ZMP
myf5
Ensembl ID:
ZFIN ID:
Description:
myogenic factor 5 [Source:RefSeq peptide;Acc:NP_571651]
Human Orthologue:
MYF5
Human Description:
myogenic factor 5 [Source:HGNC Symbol;Acc:7565]
Mouse Orthologue:
Myf5
Mouse Description:
myogenic factor 5 Gene [Source:MGI Symbol;Acc:MGI:97252]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| hu2022 | Nonsense | Confirmed mutation in F2 line | Not yet available |
| sa26293 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
hu2022
Status:
Confirmed mutation in F2 line
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:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112035 | Nonsense | 59 | 237 | 1 | 4 |
| ENSDART00000127664 | Nonsense | 59 | 237 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 4 (position 20677128)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 22020463 |
| GRCz11 | 4 | 21741438 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGGCCCCACATCAACCGGGCCATTGTCTCCAATGGGCCTGCAAAGCTTG[C/A]AAGCGTAAAGCCAGTACGGTGGACCGCCGGAGAGCCGCCACCATGAGGGA
Long Flanking Sequence:
TAAAAATTGAAAGACATAAAAACAGACATCCGAAGCCTGAGTTTCTTCACGCGAATGTTTATTGATGATAATTCCCTCTTGTAATGACCGTCACGCTGCTGAAGTGAGTGAGAAACCACCCCTCCACACAGATGTGGGAAACTCAGTAGGGGTGTTGGGTTTGGGTGGGGATCTGGATGGTGAGAGAGGGGGGTCTCTTAGCTCTGTCCTGGCCAATGGGGGCACGGTCATTAGGGCTGACCAGTGTGGGCCCCGACATATAAGAAGGGCCGTATGGCACCAGTGCTACCACACCACTCAGAAACCTTCAACACCAAACCAATCATGGACGTATTCTCCACATCCCAGATCTTCTACGACAGCACTTGCGCTTCGTCTCCTGAAGATTTAGAGTTTGGAGCCAGTGGGGAACTGACCGGGTCTGAGGAGGATGAGCACGTGCGGGCTCCTGGGGCCCCACATCAACCGGGCCATTGTCTCCAATGGGCCTGCAAAGCTTG[C/A]AAGCGTAAAGCCAGTACGGTGGACCGCCGGAGAGCCGCCACCATGAGGGAACGGCGCAGGCTGAAGAAGGTCAATCACGCCTTTGAGGCACTACGCCGCTGCACCTCGGCCAACCCTAGCCAACGCCTCCCCAAGGTAGAGATCCTGAGGAACGCCATCCAGTACATCGAGAGCCTTCAGGAGCTCCTCAGGGAACAGGTGGAGAACTACTACAGCCTGCCGATGGAGAGCAGCTCTGAGCCCGCCAGTCCCTCCTCCAGCTGCTCAGAGAGCATGGTAAATATGACTCTCTTTCTCTTATTCTATGGGGTTTAAACATGATAGACCTACAGTGAAGCTCTGCATAAACTCTTATTCCAGTGGGACTTGTCCAAAGGTCAGATAAAAGCATTTTGAATGCAGATTTTTGAGGTTTCTCTCTTCTTCATTGTGTCTAGACAAGGCAATTGTTCTGTGTTTGGTCTTTATATTTTATCTCAATAGCACACGGGGGATTGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26293
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000014818 | Nonsense | 183 | 254 | 2 | 3 |
| ENSDART00000112035 | Nonsense | 166 | 237 | 2 | 4 |
| ENSDART00000127664 | Nonsense | 166 | 237 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 4 (position 20679432)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 22022767 |
| GRCz11 | 4 | 21743742 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTAGGTTGACTGCAACAGTCCTGTATGGCCTCAGATGAATCAAAACTA[T/A]GGGAATAGCTACAACTTTGACGCACAAAATGGTAAGAATATCATATTCAT
Long Flanking Sequence:
ATGTCGATTCACAAAACATTTATGACAAAACTCTCAGGGTTTAAGAATTGAGGATATATAGTAGTAATGTCTTTCCCTCTGGACTCTTTATAGCCCAATAAAGCCTCAGTAAATCCAGCCAAACAGACACTGGCAGGAAAGTGGCGTCCGTGCTGCATTCCTGACTGACTGCATGAGCTGCGCTGCTGCCAGGATTTTCTGCAGATTTACTCCGAAAAAAGTGTCATCTTGCACAAACTGGTGTGGCTTCCACTGACTCAATCAATTCGCCTTGCCTGAAGCCCAGAATAGCGTGGGAGTCCCTGGCAAATAAGCGGCCTGTGAAAGAAAGAGATACAGAGAAGCGCACAGAATGCTCATTCACTGCCTGTGATGCTCGAGCTGTTTTGTGTACAGCTTGTTGACTGCTTTATATGTGCGTATGCTGATGGAGTTTTTGATGTTTTGTCATGGTAGGTTGACTGCAACAGTCCTGTATGGCCTCAGATGAATCAAAACTA[T/A]GGGAATAGCTACAACTTTGACGCACAAAATGGTAAGAATATCATATTCATTTAAAAAAAAAAAGAAAATTCTGCCATCATTTACTCACTCTTTACTTGTTCCTTTTTTATGTTAAATACTAAAAAAGATATTTTGAAAAATGTATGAAACCTGTAACCATTGACCTCCATAGTATTTGTTTTTCCTACTATGGAAGTCAGTGGTTACAGGTTTCCAGCTTCTTTCAAAATATCTTCTTTTGTGTTTAACATAATAAAGAAACGTTAAGAAACTAATTCAAGAAGTTAAAAGTTTGAGACAAGTAGGAGAGTAAATAGTTTTGATTTTTGTGTGAACTGTCCCTTTAAATGTGGAGTTCATGACATATATGAGCAGGAATTGTATATTACTTGATTGCCTAATTTCTCTGTAAAGTTGCTTTGACAGTTTACATTGCGCAAAGCACTACAGAAAATAAAATGAGCTGAGTTGAACAATATAATAATACTAATTTCCTGTTT
Associated Phenotype:
Not determined