ZMP
FMNL1 (1 of 2)
Ensembl ID:
Description:
formin-like 1 [Source:HGNC Symbol;Acc:1212]
Human Orthologue:
FMNL1
Human Description:
formin-like 1 [Source:HGNC Symbol;Acc:1212]
Mouse Orthologue:
Fmnl1
Mouse Description:
formin-like 1 Gene [Source:MGI Symbol;Acc:MGI:1888994]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6040 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa3326 | Essential Splice Site | Available for shipment | Available now |
sa18761 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10153 | Essential Splice Site | Available for shipment | Available now |
sa5729 | Essential Splice Site | F2 line generated | Not yet available |
sa33252 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6040
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083495 | Nonsense | 261 | 1125 | 8 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 37209239)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 37072599 |
GRCz11 | 3 | 37214457 |
KASP Assay ID:
554-3674.1 (used for ordering genotyping assays)
KASP Sequence:
CATCTTTTTTTCCCAAACAGTCTGGGTTTAATTTAGTCATGACACACCCT[A/T]GATGTGTCAACGAAATCACACTTAGTCTCAACAACAAAAACCCCAGGTTA
Long Flanking Sequence:
TGTTATTCTCAGGTTTGAGGTGGAGTCTGTGGAAAATGGTGGCTCCATATCAGACAACAGGAGGATGTCAGAGAGATCGGTGGAGGATCTTGCCAAAAATGTCAACCATTCTGCCCCACACACGATGACCAGGGCAGCGCGTGCGCTCACTGTCCGGTCAGTCATCATTACAACAAAACATAGGGATTACAGGACTCAAATGAAAAACTGATATTAAACAGACGTGCATTTTCTCAAACTCAGTGTTGATCTTTTTCTTATTCTCTGCATTTCCTAATTAGAATAACGTCACTGGCACACAGCAGAAAAACTCTGCGAATTGCCCGACTGGCCACCCAGAGAGATGATGTTCACCTCTGCATTATGTGTCTACGTGCTATTATGAACTATCAGGTATCTCAAGACAGCTTCTCTTCTCAAAAGATAATTTTAAAACAACTTTGTCTGACTCATCTTTTTTTCCCAAACAGTCTGGGTTTAATTTAGTCATGACACACCCT[A/T]GATGTGTCAACGAAATCACACTTAGTCTCAACAACAAAAACCCCAGGTTAGTGTGCATGTGTTTTCCTTTTTGTGGTATTTGTTGGTTGTTTGTGGGTTTGCATCCGCTTATAGTACACTTCATCATGTTCTTCATAGGACTAAAGCTCTCGTCTTGGAGCTGTTGGCAGCAGTGTGTTTGGTTAGAGGAGGCCATGACATCATCATATCAGCTTTTGACAACTTTAAAGATGTAAGATGACTAGCATTTCACGTATGTGCATGCATTAAAACATTTAAGATGTACTCATATTTTTTTTCGTACCCGGTACCAGGTCCGTGAAATATCATTTACATCCAAATTCTTTTAAATTTAAAGGTCCTTACTGGCCCATTACCACCATAAGAGGTTCCGTTCTCTCATCAGTTGGAATAGAAAAGTGTTTGCACAGATTATGATAGACATTTTTCTTTTATCCTATGATTACTGACTAAATTATTTACAGCAACCAAGACCACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3326
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 |
---|---|---|---|---|---|
ENSDART00000083495 | Essential Splice Site | 627 | 1125 | 17 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 37215334)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 37078694 |
GRCz11 | 3 | 37220552 |
KASP Assay ID:
554-2620.1 (used for ordering genotyping assays)
KASP Sequence:
GCAGCACCACCTCCACCTCCTCCMCCCCCTCCACTACCTGGCGCTKAAGC[A/T]CCTCCTCCTCCTCCACCACCTCCTCCTCCTTCTGGAAGTGGAGGTGCTCC
Long Flanking Sequence:
TTAAAACACTAGTGGTTGGGTTTAGGAAAGGAAGAGGGTGGGTCAGTCGATTGGTCAGTCAGTCCGTCAAACAGTCAGTCGACAGAGGCCTCTGGTTGATTTACGCGAGAACTGCCGGCACGAAAGGCACTTGCAAGAGAAAATTGAGATCTCAAAAAGTATACACAGCTGCCTCCAGAGGATTCGCAAAAAACAAAAACTGCAAAAAGCATACGTCCTGGGATGTATTTGATGCACTTCAGAAATGTAGGTACGTTTTCAGAATGAGTTGCACAAAGCACAATGTGTTCCCAGAAACATGGAGTGTTTTTAAAAAAAGAGTCTTGTACATCTGGAGAGGAAAAGAGCATGCCTGCAAATGAATTAATCAACCAACAATAATTTAACATCTATGCAATGTTTGCAGTGACTGTGCCCGATTCTGCTTCTCAAGCCCCACCCAGTCCGGCTGCAGCACCACCTCCACCTCCTCCACCCCCTCCACTACCTGGCGCTGAAGC[A/T]CCTCCTCCTCCTCCACCACCTCCTCCTCCTTCTGGAAGTGGAGGTGCTCCTCCCCCTCCCCCTCCGCCACCTCCCCCTGGTGGAGGTCCACCACCACCCCCGCCTCCACCGGGCTCTGGGCCTCCACCTCCTCCTGGAGCTCCTCCTGCCCCTGGAGCTGAAACAGGTTAACAAACTCAACTTTATAAAAAAGAATTGCAAACATGCAGTGCTCAGCATAATTGATAAACCCATTTTCAAATAGAATATTTGTATGTACTTATATATGCTGAGCACTCTACACTGAGCCTGGTGACTGTATATCCATTTTTTCTGGTGTTTTACACAGGACCAAAGGCACGCAAAACAATTCAGACAAAGTTCAGGATGCCTCTGTTGAACTGGCAGGCTTTGAAGCCCAACCAAGTGTCCGGAACGGTGTTTAGTGAGCTGAATGATGAGCAAGTGTTACAGGTAACAGCAAAAAATTACTCTCTTCCCTTTCCAAACCTGAGTGAAGT
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:
sa18761
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 |
---|---|---|---|---|---|
ENSDART00000083495 | Essential Splice Site | 632 | 1125 | 18 | 31 |
ENSDART00000083495 | Essential Splice Site | 632 | 1125 | 18 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 37215380)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 37078740 |
GRCz11 | 3 | 37220598 |
KASP Assay ID:
2259-3851.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCACCTCCTCCTCCTCCACCACCTCCTCCTCCTTCTGGAAGTGGAGGT[G/A]CTCCTCCCCCTCCCCCTCCGCCACCTCCCCCTGGTGGAGGTCCACCACCA
Long Flanking Sequence:
TCGATTGGTCAGTCAGTCCGTCAAACAGTCAGTCGACAGAGGCCTCTGGTTGATTTACGCGAGAACTGCCGGCACGAAAGGCACTTGCAAGAGAAAATTGAGATCTCAAAAAGTATACACAGCTGCCTCCAGAGGATTCGCAAAAAACAAAAACTGCAAAAAGCATACGTCCTGGGATGTATTTGATGCACTTCAGAAATGTAGGTACGTTTTCAGAATGAGTTGCACAAAGCACAATGTGTTCCCAGAAACATGGAGTGTTTTTAAAAAAAGAGTCTTGTACATCTGGAGAGGAAAAGAGCATGCCTGCAAATGAATTAATCAACCAACAATAATTTAACATCTATGCAATGTTTGCAGTGACTGTGCCCGATTCTGCTTCTCAAGCCCCACCCAGTCCGGCTGCAGCACCACCTCCACCTCCTCCACCCCCTCCACTACCTGGCGCTGAAGCACCTCCTCCTCCTCCACCACCTCCTCCTCCTTCTGGAAGTGGAGGT[G/A]CTCCTCCCCCTCCCCCTCCGCCACCTCCCCCTGGTGGAGGTCCACCACCACCCCCGCCTCCACCGGGCTCTGGGCCTCCACCTCCTCCTGGAGCTCCTCCTGCCCCTGGAGCTGAAACAGGTTAACAAACTCAACTTTATAAAAAAGAATTGCAAACATGCAGTGCTCAGCATAATTGATAAACCCATTTTCAAATAGAATATTTGTATGTACTTATATATGCTGAGCACTCTACACTGAGCCTGGTGACTGTATATCCATTTTTTCTGGTGTTTTACACAGGACCAAAGGCACGCAAAACAATTCAGACAAAGTTCAGGATGCCTCTGTTGAACTGGCAGGCTTTGAAGCCCAACCAAGTGTCCGGAACGGTGTTTAGTGAGCTGAATGATGAGCAAGTGTTACAGGTAACAGCAAAAAATTACTCTCTTCCCTTTCCAAACCTGAGTGAAGTTCTTTTGATGGGACATAACAGAAGATTATGTTTTGTAGGGACGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10153
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 |
---|---|---|---|---|---|
ENSDART00000083495 | Essential Splice Site | 632 | 1125 | 18 | 31 |
ENSDART00000083495 | Essential Splice Site | 632 | 1125 | 18 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 37215380)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 37078740 |
GRCz11 | 3 | 37220598 |
KASP Assay ID:
2259-3851.1 (used for ordering genotyping assays)
KASP Sequence:
AAGCWCCTCCTCCTCCTCCACCACCTCCTCCTCCTTCTGGAAGTGGAGGT[G/A]CTCCTCCCCCTCCCCCTCCGCCMCCTCCCCCTGGTGGAGGTCCACCACCM
Long Flanking Sequence:
TCGATTGGTCAGTCAGTCCGTCAAACAGTCAGTCGACAGAGGCCTCTGGTTGATTTACGCGAGAACTGCCGGCACGAAAGGCACTTGCAAGAGAAAATTGAGATCTCAAAAAGTATACACAGCTGCCTCCAGAGGATTCGCAAAAAACAAAAACTGCAAAAAGCATACGTCCTGGGATGTATTTGATGCACTTCAGAAATGTAGGTACGTTTTCAGAATGAGTTGCACAAAGCACAATGTGTTCCCAGAAACATGGAGTGTTTTTAAAAAAAGAGTCTTGTACATCTGGAGAGGAAAAGAGCATGCCTGCAAATGAATTAATCAACCAACAATAATTTAACATCTATGCAATGTTTGCAGTGACTGTGCCCGATTCTGCTTCTCAAGCCCCACCCAGTCCGGCTGCAGCACCACCTCCACCTCCTCCACCCCCTCCACTACCTGGCGCTGAAGCACCTCCTCCTCCTCCACCACCTCCTCCTCCTTCTGGAAGTGGAGGT[G/A]CTCCTCCCCCTCCCCCTCCGCCACCTCCCCCTGGTGGAGGTCCACCACCACCCCCGCCTCCACCGGGCTCTGGGCCTCCACCTCCTCCTGGAGCTCCTCCTGCCCCTGGAGCTGAAACAGGTTAACAAACTCAACTTTATAAAAAAGAATTGCAAACATGCAGTGCTCAGCATAATTGATAAACCCATTTTCAAATAGAATATTTGTATGTACTTATATATGCTGAGCACTCTACACTGAGCCTGGTGACTGTATATCCATTTTTTCTGGTGTTTTACACAGGACCAAAGGCACGCAAAACAATTCAGACAAAGTTCAGGATGCCTCTGTTGAACTGGCAGGCTTTGAAGCCCAACCAAGTGTCCGGAACGGTGTTTAGTGAGCTGAATGATGAGCAAGTGTTACAGGTAACAGCAAAAAATTACTCTCTTCCCTTTCCAAACCTGAGTGAAGTTCTTTTGATGGGACATAACAGAAGATTATGTTTTGTAGGGACGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5729
Status:
F2 line generated
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083495 | Essential Splice Site | 654 | 1125 | 20 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 37215650)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 37079010 |
GRCz11 | 3 | 37220868 |
KASP Assay ID:
554-3489.1 (used for ordering genotyping assays)
KASP Sequence:
ATGCTGAGCACTCTACACTGAGCCTGGTGACTGTATATCCATTTTTTCTG[G/C]TGTTTTACACAGGACCAAAGGCACGCAAAAYAATTCAGACAAAGTTCAGG
Long Flanking Sequence:
AAGAGTCTTGTACATCTGGAGAGGAAAAGAGCATGCCTGCAAATGAATTAATCAACCAACAATAATTTAACATCTATGCAATGTTTGCAGTGACTGTGCCCGATTCTGCTTCTCAAGCCCCACCCAGTCCGGCTGCAGCACCACCTCCACCTCCTCCACCCCCTCCACTACCTGGCGCTGAAGCACCTCCTCCTCCTCCACCACCTCCTCCTCCTTCTGGAAGTGGAGGTGCTCCTCCCCCTCCCCCTCCGCCACCTCCCCCTGGTGGAGGTCCACCACCACCCCCGCCTCCACCGGGCTCTGGGCCTCCACCTCCTCCTGGAGCTCCTCCTGCCCCTGGAGCTGAAACAGGTTAACAAACTCAACTTTATAAAAAAGAATTGCAAACATGCAGTGCTCAGCATAATTGATAAACCCATTTTCAAATAGAATATTTGTATGTACTTATATATGCTGAGCACTCTACACTGAGCCTGGTGACTGTATATCCATTTTTTCTG[G/C]TGTTTTACACAGGACCAAAGGCACGCAAAACAATTCAGACAAAGTTCAGGATGCCTCTGTTGAACTGGCAGGCTTTGAAGCCCAACCAAGTGTCCGGAACGGTGTTTAGTGAGCTGAATGATGAGCAAGTGTTACAGGTAACAGCAAAAAATTACTCTCTTCCCTTTCCAAACCTGAGTGAAGTTCTTTTGATGGGACATAACAGAAGATTATGTTTTGTAGGGACGAAATGACACTCATATAACTCCTTAAGGCTTTTCACACTGTGCTTAACTCTGTGTTATAAACACAGATATAAATCTAAAGACCACTTTTAACCCTGGGTAGAGGAACATTTTACAGTTTTAGAACTGTTCTACAGAGCAATTGATTGGACAGAATGTCTGGCAGGAAGTGCAAAAACTCTTTTCAAATGAGTAGAATTAACTTTCAGTAAATTTACACTCATTTCATTTGATAAAGTTGACTGTTGGGCTTTACAGTGTAGCTTTATATTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33252
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083495 | Essential Splice Site | 992 | 1125 | 26 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 37224357)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 37087717 |
GRCz11 | 3 | 37229575 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACAGTGATGTATTAGACTCCCTCGTTAAAGATGGCAAAACAGCACAGG[T/C]GAGACCCCAGGAACACACTCAGAAACACACACACTGTACTATAAATGAAT
Long Flanking Sequence:
TATTTAGTTTCAGTTGGAAGTACATCAACACACTGAAAAAAAATCTCAGCAACTTACGGTTCTCACAAACTTTAAAGCAAAATCTTTTAGAAAATCACAATAATCTCTGGATTGTTCCATTCAAGACACCTATAATTTAAGGATTGGCAGAAACTGTGATGTCAGCAACAAACTGATTCTTCATTTCAGTTCAATTCAATTCAATTCAATTCAATTCAATTCAATTCAATTCAATTCATGTTTATTCTATAGCGCTTTTACAATGTAGATTGTGTCAAAGCAGCTTAACATAGAAATTGTAGTAAACTGAATTCTCTGACCTTTGCTCTTGTCAGTGTCTCTGGACGGTGTTCTGCAGGATGTAAGATCTCTGGAAAGAGGCATGGAAGGCACCAAGAAGGAGTTTATGGTGCAGGACGACATCCCGGCACTCAAAGAGTTTGTCAAAGCCAACAGTGATGTATTAGACTCCCTCGTTAAAGATGGCAAAACAGCACAGG[T/C]GAGACCCCAGGAACACACTCAGAAACACACACACTGTACTATAAATGAATTTTTTGGTCATTTTTTTCTTCTTCTTTTTTTTCTCACAACAAGGAGGCATATGCGGCTGTGGTGGAGTATTACGGAGAAAACCCCAAGACGACACAGCCTTCCATGTTCTTCCCAATCTTTGCAAGGTTCATCAAAGCTTATAAGGTGAGAAAAAGTGTTCAGCACATACTGTACATACAGGCTGTAACATTAACTCTCGTACCAAGCACCAAGAGAGAAAACATCGGATACTTGACTGTCATTTTTAAAATTAGTTTTAAATATTTTAATAATTACCAAACAACACAACAACAATACAAGAAATACATGAAATAAGCATAATAATACAAAGAAAATAATGGTAATAATAAAAATAATAATAATAATAATAATAATAATAATAATAATTCTGTGTAATTTAGATTTTGAGTAGTGCAGTCTATGCATTACTTTAAACTGAATTAATTTAT
Associated Phenotype:
Not determined