ZMP
myof
Ensembl ID:
Human Orthologue:
MYOF
Human Description:
myoferlin [Source:HGNC Symbol;Acc:3656]
Mouse Orthologue:
Myof
Mouse Description:
myoferlin Gene [Source:MGI Symbol;Acc:MGI:1919192]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22321 | Essential Splice Site | Available for shipment | Available now |
sa22322 | Essential Splice Site | Available for shipment | Available now |
sa31933 | Nonsense | Available for shipment | Available now |
sa10226 | Nonsense | Available for shipment | Available now |
sa31934 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22321
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026000 | Essential Splice Site | 533 | 2045 | 18 | 53 |
Genomic Location (Zv9):
Chromosome 13 (position 29480793)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29126741 |
GRCz11 | 13 | 29257191 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAATTTACTGGCCTACCTGACCCATATGAGGATCTGAATTACGGCAAG[G/A]TGAGTGTAGTAAAGAAAAATGTTGTGCTATGGGACTGACTGCTGAGAGCT
Long Flanking Sequence:
TGAAGTGCAGGTGTGGATTCATTCAGAATTTGCTGTTAAATAATAATTTATCGTCATTGAATCGCTCCTTTTTAATTTTATTTTAAAACAGATTATTATTTATTTTTATATAATTTTTAGAAAAAAAGCTTAACTTTGTTCAGTACATATTTTGATTAGAACTTACTTTTGTCACCAGAAACACCCTCAGAAAATGGACTGCCATCTTCCTTTAATGGTAAAGGGAATTCTTTCATTTCATTTATTTTATTTTATTTTATTTTTTATTTATTTTATTTAATGTTATTTATTTCATTTGATTTATTTTACTATTATATCCTGTTTATTGATCTGTTGGTCATCTCTCTTAGTATCTCTAACTGAAACCTTTTTCAGTGGACACCACAGAAGCCGAAGTTGGCTTTCTTCCAGCCTTTGGGCCTTGTTATATTAACCTTTATGGAAGTCCCAGAGAATTTACTGGCCTACCTGACCCATATGAGGATCTGAATTACGGCAAG[G/A]TGAGTGTAGTAAAGAAAAATGTTGTGCTATGGGACTGACTGCTGAGAGCTATGAGAGAGAACATAATAAATTCTGTCCAACCCCAGCTACAGCCTTAGGAGGAAAATATGTCTGCAACACTTTGCCTTTAAGATACTATTGTTATGCAGTGTTTGCTTTACACAAAAAAAGAGCAAACACTTCATGCAGCCATTTCACATTCAGTCCAGCAGCTGCCTGTTGCACAGTTGTCATTTGTCAGATCAGTTGATTGTACATATGTGTGTTTCAGGGTGAAGGGGTCGCATACCGGGGAAGGGTCCTGATCGAGCTCTCCACTCAACTCAATGACAAAACTGACAAGAAGGTGGAGGACCTTTCCAACGATAACATTTTAGTGGCACAGGTAATAGCAAGCATTTTTCTGTCTGTCTTACTGAGGTCCTAATATATGATATGATATATGATATAATATATAACATGATTCATTTATTCATTTTTCTTCAGCTTAGTCTCTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22322
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026000 | Essential Splice Site | 630 | 2045 | 20 | 53 |
Genomic Location (Zv9):
Chromosome 13 (position 29482502)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29128450 |
GRCz11 | 13 | 29258900 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCAAACCACTGGCCTCTACTACTCAGTACAGCTGTGCTGTTTTTGATG[G/A]TGAGTTTCTCATAATGCCAGAGTGATAGCACATAAAAACACACTTAAGCC
Long Flanking Sequence:
ACTCGCCCCCCACCCCCAAAACGTGGACTGTTCCTTTAATTACAATAAATGTTATTATGTTGTTTTAGCCATTATGAAATCTACAGTACAGAGTAATTGCACTATCACAGAGGCTGCTTTCTGTTTAAACCAAAGAAATGTATACTAATGGTTGATGTGTCAGATCCTAAAATTAACATCTGCACTGGACAAATATTTAGCACTGCCTTTTATGCTTAACTTGAACTTCTCAGAATACAGATACTAACTTTCAAGGTAGTAATATGATAACTTCTATTGATATGAGGTCATTATAACGGAAGAATGTGCTTTTATTATGCAGAAATACCAGCGGAGAAGGAAATATTCCTTATGTGCAGTGTTTCACAGTGCCTGCATGCTTCAAGAGCCTGGAGAACCGATTCAGTTTGAGGTCAGCATAGGAAACTATGGAAATAAACTGGACTCCACATGCAAACCACTGGCCTCTACTACTCAGTACAGCTGTGCTGTTTTTGATG[G/A]TGAGTTTCTCATAATGCCAGAGTGATAGCACATAAAAACACACTTAAGCCCTTGAGACCTGCATTATTTTCCTAATTTTTTTTTTCCAAAGGAAATCACTATTATTACTTGCCCTGGGCTGATTCTAAGCCTGTTGTTATCCTCACATCTTTCTGGGAGGACATAAGTCATCGTTTGGATTCAGTGAACATCATTCTGTATATTTCTGATCGACTGGTAGGATTTTAATCTTTATGCCATTCGGCAATTCAGTGTGCTGCTAAATGATTCAGAGCAATCTCATATTTAATATGTCACTTTCTTTAGCAATCCAACATCATCTCTCTAAAGACAGCCATCTTAGCGAAAGTGTCTGACGCTCGCCTGGCTGAGATTTGGCTGAAACTTGTCACCCAAGTCATCGATGACCTTTCTAGGTAAATGCCAGAAACATTCTTATCTTCCTCTGTTTATAGCTCACACTTGGAGCATTGTTAGTGTTCAGAACAAACGTGATCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31933
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026000 | Nonsense | 667 | 2045 | 21 | 53 |
Genomic Location (Zv9):
Chromosome 13 (position 29482703)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29128651 |
GRCz11 | 13 | 29259101 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTGGGAGGACATAAGTCATCGTTTGGATTCAGTGAACATCATTCTGTA[T/G]ATTTCTGATCGACTGGTAGGATTTTAATCTTTATGCCATTCGGCAATTCA
Long Flanking Sequence:
ACTGCCTTTTATGCTTAACTTGAACTTCTCAGAATACAGATACTAACTTTCAAGGTAGTAATATGATAACTTCTATTGATATGAGGTCATTATAACGGAAGAATGTGCTTTTATTATGCAGAAATACCAGCGGAGAAGGAAATATTCCTTATGTGCAGTGTTTCACAGTGCCTGCATGCTTCAAGAGCCTGGAGAACCGATTCAGTTTGAGGTCAGCATAGGAAACTATGGAAATAAACTGGACTCCACATGCAAACCACTGGCCTCTACTACTCAGTACAGCTGTGCTGTTTTTGATGGTGAGTTTCTCATAATGCCAGAGTGATAGCACATAAAAACACACTTAAGCCCTTGAGACCTGCATTATTTTCCTAATTTTTTTTTTCCAAAGGAAATCACTATTATTACTTGCCCTGGGCTGATTCTAAGCCTGTTGTTATCCTCACATCTTTCTGGGAGGACATAAGTCATCGTTTGGATTCAGTGAACATCATTCTGTA[T/G]ATTTCTGATCGACTGGTAGGATTTTAATCTTTATGCCATTCGGCAATTCAGTGTGCTGCTAAATGATTCAGAGCAATCTCATATTTAATATGTCACTTTCTTTAGCAATCCAACATCATCTCTCTAAAGACAGCCATCTTAGCGAAAGTGTCTGACGCTCGCCTGGCTGAGATTTGGCTGAAACTTGTCACCCAAGTCATCGATGACCTTTCTAGGTAAATGCCAGAAACATTCTTATCTTCCTCTGTTTATAGCTCACACTTGGAGCATTGTTAGTGTTCAGAACAAACGTGATCATTGAGAGTTTTTATTATTATTATTATGATTATCATGAGGACAGGACAAATTAAATGAAGAAATCTAGACATTATATTTAATTGAAAAAATTTAATTATGCTGTTGATAAAAATATGACAACATTTACTGCAAAAGTCTCTAAAAACTATAAAAAATCTAAATAAATGTTTAAAATTAATTATATATTTTTTTATGAAGCAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10226
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026000 | Nonsense | 1555 | 2045 | 41 | 53 |
Genomic Location (Zv9):
Chromosome 13 (position 29504960)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29150908 |
GRCz11 | 13 | 29281358 |
KASP Assay ID:
2260-6518.1 (used for ordering genotyping assays)
KASP Sequence:
GTCCTCAGGAGTGCCTGGTCAGAATCCAYAKCATAYGTTGCCTCGACCTG[C/T]AGCCTAAAGACAACAATRGCATGGTGAGTTTCCAGTGRTGTAAAGGAACA
Long Flanking Sequence:
ATATCCTAACAAGCACATATTAACCCATTGTGTGCTTGAGATGTTCTGCTCTACGAGCGCAAATGTAGAGAACAGCGAGTTTGTGTGTGGTAGAAGAAAGAAAATTATCTGTACTCATGTTCATTTGGAATACTAGAAGACAACATTACTAAATTCCAAGCCACTGAACATTAATGAATTATACCAAGCCACAGTTTTGCTGGTCTTTATGGGAATAATCTGTTGTGTCTGTGTTCTTTAATGAGCATATTATTAATAAAAATAACAACAAAAACTTCTGTTCTCATCTCATTTATTATAGGCACTGTTACTGTTTATTGCAGTAAATCTGACCCTCAGTGATACATATTTTTCTACTGCATTGACAGGGCTCGTTTCGAGTGTATCCCTTGTCAGATGACCCAAACATCTCAGATCCACCTCGGCAGTTTAGAGAGCTGCCTGAAAGCTGTCCTCAGGAGTGCCTGGTCAGAATCCATATCATACGTTGCCTCGACCTG[C/T]AGCCTAAAGACAACAATGGCATGGTGAGTTTCCAGTGGTGTAAAGGAACACATTTTCTCTGGAATTGTACTTTACTAAGTAGTTTTGAAATGTGTGCTGCATTTGCTCCACTATTTTTCCTTAATCAATCCTGTAATTCTTGTCAAATCAAACCACGCATATAATTGCATTAGACAGACCGTCCTGAAGAACGTCCTCAAGTGTGGAAGCATTAGGAGTGTCTAAGAAGATGCAAAAGTCGTTGCACGCAATCAAGAGACTGCATTTCACTGATGAAGATAAATGATGCCTATTGTATGCCTGAAAGGGTTCAAAGTGCATAACCTAAGTGTTAACATATGGTCACAGCTACTGTAGATTAGCATTAGGTTTTAACATTAAGCTATATTTTTAATTTGCAGGGTATAAGGTGGAATCATTTTCAGAGCTTAATACTCATTACTCAGTACTCTTTAGCTTTTTTATAAGGGCTATATTTTACTCATACTTTGAGTTGTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31934
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026000 | Essential Splice Site | 2035 | 2045 | 53 | 53 |
Genomic Location (Zv9):
Chromosome 13 (position 29512467)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29158415 |
GRCz11 | 13 | 29288865 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACAGTATATTATGTGTGTTTTTAAATATTTGCCCTTTCATCTCTTTTC[A/T]GAACTACCTTTCCATGAAACTCGTAAAGCCATTTTAATAGGAAAAATTCA
Long Flanking Sequence:
TGGGTGAACTATACCTTTAACAATGTTGTTTTTGGGATGTCAGGGTAAAGTGGAAATGACTCTGGAGGTGGTAGAGGAGAAAGAGGCGGATGAGAGGCCTGCTGGGAAAGGAAGAGATGAACCCAACATGAACCCCAAACTAGAGTCTCCAAAGTAAGAACATCAGTGTTTGGTTGTTCGCTATAATCTTTCATTAAAGGATGTGAGTAATACTGTGTGTTGTACTATGTTCAAACAGCCGTCCAGATACATCTTTCCTTTGGTTCACAAATCCATGCAAGACCATGAAGTTCATCGTGTGGCGCAAATACAAATGGCTCTTCATTGGATTAATTATTCTCATACCTGTGATCCTGTTTATTGGAATCCTTTTGTATTCTTTCCCGGTAAGTGTTTTCCTGATATTGTAAGTTAATGTGGGAATTGATTAAAATTCTTATGTTAGGATCACTACAGTATATTATGTGTGTTTTTAAATATTTGCCCTTTCATCTCTTTTC[A/T]GAACTACCTTTCCATGAAACTCGTAAAGCCATTTTAATAGGAAAAATTCAAGATTTGGAAACTGCAACTTGCACTGGACACAGTCAATGGAGAAATTGAATTTTATTGATGTCATTCTCTGCAAAAAGACTTGAATCTTTTATATATGACAAGTGATATGCTTTTTTTTAGACAACACTGGGTTGGCAGATTGCGAATGCTGCTAAATGTTGCACTATATTACTTTGTACAATCTCTGAAAGTTGCTTTTTTTGTTTAATTGTTCATATACAGGAACGCGAATTAATAATACTTCTTAGTAATACTAATGTTAGGGTTGTTTTGTTGTTGTCATTTACAGTACAATCATTTTTCTATTCAATTAAATCCAAATGTATCTACTCTTTGTTCATTCTGCATTAGTCAACAGTTTCTTGTATTCATCTTTTTTAATATTAGCAATAGTAATTTTATGTAATTAGTAATTAAATGTTAAAAAGTAATTAAATGTAGATCTTTAA
Associated Phenotype:
Not determined