ZMP
FAT4
Ensembl ID:
Description:
FAT tumor suppressor homolog 4 (Drosophila) [Source:HGNC Symbol;Acc:23109]
Human Orthologue:
FAT4
Human Description:
FAT tumor suppressor homolog 4 (Drosophila) [Source:HGNC Symbol;Acc:23109]
Mouse Orthologue:
Fat4
Mouse Description:
FAT tumor suppressor homolog 4 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:3045256]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6331 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1616 | Nonsense | Available for shipment | Available now |
sa14018 | Nonsense | Available for shipment | Available now |
sa10891 | Nonsense | Available for shipment | Available now |
sa45505 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10334 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6331
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067146 | Nonsense | 210 | 2485 | 1 | 24 |
ENSDART00000122984 | Nonsense | 212 | 2702 | 1 | 22 |
ENSDART00000131031 | None | None | 2346 | None | 10 |
Genomic Location (Zv9):
Chromosome 14 (position 455954)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 424447 |
GRCz11 | 14 | 447340 |
KASP Assay ID:
554-4456.1 (used for ordering genotyping assays)
KASP Sequence:
CAGATTGCAGCCAGTGATCTGGATGAAGGTGCAAACGCTGAWATAACCTA[T/A]CTTTTAGATGAGGGGACYCCTTTTCAGATTGACCCCAAGGCTGGGACTGT
Long Flanking Sequence:
GTGCGCATCGTGGTGCTGGATATCAATGATAACGCGCCCGTGTTTCCCGACGCGTCGATAGTGGTGTCGTTTAAAGAGGACGCGAGCAGCGGGCGGCAGGTCATTCTGGACACCGCCACCGACGCGGACATCGGTAGCAACGGAGTGGATCACACCACATACCGGATCATCAGCGGGAACGACCAGCGGAAATTCCGCCTGGACATCACCGTCAACCCGAGCGGAGAGGGCGCGTTTTTACACCTAGTCTCCACTGGAGGGCTGGACAGAGAAACGACTCCATTCTACCAGCTGCTTATTCAAGTGGAAGATAAAGGAGAGCCCAAAAAGTTTGGCTATCTTCAAGTAAACGTCACTATTCAGGATATAAACGACAACCCTCCCTCTTTTGACCATGAGCAGTATCAGACTAGTGTGTTTGAGGATGCTGCCGTCGGCTCTAGTGTGCTGCAGATTGCAGCCAGTGATCTGGATGAAGGTGCAAACGCTGAAATAACCTA[T/A]CTTTTAGATGAGGGGACTCCTTTTCAGATTGACCCCAAGGCTGGGACTGTTGTTATAAAGGAGGGGTTGGATTACGAGACTAAAAGGGAGTATTCTCTCACCATCCACGCTGTGGATAACGGCGTCCCTTCACTTTACACTAGAACTGAAGCTACTGTTAAATTGCTCGATGTTAACGATAATGACCCCGTTGTTAAATTTCGATACTTTCCTACGACTTCCAAATTCGCGTCAGTGGATGAAAACGCCCAGGTGGGCACTGTTGTAGCACTGTTGACTGTTTCTGATTCAGACTCGTCCACCGCCAACGGCAACATCTCAGTTTCTATACTTGGCGGAAACGAGCAAAGACACTTTGACGTGCACAGTTCGCCCGTCCCCAATTTGAGTCTGATCAAAGTGGCCAGCGTGCTAGACCGAGAGCGCATTTCATCCTACAACCTCACTGTTTCAGTGTCAGATAACGGCAAGCCCTTGGCCCGCTCGTCTTTCGCTAGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1616
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 |
---|---|---|---|---|---|
ENSDART00000067146 | Nonsense | 712 | 2485 | 3 | 24 |
ENSDART00000122984 | Nonsense | 929 | 2702 | 1 | 22 |
ENSDART00000131031 | Nonsense | 492 | 2346 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 14 (position 453805)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 422298 |
GRCz11 | 14 | 445191 |
KASP Assay ID:
554-1557.1 (used for ordering genotyping assays)
KASP Sequence:
ACCAGCTCTCRTATGAGGTCACCATTCTCGAATCAGAACCCGTCAATAGT[C/T]GATTTTTCAGAGTTGAGGCTACTGATAAAGACTCTGGCGTCAATGGGGAA
Long Flanking Sequence:
AGATTACAGCGTTAGGGCTGATAGACAGAGAAGAGCAGGCTTTCTATCAGCTCAGGGTGATCGCTAGGGCCGGGGAGGTCACAGGGGAAACTTTAGTGAACATTACAGTCAAGGATTTGAACGATAACGCGCCTAACTTCATGCATAGCGTCGAGCATGTTAGTGCTGTTGAAAACTGGGCTACAGGTCATCACATATTCCAAGCTAAAGCTTCAGATCCTGATGAGGCGACCAATGGGATGATTGTATACAGTCTCAAGCAAAACCCTAAAGGCTTGTTTCACATCCACGAGAAGCATGGCTTAATCTCTCTCACCGGCCCTCTTGAAGTCACCACGAGTTCATATCAGCTGGAGGTCGTGGCTTCTGACCTGGGCGTCCCTCAGCGCACGTCAAGCCTATTCCTCACTATTAGTGTGTACGACGTTAACGATAACGCTCCAGTCTTCGACCAGCTCTCGTATGAGGTCACCATTCTCGAATCAGAACCCGTCAATAGT[C/T]GATTTTTCAGAGTTGAGGCTACTGATAAAGACTCTGGCGTCAATGGGGAAATCGTGTATGATATCATTAGCGGGAACACGCGTGATGTTTTCGGGATTTTCCCTGACGGGCAGTTGTATATAAAGGCAGATCTGGATAGAGAGGTGCAAGATCGCTATAGTTTATTAGTGGTGGCTAAAGACAGAGCGGTCGAGTCTCTGAGCGCTAGTGTTAACGTGAGCATCCTCCTGGATGACATCAATGACAACCGTCCGCTCTTTAACAGCACTAACTATGTGTTTCACTTCGAGGAAGAGCAGGAGCGAGGCGCTCTAGTTGGACGGGTGTTCGCTGAGGATAAAGACTTCGGGCCTAACAGTGAAGTGCGGTATTCCTTTGAAACGCCGCAGTCGAATTTTGAGCTCAACGCAATCACTGGCGTATTAACAAGCACTCTACAGTTAGACCGAGAGTCTTTAATGAGGCAGAGAGGCGCCGCGGTGTTCAGCTTTACAGTGCTG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa14018
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 |
---|---|---|---|---|---|
ENSDART00000067146 | Nonsense | 818 | 2485 | 4 | 24 |
ENSDART00000122984 | Nonsense | 1035 | 2702 | 2 | 22 |
ENSDART00000131031 | Nonsense | 706 | 2346 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 14 (position 453163)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 421656 |
GRCz11 | 14 | 444549 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAARGACATTTACCAGGCCTCGATYGCAGAATCCGCCCAGAACATGACA[C/T]AGCTGCTCCGAGTGTCCGCCTCAGATGTGGACGAAAACAAAAACGGCCTC
Long Flanking Sequence:
AGGTGCAAGATCGCTATAGTTTATTAGTGGTGGCTAAAGACAGAGCGGTCGAGTCTCTGAGCGCTAGTGTTAACGTGAGCATCCTCCTGGATGACATCAATGACAACCGTCCGCTCTTTAACAGCACTAACTATGTGTTTCACTTCGAGGAAGAGCAGGAGCGAGGCGCTCTAGTTGGACGGGTGTTCGCTGAGGATAAAGACTTCGGGCCTAACAGTGAAGTGCGGTATTCCTTTGAAACGCCGCAGTCGAATTTTGAGCTCAACGCAATCACTGGCGTATTAACAAGCACTCTACAGTTAGACCGAGAGTCTTTAATGAGGCAGAGAGGCGCCGCGGTGTTCAGCTTTACAGTGCTGTCCTCAGATCAGGGTCTTCCCAAACCCCTCAAAGACCAGGCCAAAGTGCAGGTGTACATACAGGACATCAACGACAACCCGCCCAAGTTCACTAAGGACATTTACCAGGCCTCGATTGCAGAATCCGCCCAGAACATGACA[C/T]AGCTGCTCCGAGTGTCCGCCTCAGATGTGGACGAAAACAAAAACGGCCTCGTCCACTATGACATCACCGAGGGGAATGAGGAGAAGCAGTTTAGCATCGACAGCAATTCCGGTCAAGTTACTCTAGTGGGGAAACTAGACTACGAAACAACACCCTCTTACTCCCTCAAAATCATCGCAGAGGATTCTGGGAGCGTCCCTCTGTCTTCAACCTGCGTGCTGAGCATCAGCGTTCTGGATGATAACGATAACTCTCCGTCATTCCCCAAATCTACACTCTCAGTGGATGTGCTGGAGAATATGAGGATCGGGGAGCTGGTCGCCTCTGTGACCGCCACCGATTCCGACTCCGGATCCAATGCTGATATCACATACAGCATCTCCGCCACTAATAACCACGGCACATTCAGCATCAGCCCCAACACCGGCAGCATTTTCCTCGTCAAGAAGCTCGATTACGAAACCCAGTCTCTTTACAAACTCAACGTCACAGCTAAAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10891
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067146 | Nonsense | 874 | 2485 | 4 | 24 |
ENSDART00000122984 | Nonsense | 1091 | 2702 | 2 | 22 |
ENSDART00000131031 | Nonsense | 762 | 2346 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 14 (position 452995)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 421488 |
GRCz11 | 14 | 444381 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTACTCTAGTGGGGAAACTAGACTACGAAACAACACCCTYTTACTCCCTC[A/T]AAATCATCGCAGAGGATTCTGGGAGCGTCCCTCTGTCTTCAACCTGCGTG
Long Flanking Sequence:
CTCTAGTTGGACGGGTGTTCGCTGAGGATAAAGACTTCGGGCCTAACAGTGAAGTGCGGTATTCCTTTGAAACGCCGCAGTCGAATTTTGAGCTCAACGCAATCACTGGCGTATTAACAAGCACTCTACAGTTAGACCGAGAGTCTTTAATGAGGCAGAGAGGCGCCGCGGTGTTCAGCTTTACAGTGCTGTCCTCAGATCAGGGTCTTCCCAAACCCCTCAAAGACCAGGCCAAAGTGCAGGTGTACATACAGGACATCAACGACAACCCGCCCAAGTTCACTAAGGACATTTACCAGGCCTCGATTGCAGAATCCGCCCAGAACATGACACAGCTGCTCCGAGTGTCCGCCTCAGATGTGGACGAAAACAAAAACGGCCTCGTCCACTATGACATCACCGAGGGGAATGAGGAGAAGCAGTTTAGCATCGACAGCAATTCCGGTCAAGTTACTCTAGTGGGGAAACTAGACTACGAAACAACACCCTCTTACTCCCTC[A/T]AAATCATCGCAGAGGATTCTGGGAGCGTCCCTCTGTCTTCAACCTGCGTGCTGAGCATCAGCGTTCTGGATGATAACGATAACTCTCCGTCATTCCCCAAATCTACACTCTCAGTGGATGTGCTGGAGAATATGAGGATCGGGGAGCTGGTCGCCTCTGTGACCGCCACCGATTCCGACTCCGGATCCAATGCTGATATCACATACAGCATCTCCGCCACTAATAACCACGGCACATTCAGCATCAGCCCCAACACCGGCAGCATTTTCCTCGTCAAGAAGCTCGATTACGAAACCCAGTCTCTTTACAAACTCAACGTCACAGCTAAAGACAGCGGGAGGCCGTCCAGATCCTCTTCAATCCCGGTTATCATTCATGTACGAGATTTTAACGACAACCCTCCTGTTTTTACACCAGGAGACATTTTTAAATCGATCCCCGAAAACCTCCCGATCTCCACTTCTGTGATGTCCATAACAGCTCACGACACCGACGCGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45505
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067146 | Essential Splice Site | 1700 | 2485 | 16 | 24 |
ENSDART00000122984 | Essential Splice Site | 1917 | 2702 | 14 | 22 |
ENSDART00000131031 | None | None | 2346 | None | 10 |
Genomic Location (Zv9):
Chromosome 14 (position 401926)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 378910 |
GRCz11 | 14 | 389496 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCACACAGAAACACCAACTGACCCAGCTGGGAAAATAATAAGTTATGC[A/G]GTGTTTTAGATGTGGTAAAGTCGATATAGATATGCAGTATTTTTATTTAG
Long Flanking Sequence:
TACAATTAAAAGATAATATATTGTGTGCATTACATTGATGAACAGACTACATCCTTAAAAAAAATTCTCAAACATGGATTAACCAAACGTTGGGTCATTTTTTTTTTACCCAAAAAGTTGGGTTTGTCCATATCTGACCCAGCATTGAGTTACAACAGCCAAGCATTTTACAGTGTAACTTGCATAAAAAAAAATAATCAGTTCATTCCTTCCTTCAGCTTAGTCCCTTTATTCATCAGCGGTCACCACAGTGGAATGAACCGACAACCTATCCAGCACGTTTTACACAGCAGATGTCCTTCTAGCCACAACCCAGCTCTGGGAAACACCCATACACACTCATTCACACACACACACACACACTCATACACTATATGGCCAATTTAAAGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCATGTGAACATGAGGAGAACATGCAAACTCCACACAGAAACACCAACTGACCCAGCTGGGAAAATAATAAGTTATGC[A/G]GTGTTTTAGATGTGGTAAAGTCGATATAGATATGCAGTATTTTTATTTAGTACATACATTTAAACAGTTGTATAATCAGTGTTAAAGTGTGTGAGGCAGCAGACAGCAGATCTCCCAGGATCAGACACGGGTCACCGTGATTCAGGACTGAATGAATGAGAACACACATACTCACACACACACACACACACACACACACGTTTCCTTGTGCTCATCAGATAAACGCTAAGCTGACACCATGCTAATCTCTTTGTCTTCCCAGTGAGGATGAGGCGATTAGAGCGTGTGCTAGCAGCTTATTAGCATGTGTTATTAGTTCCACTAATCTGCAGGAACAACAGGCTCTGGAGGACTCTGAGCAGCGGGAAATCTGCCCTGTGTTTACCAGCAGCCTTTATTCTACTGTACTGCACACACCATGATCAACTCATGCATGCTGAAGATCAGTGTTAATCACATTCAGTGTTGGGTCAAATAGGGACATACCCAACCGCTGGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10334
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 |
---|---|---|---|---|---|
ENSDART00000067146 | Essential Splice Site | 2477 | 2485 | 24 | 24 |
ENSDART00000122984 | Essential Splice Site | 2694 | 2702 | 22 | 22 |
ENSDART00000131031 | None | None | 2346 | None | 10 |
Genomic Location (Zv9):
Chromosome 14 (position 389605)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 366589 |
GRCz11 | 14 | 377172 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACTTCCTTTCCAATYACTACCTCAGTTTCTTGCGCATCGCCAATTCACA[G/A]TTAGCCGGTCTAGGCACTGGAGTCCAGATCTATGGGGTGTTTGAACTTAA
Long Flanking Sequence:
CGAGAGCAGATAAGCGATTTCTACCTCTCTGTGCTCATCAAAGACTCAGGAATTCCTCAGATGTCCTCAACAGGAACTGTCCACATCAAAGTCAATGATCAGAATGATAATCCCTCGGAGTCTCGCTCTGTGGAGATCTATGTCCATTATTTTGGAAATATGTTCCCTGGAGGATCCCTGGGGGTGGTGAAGCCACAGGATCCGGATATCCAAGACACGTTTCAGTGTTCTCTGACTCCGCCAGCGGCTCTCCTCTTCAGCATTCCCACCGGAACCTGTGACCTCATCTCTAACAGTCGCTCCACAGATGGAACGTTTGATTTATCAGTGCGTAGCAACGATGGCGTCCACAGTGCTGTCAACAGCCATGTGCGTGTTTTCTTCATTGGGTTTAACAATGCCACAGTGGACAACAGCATCCTGATACGTGTCACCACCAAAAGCGCAAGTGACTTCCTTTCCAATCACTACCTCAGTTTCTTGCGCATCGCCAATTCACA[G/A]TTAGCCGGTCTAGGCACTGGAGTCCAGATCTATGGGGTGTTTGAACTTAACAACAGTACTTTTTTAACAGCTGCAGTCAAGAGAGGTCACAGCCAGTACGTCAATCCAAGTGGAGTAGCAACATTCTTCCAGAGCATTAAAGAGGTTCTGCACAGACAAAGTGGAGTTAAGATTGACTCCGTGGACCATGATCCCTGCTCCCACAATCCATGTCAAAATGGGGGCAGCTGCAAGAGGCGGCTGGGTGTTGGCCCAGAAATGAAGACTGAGGAGAGTGTCCCGGTTATCCTCGTCTCAAATCAGCCCCTACAGCCGTACGCCTGTAACTGCAGGCCAGGGTATGCCGGTGCCCTTTGTGAAACGGATATCGATGAGTGCCAGCCGACACCTTGCCACAATGGTGGAACTTGCCACAACTTGGTGGGAGGATTCTCATGCACGTGCCCAGACGGTTTCACTGGGATGGCTTGTGAGAGGGACGTCAACGAGTGCCTTTCGAA
Associated Phenotype:
Not determined