Busch Lab

ZMP

FMN2 (2 of 2)

Ensembl ID:
ENSDARG00000023318
Description:
formin 2 [Source:HGNC Symbol;Acc:14074]
Human Orthologue:
FMN2
Human Description:
formin 2 [Source:HGNC Symbol;Acc:14074]
Mouse Orthologue:
Fmn2
Mouse Description:
formin 2 Gene [Source:MGI Symbol;Acc:MGI:1859252]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa42903 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa42903
Status:
Mutation detected in F1 DNA
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
ENSDART00000037716 Essential Splice Site 194 247 7 7
Genomic Location (Zv9):
Chromosome 17 (position 19603465)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 19753476
GRCz11 17 19773312
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTATTTCCTGTATGATTGCGGTTCAGACTTTCCACTGTTTGTGTGTC[A/G]GGATGCAGGTAAAGAAACGTGCACGTATCCACTTCCAGAACCTCAGGATC
Long Flanking Sequence:
TTTGGTTTCATCACTTTGATTTGCCTTGCTTTCCCTTCACCATATAGACAAATGGCTGCTGTGAATGAGCAGAGCCCTCTGATTGCTCGATGCCCTTTTTGGACGCAGATTAAAAGGCTGTATTATAAATACCGTCAACAGTGGGTCCAGATGTTGTGATTATGAGGCCGTGTCCAAATTGATAAAATATGATCCACAGGTTGTCGAAGTGCTTCTAGCTTTGGGCAAATAATAAGGAGAGTGCATGTGTTTGTGTGTGTTTGTGTGTGTATGCATGCGAGCAGCTCTCTGACAGACGGAACGATATTGAGATTGATTTGTTGTGTTTGATGTTTTTGATTGTTTCTGGAATTATAATGATCTTTGCACATTGATCCATTTGAACAGAATTCACATTTAAATCAAATCATCAATTGCCATAGATATGATCTTATAAACACAACATTCTTTGTTTTATTTCCTGTATGATTGCGGTTCAGACTTTCCACTGTTTGTGTGTC[A/G]GGATGCAGGTAAAGAAACGTGCACGTATCCACTTCCAGAACCTCAGGATCTATTTCAGGCATCGCAGATGAAGTTTGAAGATTTTCAACGTGACCTCCGCAAGCTACGGAAAGATCTAAATGGTGAGATGGAGAAGATTAATAGACATAAGCTATGCATGTACATGGTGTCACATGCGTGCACACACATGTGGACATACAGATATATTGACAACTCATACAAGTGTGCATATACAAAACACAGAGACATGTTTCGTTTGTATACACCAGCGCCAGTGACCCATGCTCTCCTTTAGAAGGCTCATTGATTTTCAAATGGCTGTTTTTATTGAGCCCCCAGCTGGCTGCCACAATGATCAATATTGCAAATGTGGTTTGTTAAATGCCCCAGCATGTAAATAAATGAGAGAGAGGGTCATTTTCAGCACTTTTCCTAGCAGGCTTACCTGTTACTACAGGCCTCAAGCACTTAACTCTTGCTTTCTGCAGGTGAATAGTCTC
Associated Phenotype:
Not determined