Busch Lab

ZMP

frmd8

Ensembl ID:
ENSDARG00000073696
ZFIN ID:
ZDB-GENE-090812-5
Human Orthologue:
FRMD8
Human Description:
FERM domain containing 8 [Source:HGNC Symbol;Acc:25462]
Mouse Orthologue:
Frmd8
Mouse Description:
FERM domain containing 8 Gene [Source:MGI Symbol;Acc:MGI:1914707]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa41676 Nonsense Mutation detected in F1 DNA Not yet available
sa21752 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa41676
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114457 Nonsense 369 471 8 10
ENSDART00000135493 Nonsense 369 471 9 10
Genomic Location (Zv9):
Chromosome 10 (position 27592092)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 26994886
GRCz11 10 26956599
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTTACTGTTCATTTTATTCTCTAGGCTGAACTTATGAGTGGTCTTATC[G/T]AGTTTTGTGTGGAGTTACGCTCTGTTAGTGAGTCAGCAGCCACAGGTACA
Long Flanking Sequence:
AAGCAAGTTAATCATGGCACATAAATACACTTTGACAGTTTCATCCAATAAACCCTTGTGTGCTGTTGGGAATGTGTTCATCCACTCTGGGGTGATTTTCAAGTCTTAATTTGGCCACAACTTTCTCTGTATTTCAGCAAATTGAATGATTTTTGGTGAATTTATTTTTGTTTTTATGAAAATGCTTTGAAAAAAAGCTCAACAATACACTGTAGGCAGATGTACTACCCTTTCATTATGTTTGGGGCTGTTTTTGCCTAATTGACTGCCATTATAAGTACCAAGACTTTTTTTTTGATTGCTAAGCCATGACACCATATCATCATGCAGTTTTGATCATTACTGTTTTTCTCTTTTGGGAATAAGTCAAATCTAAATGCTTTCAAACCTAATACATTAATTTTCATGTGCTTATTTTGTTCATATCTGTGTATGTAAAATGTAAATATTAATTTACTGTTCATTTTATTCTCTAGGCTGAACTTATGAGTGGTCTTATC[G/T]AGTTTTGTGTGGAGTTACGCTCTGTTAGTGAGTCAGCAGCCACAGGTACAGACGGTGAGGTCACGCCTTCCCATGAACCTACGAGTCCAGAAACCAACAACAAAACCAGAGAGCGACGGCAGGGGAAACTGCGCAGACAGAACAGTGTGGTCTGTAGCCGAGTCCATTCCCTGAGCACCATCAACTATGTTGATGACGGTATGACTCCTTAAAATCATTTTGTTATGACATCTTTTTTTTATTTTTTATGAAAGTCTGTTCCCGCCACTAAATAATAATAATAATAAAAAAACTATAATAAAAGTCAGAATTTTAAGTTGTGACTTATTTTAACTTCTGACATTATAACTTGGAAATCTGACATTGTATGACGGAATTGCGACTTTATTACTCGGAACTCTGATTTTATAACTTGGAAATGTGGATTTATAACCCAGAGCTCTGACTTTATAACTCCAAATTGCAAATGTAAAACTCTGAATTGCGACTTTATTACTCGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21752
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114457 Nonsense 466 471 9 10
ENSDART00000135493 Nonsense 466 471 10 10
Genomic Location (Zv9):
Chromosome 10 (position 27593399)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 26996193
GRCz11 10 26957906
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTACAAGGCAAGCGCAGCCTCCCACTTACTCTGCTGTTCAGGTGACT[G/T]AAAGTTTAGAGCAAGGGTGAACCCAGGCCTCAACACTGCCCTCTTCTGCC
Long Flanking Sequence:
AACTCTGACTTTATAACTCGAAATTGCAAATTTATAACTCGGAATTGTGACTTTATAACTCGAATTGCAAATTTATAACTCGGAATTGTGACTATAACTCGTAACTCTGACTTTATAACTCGGAATTGGGAATTTTTAACTCAGAATTGCGACTTTATAACTCAGAATTTTGACTTTAGAACTCGGATTTGCAAATGTATAACTCGGAATTGCGACTGCATAACTTTGTAATTCTGACTTCATAACTCGGAATTTCGACTTTATAACTCGGAATTCTTTATAGTTTTTTTTTTTACTTTTTATTTTTTATAATTCAGTGGCAGGAAGGGGCTTCCATAGTTTTTCCTATTTATCATACAGAAATAAAGACCTGGGACAAAGCTTATTTTAATTTTTCCATTGTTTCAGGCAAAGAAATCAAACGTTTGAAACCCAAAAGAGCAGCTTCTTTCTTTACAAGGCAAGCGCAGCCTCCCACTTACTCTGCTGTTCAGGTGACT[G/T]AAAGTTTAGAGCAAGGGTGAACCCAGGCCTCAACACTGCCCTCTTCTGCCCGGTGACCAAAACTACATCTGTCCATTGAGATTCTCAGAGACGCAGTGCAAAACCATCTGAATGGACAGATCGGACCAAGATCACAGACCGAAGAGCTGAACCACTATTTATAGATGATTTGTGCATGATGTCGCAAGTTTAAGTTAAAGCTTTTTCTCTGTTGGCTGTTAAAAAATAAGAATGTGAAATTAAGTTTTCTTTTCCGTCAAACATTTTGGTGTAAGAGCAAGGCTAAGGGAAGCGATCTGAAAGCTCTGGGTCGGTCACTGTTCTGAATGTAGATTCTACTATGCAACCATCAAACCAAACTACATCCCAGTGGCTGTACATCAATAATTCCTCACTTTGATCCACTAATACTGCTAAAACCAGACCTGCTGCACCAAAGGAAACAATCAAAGCCTTTAGTATAGGTTGTAAAACTCCTATATGCAAAACCAGCGCTGCAG
Associated Phenotype:
Not determined