGTACCATGATAAATCAAAACTGGGAGGCTAAAATGGGCTTCAGGAGGGGGAAGGCCAAAACAACAAACAAAAGTACACTCTAGCTAGTTAGGGAGAAAAGAAGTCAAATTAAATTAACACCAGAAATGTACAGGAATGTACATTACCATGAGCAAAGAGTCAAAGGGTTTTAGAAATAAAATGGCACCCACCTTCCTACAGCTTCCACACACAAAGTTAAGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12460
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 |
---|---|---|---|---|---|
ENSDART00000058522 | Nonsense | 1587 | 3079 | 36 | 59 |
ENSDART00000132248 | Nonsense | 1650 | 3142 | 37 | 60 |
ENSDART00000136922 | None | None | 148 | None | 5 |
ENSDART00000144261 | None | None | 182 | None | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 23365994)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 23479381 |
GRCz11 | 20 | 23378481 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTWCCGTTTCCACCCACTGGCGGCTGCTGGTCACCAMTGGTCGATTACT[T/A]GCCTGAAACCACCACACCTGGAGTCTCCCTGCACAGGTAAARAACCTGCK
Long Flanking Sequence:
AAATCTACTTATCCAAAATTTGTATTTAATCAAAATAACTGAGTTTTGATATTATTAATGGTAGGAAATGTACAAAATGTCTTGATGAAACATGATCTTTACTTAAACCTAAATTTATTATTTCTTTTAGCAATACTGTATATTTTACAGTAGGCTATTGCGAAAAATATACCCATGCCACATAAGACGATTTCTGAAGAATCGTGTGTCATTCCATTATTTTAACACTGGTGGTCAAATTATTACTGCTTAAATGTATTTTTGGATTAAATACATCTACTATTAGTGAGCATAACAAACTTTTTTTTTCTTGTTTAACAAGAGGATAAAATCTTAGTGCAACTCTAAGCTTTTCGACATTAATAACATGTGGTTACTCCCTCTAGGTGACTCTATGCCTGTCTATGCTAACTGGCGTCTGAAGGTAATGGACCATAACCGGCCAGAGCCCCTACCGTTTCCACCCACTGGCGGCTGCTGGTCACCACTGGTCGATTACT[T/A]GCCTGAAACCACCACACCTGGAGTCTCCCTGCACAGGTAAAAAACCTGCTCACTGTGTCTTATATGGATTCAGTGTTGTTTTTCTTAACCACGGACCTCTGACAACACATTCTCATTCCTTTTCAGATGTAACATCGCTGTGATCTTGCTGACGGACCTCATTGTAGACCATGGGGTAAAAGTGGAATGGAGCGCGTACCTTCATCTGCTACTGCATTCCATATTCATAGGTAACACATACACACGTATACTGTTTATAAAAAGCATTAGCACTAGATTGTGCTACATTAAATATAACATAATGATTGTTTGTGTAGGTTTTGACCATCAGCACCCAGAGGTCTATGAGCACTGCAAGCGTTTACTGCTTCACCTGCTGGTGGTTCAGGGCACCAACAGCAGCGTCCAGTCACTGGCGTCTGTACTGCTTCGCAACCGTGAGCTGAACGAACCCAGAGTTCTGACCGTCAAACCCACTCTTCAGGAGTTTAACCTCACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43429
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058522 | Essential Splice Site | 1599 | 3079 | 36 | 59 |
ENSDART00000132248 | Essential Splice Site | 1662 | 3142 | 37 | 60 |
ENSDART00000136922 | None | None | 148 | None | 5 |
ENSDART00000144261 | None | None | 182 | None | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 23366031)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 23479418 |
GRCz11 | 20 | 23378518 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGTCGATTACTTGCCTGAAACCACCACACCTGGAGTCTCCCTGCACAG[G/A]TAAAAAACCTGCTCACTGTGTCTTATATGGATTCAGTGTTGTTTTTCTTA
Long Flanking Sequence:
ACTGAGTTTTGATATTATTAATGGTAGGAAATGTACAAAATGTCTTGATGAAACATGATCTTTACTTAAACCTAAATTTATTATTTCTTTTAGCAATACTGTATATTTTACAGTAGGCTATTGCGAAAAATATACCCATGCCACATAAGACGATTTCTGAAGAATCGTGTGTCATTCCATTATTTTAACACTGGTGGTCAAATTATTACTGCTTAAATGTATTTTTGGATTAAATACATCTACTATTAGTGAGCATAACAAACTTTTTTTTTCTTGTTTAACAAGAGGATAAAATCTTAGTGCAACTCTAAGCTTTTCGACATTAATAACATGTGGTTACTCCCTCTAGGTGACTCTATGCCTGTCTATGCTAACTGGCGTCTGAAGGTAATGGACCATAACCGGCCAGAGCCCCTACCGTTTCCACCCACTGGCGGCTGCTGGTCACCACTGGTCGATTACTTGCCTGAAACCACCACACCTGGAGTCTCCCTGCACAG[G/A]TAAAAAACCTGCTCACTGTGTCTTATATGGATTCAGTGTTGTTTTTCTTAACCACGGACCTCTGACAACACATTCTCATTCCTTTTCAGATGTAACATCGCTGTGATCTTGCTGACGGACCTCATTGTAGACCATGGGGTAAAAGTGGAATGGAGCGCGTACCTTCATCTGCTACTGCATTCCATATTCATAGGTAACACATACACACGTATACTGTTTATAAAAAGCATTAGCACTAGATTGTGCTACATTAAATATAACATAATGATTGTTTGTGTAGGTTTTGACCATCAGCACCCAGAGGTCTATGAGCACTGCAAGCGTTTACTGCTTCACCTGCTGGTGGTTCAGGGCACCAACAGCAGCGTCCAGTCACTGGCGTCTGTACTGCTTCGCAACCGTGAGCTGAACGAACCCAGAGTTCTGACCGTCAAACCCACTCTTCAGGAGTTTAACCTCACAGGTGCTCTTTGCCTTTTTGACTCAAAGTTCCCACCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18085
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058522 | Essential Splice Site | 2701 | 3079 | 52 | 59 |
ENSDART00000132248 | Essential Splice Site | 2764 | 3142 | 53 | 60 |
ENSDART00000136922 | None | None | 148 | None | 5 |
ENSDART00000144261 | None | None | 182 | None | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 23390171)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 23503558 |
GRCz11 | 20 | 23402658 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGACGATCGGTGCGAGGAAGAAGAGGCAGATTTTTATGGACTTTCCAG[G/A]TTGGTCTATGATTTCKGTTGCGGTMATTCATAGGGTGAATAWTTGACTCA
Long Flanking Sequence:
AATATTGTTCTAATATCATGCATCTCTAATTGAAATGAGCATTGAAAAGAGCTTGACCAAAAATACAGTTTGCTCTATTTTTATCATTATTTCATTCTTTATTATGTCTGTTTGCAGGATGCCAGTGTAACAGCTGGGGATGAATTAAGCAGCAGTGTCAGTGAGGATACGGGGTTTGGCAGTGCCCCCCCTCTGCCCTCAGACCCCCCCGAGCTCTGTGACTTACATGACTCCCAGGACCCCACAGACGACCTGGATCCAGCCCCACCACCTCCACCAGCCATGGACAGCCCGCCTGGGTCCCTCTTTGATGACGAACCAGGGATTACACCCTCCGTCATAGACACCACGTTAGACTCCATGTGTGAGGAGGAGACCGTCCTGCCACTAGTTTTGAACTCGGCCCCTGATTCAGTCTGTGAGGATGATGTGACACTCGCTTTGAAAGAGCTGGACGATCGGTGCGAGGAAGAAGAGGCAGATTTTTATGGACTTTCCAG[G/A]TTGGTCTATGATTTCTGTTGCGGTAATTCATAGGGTGAATATTTGACTCAATGATCGGTTCTGTTTAAAAAACTTTGTTGTTGTATGCTGCCTACAAAGATAGCTCCCTTTAAAGGCAGCATCCAAACCAAAATGAAACCTAAAAAGTTGATCTGAACACTCACTTGTTTTCTCGCATGAAAAATAACATCCATATGTAATCATAAAAATTTGAAATCATGTATAGTAGTCTGCATTTGAAGTTGATCATTATCATTAAAGACTTCCTAAAACCTAAACAAATAACCATTTTTGTTTTGGGACAACTTTGGTGTCCAACTTTTGATCCTCTTTAATGTTAGATACTCTAGTTAGTACTTTAAAAAAAAAAAACTTTCATTTGTTCCTAATAAGTGCTTATTGACATAGTTGTAAACTTATAACAGCTTTCTACATCCGTAAGGGGTTCAGTATCATAAAGACTTTGTTCTCAGGCAGATGTTTTAAAATCTAATTTCAAG
Associated Phenotype:
Not determined