ZMP
wu:fd60h05
Ensembl ID:
ZFIN 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 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22145 | Nonsense | Available for shipment | Available now |
sa42073 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35342 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44769 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35341 | Nonsense | Available for shipment | Available now |
sa45469 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45468 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22145
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 |
---|---|---|---|---|---|
ENSDART00000111897 | Nonsense | 65 | 1612 | 4 | 41 |
Genomic Location (Zv9):
Chromosome 12 (position 35195988)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 33600097 |
GRCz11 | 12 | 33701080 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCCCATTTGTTAAATCAGTTATTTGGTGTTTTGTTGATTAGGATGGAT[G/A]GTGCCAAGCACAGGGTTATCCACTTCAGAGGCCTTTGACGTCCCTTGACC
Long Flanking Sequence:
TTTACCAGATTTATCTAAAATAACTCACAAATGAAGAAGTACTTCAGATCTTATATAAAATGTATAGACGCTATGACAAATGGAAGTTAGTTTAGCACCTTATTTATTTTCTTATTTTTTATTATCGAATCCTTTTCACAGGGTGTTTTAAGAGGAAAAAGCAAAGAGTGTGTTTCCTACAGGTGGTTTGTAAACCCCACTCACCAGTGTAAAGCACACTCAGAATCACACAGTGTTTTCCTAGGAACATGGAGAGTTTATACGAAGGTGTTTGGTGCATATGGAGAGTAAAAAGGAAAGAGTTTGTTTTCTATAGGTGGTTTGTAAACACCACTTACCTGTGAGAAGCACATTAAGAATCGCACAATGTTTTTTTTTTTTTGAAGTATGTATTAGAGTGTCTGGTGCATATGGAGAGGAAATACTGTCTTTTCTATATGTGGTTTTGTCGAGCCCATTTGTTAAATCAGTTATTTGGTGTTTTGTTGATTAGGATGGAT[G/A]GTGCCAAGCACAGGGTTATCCACTTCAGAGGCCTTTGACGTCCCTTGACCATGAGGATGCCCGTACAGCTTTGGAAATCTACAAACTGGTCAGTACGAAATTTAAAGGCATTTGTTCATACATAATTTGCCTGATTATGTACAACATTTTATTCTACAAAAAATATGTTAGAATGTGTTTATTTTCTGGCTCTTTGCAGTATTTATTAAATTATTAAGTGAAACTATCTCCTTTGACTTTAATAGTATGTCAAAAATGTAAATAAGAGCTTTTAAAGTCGACTTCATCCAATGTTTAAATCGTTGTTCTAGAAATGTATGCTAATTAGTGCATATTTAATTTGATGCCTCATTAGAATATGTAAACATAACATTTTAGAAAGCTTGTAATACAAGAAATCATAACATAATCAATTAAACTGGGTAGGTATGATGATAATCAGTTAATCTTGTTTACCCAATATTTACCTGCTGTGTCTTGCTTTAACATAAACCTTCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42073
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 |
---|---|---|---|---|---|
ENSDART00000111897 | Essential Splice Site | 691 | 1612 | 18 | 41 |
Genomic Location (Zv9):
Chromosome 12 (position 35179132)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 33583241 |
GRCz11 | 12 | 33684224 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGGCACTAGCCATTCTCAAATCTCAGGGCCCTGTCAGTCATCAGAAG[G/A]TAGACGATATTGAACCAAATGAGATGTCATAATGTAGTGCTTTAATTGAT
Long Flanking Sequence:
AATGAGTTATTAAAACTATTATGTTTAGAAATCTGTTGAAAAAATCTGCTCTCTGTTAAACAGAAATTGAAGAAAAAAATAAACAGGGGAGCTAATAATTCAGGCGGGTTAATAAATATGACTTCAACTGTTTCTATTCTAGTAGTATATTATATAGCAGTAACGTAGTGTTTTAATTTCCTACTCTGGAAGTTAATGGGTAAAAGTTTCCAACAATTTAAGAAAAAGCTATTTGTGTTCAACAGAAGAAAAAACATACATAAATAATGTAGATAGCAATGATCACTGCGAGTTTCATTAATTTAATACAACCTCTGCTGTTACTGAATGTTTGCATAATGTTCTGTCTCTTGACATTTTTATCTAAGAGTGATTTCCAGATAAAAATTGAAGGATTTGTTCTACACAGGGTTCCGGCCAAACAATTTCTCAAGAAAAATGACCCCAAAGATGAGGCACTAGCCATTCTCAAATCTCAGGGCCCTGTCAGTCATCAGAAG[G/A]TAGACGATATTGAACCAAATGAGATGTCATAATGTAGTGCTTTAATTGATAATTTGAGAATGCAGAAATTGATTGTGACTCTTCTATGTGTTTGTGCTGCAGAAACAGTGGGTAGAGAAGCCCCCTTCACCCCCTCAGCAGCTTGAGTCCCGTGGGCCTCGCTCCATCTCCAATAGCATGAAACAGAAGCAGCTTTCGCTAGCTGATCTGTTCGGTTCTCAGCGCTCTCAGCCTCTGCCTCGTGCTCGTGAATCCATACCTTCTCCACCGCCCCCCATCCCCGACCCACCGAGACAGCCTGCACCTGCTCTCAGTAAGACATTTGCAAATTATTCAGTATGGCGCATCTGTAAATGCAGTGTATGTAGTGTTTCAGATATGTCTAAAGGGGGTCTTTTATGCACTTTTAATGTCCTTTAGTGTGAACTGTTGCTTATTGAAAAGGTTCCGCCCTCGTTTGAATAGGAGGCGTGGACTGAACGAAAACAGATTTACGTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35342
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 |
---|---|---|---|---|---|
ENSDART00000111897 | Nonsense | 982 | 1612 | 26 | 41 |
Genomic Location (Zv9):
Chromosome 12 (position 35174105)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 33578214 |
GRCz11 | 12 | 33679197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCATTTCCATTTGCAGAACTCAGAGTATGTGATCGCAGTGAAAAGCTA[T/A]GTAACAGATGACAAGAGCTTGCTGAGCTTCCACAGAGGTGACGCCATTAA
Long Flanking Sequence:
TTGGAACTGCATTCCCAACAGGCACCACAAATCGCTGCTGTTATTCGCCTCTTCCTCATGGAGTTGATTAAGGTGCTTTTATTAAGTTTATTCACCAAAAATGTAAAATCTTTCATCATCATTTATTCACTCTCCACTTGTTCCAAACCTGTTTGAGTTTCTTTATTCTGTAAAAAAACAAAAACAAAGTATTGTTGGAAAGGAGCACCCATTGAGTTCTATAGTATATTTTGTTCCTTGTTTGGAAATGCACAACCGTCTTTCAAAGTTGGAATAATAGCTAGTGGTTTAACCTTTCATTTAAAAGAGTTAATGTGGGTTACAGTTTTATGTCATAAGTATTGTAGTGATGTTTCAAAAGTTTGTATGGGGAAATTTATTGATAAAATTCATAAATCAATGTTTAGTATTGTAATTGTTATTTCTTTGATGTTATAAAGAATATTATCCTCTCATTTCCATTTGCAGAACTCAGAGTATGTGATCGCAGTGAAAAGCTA[T/A]GTAACAGATGACAAGAGCTTGCTGAGCTTCCACAGAGGTGACGCCATTAAACTCTTGAACATGGACGGACTCAAGGATGGTAAGAAGAAAGCATGAAAAAACATGATGAGGAAGGGTAGGGTAAGGTAGGATAGGATAGTTAGGGTAGGGTAGGGTGTGGCTCTGGACTACATAACAAATAAGTGCAATTTATTTAAAATTGGGATTTATACATCACCTGAAAGCTGAATAAATTACAATGATTTAAGGTAGAGTAGGATATGGTAGGGTAAGGTATGGCTGGGTAGGGTAGTGTAAGGTAGGGCTGGGTAGGGTAGGGTGAGATAGGATAGGTTAAGGTAGGGTTGGGTAAGGTGAGGTAGGATCAAGTAGTTATCGCTACAGCCCGGAGACCTCCAAGTGGGAGGGATTACACTGCAAGTTGGTTGGGTGACCTCAAAGTGGGAGGGCCTTATGCCACAAGTAGGTTGGGATTAGGTGGTGTAGGTGGAGTAAACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44769
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 |
---|---|---|---|---|---|
ENSDART00000111897 | Nonsense | 1451 | 1612 | 38 | 41 |
Genomic Location (Zv9):
Chromosome 12 (position 35161586)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 33565695 |
GRCz11 | 12 | 33666678 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCCCATCTGACACTCTTATTTCTAAACCCGGCCAGTGCTGAGATAAAG[C/T]AGTATCATCCCCGGATGGATGGACTCAACTCTACTGATGAAAGACTCCTT
Long Flanking Sequence:
AAGAGATTTTTTCAACCTATTTCCAAACATAATAACTCATTTCTTATTACTGATTTCTTTTATCTTTGCCATGATGACAGTAAATAATATTTGACACTTCTTAAAGTGACATTTAAAGGCTTAACTTGGTTGATTAGGTTAACTGGGCAGGATAGGAACTATAGCACTATAGAAAACATTATAAAGTGGCTAATAATATTGACCTTAAAATGTTTAAATGTGTAACATTTCACAATATTACTGTTTTCCGTTTTTCAGCTTGTGGCCAGTTATCTGGAAGGGAAAATGTTTCTGTCCATGAACAGTTCTACAGTTTACCAGCAGGTGGCAGAACTGACCGCTCTTCAACACCTTGCGCTTGGACTAAATAATCTGCCCTCAAAGTAATTTCATACATCTCACACAGACGGATTTCTAAAATATCAAATGAAACCTGCATCCATTAATTGTTTCCCCATCTGACACTCTTATTTCTAAACCCGGCCAGTGCTGAGATAAAG[C/T]AGTATCATCCCCGGATGGATGGACTCAACTCTACTGATGAAAGACTCCTTGCTACGATACGAGCGCAGTTTTCAACCTTAGGCCCCATCAGCCCTCTTGATGCCAAAGCTCGGTTTATCAGTGAGTGAACAAATCTGTCCAAACATGCTCCCAGGTTATTGTTACACAATTATAATGAATGATTTTACATCCAAAACAAACTCTTAAAACAGATGTGGGGTAAGTTACTTAAAAAAACTCATTAATTACTGATGAAAATTAAAGGAATAGTTCACCAAAAAATAAAAAATGTTCATAATTTACTCACCCTCCACTTCTTCAAAACCTGTTTGAGTTTATTTCCTCTGTTGAACACAAAACAATATATACTTAAGAATGCCGGAAAAAGTAGCCTTTGACTTCCATAGTGGTACATTTGTATTTAATTTACTTCACTCAATACATACATTTCAGTGCATAGTAAACCAAATTTAAGATTGTAATTATTCAAATTTGAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35341
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 |
---|---|---|---|---|---|
ENSDART00000111897 | Nonsense | 1471 | 1612 | 38 | 41 |
Genomic Location (Zv9):
Chromosome 12 (position 35161526)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 33565635 |
GRCz11 | 12 | 33666618 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCGGATGGATGGACTCAACTCTACTGATGAAAGACTCCTTGCTACGATA[C/T]GAGCGCAGTTTTCAACCTTAGGCCCCATCAGCCCTCTTGATGCCAAAGCT
Long Flanking Sequence:
TATCTTTGCCATGATGACAGTAAATAATATTTGACACTTCTTAAAGTGACATTTAAAGGCTTAACTTGGTTGATTAGGTTAACTGGGCAGGATAGGAACTATAGCACTATAGAAAACATTATAAAGTGGCTAATAATATTGACCTTAAAATGTTTAAATGTGTAACATTTCACAATATTACTGTTTTCCGTTTTTCAGCTTGTGGCCAGTTATCTGGAAGGGAAAATGTTTCTGTCCATGAACAGTTCTACAGTTTACCAGCAGGTGGCAGAACTGACCGCTCTTCAACACCTTGCGCTTGGACTAAATAATCTGCCCTCAAAGTAATTTCATACATCTCACACAGACGGATTTCTAAAATATCAAATGAAACCTGCATCCATTAATTGTTTCCCCATCTGACACTCTTATTTCTAAACCCGGCCAGTGCTGAGATAAAGCAGTATCATCCCCGGATGGATGGACTCAACTCTACTGATGAAAGACTCCTTGCTACGATA[C/T]GAGCGCAGTTTTCAACCTTAGGCCCCATCAGCCCTCTTGATGCCAAAGCTCGGTTTATCAGTGAGTGAACAAATCTGTCCAAACATGCTCCCAGGTTATTGTTACACAATTATAATGAATGATTTTACATCCAAAACAAACTCTTAAAACAGATGTGGGGTAAGTTACTTAAAAAAACTCATTAATTACTGATGAAAATTAAAGGAATAGTTCACCAAAAAATAAAAAATGTTCATAATTTACTCACCCTCCACTTCTTCAAAACCTGTTTGAGTTTATTTCCTCTGTTGAACACAAAACAATATATACTTAAGAATGCCGGAAAAAGTAGCCTTTGACTTCCATAGTGGTACATTTGTATTTAATTTACTTCACTCAATACATACATTTCAGTGCATAGTAAACCAAATTTAAGATTGTAATTATTCAAATTTGAGTCACTTTTGGTCTTATTTTTATAATATTTTAAGCTTTTTAAAGAGTTTACTCCAAAATGTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45469
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111897 | Essential Splice Site | 1535 | 1612 | 39 | 41 |
Genomic Location (Zv9):
Chromosome 12 (position 35159153)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 33563262 |
GRCz11 | 12 | 33664245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCGCAGTCAATCATGAAGTCATAACCGTCCTCGATCCTAAAACACTGG[T/G]ACGCCACACTTCATCTCACAGTCCAACATGTTTCCTGTGATGTTCTGATA
Long Flanking Sequence:
CATAACAAAATGGTAGTCAATATTCATAGTGTGTTGTGTAGTTTTTGCTAAAATTTCAAAGCATGTTCCTAAAATATGTGTCAAAATAAGATTTGTCACCAAAAAGCTTTCCATTTGCTGAAACACAAAGAAAGTCGTGGCCAAATTAAGACTTAAAATCACCCAAGAGTGGACGAAAACACCCCCAACAGCACACAAGGGTTAAGAAATAAGCACAAATGTCTGGACATGTCAAAACATTCAAAGGGTCCTGAAATCACCTCAGACCCCGGAGAATTAAATGACCTAAAAATAAACAGTAATTACTTCTCGATATGTGAATTGATATAAGTATAATTATACCCAACACTGCTCCTATCTTCCAGAGAGTATCAGTTCGCTGCCTCTCTTTGGTTTTGACATCTTCACGGCTCAGAAAGTCAGTCATCGCAGCTGTCCTTCGCCTTCCCTGGTCGCAGTCAATCATGAAGTCATAACCGTCCTCGATCCTAAAACACTGG[T/G]ACGCCACACTTCATCTCACAGTCCAACATGTTTCCTGTGATGTTCTGATAATGTAAACTATCACAATCTTTGCAGAATGCGTGTTTGACGATGTCCATGGAGGATGTGTTGTCCTTGCGCTCAATCCGTCCCAAAAAAGACAAGCTGCCATCAGTTGAGATCAGCTTTGGTGGCCAGACTCAACACAAGACTCTCAGCTTCAATCTCAAGCAGGTATGTTTGTCAAAGTCCAAGTCATAGAGAGTTTGAATCTCCCATAAGATGCATTTGAAAATATGACATGTTGCAGGTCTGCAGAGAGAATTGTTTATAAATCTGTTTCAATTTCAAAGCAATTCAGTATTCAGATACAATTCAGATACATTTCTGTCTTAATAAAAGCTCTATTTTATGCTCAAATGTTAAAGATTTTTCAATCATAAATATTAGATTTGTAATTGTATTTTTTTTTATATTAACAGTTGTTAATAATTTTAATAAAGCTAATAAAATATAGTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45468
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 |
---|---|---|---|---|---|
ENSDART00000111897 | Nonsense | 1547 | 1612 | 40 | 41 |
Genomic Location (Zv9):
Chromosome 12 (position 35159043)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 33563152 |
GRCz11 | 12 | 33664135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCACAATCTTTGCAGAATGCGTGTTTGACGATGTCCATGGAGGATGTGT[T/A]GTCCTTGCGCTCAATCCGTCCCAAAAAAGACAAGCTGCCATCAGTTGAGA
Long Flanking Sequence:
CCATTTGCTGAAACACAAAGAAAGTCGTGGCCAAATTAAGACTTAAAATCACCCAAGAGTGGACGAAAACACCCCCAACAGCACACAAGGGTTAAGAAATAAGCACAAATGTCTGGACATGTCAAAACATTCAAAGGGTCCTGAAATCACCTCAGACCCCGGAGAATTAAATGACCTAAAAATAAACAGTAATTACTTCTCGATATGTGAATTGATATAAGTATAATTATACCCAACACTGCTCCTATCTTCCAGAGAGTATCAGTTCGCTGCCTCTCTTTGGTTTTGACATCTTCACGGCTCAGAAAGTCAGTCATCGCAGCTGTCCTTCGCCTTCCCTGGTCGCAGTCAATCATGAAGTCATAACCGTCCTCGATCCTAAAACACTGGTACGCCACACTTCATCTCACAGTCCAACATGTTTCCTGTGATGTTCTGATAATGTAAACTATCACAATCTTTGCAGAATGCGTGTTTGACGATGTCCATGGAGGATGTGT[T/A]GTCCTTGCGCTCAATCCGTCCCAAAAAAGACAAGCTGCCATCAGTTGAGATCAGCTTTGGTGGCCAGACTCAACACAAGACTCTCAGCTTCAATCTCAAGCAGGTATGTTTGTCAAAGTCCAAGTCATAGAGAGTTTGAATCTCCCATAAGATGCATTTGAAAATATGACATGTTGCAGGTCTGCAGAGAGAATTGTTTATAAATCTGTTTCAATTTCAAAGCAATTCAGTATTCAGATACAATTCAGATACATTTCTGTCTTAATAAAAGCTCTATTTTATGCTCAAATGTTAAAGATTTTTCAATCATAAATATTAGATTTGTAATTGTATTTTTTTTTATATTAACAGTTGTTAATAATTTTAATAAAGCTAATAAAATATAGTGCTTTTCATTTGTTTGAATTTTTCAAAATATTTTTTTCTGTAATATATTAAAATATATTATAAAAATAAATAATTATTATTATAAATTAATTAAAAATTTAAAAATAAAAAAT
Associated Phenotype:
Not determined