ZMP
fmn1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate formin (Limb deformity) (FMN) [Source:UniProtKB/TrEMBL;Acc:Q5RIQ
Human Orthologue:
FMN1
Human Description:
formin 1 [Source:HGNC Symbol;Acc:3768]
Mouse Orthologue:
Fmn1
Mouse Description:
formin 1 Gene [Source:MGI Symbol;Acc:MGI:101815]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11299 | Nonsense | Available for shipment | Available now |
sa43462 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39286 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1135 | Nonsense | F2 line generated | Not yet available |
sa29378 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11299
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 |
---|---|---|---|---|---|
ENSDART00000019819 | Nonsense | 40 | 1303 | 1 | 13 |
ENSDART00000136804 | None | None | 443 | None | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 29462790)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 29534003 |
GRCz11 | 20 | 29436882 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCACTGTCTGAGGAAAATACAAATATKATTAATTTTCACTCTTTGACT[G/T]GAAAAGGAGATGTTCATGGTCAACAAACATGTATTCAAAGGCAGGATGGT
Long Flanking Sequence:
AGCATCTCTGCTTTAATGCACTTTTCCTGGCATCCTTGATTCTGGAAACTTCATGAAAGGAAAAAAAAAAGACAAATTGTGTAGACTTAATAAAAACAGAACAGCTTTTTAAAAGCAGAAGAAGACTTGTCTTTGGAATTGGTCAGAACTCTTAACCATTTGCAACCTTTTTTTAGCATAAGGACCAAAAATTCAGGATTGGTTAAATGGATTTGGGAATAAACCTGGAGTGGATTTTGTAACTAAAGTCACACATCTAATTTTACCCTCTGGAGATTTATACTTTGACTCGCTTCTAGTTTTTTGAACTGGTGGAATGGGTTTTTGCAAATACAGACATAGTTAATTTGATTTTAAACAGCCTATACGCCAAACTAGAGGAAATGGAGAGTCCGCCAACGAATTCGTTTTTGGACAAATTAACAAACTTGTTTACTAAACATGAACCCCAATCACTGTCTGAGGAAAATACAAATATTATTAATTTTCACTCTTTGACT[G/T]GAAAAGGAGATGTTCATGGTCAACAAACATGTATTCAAAGGCAGGATGGTTTTGATGATCAAGGTGATGATTTTGTTAAGACTTTGCATGCAAATGCTGATGTTAACAGATCAGAGCATCAGAATGATGAGAAAACTGATTCTTCATCAAGAGAAGATCTATTGGACTTTGCCTTGGATGATAATCATGGCAATAAAACATTAGCAGCAGGCCAGGCTGACCAGGATGTAACAGATGGTCAAGCTGACACACTGCCTAAATCACTTAGCCCAGTCTCAGCCAGTGCTAAAAGTCTGGACAAACAACTTGAGGATACAGCAATCTGTACAGAGGATAATGAGCTTGTTTTGAAAAGAGGAGAGTTTATTTCAAAAATGAGCAATGACAGGCTCATTGAAGATGTATTGAACAAGAAAGATGTTGAGGAATCAGAAAATGTGGGGCTTACGCATAATGAGAAAGAAGAAGGCCACAAAGACGAAACCAGCATATTCAACAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43462
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019819 | Nonsense | 568 | 1303 | 1 | 13 |
ENSDART00000136804 | None | None | 443 | None | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 29464374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 29535587 |
GRCz11 | 20 | 29438466 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTAAAGGCTTTCTTTACAGTTAAATCTGCCAAGAAGGACTCTTCTAAT[C/T]GAAAGGACCTGGATATTGTGAAGAAGAAGATCAACAGGGACAAAGAAGTC
Long Flanking Sequence:
TGGAACCTTCAGAACCACTGGAGACTGAAATGCATACAGAGGGAGAAATTAATAAGGAAAATGAAGAGACCATTGAGAACACCACTGAAACCGCTAAAGTGGTAAAAGAGAAACCGCTTCAACTGTCGACGCTATTCAACGGGCTGCTCAGCCCTAAGAAAGAAGTTCTTGAGGAGAAAGACGAACCAGGGCAACCCCGAAGCACTTCCAAACGAGGACTTTTTACAGATCAGTCAAACAAGAAAGAAGTGAAAGCGGACTTCCTGGAACAGCTCACCCAATTCCTGAGCAAGGGGGAAGGAAAGAGAAAGCAAGAGAGCATCTCGAGCCCCCCAATGTCTCCAGTCAGTCAGGAAACTGTAGAAAATCCAGAGACAACTGTAGAGGAACCGGTCATTCCCCAGTCTGAGGAAACCAACAAATCTAGCAATGCAGAGACAGCCCTGGGCGCACTAAAGGCTTTCTTTACAGTTAAATCTGCCAAGAAGGACTCTTCTAAT[C/T]GAAAGGACCTGGATATTGTGAAGAAGAAGATCAACAGGGACAAAGAAGTCCTTAGAGCTTTCTTTGACAGAAACTCAAGCAAGTCTCCAGAGATCAAAGACACTACTGATTGCAAAGTATGATATAATGGTTATATTTAAAATACAGATGGTTATGTGTAAAATACTTGTTTATTGGTAGTATCGGTAGTAACAAGTTCATATAAAAAGTCTTATTTTCTGTTAAGTTAATATTTGAATTATAATATTTATTTTTATTTAAATAAGTCATTAATTTATTCATTTTTGTTCCCTTATTTATTAGGGATCGCAGCTTAGTCCCTTATTTATCAGTGGTCGCCACAGTGGAAAAAAACATTATTTTGTTTTAAATGCACCAAATGCATGCATGCTCACTTTTATTTTTTTATTTATTGTATTTTTCCTTTTTTTTTCATTTATTCCTTTTTTTTCAGCTATGTCCTTTCATAATCAGGGGTCGTCACCTTTTTGCTGTGAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39286
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 |
---|---|---|---|---|---|
ENSDART00000019819 | Nonsense | 690 | 1303 | 4 | 13 |
ENSDART00000136804 | None | None | 443 | None | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 29468292)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 29539505 |
GRCz11 | 20 | 29442384 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGAAGAATGAGCAGAATTTGTCCAGACTCAGCGCAACCATTGCAAGCT[T/A]ACAAAGAGAGAGAGACAAAGTTCACCACAGAGAACACCAACATGTTGCTG
Long Flanking Sequence:
ATGGGGTTCTTCTCTAAAGAAGTTACTCCACTCCATTAAGAGCATCCTTATGAGCGTTTTGTCACTACATCGTTCTTTTCCCAAACGATGCATTGTACTATGATAGTTCAGCCGTGAGTTGCATCGTTGTTTTAAAACGCACCCCTGATCTGTTCTCTGATCTGTTTTCAGAGCATCAGGCAGCGCTTCTACAACTAAAAAGAGAATGTAACGAAGAGGTGGAGAAATTACAGGTGAGAAACTCCAGAAAATAACAATATAATTGAACTTTTTTTAGTTGACAAATATAAAGCATATATATTGTGGCCTTTTTGCATACAGTATAGCAGACACTATCCAAAATGTAACTTTTTACCAATTGATGTATTTTCTGGGAATGTATGTTTATATTTGTTGTTGTTTGTATGCTTTAATGCAGACTGACTTCAGACTTGAGCTCTTCCGCATACAAGAGAAGAATGAGCAGAATTTGTCCAGACTCAGCGCAACCATTGCAAGCT[T/A]ACAAAGAGAGAGAGACAAAGTTCACCACAGAGAACACCAACATGTTGCTGTGTCCACCGAAGACGATATCAAAGCACGGGCCGTCCGATCGGTGTGCATTCAGACAGACAGAGAGACATCCATCAACTCTGAGGAGGCCAAAGAAACCCACAGCAACAGTCTTGACCCCCTGTTTAAAAATGGTGACCTAAACAACTCAACCAAAAACTTGACTGGCAAACAAAAGACAGTCCCTCCTCCATCAGCTCATCCGCCTCCATCACCTCAGTTACAGTTGGAAAGCAGTAAGATCACACCTCCAACTCCACCTCCTCTGCCTGGTCCTTGTACTCCTAATATACCTCTTGCTCAGCCACCGAATAAGCATGTGAATGTGCCTCCTCCACCTCCTCCTCCTCCGCCTCCTCCCATGACAGGGTCTGGTCTTCCACCACCACCACCACCACCTCCACCTATGACAGGGTCTGGTCTTCCACCACCACCTCTACCACCTCCACCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1135
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019819 | Nonsense | 985 | 1303 | 5 | 13 |
ENSDART00000136804 | Nonsense | 69 | 443 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 29471625)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 29542838 |
GRCz11 | 20 | 29445717 |
KASP Assay ID:
554-1046.1 (used for ordering genotyping assays)
KASP Sequence:
TTTGCTAAAGCCACATCGCCCACCAAAAGAAAGCCCCTATCTGATGCCTA[T/A]GAGAAGAAAACCAAAGCCAGGAAGGTAGCACKCTTTCCTCAAGATCAGAA
Long Flanking Sequence:
CACCTCCGTGCTGCTGCAATGTTATTTGACTCCTCATGAAAGCTTTCTGCTCTCTCCCGGAGCATTTTGTCAAGCCAAAGCAGAACCCAGTCAAGCTTAGCTGTGCGCCGTCGTCCTGGCTCCTTAATTATTTTTATGGGAGAGAAAATTTAGCAAGTCAGATTACTCACATTGAGCCCCTGTTGATTTTCCTTTTCCTGCTCATAGGCACGGTTGCCCAGCAACAGTTAATAACTCATGTAACTTGGGCTTTTACAGATGCCAGTATTTGAAAAGGTTTTCTATAAGTGTATGAGTGTGAAGGTTCAGTTTTGATAACCCTTAAAAAGAAAAGGTCGAATTTTCAAGAAACATAAAGTCTTTTGTTATCTGTGTTTTTTTAGGAACGATGTTCTGTGGAGTTCCCTGAAGGAGCCAGAGATAATAAACACCAATGAGTTTGCAGAACTGTTTGCTAAAGCCACATCGCCCACCAAAAGAAAGCCCCTATCTGATGCCTA[T/A]GAGAAGAAAACCAAAGCCAGGAAGGTAGCACGCTTTCCTCAAGATCAGAAAATGGCATAATGCAGAGCAGGTCTTATCTAGAATGCCTGTGTCATTCACTATGTACATTTGTGTTGTTTTGCTCTCTAGATGACTTCTTGATGTAGTTCTTATATATAGCTACATAAAATGCTAGGTTGTTGGATTTGCTCACGTAATTAAAAAAACTGTCAATTCATAAATGTCTGATAAAATGCAGAAATGTGGGTTATGGTGACATTATTCTCTTTTCAATTCATTGAAACAATTTGTTGTTATAAGGAAACTTATCATCACTTGTAGGGGCACATTATCATTAACTCATTCTTTTATACTCGTGACTGTCTATCTGTTGTGTTTACATCAAAAAACAAAGTATTATCTACATCCAAATGAACAGTTTAAACATATGAGTTAATGAGTAAGATTTATTTAATGATAATGTGCCACTTCAAGTAAAGTCATGACATAACATATTTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29378
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 |
---|---|---|---|---|---|
ENSDART00000019819 | Nonsense | 1300 | 1303 | 13 | 13 |
ENSDART00000136804 | None | None | 443 | None | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 29489848)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 29561061 |
GRCz11 | 20 | 29463940 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATTTATGGGCTCTGTCACATCGGCCAATCCCTCACGTCTACCCTGTTC[A/T]GATATGAAGTTTAGTTGGTCTCTGAGACAATCCGTCTCTCTAGATGATTG
Long Flanking Sequence:
AATAAAGTGGCTGGTGAGTGTACATGTACACTTATTTACTATAAATCCACTTAGTAAGAAAACATATGCATTGAAAATTCTACAAGCTTCAGTGTGGCATTTATTATTTAAGATTTTGGAATAAAAAACGCTCATGGTGGTCTAACATTAAAATGTCAGACTGTTCAATTTTGGATAACATATGGTGTTAAAGATTATTTTACAATGACTGGCCTCTGTGAGTTGGACCCAGTCAGGGACTTTACTCTGACCCAATGTTATTGTTTTTGTCTCGTACAGTTTGCGAAAAGGACGTCCTAACTGTGTGTACCAACTCGTCTCAAGAGCACATTCATCCCTTCCAGGAGAAAATGGACTTTTTCATTGCCAGCGGTGAGTTATGTTATAATGCCAGAGATTATCCCGCATTACCTTTCAGAAGAGGATCTTTATTCAGAGTTTTTAAGTCTTGTATTTATGGGCTCTGTCACATCGGCCAATCCCTCACGTCTACCCTGTTC[A/T]GATATGAAGTTTAGTTGGTCTCTGAGACAATCCGTCTCTCTAGATGATTGATGGAGAGCAGCACAAAAGTTTGTTTAGATGGTACGCAGGATTGTTTTGTTGTGCAGATCGTATGCAAAGATGTAAACTGATTGTCGTTTACTATAGACGACGGCAGCTATGGTAGACAAACATGTTTTATTCTGTTTGTAGTTTATGTAGAATATAACGGCAAGTGTAAACCAAAGCTTCTCTTTTCTTCGCATTCTTCCTACTACAACCATTTGATTGTCTCGACTGCGCTGATAAGAAGGCACACATCCTGCAGTCATGAAGAATATCTGCTGTGTGCCCTTTTGGGCACCTGATAAGCGTCTGTGACTGATACCTGAAGACCGATACAGAGATTGGAATCAGGGAGACTTTGGCAATGAAGGAGACTTGTCAGTATAGGAGAAACTACAATTTTGACATTTTCTCAGAAGTAAAAGGCTGGGAATTTGGCGCAATATTTGTTTTGG
Associated Phenotype:
Not determined