ZMP
MYOM1 (1 of 2)
Ensembl ID:
Description:
myomesin 1, 185kDa [Source:HGNC Symbol;Acc:7613]
Human Orthologue:
MYOM1
Human Description:
myomesin 1, 185kDa [Source:HGNC Symbol;Acc:7613]
Mouse Orthologue:
Myom1
Mouse Description:
myomesin 1 Gene [Source:MGI Symbol;Acc:MGI:1341430]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15474 | Nonsense | Available for shipment | Available now |
sa34248 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa34247 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa34246 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11567 | Nonsense | Available for shipment | Available now |
sa21150 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15474
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 |
---|---|---|---|---|---|
ENSDART00000087099 | Nonsense | 675 | 1656 | 20 | 43 |
Genomic Location (Zv9):
Chromosome 7 (position 74389198)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 71534588 |
GRCz11 | 7 | 71726380 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCACAGACAGCTGGCAGCGAGTGAACACTGAAATCCCAGTGAAATCTCCA[C/T]GMTTTGCTCTCTTTGATCYGGCCGAGGGCAAATCTTACCRCTTCAGAGTT
Long Flanking Sequence:
TTTATGTCTGGTGACTGGGCTGGCCAATCCTGTATGAGGAGTGCTTTCCTGCTGGATAATTGTCCTTGTCCCTCTGCTGTGGTTTGTAATGTAATGGGCAGCACAAATGTCTTGATACCTCAGGCTGTTGATGTTGATCATCCACTCTGCAGATCTCTCGCACGCCCCCATACTGAATGTGACCCCAAACCAGGATTTTTCCTTCACCAAACTTGACTGATTTCTTTGAGAATCTTGGCTCCTTGCGGGCTCCAGTAGGTCTTCTGCAGTATTTGTGGTGATTGGGATGCAGTTCAACAGATGATTCAGCAGAAAAGTCCACCTTCAGACTATAGCTCTTACTATAAGTTACTGTATTATTTTTTTCAGATGGGTAACTGCTGTAATTAGTAACTCATTACTGGTAATTTGTCTTGATAAGCGTGTGTGTGTTTGTGTAGTGTGTGTCAGGCACAGACAGCTGGCAGCGAGTGAACACTGAAATCCCAGTGAAATCTCCA[C/T]GATTTGCTCTCTTTGATCTGGCCGAGGGCAAATCTTACCGCTTCAGAGTTCGCTGCTGCAACTCTGCTGGTGTTGGAGAACCATCAGAACCCACTGACGCCACAACGGTTGGAGACAAATTGGGTATGATTCTGTCATGAAGAGCTCATTTGATGATTTACGTTGGCGAGATTTAGCCAATTTATAACATCAACATGCTAGAATGTGTGGTAAACATGCTGGAAATGTGCTAATAAAAAGCTAATTCACACTGCCAATGTGCTAAAACTTGGTAGATATGGGCTAGACCCATGTTTATTAATGCTAGCAACCGGGGCCGGGGTGTCCATAGAGGCGACCTTGGTCGGCCAGTTCAGCTTGCTCTGGCTCTGCTAGCAACACGTTAAAACGTAAGCCATGTGATAAAACTAGGGCTGCTACTCGCTTGAATGGGGTAAACATGCTGGAAACGTGTTAATGAAAAGCTAACTCATAAATTTAATATGCTAAAACTTTCTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34248
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087099 | Essential Splice Site | 1214 | 1656 | 29 | 43 |
Genomic Location (Zv9):
Chromosome 7 (position 74375038)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 71520428 |
GRCz11 | 7 | 71712220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTGACACACACTGATGGAGCGTCTGCCAGCTACACGTTCTCTGAAGAAG[G/A]TCGGATTATCTGTTTTCTGCTTTTTTGTTTTTGTATTTATAAGTGTGCTC
Long Flanking Sequence:
TGCTGTCTTTATAGTCCTTGTAATCAGTCTATGTCAATCCTCCGACTGTGTGTATGCAATCAGTCATGATCAGGAACTGGTTGTGTGTGTGTGTGTGGTGCATGACTGGATTTTGTAGTCCATAAATGGCAGATTTGTAGTCTGTTAGCGATCTGCAGCCACTAGGTCGCTGATAATCACAACACTTACGATGACCTGCAACAATCTCAAGTGCTAGTTGAGTTATGATGCTTTTCGCCAACAGGCTATAACGTTACGACCAGTCGCACAATCATTTTGACCATCTACTTAGGCTTTAGATGCTTTTGGTAATCGCAGCCCAAGTCAAGCCACATTTACAGAGCTTTAATTACAAAAGTCATCTTGTAATAAGTCTTCAATGCTGGTCTGCAGGTCCAAAGCCATCTTTAACTCTCCTTCAGAGGAGGATCTGGGCATCTACTCTTGTTTCGTGACACACACTGATGGAGCGTCTGCCAGCTACACGTTCTCTGAAGAAG[G/A]TCGGATTATCTGTTTTCTGCTTTTTTGTTTTTGTATTTATAAGTGTGCTCAAGTTATTGATTCTGCTCACTTGATCTGCTCTTAACAGCTCTGAAAGAACTGCTGAAGGTCAGCCACGACCACAAATTCCCCAGTGAGTTTTGTTGTTGTTGTTGTTGTTTAGTTTACAGCAGGGGTCACCAACCTTTATGAAACTGAGAGCTACTTCTTGGGTACTGATTAATGTGGAGGGCTTCCAGTTTGATAGACACTTGTCAAATAACAAATTTGCTCAATTTACTTGTAATTATACTTTATGTTTTTGGTAATAATAAATGATATTCATCCATGTGAAGACACTGATCATGTAAATGATTCTTACAAAAGTTATCAACAACGATTTAACAGGGTAGGAAATACCCTGTATTTAATGTATCAATGTGCAACACTTTATTATTATACATCTCTGCAAATATTTATATTTTTTAATGATTACTTCGATATAAGATGAAGCTTACTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34247
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087099 | Essential Splice Site | 1276 | 1656 | 32 | 43 |
Genomic Location (Zv9):
Chromosome 7 (position 74370767)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 71516157 |
GRCz11 | 7 | 71707949 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAGGTAATAATAATACATTTTAAACTAAACTACTCCGGTGTGTTGTA[G/T]AAATACAAGATGAACTTTGACAAAAACACTGGCATCATTGAGATGTTCAT
Long Flanking Sequence:
GTTGTAACGAACATATTAATGCAAACTGTTGCGTACATTTTTTTTGTTTTGTCTAAACAATATTTTTTAGAGTGTAGATTATTTATTTTTCTATTTGTATTTGGTGTTTGGTTGAAATTAAAGTATGTTAATCTTAAGGATATCTATAAGCTAGTGTGCTCCAAGAACATTGACAAAAGGTGCATTTAGAAGATATAAACCTGATATAAACATCCAAAGCTTGCAGTTTGTCAATTTCCGCCTGAATAGATCAACGATTTGTTTGACGTCCTCTCATACTTCAGTTTCTCATCAAATCTCCTGACCAATCAAATGCTCTCTAGTATCTGATGTGCCCCGCCCTCTCTTCCACGTTTCAGTTGAAATTATATCAAACATTGAATAAAAAAAATGTACATTTCAAAGCACTACACGGTAAACCTCACACCTCACATATCAGAATGAATCGCATCAAAGGTAATAATAATACATTTTAAACTAAACTACTCCGGTGTGTTGTA[G/T]AAATACAAGATGAACTTTGACAAAAACACTGGCATCATTGAGATGTTCATGGAGTCTCTGGGCAAAGAGGACGAGGGCACGTTCACTTTCCAGCTTCAAGACGGAAAAGCCACCAACCAGTCCAGTCTAGTGCTAATCGGAGATGGTACGTCTGAAAATGAATGGATTTCCTACATACAGCACATGCATCTGATTTACAGAGTGTGTATCAGGGATGTTTTCTTGTTTCTTTCAGTGTTTAAGCAGTTGCAGAAGGAATCAGAGTTTCAGAGGAAAGAATGGCATAGAAAGCAAGGTATGAGTATAGTGTATGCACTAAAATATTATGTGTGCATAAAAAAGTCATATAAACAGTCTAAGTTCACATTAGTTTACTGTTTGAGTGGTCTCACATGATCATTTTTTAAATAAAAAAAAATATACACTCACCGGCCACTTTATTAGGTACACCTGTCCAATTGTTCGTCAATGTGAATTTCTAATCAGCCAATCACATGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34246
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087099 | Nonsense | 1339 | 1656 | 33 | 43 |
Genomic Location (Zv9):
Chromosome 7 (position 74370485)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 71515875 |
GRCz11 | 7 | 71707667 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGTGTTTAAGCAGTTGCAGAAGGAATCAGAGTTTCAGAGGAAAGAATG[G/A]CATAGAAAGCAAGGTATGAGTATAGTGTATGCACTAAAATATTATGTGTG
Long Flanking Sequence:
AGTTTCTCATCAAATCTCCTGACCAATCAAATGCTCTCTAGTATCTGATGTGCCCCGCCCTCTCTTCCACGTTTCAGTTGAAATTATATCAAACATTGAATAAAAAAAATGTACATTTCAAAGCACTACACGGTAAACCTCACACCTCACATATCAGAATGAATCGCATCAAAGGTAATAATAATACATTTTAAACTAAACTACTCCGGTGTGTTGTAGAAATACAAGATGAACTTTGACAAAAACACTGGCATCATTGAGATGTTCATGGAGTCTCTGGGCAAAGAGGACGAGGGCACGTTCACTTTCCAGCTTCAAGACGGAAAAGCCACCAACCAGTCCAGTCTAGTGCTAATCGGAGATGGTACGTCTGAAAATGAATGGATTTCCTACATACAGCACATGCATCTGATTTACAGAGTGTGTATCAGGGATGTTTTCTTGTTTCTTTCAGTGTTTAAGCAGTTGCAGAAGGAATCAGAGTTTCAGAGGAAAGAATG[G/A]CATAGAAAGCAAGGTATGAGTATAGTGTATGCACTAAAATATTATGTGTGCATAAAAAAGTCATATAAACAGTCTAAGTTCACATTAGTTTACTGTTTGAGTGGTCTCACATGATCATTTTTTAAATAAAAAAAAATATACACTCACCGGCCACTTTATTAGGTACACCTGTCCAATTGTTCGTCAATGTGAATTTCTAATCAGCCAATCACATGGCAGCAACTCAATGCATTTGGGCATGTCGATCTGCTGCAGTTCAAAGCGAGCATCAGAATAGGAAGAAAAGGTGTTTGTTGGTGTCAGACGGGCTGGTCTGAGTATTTCAGAAACTGCTGATCTACTGGGATTTTCACGCACAACCATCTCTAGGGTTTACAGAGAATGGTCTGAAAGAGAGAAAATGTCCAGTGAGCGGCAGTTCTGTGGGCGCAAATGCCTTGTTGATGCCAGAGGTCAGAGGAGAATGGCCAGACTGGTTACAAAAAGGCAAGAGTAACTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11567
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087099 | Nonsense | 1378 | 1656 | 35 | 43 |
Genomic Location (Zv9):
Chromosome 7 (position 74369090)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 71514480 |
GRCz11 | 7 | 71706272 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAATCTGKGCTGTAGGTTGGKAACATGAAGAAAGACTCGACGGCRTTGTG[G/A]TATAAAGATGGACGGGAGGTGAAGGTCGACGAAAAACTGGATTTCTCTGA
Long Flanking Sequence:
TGAGTATTGTTGCTGACCATGTCCATCCCTTTATGAGCACAGTGTCTCCATCTTCTGATGGCCACTTCCAGCAGGATAACGCACCATGTCATAAAGTGTAAATCATCTCAGACTGGTTTCTAGAACATGACAATGAGTTCACTGTACTCAAATGACCTCCACTGTCACCAGATCTCAATCCAACAGAGCACCTTTAGGATGTGCTATATACATAACAAAACCAAAACAAAGAAAAAATCTATGTGTATGTTAGCGCCATTGCAGAGACTGTGTCTGTATGCTAATCAGTCTGTTTACACTCTGTCAGGTCCACACTTTGTGGAGTATCTTGGTTATGAAGTGACACCTGAATGCTGCGTCAGACTGAAGTGTAAGGTGAGCTGACGTCTCTCTACACTCCAACACTCACAGACACTCATTCAGCTCTCTGATTCTTCAATAATCATGTGCTAATCTGTGCTGTAGGTTGGTAACATGAAGAAAGACTCGACGGCGTTGTG[G/A]TATAAAGATGGACGGGAGGTGAAGGTCGACGAAAAACTGGATTTCTCTGAAGGAGTGTTAACTTTGGAGATCGCACAGGTGAGCGGCAGAAACTTAAAAGCTAAACAGACAAAAACTGGTCCTCCAGTAGCTAACGTAGGGAAGTATGCTAGTGCTAGCATCGCAAAAGTTTGTGGGAAAGCAAAAACTGATCAAATGTGGACCTTCAATGCAATGCAACCAGTTAATCATGACAAAATCATGCTAGCAATATGTTCACACCAGCTAAGTCATGTTAGCCTGGGGTAAAACTGTTAGCAGCATGCTAATTCCCCTGCTTAAAACAAAACAGCTAAAACAGCTAAAGCTGGTTGGCTGGTCTTAGCTGGTTTTAGCAGGAAGTTGCTGGATTTAGTCTGGCCAGACTGGTTAAGCTGGTCTCTCAATCTGGCCAGGCTGGTTTTAGTTGGTCTCTCAGCCTGGTCAAGCTGGTTTTACCTGGTCTCCCAATCCTGGCCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21150
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 |
---|---|---|---|---|---|
ENSDART00000087099 | Nonsense | 1379 | 1656 | 35 | 43 |
Genomic Location (Zv9):
Chromosome 7 (position 74369087)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 71514477 |
GRCz11 | 7 | 71706269 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTGCTGTAGGTTGGTAACATGAAGAAAGACTCGACGGCGTTGTGGTA[T/G]AAAGATGGACGGGAGGTGAAGGTCGACGAAAAACTGGATTTCTCTGAAGG
Long Flanking Sequence:
GTATTGTTGCTGACCATGTCCATCCCTTTATGAGCACAGTGTCTCCATCTTCTGATGGCCACTTCCAGCAGGATAACGCACCATGTCATAAAGTGTAAATCATCTCAGACTGGTTTCTAGAACATGACAATGAGTTCACTGTACTCAAATGACCTCCACTGTCACCAGATCTCAATCCAACAGAGCACCTTTAGGATGTGCTATATACATAACAAAACCAAAACAAAGAAAAAATCTATGTGTATGTTAGCGCCATTGCAGAGACTGTGTCTGTATGCTAATCAGTCTGTTTACACTCTGTCAGGTCCACACTTTGTGGAGTATCTTGGTTATGAAGTGACACCTGAATGCTGCGTCAGACTGAAGTGTAAGGTGAGCTGACGTCTCTCTACACTCCAACACTCACAGACACTCATTCAGCTCTCTGATTCTTCAATAATCATGTGCTAATCTGTGCTGTAGGTTGGTAACATGAAGAAAGACTCGACGGCGTTGTGGTA[T/G]AAAGATGGACGGGAGGTGAAGGTCGACGAAAAACTGGATTTCTCTGAAGGAGTGTTAACTTTGGAGATCGCACAGGTGAGCGGCAGAAACTTAAAAGCTAAACAGACAAAAACTGGTCCTCCAGTAGCTAACGTAGGGAAGTATGCTAGTGCTAGCATCGCAAAAGTTTGTGGGAAAGCAAAAACTGATCAAATGTGGACCTTCAATGCAATGCAACCAGTTAATCATGACAAAATCATGCTAGCAATATGTTCACACCAGCTAAGTCATGTTAGCCTGGGGTAAAACTGTTAGCAGCATGCTAATTCCCCTGCTTAAAACAAAACAGCTAAAACAGCTAAAGCTGGTTGGCTGGTCTTAGCTGGTTTTAGCAGGAAGTTGCTGGATTTAGTCTGGCCAGACTGGTTAAGCTGGTCTCTCAATCTGGCCAGGCTGGTTTTAGTTGGTCTCTCAGCCTGGTCAAGCTGGTTTTACCTGGTCTCCCAATCCTGGCCAGGCTG
Associated Phenotype:
Not determined