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 is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11299 | Nonsense | Available for shipment | Available now |
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