Busch Lab

ZMP

myf6

Ensembl ID:
ENSDARG00000029830
ZFIN ID:
ZDB-GENE-040309-2
Description:
Myogenic factor 6 [Source:UniProtKB/Swiss-Prot;Acc:Q6VNZ9]
Human Orthologue:
MYF6
Human Description:
myogenic factor 6 (herculin) [Source:HGNC Symbol;Acc:7566]
Mouse Orthologue:
Myf6
Mouse Description:
myogenic factor 6 Gene [Source:MGI Symbol;Acc:MGI:97253]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
hu2041 Nonsense Confirmed mutation in F2 line Not yet available
sa16975 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
hu2041
Status:
Confirmed mutation in F2 line
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
ENSDART00000040266 Nonsense 84 239 1 3
Genomic Location (Zv9):
Chromosome 4 (position 20653734)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 21997069
GRCz11 4 21718044
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAGGCGCACTGCGAGGGTCAGTGCCTCATGTGGGCTTGCAAGATCTG[T/A]AAACGGAAATCTGCTCCTACTGACCGGCGAAAGGCCGCCACTTTGAGAGA
Long Flanking Sequence:
CTTTATATATATATATAACTTGTTTTAATCTTGTTTTAATAGTATTAAAACAAGTAGTTAGTAAAACACCCAGTTGAGTGTTTCCTATATTTTTCATTTGGGCACCAGAAGGCCTATTGAATTGAATCTGAAGCCCCGCAACAGCTAAGCGCTGGATAGAATTTCACATGCTATATTTAAGTCTCCCAACTTGTGTCACAGGGCTATTTAAATGCCAACAGTCTTACTGTCAAAACAGCCTACAACAACATGATGGACCTGTTTGAGACCAACGCTTATTTTTTCAATGATTTGCGTTATCTTGAGGGGGACCATGGGACCTTGGATATGCCAGGAGTGTCCCCATTGTACGAGGGGAATGACAGTCCTCTGTCCCCAGGTCAGGATCCTGTCCCGTCGGAAACGGGGTGCGAGAGCAGCGGAGAGGAGCACGTCCTCGCTCCACCGGGGCTCCAGGCGCACTGCGAGGGTCAGTGCCTCATGTGGGCTTGCAAGATCTG[T/A]AAACGGAAATCTGCTCCTACTGACCGGCGAAAGGCCGCCACTTTGAGAGAACGAAGGCGGCTCAAAAAGATCAACGAAGCTTTTGACGCGCTAAAGAAAAAGACGGTGCCTAATCCGAACCAGAGGCTGCCCAAAGTGGAGATTTTACGCAGTGCGATAAACTACATTGAGAAACTGCAGGACCTCTTGCATTCGCTGGATGAGCAGGAGCAGAGCAATGACACTGACCCTTACACATACAACCTGAAGGAAAACCATGTAAGCCCATCCATTTGCTCTGGATCCACGTGGTGCTTTGACTCTGCGCACAGCTAATGCTATGATTTGTGTTTCAGAGTTACATTAAGAGTATTATTAATGTTTTTTCCATCATGATTGCCTGTTCAGGTGACTCCCAGTGAGTATCATTGGAAAAAGACCTGCCAGAGCTGGCAGGAGAACCCAGATCATTCCAGCTCCCAGATGGCAGGTCATAGAGAAGGTTGGTACAGAGCAGGATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16975
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
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040266 Nonsense 176 239 2 3
Genomic Location (Zv9):
Chromosome 4 (position 20654139)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 21997474
GRCz11 4 21718449
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAATGNNNNTTTTTCCATCATGATTGCCTGTTCAGGTKACTCCCAGTGAGTA[T/A]CATTGGAAAAAGACCTGCCAGAGCTGGCAGGAGAACCCAGATCATTCCAG
Long Flanking Sequence:
GGGTGCGAGAGCAGCGGAGAGGAGCACGTCCTCGCTCCACCGGGGCTCCAGGCGCACTGCGAGGGTCAGTGCCTCATGTGGGCTTGCAAGATCTGTAAACGGAAATCTGCTCCTACTGACCGGCGAAAGGCCGCCACTTTGAGAGAACGAAGGCGGCTCAAAAAGATCAACGAAGCTTTTGACGCGCTAAAGAAAAAGACGGTGCCTAATCCGAACCAGAGGCTGCCCAAAGTGGAGATTTTACGCAGTGCGATAAACTACATTGAGAAACTGCAGGACCTCTTGCATTCGCTGGATGAGCAGGAGCAGAGCAATGACACTGACCCTTACACATACAACCTGAAGGAAAACCATGTAAGCCCATCCATTTGCTCTGGATCCACGTGGTGCTTTGACTCTGCGCACAGCTAATGCTATGATTTGTGTTTCAGAGTTACATTAAGAGTATTATTAATGTTTTTTCCATCATGATTGCCTGTTCAGGTGACTCCCAGTGAGTA[T/A]CATTGGAAAAAGACCTGCCAGAGCTGGCAGGAGAACCCAGATCATTCCAGCTCCCAGATGGCAGGTCATAGAGAAGGTTGGTACAGAGCAGGATTTAACTTCATTTACGGTTTCTGATGGTTTCTTGGGCTGGTTGTCGGTTTGCTTTTGTTAGCTTGTATCTGTGCATAACTGGAAATGCTGGTAGCTTTATTCAAGGTTGAATAAGTTGCTGTGAAGGTTGGTAGTTTATTTGGACTTTTTGTCATTATACAGCAATGTTAAAATCTGGTAAAGAGCAGAGTTAGCATTGCTTTTGTCATGTTAACCCTGCATGAGTGTGCTAGACATCAATAGAGAAACACACACGTTGTATCTTTTACATGCTCAACTTTATTATTTTAAATGTAGACGCACGACAACCATGATCAACATTTAAGCTACATCGTCATGGGACTCATGTGGTCTGAAGCGCTCAGATTTTCCAGACGTGTCTGCACTATGGAAAATGTTCAGGGCCA
Associated Phenotype:
Not determined