Busch Lab

ZMP

FMNL1 (2 of 2)

Ensembl ID:
ENSDARG00000075519
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 is 1 allele of this gene:

Allele Name Consequence Status Availability
sa13898 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa13898
Status:
Available for shipment
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Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111516 Essential Splice Site 883 953 27 29
Genomic Location (Zv9):
Chromosome 24 (position 38084241)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 36699160
GRCz11 24 36586916
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCGTCCGCCTTCTTYCCCGTCTTCACACGCTTCWTCAAAGCATACAAG[G/C]TGGAGAAATCATCACACACACACNNTGATCATCTTAAACACATACTKTACAT
Long Flanking Sequence:
CTGTACCTGTTTGTGTCTGTTTATGTGTGTTTGTGCCTGAATATGTGTCTGCATATTCATTCTGGATATGCATATGTGTGTTTCTGTACATGTGTGTCTTTATCCGTGTGTATTTGTACACATACACACACACATTGAGTTTTCATGTTTTATAGTGTCTTCCCATAGACGTAGGGATTTTTACACTGTACACACGGTATATTGTATCCCCCTACCCCAACTCTATGCAGTTTTACAGTTTGACAATTCTTCAACGTGTGACTTATAAGATGTTTTCCTCAGGGGGACAAAATAAATGTCCCCACAAGGTCACAAATCACTGATATTACTACACATGAGGGAACCACACATACACAAACACACACACACACTAACACCTTCTGCATGTGTGTCCACAGGAAGCCTATCAGTCTGTGGTGGAGTATTTCGGAGAGAATCCCAAATCCACTCCTCCGTCCGCCTTCTTTCCCGTCTTCACACGCTTCATCAAAGCATACAAG[G/C]TGGAGAAATCATCACACACACACTGATCATCTTAAACACATACTGTACATTACACTGCTGTCGCTGTGAGCCAACAAAACCATGAAGATGCTGAAAGCAAGCAAACAAAATACTTTGATAGACTTAAAGTCAAACTTACTTGCATTTTCACTGACACAGCATCTGAAGTAGACATAATAAGAGTGAAAATATGAATGAAGCAGTATTTTCTTGTAGACAAACTCCACTAGTACTAGTCTTTCTTTTTGAACTTGAAACTTTTAAATAAATAAAAAATATACAAATATAAAAAAATATACAAAATATACATGTTCACCAACCGTTCTGAATCAACCAGTCTAACAGGGGTCACCAATCTCGTTCCTGGAGGTCCGGTGCCCTGCAGGGTTTAGCTCCAACTTGCCTCAACACACCTGCCTGGGTGTTTCAAGTATACCTAGTAAGACCTTGATAAGCATGTTCAGGTGTGTTTGATTAGGGTTGGAGCTAAAATCTGCAGG
Associated Phenotype:
Not determined