ZMP
ENSDARG00000070174
Ensembl ID:
Human Orthologue:
MYO15B
Human Description:
myosin XVB pseudogene [Source:HGNC Symbol;Acc:14083]
Mouse Orthologues:
Myo15b, Myo3b
Mouse Descriptions:
myosin IIIB Gene [Source:MGI Symbol;Acc:MGI:2448580]
myosin XVB Gene [Source:MGI Symbol;Acc:MGI:2685534]
myosin XVB Gene [Source:MGI Symbol;Acc:MGI:2685534]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12019 | Nonsense | Available for shipment | Available now |
sa40118 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa26121 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12795 | Nonsense | Available for shipment | Available now |
sa33251 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12019
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 |
---|---|---|---|---|---|
ENSDART00000102784 | Nonsense | 295 | 634 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 37032841)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36896201 |
GRCz11 | 3 | 37038059 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAAGTGGAGAGCTAYGCGTCCTTCATTGGCCAGGCTCTAGAGAAGACC[C/T]GAGGCAGAGAGTGTGTGCCCTCGTGGGAGGAGATTCAAGGGCTGATGGGA
Long Flanking Sequence:
ACTGTCTGACTGTCTTTTTGGGAAAGGCTATGAGGAGTCCATTACAGTAATCCACCCTGGTGCTGATAAAAGCATGAACAACTTTCTCTAAGTCTTCACTAAAAACAAAGCATGTAATTCTTGCAATGTTTTTGAGATGATAGTATGATGATTTAGTTACTGCTTTTGCTGTGCATTGTATAATCAGGTAAACTATGTTTGAAGATATTTCTCCGTGAATCAGACTTTAAATATATGTATTGTGATTAAAATCTCCCAACACAAATTGATGAAGTGTGTGACAAAAGAATGACTTGAAAGTACATTTTGGATATTTTCTTCACATTAAACTGAAAAGATAAAAACGCTTCATGAAAAGCCCAACATCTAAAAACAGTGCCTTTGCTTGTATTGTAAACTTTGTTTTTTGTTTTCCTCCATGTTTCAGGGTTCAGAGTTTGAGTGTGGACCCAGAAGTGGAGAGCTATGCGTCCTTCATTGGCCAGGCTCTAGAGAAGACC[C/T]GAGGCAGAGAGTGTGTGCCCTCGTGGGAGGAGATTCAAGGGCTGATGGGAAGACAGGAGATACTGTGTACTGTGCATTACCCTGGACCAGGCTGCTGCCAGATACCCATCACCTCACACACCACAGCTAATGAGGTTCGGTTTCAATCCTTTCCTACAACTCTGACTCACTAAAAAGTTATTTAGTTATTTTATGATGAATTATACTATACTATTATAGATGCATAAACATTTTGAGAATTGTGAGATTTTTATTCTGAGTAGAAAATTCTGAATTCTATGATAAAAAAAAATCACAATTCCAAGACTTAAAGGTCCCATGTAGTGCATTTTTATTCAATGTTTAATTAAATTTCAACCAAAACACGAAGAGGGTGGGACATAGTGTAGCTCCTCCCCTTTAAAAAAAACAGGCAGTAGCATTTTGTTTTATCACAGCTCAGCCAGTGAGAGGGGTTGAGCTCAAGTGCATAAAATGAGAACTGGCTTGAAAGGGGTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40118
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 |
---|---|---|---|---|---|
ENSDART00000102784 | Essential Splice Site | 339 | 634 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 37032976)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36896336 |
GRCz11 | 3 | 37038194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCAGGCTGCTGCCAGATACCCATCACCTCACACACCACAGCTAATGAG[G/A]TTCGGTTTCAATCCTTTCCTACAACTCTGACTCACTAAAAAGTTATTTAG
Long Flanking Sequence:
GATGATAGTATGATGATTTAGTTACTGCTTTTGCTGTGCATTGTATAATCAGGTAAACTATGTTTGAAGATATTTCTCCGTGAATCAGACTTTAAATATATGTATTGTGATTAAAATCTCCCAACACAAATTGATGAAGTGTGTGACAAAAGAATGACTTGAAAGTACATTTTGGATATTTTCTTCACATTAAACTGAAAAGATAAAAACGCTTCATGAAAAGCCCAACATCTAAAAACAGTGCCTTTGCTTGTATTGTAAACTTTGTTTTTTGTTTTCCTCCATGTTTCAGGGTTCAGAGTTTGAGTGTGGACCCAGAAGTGGAGAGCTATGCGTCCTTCATTGGCCAGGCTCTAGAGAAGACCCGAGGCAGAGAGTGTGTGCCCTCGTGGGAGGAGATTCAAGGGCTGATGGGAAGACAGGAGATACTGTGTACTGTGCATTACCCTGGACCAGGCTGCTGCCAGATACCCATCACCTCACACACCACAGCTAATGAG[G/A]TTCGGTTTCAATCCTTTCCTACAACTCTGACTCACTAAAAAGTTATTTAGTTATTTTATGATGAATTATACTATACTATTATAGATGCATAAACATTTTGAGAATTGTGAGATTTTTATTCTGAGTAGAAAATTCTGAATTCTATGATAAAAAAAAATCACAATTCCAAGACTTAAAGGTCCCATGTAGTGCATTTTTATTCAATGTTTAATTAAATTTCAACCAAAACACGAAGAGGGTGGGACATAGTGTAGCTCCTCCCCTTTAAAAAAAACAGGCAGTAGCATTTTGTTTTATCACAGCTCAGCCAGTGAGAGGGGTTGAGCTCAAGTGCATAAAATGAGAACTGGCTTGAAAGGGGTGGGGCATGTCAGATACTAGAGATCATTTGATTGGGTATGGTTTGATGAGAAACTGAAGTTTGAGGTTATGTGAATAAAATCGTTGATCCATTTAGGCGGAAGTGACAAACTATAGGCTTTAAATGCTTATATCAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26121
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102784 | Nonsense | 362 | 634 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 37034639)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36897999 |
GRCz11 | 3 | 37039857 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGAGCGCCTCGGGCTGCAGGACAGCCGAAACACGTTTGGTCTTTTTGAG[C/T]AGAATGCATGCTGGGAAAAAGCTATAGGAGGCAGCACAATAATCGCTGAT
Long Flanking Sequence:
AGCAACATTTTGTGTCTGCTGGTTTGTTTACTTGCAGAAGTTCATTAGCATTTTCCCACACGTTAATTCTGACCAATCGATAAACAGTTTAGGAACTATGTTCAACAACATCTGGCCAATGAGAGATGTGGATTTTGTCAGATGACTGCATTTTGGTTCTTTTCAACTGGAACGGACCAAAGCAATCAGTGTGGTGTGAAAACAACCCGAAGATGGCAGAAACTGCAACAATTTATTGCTCTTGGTCTGGACCAAATGAAGTGAACTACAGATGTGAAAGCACCATAAAACACTTTATTTTAAATTCATGGGACCTTTAAACTACTGTGATATTAAGCATATGGTGATAGTTTTTCAATGACACTAAACTAACACTTTTCTTATGATACTGAACTAACAGCGATTCTCTTTGTGATTTGATTTCATCTGTCTAGGTGGTGAGGAAGATGGCGGAGCGCCTCGGGCTGCAGGACAGCCGAAACACGTTTGGTCTTTTTGAG[C/T]AGAATGCATGCTGGGAAAAAGCTATAGGAGGCAGCACAATAATCGCTGATGTCATCACCAGATTTGAAAAGTAACTCTGTCTTTTACTAAATGTTTTTAACTTGCTGCTTTAGGTAGAATACAATAAATATTTTAAGTTGCCAAACCAAAATGACCACATCACTATTATATATCGATTTTAAAGGGTTCATGACATGGATTGTTTTTTTTTTCATCAAATTTTTTTTGTTATTTTGAAATTATGTAAATGCAAAAAATATGGTGTAGATGATCAGGATATAACAGTGGGCATATAAAAATACACGCAATAAACAAAATACAGTACAACAAGAGGTTGTTAAATAATAAAATTAATAATAATTATGCTAACAACAACAACAATAGTAAAAATAAAAAGTATAAACTAAAGAATAAATAACAGATGTACTAGAACAAAACAAAAAATACACTTAAGATGGCAGCAGTGATTATAATTGGTGTGTAATTGATTTCCTATGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12795
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 |
---|---|---|---|---|---|
ENSDART00000102784 | Nonsense | 452 | 634 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 37038969)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36902329 |
GRCz11 | 3 | 37044187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGCTTGTGAGGAAGATCTTCTTTCACTGGCGGCGCTGAGGCTGCAGTA[T/G]CTGCTGGGGGATTTCAGCGCCCTYTCTCCGTACCCGGCGCTAGAGCAGCT
Long Flanking Sequence:
TTGCTTGTACATATTTAGGGCTGGTGTTCTCAAGTCAAGCGAGCCCAAACATAACATGAAAATGCAAGCTGGCTTTTATCTAGATTTATCGAGATTATTGTACACATAGCTCACTATAAACACTTGTAGTTCACTTAAAACTTTCCTAACTTTATAAATCATTATTAAAGGTTCTAGTGGTATTTGTAAGGAATTGGATGCAAGCTGTTTTGTGAATCATTCAACGCCATCTGCTTTAAAAATTAAGCTCTAAATTTAAGAGAGAATAGCAATGCATTTTGAAAATATCAGAACTAATTCCTGGAATAATTTTTCACCACAAATACTTTAGCTGTGTTCATCAGCTAATTAAATAGTGTTAAAACAGCCTTGTAGTGAACTTTATAAATTGAAGCCGGCTTCTTCCCTTCTCTCTGCCAGTGTCATGAGATGGTGGTGCGAGGGCAGCTGCCAGCTTGTGAGGAAGATCTTCTTTCACTGGCGGCGCTGAGGCTGCAGTA[T/G]CTGCTGGGGGATTTCAGCGCCCTCTCTCCGTACCCGGCGCTAGAGCAGCTCTTTCCAGCAGAGGTGGTGGAGGCCCGAGCCCTGCTGGCCCCCGTCGATCCCCCCGGCTGCCCGTCCTTCCCTGGGGGTCTGCTGGCTGGGACGCTGTGGGGGCACAAGCGACGACAGGAACAGGACCAAAGGCTGCGGGCCAGGCTGAGGGAGGAGGGGGCTGTGGTGATGTCCACTATTCTAGAGCGCTGGAAAGCCCTGGTGGGATACAGTGGCAGGGACAGCATGGCTGCTTATCTTACCATTGCCCGGCAATGGTCAGGGTTCGGCTGCACACTCTATGAAGTGGACTTTTATATAGTAAGTTGGCAAACTTTTGGAATAATTAATTTTTTGTATTTGAAAAAATTACTTTATTTTCACCAAAGGTGCATTAAACATGTGGTATATACATAAATTATATGTAAATAGAGTAGTCAGATATATGAACTGTACCTTTATTTGACCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33251
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 |
---|---|---|---|---|---|
ENSDART00000102784 | Nonsense | 591 | 634 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 37040834)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36904194 |
GRCz11 | 3 | 37046052 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCTCAGAAGTTGTGGCTGGGTGTAGCGGCATCCTGCGTGACTCTGTA[T/A]CGTCAGGGCGAGGCTGAAGCGCTGGAGTCTCTGCCCATCACTCAGATCTG
Long Flanking Sequence:
TGACATAAACTGTCTGTTCTTATCCATGCGTAGTCAAACTGCAGATTGATGTGCTGTTTGCACAATGTTATTATGCAAAGACACGTTTCAATACAATTACAATTTCACAAAAGTATATTTATACAAAATCAGCACGAATCAACATCGATTTTTTTTAAGTTTTAAATCAGCATATTAAAATAATTTCTGAAGAATTATATAACACTGAAGACTGGAGTAATCACAGCAATACAGTGCATTTTAAAAACATATGAACAGAAAATTACATGCGTTTCTATTTTAAAATATATTTGATCAAATGCTATTATTTTAATTTAATAGTTTTTGTATTGGATAAATGCAGTCGTGGTGAACATAAGAGGACAACAAAAAGTGTGTATTTTGGTGTTTAGAGAATGCTTTAAGCAGTGTCTGACATCCATATATGTTCCTCAGAGCTCAACAGGAAGCTTCTCTCAGAAGTTGTGGCTGGGTGTAGCGGCATCCTGCGTGACTCTGTA[T/A]CGTCAGGGCGAGGCTGAAGCGCTGGAGTCTCTGCCCATCACTCAGATCTGCTCATATGGAGTGTCTGATAGCAACACGTTCAGGATCACTGCAGGAGATCGAGACCTGCTCTTTGAGACCACCAAGGTAAGCGGGCAATATAAAAAATGTTGCATCATCAATATCCCTATCTGCACAATCTGTGCTATGAATGCGAAAGATTCTGGTTGATTTAAAAGTGGTCAGACTTATGGTATTAGTTCAGCCTGTTGTGATAATTAATAAATTGACTTGTCGTGCAATAAATGGTCATTCCTTTAATAATTTATAGTGACACAAGGCATTGCCTGTTGTGCTTACTTAAATAATATGATAACAACAAGGTACTTACCATAAAGCCCATAACCAGCATTTAACCCTGCTGTGGTGTTTGCCTCAAACTTCTGGAAAACCAACACTTTCCAAATTAAACTGTATGACATTTCAAATACAGTCACTTGATAGTGTGAACTAATCTGACA
Associated Phenotype:
Not determined