ZMP
si:ch73-60e21.1
Ensembl ID:
ZFIN ID:
Description:
Wu:fb74h11 protein [Source:UniProtKB/TrEMBL;Acc:Q6NXC0]
Human Orthologue:
FMNL3
Human Description:
formin-like 3 [Source:HGNC Symbol;Acc:23698]
Mouse Orthologue:
Fmnl3
Mouse Description:
formin-like 3 Gene [Source:MGI Symbol;Acc:MGI:109569]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37715 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10571 | Nonsense | Available for shipment | Available now |
sa24340 | Nonsense | Available for shipment | Available now |
sa43989 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37715
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 |
---|---|---|---|---|---|
ENSDART00000023359 | None | None | 390 | None | 11 |
ENSDART00000109023 | Nonsense | 567 | 992 | 18 | 27 |
ENSDART00000144554 | Nonsense | 60 | 485 | 3 | 13 |
ENSDART00000147440 | None | None | 468 | None | 14 |
Genomic Location (Zv9):
Chromosome 23 (position 25717770)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25503890 |
GRCz11 | 23 | 25430431 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCTCCACTCAGATTATGTGCTTTTGTTTTGACATACAGGAATTGGATT[T/A]AGAAAAGTTTGAGGAGCTGTTCAAGACGAAAGCTCAGGGTCCCGTGGTGG
Long Flanking Sequence:
GGCTGATTTAAACAATTATAAACAACATATAAACATTTTGATGTTCGGATAGCGATTCCAATGCAGAAGAATCACTTCCTGCCCTTCATCTGAATTGAGCATCAATGACGTCATGTAAAAACAACCTGTAGCACACTTACTTTCACATTACTTTGCTTAAAAAGTAACCTAGTAACATATTTAAAAATGACTTAAATTACTTTTAAAGGTAACTTTACCTAATGCATATATTAGTTAAGATAATAATCTGACTGTAAAGTTTTTATTTCCTCTCTTAGCAATACGCATTAAGAAACCTATAAAAACAAAGTTCCGCCTGCCTGTCTTTAACTGGACTGCACTGAAACCCAACCAGATCAATGGCACCGTTTTCAACGAGATTGATGATGACCGTGTTCTCGAGGTGATGTTGAGCATGATTTACGTTATTTTGAGAGTGTCCTTCATTAAGCTCTCCACTCAGATTATGTGCTTTTGTTTTGACATACAGGAATTGGATT[T/A]AGAAAAGTTTGAGGAGCTGTTCAAGACGAAAGCTCAGGGTCCCGTGGTGGATCTGTCATGTTCAAAGAGCAAGGTCTCCCAGAAGGTCATCAACAAAGTTCAGCTGCTAGATGCCAATCGATCAAAGAACTTGGCCATCACTTTACGCAAGGCCAACAAGACCACAGAGGAGATTTGCAAAGCCATTCAAACGTATGCACACATACAAAAGTATTTCTACATATGTTGTGTTCATCTCTTCTGAGATTAATATGTGCTATTTCTGTGTTGAAGGTTTGATCTGAAGGCACTGCCAGTGGATTTTGTGGAATGCCTGATGCGGTTTCTGCCCACAGAGGCCGAGAGTAAACTGCTGCGTCAATACGAGCGGGAGAGGAGACCGCTGGACCAGTTGGCGGAGGAAGACCGCTTCATGCTGCTCTTCAGCAAAATCGAGCGGCTCACTCAGAGGATGAGCATCATCACGTTTGTGGGCAACTTCAATGATAATGTCAACATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10571
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 |
---|---|---|---|---|---|
ENSDART00000023359 | Nonsense | 5 | 390 | 1 | 11 |
ENSDART00000109023 | Nonsense | 607 | 992 | 18 | 27 |
ENSDART00000144554 | Nonsense | 100 | 485 | 3 | 13 |
ENSDART00000147440 | None | None | 468 | None | 14 |
Genomic Location (Zv9):
Chromosome 23 (position 25717889)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25504009 |
GRCz11 | 23 | 25430550 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAAGGTCTCCCAGAAGGTCATCAACAAAGTTCAGCTGCTAGATGCCAAT[C/T]GATCAAAGAACTTGGCCATCACTTTACGCAAGGCMAACAAGACCACAGAG
Long Flanking Sequence:
AACAACCTGTAGCACACTTACTTTCACATTACTTTGCTTAAAAAGTAACCTAGTAACATATTTAAAAATGACTTAAATTACTTTTAAAGGTAACTTTACCTAATGCATATATTAGTTAAGATAATAATCTGACTGTAAAGTTTTTATTTCCTCTCTTAGCAATACGCATTAAGAAACCTATAAAAACAAAGTTCCGCCTGCCTGTCTTTAACTGGACTGCACTGAAACCCAACCAGATCAATGGCACCGTTTTCAACGAGATTGATGATGACCGTGTTCTCGAGGTGATGTTGAGCATGATTTACGTTATTTTGAGAGTGTCCTTCATTAAGCTCTCCACTCAGATTATGTGCTTTTGTTTTGACATACAGGAATTGGATTTAGAAAAGTTTGAGGAGCTGTTCAAGACGAAAGCTCAGGGTCCCGTGGTGGATCTGTCATGTTCAAAGAGCAAGGTCTCCCAGAAGGTCATCAACAAAGTTCAGCTGCTAGATGCCAAT[C/T]GATCAAAGAACTTGGCCATCACTTTACGCAAGGCCAACAAGACCACAGAGGAGATTTGCAAAGCCATTCAAACGTATGCACACATACAAAAGTATTTCTACATATGTTGTGTTCATCTCTTCTGAGATTAATATGTGCTATTTCTGTGTTGAAGGTTTGATCTGAAGGCACTGCCAGTGGATTTTGTGGAATGCCTGATGCGGTTTCTGCCCACAGAGGCCGAGAGTAAACTGCTGCGTCAATACGAGCGGGAGAGGAGACCGCTGGACCAGTTGGCGGAGGAAGACCGCTTCATGCTGCTCTTCAGCAAAATCGAGCGGCTCACTCAGAGGATGAGCATCATCACGTTTGTGGGCAACTTCAATGATAATGTCAACATGCTGACTCCGGTGAGCAAATAGAAGTGTTGGGAAACTTTGTGGGGTTTCAGAAAAATTTATTTTCAGTGATGTTCATCAAGTGATTTTGTTTGTTTGTTTGTTTGATATGGACGAACATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24340
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 |
---|---|---|---|---|---|
ENSDART00000023359 | Nonsense | 9 | 390 | 1 | 11 |
ENSDART00000109023 | Nonsense | 611 | 992 | 18 | 27 |
ENSDART00000144554 | Nonsense | 104 | 485 | 3 | 13 |
ENSDART00000147440 | None | None | 468 | None | 14 |
Genomic Location (Zv9):
Chromosome 23 (position 25717902)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25504022 |
GRCz11 | 23 | 25430563 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGGTCATCAACAAAGTTCAGCTGCTAGATGCCAATCGATCAAAGAACT[T/A]GGCCATCACTTTACGCAAGGCCAACAAGACCACAGAGGAGATTTGCAAAG
Long Flanking Sequence:
ACACTTACTTTCACATTACTTTGCTTAAAAAGTAACCTAGTAACATATTTAAAAATGACTTAAATTACTTTTAAAGGTAACTTTACCTAATGCATATATTAGTTAAGATAATAATCTGACTGTAAAGTTTTTATTTCCTCTCTTAGCAATACGCATTAAGAAACCTATAAAAACAAAGTTCCGCCTGCCTGTCTTTAACTGGACTGCACTGAAACCCAACCAGATCAATGGCACCGTTTTCAACGAGATTGATGATGACCGTGTTCTCGAGGTGATGTTGAGCATGATTTACGTTATTTTGAGAGTGTCCTTCATTAAGCTCTCCACTCAGATTATGTGCTTTTGTTTTGACATACAGGAATTGGATTTAGAAAAGTTTGAGGAGCTGTTCAAGACGAAAGCTCAGGGTCCCGTGGTGGATCTGTCATGTTCAAAGAGCAAGGTCTCCCAGAAGGTCATCAACAAAGTTCAGCTGCTAGATGCCAATCGATCAAAGAACT[T/A]GGCCATCACTTTACGCAAGGCCAACAAGACCACAGAGGAGATTTGCAAAGCCATTCAAACGTATGCACACATACAAAAGTATTTCTACATATGTTGTGTTCATCTCTTCTGAGATTAATATGTGCTATTTCTGTGTTGAAGGTTTGATCTGAAGGCACTGCCAGTGGATTTTGTGGAATGCCTGATGCGGTTTCTGCCCACAGAGGCCGAGAGTAAACTGCTGCGTCAATACGAGCGGGAGAGGAGACCGCTGGACCAGTTGGCGGAGGAAGACCGCTTCATGCTGCTCTTCAGCAAAATCGAGCGGCTCACTCAGAGGATGAGCATCATCACGTTTGTGGGCAACTTCAATGATAATGTCAACATGCTGACTCCGGTGAGCAAATAGAAGTGTTGGGAAACTTTGTGGGGTTTCAGAAAAATTTATTTTCAGTGATGTTCATCAAGTGATTTTGTTTGTTTGTTTGTTTGATATGGACGAACATTCCTGGAATTTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43989
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023359 | Nonsense | 189 | 390 | 5 | 11 |
ENSDART00000109023 | Nonsense | 791 | 992 | 22 | 27 |
ENSDART00000144554 | Nonsense | 284 | 485 | 7 | 13 |
ENSDART00000147440 | None | None | 468 | None | 14 |
Genomic Location (Zv9):
Chromosome 23 (position 25719212)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25505332 |
GRCz11 | 23 | 25431873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACATTGCTCTGGTCGTCAAAGAGAAATATCCTGAACTGGCTAACTTCTA[C/A]AATGAACTGCACTTTGTGGATAAGGCCGCAGCAGGTTGGTGTTATTTTGT
Long Flanking Sequence:
TAGAAAGAAACATATTCTTGATACAATACCACATAATTCATATTTTGAAATGACATTTCTTATTTAAATCCACAGCAACTCAACGCCATCATCGCAGCATCAGCTTCAGTGAAGTCCTCTCCAAAGTTAAAGAAGATTCTTGAAGTAAATATCTACCTTATTATAAAGGCTCAGATTCATCCCAAAATCATCTACTATTTTGCATAATTATCCTTTTGTTTTGCCTCCACACAGATCATTCTGGCCTTGGGCAACTACATGAACAGCAGTAAAAGAGGTTCAGTGTATGGTTTCAAACTTCAGAGTCTGGATCTGGTGAGCTGAGAGGGAGAAAAGGTTTCAGTGAAGGTGTTGTTCAATTATAGTGCTGATTTTACTCATGATGTTGTTTCTGTCCTCTCTCAGCTGCTAGATACTAAGTCTACTGACCGGAAGATGACACTGCTCCACTACATTGCTCTGGTCGTCAAAGAGAAATATCCTGAACTGGCTAACTTCTA[C/A]AATGAACTGCACTTTGTGGATAAGGCCGCAGCAGGTTGGTGTTATTTTGTGTTATAGGATGTTAAACTGAACGTTTGGACTACATTAATTAGCCTTTCAAAAATGTAATAGCTAAATATCAGAGGAAATACATCAGTCAACACAGTGTGACAGGTTTGTGTTGTTTGGCTTTATTTAGAAGATGAGTCAGTTCTTAATTTGTGAAATTAGTGAAGCATAAATTGTTTAATTATGTTCATTATTACTTCGGTCCTCAATGTCACATGATCATTCAGAAATCATTTGAATCTGGTTTGGTGCTTATGAAACATGTATTTTATATTGTTGTTGCTAAATTAATTCCTTATTGTAAAGCTTTGGTCAAATTTCTGTATAGTAGCTTCTATATGAGTTATTGCTCATTTGAACCCACTATTACTGTCTAATATTCATGCAAATATTATTTGTGTTGTGTGTATGGTTACATAGTTTACCATTTACATAGGGTGTATGGTTTCATA
Associated Phenotype:
Not determined