ZMP
LOC100332329
Ensembl ID:
Human Orthologue:
MYO9B
Human Description:
myosin IXB [Source:HGNC Symbol;Acc:7609]
Mouse Orthologue:
Myo9b
Mouse Description:
myosin IXb Gene [Source:MGI Symbol;Acc:MGI:106624]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30432 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30430 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30429 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30428 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30754 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30432
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 |
---|---|---|---|---|---|
ENSDART00000112478 | Nonsense | 392 | 1825 | 11 | 44 |
Genomic Location (Zv9):
Chromosome Zv9_NA735 (position 155958)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 5010844 |
GRCz11 | 22 | 5395219 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACATGCGGCCGGATATCGTGGCTCTCTTGCGGAGCAGTGACCGGTTTTA[T/A]GTCCGCCAGCTGATCGGGATGGACCCGGTGGCCATGTTTCGATGGGGGAT
Long Flanking Sequence:
TCCAGTGATGGAACCAGCATTCGTCATCCTCCATTTTGCTGGGAAGGTTAAATACCAGATTAAGGTAAAGGATGCAGAAGATAAGAAATCACAATATATCCTATTATAACATATATATTTTATTTTTAAGTCAAAATTAATTTCAAATTACATTTACAAAACAGTTTGTGTGGTACACCTAGTAAAGTTTTACATTTTTCAAGTTCATATAGATTAATTAAATTACAGTCGTTTTTATTAGTATTATTAATAATGTCGGTTTGTGCTATTTGTTATGCCTATATAAGTATAATTAAATTGGAGAGAAAAAAAAATTCTATAAAAAGATAATAAATCAATTATTCACAATTTAGGTAGTAATATTGTTAGCATTACTATTAATACCCTGTTATTGTTCTATTTGTCTGTGTTGATTATCTGTGGCAGGATTTCCGTGAGAAGAACACTGATCACATGCGGCCGGATATCGTGGCTCTCTTGCGGAGCAGTGACCGGTTTTA[T/A]GTCCGCCAGCTGATCGGGATGGACCCGGTGGCCATGTTTCGATGGGGGATCCTCCGTGCCACTGTTCGTGCTCTGGCTGCCTTCAACGAGGCCGGTCGACGCTGGGCAGCCAAGACTGCGGGTAACCCATGGATTAGTTTCAGATTATCCCAAAACTTTGGATTTTCAAGGTCTGAGATGGTGTTATTTATAGCCTGCACGTGAGAAAGCTGGCCAGTGACGCAAGTAGTCATTTTTAGAAGGATTTGAGTGTGATTAAACTAAGAAGGGATATTAAAAATTATGGAGCCAAGCAGTAGATGGGCAGAATGAGCCAGCAAAACCAATCTTTATTAAAAGCATTTCAGGATTGTTTCAGCTACAATAGATAAAACAAGATTAGAGATGCATTTATTAGTAAAATTACTCAAAGTTTGTGCTAAATAACAATTTAGAATATTTATTTTGCTACCGCACTTTGTTATTCTTTAAGTGAACATTTAATCTGTGCAAGTTGATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30430
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 |
---|---|---|---|---|---|
ENSDART00000112478 | Nonsense | 856 | 1825 | 22 | 44 |
Genomic Location (Zv9):
Chromosome Zv9_NA735 (position 146330)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 5020129 |
GRCz11 | 22 | 5404504 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCCAAACTTCCACCATCGAGAAGTCTGGAGAAACGGGAGCTTAGGAGA[C/T]AACGTGGCCTAGAGCATAACCAGAGAGAAAGTGAACGAGCAGCTTCAGTC
Long Flanking Sequence:
AGCTCAAAGAGGAAGAAGATAGAGCAAGGCAAGCCAGAGAGAAAGAGGAAGCAGTCAGAAAACAAAAAGAGCAAGAGAAAAGGGCTGCTCAGCTTGCGTTTGAGGTTGAACAGCAAGAGAAGGAGAAGCCACTACAACAAACAGAAGTACCAATATCAGGAAAGCATCCTGACCAAGACAAGACACTAGTGCTGGATCACGATAAAATTCCTGTCGGTGTAGAAATTGAAAGTAAAAGCAAGGGCAATCTGGATGATGCGTCTGTGTCAAAAGTGCAGAACCGTTCTGAAAAAGTTACTCATGCAGAGGCTGGTCCTCAACCTGAGGTCAAGGAGCAAGAGAAGCAAAGTGAGAATGAATCCATCACTCCTCCCAGAGATGAAAATACACAATCGAAACCTATGACTCCAGAAACACCAACTGGGCAAGTCCAAAACCGGACTCCTTCGATCTCCAAACTTCCACCATCGAGAAGTCTGGAGAAACGGGAGCTTAGGAGA[C/T]AACGTGGCCTAGAGCATAACCAGAGAGAAAGTGAACGAGCAGCTTCAGTCGGAAAAGAGGAAACATCCTTGAAAAGCGTGACTCTTGATAGTCCTGGAAAAGCGGACAACAAGTTAAAGGAGCGGTCTGATAGCAAAACTCTTGATAGTCCTGGAAAAGCAGACAACAAGTTGAAGGAGCGGTCTGATAGCAAAACTCTTGATAGTCCTGGTAAAACAGACAACAAGTTGAAGGAGCGGTCTGATAGCAAAGAGTTGGATCAATACACCTTTGTAGCTTGGAAAGGAGACAAGAACAAGAAGGATCCTAAGGATGCCCCACAGGAACTTGTCCGACCCACTACCTTACCCTTGGATATCCCTTCTCCGGGGATCAGAAGAAATGGCTGTAGTGACTCTGCAATTGCATCTCAATCTGGGATTTCCAAAGAAGAAGCCAGCAAGAAGAAGGAACCATTGAGGAGCAACACTCAGCCAGAAAACCTCATAGCAGGACCTCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30429
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112478 | Nonsense | 1374 | 1825 | 36 | 44 |
Genomic Location (Zv9):
Chromosome Zv9_NA735 (position 132058)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 5034401 |
GRCz11 | 22 | 5418776 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATTAAAGATATACTGTTGTTTGTGTGCTGTGGATCTAGTGTGAAGAT[G/T]AGCCTGGATCCAATCACTTTGGTGTACGCGTCGGCAACCTGGTCAACAAT
Long Flanking Sequence:
TATCCATATCAAACACACCTGAACCAATTAATTAGGACCTGAACACCACATGATAATTACAGGCAGGTGTGTTTGATATGGATTGCAACTGAAATCTGCAGGAAGGTGGCTCTCCAGGAAAAGGGTTGGCCACCCCTCGGTTAGTGGAATAGGATGGTTATTGGAATGAATAATGGAAGTCAATGGTCACAGATTTCCAGGGTTAACTTTGAATAATAACAATAGTCTCCCATTCGCTAGCTTTATTTTTATCTTGCCCAAATTACTAAACCCTAAAAACCCCAGAACATTCCCCAAACAAAACCCCTGCGCCTCTTAGTGGACACCGAGCAAGCATAACTTAACATCCAGCATTTTTTTTTGTTTGTAAATATCTTTATCGGTGTTTATCAGAAAACAGAAAGTCAAACAGGTTTGGAACAAGTGAGTAAATGATGAGAACTTTAAGCTTTTATTAAAGATATACTGTTGTTTGTGTGCTGTGGATCTAGTGTGAAGAT[G/T]AGCCTGGATCCAATCACTTTGGTGTACGCGTCGGCAACCTGGTCAACAATAAAACTCCAGTGCCGATTGTGCTGGAGATAATGCTGGAACATGTGGAAATGAACGGCCTATACACGGAGGGCATTTACAGGAAATCCGGCTCTGCCAACCGCATGAAGGAGCTCCACCAGCTGCTGGAAGCAGGTAAACCATTAGGAAGATCAGGATAACTCTGTAGCACACCGGGAAGGCGACTTGTCTGTATTGTCAGTCATACTACTGGGTGACTTATCCTCAACAATGCTTGATTCTGATTGGTCAATAATGACATTCAAAGATATGTAATTCCCAGATAACAACCACTGAAACTAATAACACTTTTTGTACTATGAATCTTCCTGACCATTAGTGAATATATTCATATACATATTTTAATGCTTAAAGGGCAGCTATCATGCCCCTTTTTACAATATTTATAAAAAGTCTTTGATAAGTCTAGACTGTAGACTGTTGCTTGAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30428
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 |
---|---|---|---|---|---|
ENSDART00000112478 | Nonsense | 1483 | 1825 | 38 | 44 |
Genomic Location (Zv9):
Chromosome Zv9_NA735 (position 129433)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 5037026 |
GRCz11 | 22 | 5421401 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACTTGTTAGAACTTCTGTTGTCTTTCTGCCGCAGAACTACCTGAGAAG[C/T]AAGAGCAATTGCAAGCGATTTACAGAGTTTTGGAGCAGCTGCCGACGGCC
Long Flanking Sequence:
TGTTATTGCAAGTAGTATAATCTGTACTTCACATCAAGGACCACAATGGAAATAAGTTTTGTTTGAGTATATTCTTGACGCACTAAGTGTATTCACTTTTTTGTCAAATCAAAAAGAAAAGAAAGAAACCTACCTTGGAATGTCATGACTGACCAATCAAAATCAAGTATTCTGCAGAGCCGTGTAACAATCTGTGATAACAACCAGCTGGATGTACATTATACCTTACTTAATGCTGATAAATGATTGTGTTTAATGACCACATATGTGTGTGTAGGCCCAGAGAACGTGTGTCTGGAGGATTACCCCATCCATGCTGTTACCGGTTTGGTCAAACAGTGGCTCAGGGAGTTGCCAGAACCTCTCATGACCTTTACGCACTACAACGACTTCCTCTATGCCATAGGTTGGTCCTTATTATGGCTTTGTGTTGTCTTTTTAGTAGCCTTCAGACTTGTTAGAACTTCTGTTGTCTTTCTGCCGCAGAACTACCTGAGAAG[C/T]AAGAGCAATTGCAAGCGATTTACAGAGTTTTGGAGCAGCTGCCGACGGCCAACTTTAACACATTGGAAAGACTCATTTTCCACCTTGTCAGGTACGTTTATGCAGTACTCTAGAATTGTGGGTACATTTGATTCTCCATGATCAGCCTTGTTATTTTTCAAACACATAAAACTTAATGGAATAATTTTGAATAACACCATAAATTGTCAAGTTATATCTAAAAATAATGTTTGCATGTGTATTTAGCCACATTTTGTCTTAAAGATATTAGCTTGAAGTCAAAACTTGCTATGTTTATTTTGCTAGCTCACATTGATATTCCTAAAGTGAATAATTAATCTGTGCAAGTTAATCTACTGGGAAATAAGTGTTTGTTTTGGTAATCTTCAATGAAAGTCTGAGCATTTGCTTTAACGTGTGTTGGTCCTTCTATTGATGTCATCTGAGCGCTTTCATAGCATATTCATACCCTCACTTACCGTTAGTTTGCTATTTAGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30754
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 |
---|---|---|---|---|---|
ENSDART00000112478 | Essential Splice Site | 1615 | 1825 | 42 | 44 |
Genomic Location (Zv9):
Chromosome Zv9_NA735 (position 124005)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 5042454 |
GRCz11 | 22 | 5426829 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTCAGTTTTGTTACCTTGAGTTAAAGTTGGTATTTGTTTGGACTCTA[G/A]ATTCGGGAAAAGCCATCTTCTGACCTTTGTGTTGTACCTGAGAACGAGCC
Long Flanking Sequence:
AACCGCTCAATGAAAGCAAGGCATTTGTCTTTGTTTTCTGATTGTTTGAGTCCCACAAACCTTTGAAACTCATGCCTTGAAGGTTTTCCATACTTTGAATTGTGTTTAGTTCCTCAATACCATAACATCCATCCGAATAGTTGTCATTCTTTCCCAAAAAACCTTTTTTTTTTCATCAAGACTCACTTATGAAACATCTCTGTGTACTAACTGTGTACTAAGACCGAGAAGAGCCAAGCTTTAATTAGGAAATGATCTAAACCTATCTAATAGTTATCCAAAATGCTTATAGTCTAATCTGATTCAATGCTTTATGCTAAGCTAAGCTAAAAGTGTTGCTACCAGACCAGGAAATCAGCTGAATGGATTCAAAAACAGAAAACTCAACTCTTTATCTTTGGGTAGCTTGTAAAATGAGCCTATTGTCAAAAAGTGGAGTGTTGTTTAAATTGTGTCAGTTTTGTTACCTTGAGTTAAAGTTGGTATTTGTTTGGACTCTA[G/A]ATTCGGGAAAAGCCATCTTCTGACCTTTGTGTTGTACCTGAGAACGAGCCACTGGATTCAGACACTGAGGCTGAGCGGAGCCTGGTGGAGCGGATCAAGTCCATCAAGCAGGAAAAGTATGTAGACTGAGATCCCAGGACCAAATGTACCCCTTGAGTCCAGGGATTAACTCAGTCCTTGTCTAGAGCAGCTTATTTGATTTAAACAATATTAGTGTCATTTTGAGCAAAGGTGATACTGAAAGTCTGTACCAACCACTGATATTTTCTTTCAATCTAGACTCAAAAACGGTGATGGTATGGTACTTTTTCAAAGGATTTAATTTGTTCTCCTGTACCTTTTATGGACTTACATGTACAGTTTAGGTCAGGGGTGCCTTCCTATCTCATCCACCTTTTTGCAGCGTTCAGCTCCATCCCTGGTCAAACACAGGAGCACTGAAGGAGCACTTGGTAAAGACAGGTGCTTTTTATCAAGGTTAGAACTGAACTCTACAGGAA
Associated Phenotype:
Not determined