ZMP
myo9b
Ensembl ID:
ZFIN 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 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19821 | Nonsense | Available for shipment | Available now |
sa32969 | Essential Splice Site | Available for shipment | Available now |
sa31289 | Nonsense | Available for shipment | Available now |
sa16154 | Essential Splice Site | Available for shipment | Available now |
sa15461 | Essential Splice Site | Available for shipment | Available now |
sa17368 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19821
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088040 | Nonsense | 334 | 2227 | 4 | 56 |
ENSDART00000131590 | None | None | 678 | None | 16 |
ENSDART00000144807 | Nonsense | 334 | 998 | 5 | 22 |
The following transcripts of ENSDARG00000077410 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 37448755)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37745465 |
GRCz11 | 2 | 37727922 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACTCAACGCAAATTCCTTGTCTGCTTGTTATCTGACCTACAGGAATTA[T/A]CATGTTTTTTATTACCTTTTGATTGGCGCCTCAGAGGAGGAGAGAGATGA
Long Flanking Sequence:
TGAGTTACTAAACCACCCACGAAGGTGCGCACCTTACTTTGTCCAGCAAGTTGGAGAGCAAGCTTTTTTCACTATGCTGATTGAATATGTTTTTAAAGACATGTCTGAAGTACCGTTATGTTTTCTCAATCAGGAAGTGATGTTTTTGTTAGACTGAAGTTGCTAGGCAGCAGAGACAGATTAAGACAGACCTCTTATATTTTCTGGTCCCATTCTCTAAAATAATTATCGGAAAGTCTAGCTATTGCTGGCATTGATCTGAAATTCCTAATACAGCTTTTGTTCAATGTTTCAGGGCTGTTGTTGAGAAGTATTTACTAGAGAAATGCCGCCTAGTGTCCAGAGGAAAAACTGAAAGGTAATAAATTGGAAACCATTTTATATATATCAATTTTATCCATATCCCTTTTACGTTTGAACTCCTTAGTGTCACAAGTGGAATTAAATGTATTACTCAACGCAAATTCCTTGTCTGCTTGTTATCTGACCTACAGGAATTA[T/A]CATGTTTTTTATTACCTTTTGATTGGCGCCTCAGAGGAGGAGAGAGATGAGTTTAAGCTTCTGCAGCCTAATGACTACCACTACCTCAAAGAGGTAAGGATTATCTTAGTTTTTCTTGTCTTTGCTGAACAAATTTTTTTGTCATCATTTACTTATCGTCCACTTGTTTCAAACTTGTTAGACTTTCCTGTTTCTGTTAAAGATAAATGCAAGTATTTTAAAGATTGTGAGAAACTAGTAACCATTGACATGTCTATTTTGTTTAAGTCAATTGTTGGACTTTCTTCAAAAAATCTTCTTTTCAAGAGAAGAAAGAATCTAATAGTCTTCTAATGTTCTTACTGTATGTCTTATTGGATTATTTGCTTTTTTTGTTATTGTTAAAATATCACAGCTAAGCTTTTCCATTAATTATCTGTTTTTCAACTTAACCTCACAGGAAATGCCAATTTCAGAGGATCAAGCTGAAATGACACATGAATTCCGGAGACTTCATCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32969
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088040 | Essential Splice Site | 489 | 2227 | 8 | 56 |
ENSDART00000131590 | None | None | 678 | None | 16 |
ENSDART00000144807 | Essential Splice Site | 471 | 998 | 9 | 22 |
The following transcripts of ENSDARG00000077410 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 37444982)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37741692 |
GRCz11 | 2 | 37724149 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTAATTCAGTCATGTGTTAAGTACAAATCTATAAATAACTCTGTCTTT[A/T]GGCTATTACTGCCAGAGACTCTATGGCCAAGTCTTTGTACAGTGCCCTGT
Long Flanking Sequence:
GTGTCCACGTTTTCTGTAGACAGCACAAAGTCTGACATTCCTGGAGGGAAATACAAAAATTAAAGTTTACTATGAGATTTGGATATTGCATGAGACTAACAAGAAACTATCACATCAGTTGAATATTGCTGTTTGTTTGTTGCTTTGATCTGTTAAAGTGATTAAATGTAATGTAAAAATTGAGCTGTTATATAAAGCATTACACATTGACAGACTCGTGTTTTCAAATGTTTAAATGTCGTCTTTATTACCATAAAATATGTCTTACATCATTGCTTTTCAATTCCAGGTTAAAGTTGAGCTGCTTGTTGAAGCACTGACTACAAGGAAAGCAATGACTGCTAATGACAAGCTGATTCTGCCTTACAGCCTCAATGAGGTAAATTATAATATAACCGATAATATAATAGTGATGCATGTGATGACATTTTCTGCTATGTACTGATCATTCATTAATTCAGTCATGTGTTAAGTACAAATCTATAAATAACTCTGTCTTT[A/T]GGCTATTACTGCCAGAGACTCTATGGCCAAGTCTTTGTACAGTGCCCTGTTTGATTGGATCGTCCTGCGAATCAATCATGCTCTACTCAACAAGAGAGATTTGGAGGACTCTGTACCGGTACATAAATACACTATATATTAGGCTTATGATGGTATCAGTTTTATATCTAAACTTTTTTGGGATTAAATGTTGAAGCTTGTATCACGGTAAGTGGTATTAAAAAACTGAGCTGAGCTGCAAAAGAGGTTGCTTTTAACTGATATAATCAGGGCTTGACATTAACTTTTTTGATTACCAGCCACTGTGGCTAGTAGTTTTCCAACATTAATGGCCATCACTTTTTCCTCTAACCAATTTTGTTGTTGGTAAAATATATTTCATACATTCATAAATTTAACTTTGTCTTGCTAAAATACTATTAGATGTTATGACTCCTTATTCATTTCACTTTTTGTGTGTTATGTATGACCTTGTTCTATGAGCAAATGGATTGTGGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31289
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088040 | Nonsense | 887 | 2227 | 20 | 56 |
ENSDART00000131590 | None | None | 678 | None | 16 |
ENSDART00000144807 | Nonsense | 830 | 998 | 18 | 22 |
The following transcripts of ENSDARG00000077410 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 37430860)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37727570 |
GRCz11 | 2 | 37710027 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTATGTCTTGGTCTGTTCAGGCATCCCTAAGCAAGTTGTTGGAAACCT[T/A]GAGGAAAGCAGAACCTTTCTTTGTTCGCTGTATCAGATCAAATGGGGATA
Long Flanking Sequence:
GACTCAAAATCACCTCCAAGTGGATGAAAACATCCCTAACCTCACAAAAAGGGTTAATTGGTTATATTCAAAAATGCGAGTAATAACACTAAGCTTTACTGTCCTCTACAGAATCTCATCGACTCACACTCTCTGAAGTTCATCATGGCCCTGACACAGCACAACCGCGTGACCAGATCCCTGCTCCATCTGCACACCAAGAAGAAACCACCTAGCATCAGCGCTCAATTCCAGGTTCAATATTATCATCTTAGCGTGGAAAAAAAAATGCATGGAGTAATCTCCAGCATCTGAGGTTTCAGGGATCAGTTTGCTCCGGCTCTGTGAAAGCCTGTTTTGTGGTAGTTGTAAATGAGATAAAAGGCTCAGACCCCCTAAGCTGTGGGGAGGTTTTGATATGATTTGCAGGGGTTTAATGGATGCTGATGGACAAATCAATGAGTCACATGCTTTTATGTCTTGGTCTGTTCAGGCATCCCTAAGCAAGTTGTTGGAAACCT[T/A]GAGGAAAGCAGAACCTTTCTTTGTTCGCTGTATCAGATCAAATGGGGATAAGGTATGGCGGAGAGCTTTCGTTTGAAGATTTGTAACAAATCTGTGGAATCTGTTTATGTTTTGGGTGATAAATGTTGATGCATACATGTTGGTGGATGTGTTTACAGAGGGAAATGCACTTTGATGATGCTCTAGTTCTTCAGCAACTGAGATACACCGGCATGTTACAAACCGTTCGGATTAGAAGGTCTGGATATGGAGCCAAATTCACCTTTAGGGTAATGTACTGAAATACTTTTTAAAATGTGTAACATTTCATTAGGGCTAATAATTGAATGGAATAAAGTAATAATTTTTTTTCAAATATTTGTAAATGATTAATGTAATGACTAATGATGCCTGAGTTTGAGGAGTAATTTAATAAAAAAGAGCAGAGATTAATAAGTAGTTTTTCTTAGGATATGCATATTGATTTTTGTTTTATGTCTAGTCATAAAGGTACTTATCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16154
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088040 | Essential Splice Site | 904 | 2227 | 20 | 56 |
ENSDART00000131590 | None | None | 678 | None | 16 |
ENSDART00000144807 | Essential Splice Site | 847 | 998 | 18 | 22 |
The following transcripts of ENSDARG00000077410 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 37430807)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37727517 |
GRCz11 | 2 | 37709974 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAAGCAGAACCTTTCTTTGTTCGCTGTATCAGATCAAATGGGGATAAG[G/A]TATGGCGGAGAGCTKTYGTTTGAAGATTTGTRAYAAATCTGTGGAATCTG
Long Flanking Sequence:
TTAATTGGTTATATTCAAAAATGCGAGTAATAACACTAAGCTTTACTGTCCTCTACAGAATCTCATCGACTCACACTCTCTGAAGTTCATCATGGCCCTGACACAGCACAACCGCGTGACCAGATCCCTGCTCCATCTGCACACCAAGAAGAAACCACCTAGCATCAGCGCTCAATTCCAGGTTCAATATTATCATCTTAGCGTGGAAAAAAAAATGCATGGAGTAATCTCCAGCATCTGAGGTTTCAGGGATCAGTTTGCTCCGGCTCTGTGAAAGCCTGTTTTGTGGTAGTTGTAAATGAGATAAAAGGCTCAGACCCCCTAAGCTGTGGGGAGGTTTTGATATGATTTGCAGGGGTTTAATGGATGCTGATGGACAAATCAATGAGTCACATGCTTTTATGTCTTGGTCTGTTCAGGCATCCCTAAGCAAGTTGTTGGAAACCTTGAGGAAAGCAGAACCTTTCTTTGTTCGCTGTATCAGATCAAATGGGGATAAG[G/A]TATGGCGGAGAGCTTTCGTTTGAAGATTTGTAACAAATCTGTGGAATCTGTTTATGTTTTGGGTGATAAATGTTGATGCATACATGTTGGTGGATGTGTTTACAGAGGGAAATGCACTTTGATGATGCTCTAGTTCTTCAGCAACTGAGATACACCGGCATGTTACAAACCGTTCGGATTAGAAGGTCTGGATATGGAGCCAAATTCACCTTTAGGGTAATGTACTGAAATACTTTTTAAAATGTGTAACATTTCATTAGGGCTAATAATTGAATGGAATAAAGTAATAATTTTTTTTCAAATATTTGTAAATGATTAATGTAATGACTAATGATGCCTGAGTTTGAGGAGTAATTTAATAAAAAAGAGCAGAGATTAATAAGTAGTTTTTCTTAGGATATGCATATTGATTTTTGTTTTATGTCTAGTCATAAAGGTACTTATCTATAAAGTAATATTACTACTTTCATCTTTAATATGACTCAGTAAATGTTAATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15461
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088040 | Essential Splice Site | 941 | 2227 | 21 | 56 |
ENSDART00000131590 | None | None | 678 | None | 16 |
ENSDART00000144807 | Essential Splice Site | 884 | 998 | 19 | 22 |
The following transcripts of ENSDARG00000077410 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 37430589)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37727299 |
GRCz11 | 2 | 37709756 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCGTTCGGATTAGAAGGTCTGGATATGGAGCCAAATTCACCTTTAGGG[T/A]AATGTACTGAAATACTTTTTAAAATGTGTWACRTTTCATTARGGCTAATA
Long Flanking Sequence:
ATGGAGTAATCTCCAGCATCTGAGGTTTCAGGGATCAGTTTGCTCCGGCTCTGTGAAAGCCTGTTTTGTGGTAGTTGTAAATGAGATAAAAGGCTCAGACCCCCTAAGCTGTGGGGAGGTTTTGATATGATTTGCAGGGGTTTAATGGATGCTGATGGACAAATCAATGAGTCACATGCTTTTATGTCTTGGTCTGTTCAGGCATCCCTAAGCAAGTTGTTGGAAACCTTGAGGAAAGCAGAACCTTTCTTTGTTCGCTGTATCAGATCAAATGGGGATAAGGTATGGCGGAGAGCTTTCGTTTGAAGATTTGTAACAAATCTGTGGAATCTGTTTATGTTTTGGGTGATAAATGTTGATGCATACATGTTGGTGGATGTGTTTACAGAGGGAAATGCACTTTGATGATGCTCTAGTTCTTCAGCAACTGAGATACACCGGCATGTTACAAACCGTTCGGATTAGAAGGTCTGGATATGGAGCCAAATTCACCTTTAGGG[T/A]AATGTACTGAAATACTTTTTAAAATGTGTAACATTTCATTAGGGCTAATAATTGAATGGAATAAAGTAATAATTTTTTTTCAAATATTTGTAAATGATTAATGTAATGACTAATGATGCCTGAGTTTGAGGAGTAATTTAATAAAAAAGAGCAGAGATTAATAAGTAGTTTTTCTTAGGATATGCATATTGATTTTTGTTTTATGTCTAGTCATAAAGGTACTTATCTATAAAGTAATATTACTACTTTCATCTTTAATATGACTCAGTAAATGTTAATATTTTTAAAGATTATTGCTTTAAAACATGAAACAAATGTTTGTACTGTTCTAGATACTGTTGGAAGAGACATTCTGTACTGTAATGTTAGTGTTAGGGATTCATTTGTGTATGTATATGTGTGTCTGGGGGAGTGTCTGTCTGTCTATCTATCTTTTTTCAAACAGTTTTTATCTATCCGTCTGTCTATCCCTCTATCCGTCTATCTGTCTATCCGTCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17368
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 |
---|---|---|---|---|---|
ENSDART00000088040 | Nonsense | 1077 | 2227 | 25 | 56 |
ENSDART00000131590 | None | None | 678 | None | 16 |
ENSDART00000144807 | None | None | 998 | None | 22 |
The following transcripts of ENSDARG00000077410 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 37426499)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37723209 |
GRCz11 | 2 | 37705666 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATKTAACACTTTTACAGTATTTATAATTTATTTGTGACCMTCTTCACMCT[C/T]AAATGTATTGCAAATWYGTTTGGGAAGCTAAATAAATGATAATMGAGCCA
Long Flanking Sequence:
AAAAGTGATCTTTCTAATGTGCTAATTTGCCATTCTATTATGATTAGCTATAATTAGTGCTAAATCACAAATAATAGTTGTGAAATAAAAAAAATCTGCTTTGTGTTTTTAAGTAAACTGACAATATTATTGCAAATTAGATTTTTTAAAAACTTTTTTTAATTAGTTGAAATGTCACATTAAGATCATTTATTTGAAATAAACATTACATTATACGTATATTTTAAATGCATTTACTGTCACTTTTTATCAATCTAATGTATCTGATGAAAAAAAATATTAAAAACAAAGTTGTTTTCAATATGCTTCTTACAAAAAAGTCATATTAGTATACTTTATGATAATGCCATGGATTTCACAAAATATATAGCAGCACAACTGTATTCGATATTGAGATTCAAGTGGAAAAAAATATTTGTACTTTGTCCTGCACTTTATACTGCATATATTATGTAACACTTTTACAGTATTTATAATTTATTTGTGACCATCTTCACACT[C/T]AAATGTATTGCAAATATGTTTGGGAAGCTAAATAAATGATAATCGAGCCATTTTTTCCTCCTCTCATTCCACAGCGATCATGGCGTTATGTGCGTGAGACGTACAGATGCAGAGCTGCTATTGTGATTCAGATTGCATGGCGAAAGTCCAGGCAGAGAGCAGAGCAAGAAAAACTCAAAGCACAGGCGTATGTCAAGGTTATCTTTGGTTTGTTTTTGTTCAGGTTTTGTTCAAAAGTCTTAGTAATTTGTTTGTCCTTTTTAGATTTCAGAGAGATCTGAACAAGATTGAGGAGAAGAAGCCCAGCCAGCCCAAACCACTGCCTTCACTGCCTAATGAATCCCGCACAGCTGAATCAAAGAAAACTGATGAACCGAGACCACAGTTAAACACAGACACCAAACCTAAAATCCCAACACAACCTACTCCGGGAATCACAAAGCAACTTAGCGTTAAAGAGGACCGACTGGGTCGGAGTAATCGAGGAATGGTTGGCAATA
Associated Phenotype:
Not determined