ZMP
myh11a
Ensembl ID:
ZFIN ID:
Description:
myosin-11 [Source:RefSeq peptide;Acc:NP_001019619]
Human Orthologue:
MYH11
Human Description:
myosin, heavy chain 11, smooth muscle [Source:HGNC Symbol;Acc:7569]
Mouse Orthologue:
Myh11
Mouse Description:
myosin, heavy polypeptide 11, smooth muscle Gene [Source:MGI Symbol;Acc:MGI:102643]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20640 | Nonsense | Available for shipment | Available now |
sa11268 | Nonsense | Available for shipment | Available now |
sa15692 | Essential Splice Site | Available for shipment | Available now |
sa7029 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20641 | Nonsense | Available for shipment | Available now |
sa16962 | Nonsense | Available for shipment | Available now |
sa40634 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16661 | Essential Splice Site | Available for shipment | Available now |
sa20642 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20640
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 |
---|---|---|---|---|---|
ENSDART00000041142 | Nonsense | 29 | 1974 | 2 | 41 |
ENSDART00000138858 | Nonsense | 29 | 133 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 6 (position 9227144)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8333520 |
GRCz11 | 6 | 8569059 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTTCACGGACAAAGACTTCATCAACAGCCCCGTGGCCCAGGCCGATTG[G/A]TCAGCCAAAAAGCTGGTGTGGGTCCCCTCCGAAAAGCACGGCTTCGAGTC
Long Flanking Sequence:
GGAGGCGGGACATGTCAGATACTAGAGAGCATTTGATTAGTCACAATTTGATGAGAAGCTGAAGTATGAGGTGACGGGAAAAAAACGTTCATCCAATTACGCAGAAGTGACAAACTACAAGCTTTACATGTTTATTTCTTCTTGAATATATCTTCTAAACGTGATTTTTGTCACTGTTTTGGAGCACACTAGCTTATAGATATCCTAAAATACAAACAATACTGATACTAACATCTAAAAAATTTTATTTTATTATAATGGGACCTTTAAATAAATGTTTAAAAGCCAAAAAAACTTAGCATTATTAATATTTCTGTATAGTCATACACACAACAAGACCACAATTTATAAAGCATTGTACTTATCAATCAGTTTTTCTCCTTAAATTTGCAGTTGTCTTAACCCAGCACCAAGATGACGAAGAAAGGCTTGAGCGATGATGAGAAATTCCTTTTCACGGACAAAGACTTCATCAACAGCCCCGTGGCCCAGGCCGATTG[G/A]TCAGCCAAAAAGCTGGTGTGGGTCCCCTCCGAAAAGCACGGCTTCGAGTCTGCCAGCATCAAAGAGGAACATGGAGACGAGGTGCTGGTGGAGCTAATGGATAATGGAAAGAAGATCACCGTCAACAAGGACGACATCCAGAAGATGAACCCGCCCAAGTTCAGCAAGGTGGAGGACATGGCGGAGCTCACCTGCCTGAATGAAGCCTCCGTCCTGCACAACCTGAGGGAACGCTACTACTCCGGCCTCATCTACGTGAGTATGACAGGGGTTATTCAAATATCTGGGGGATGCAACTGTTCAGAAATCAGAAATATTTGAAAAGAAATTGAAAAGGACTTAGTTAAATCAAGTCATATTTACAGCGGAGAGAACAAGTATTGAGCACGTCATGTTTTTCCTGGGAATAATATTTCTAAAGGAGCTGTTGACAAGGAATTGAACCAAATTTTGGTTTTGGTTTATTGCTCAGCTGTGAGTTTTTCACAGACTTTAACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11268
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041142 | Nonsense | 427 | 1974 | 12 | 41 |
ENSDART00000138858 | None | None | 133 | None | 3 |
Genomic Location (Zv9):
Chromosome 6 (position 9260748)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8299916 |
GRCz11 | 6 | 8535455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTMCCATTACAGGCTGATTTTGCCATTGAAGCTTTAGCTAAAGCTATGTA[C/A]GAACGCTTGTTYCGTTGGATCCTTCTAAGAGTCAACAAAGCGTTAGACAA
Long Flanking Sequence:
TCTTGGTACGTTTCAAATATTGCAGTCTTTTAAAAGATAATCAATTCTGATAAATGTTTTGTTTTTTGTTAGATGTCCTCAAAGTAGTTTCAACTGTGCTGCAGTTGGGTAACATTGAGTTCAAGAAAGAGAGGAACCAAGAACAAGCTACCATGCCAGACAACACAGGTCAGACAATGCAAAGTTATAGACTTCTCAGATGAATGTAAATCAACTCTGCAGACCAAAATAACGTGTTAATGTGTATCTGATTTTCAGCTGCACAGAAAGTTTGCCATCTTCAAGGCATCAATGTGACAGACTTCACAAGAGCCATTCTGACACCACGTATTAAAGTGGGTCGTGAGGTTGTGCAAAAGGCCCAAACCAAAGAACAGGTGACGAAAGTGCCTAGTCGTGCTGTGATGTTGTGAAACAGAGTTTTGATGTACAATATTATTAATACCCTTTCTCCCATTACAGGCTGATTTTGCCATTGAAGCTTTAGCTAAAGCTATGTA[C/A]GAACGCTTGTTCCGTTGGATCCTTCTAAGAGTCAACAAAGCGTTAGACAAGACGAAACGCCAGGGTGCATCTTTCCTGGGGATCTTGGACATCGCTGGCTTTGAGATATTTGAGGTTTGGAAAAACAAATTAAGAAAGTAATTAAGTGAAGTTTATTCATGAACTAATTTCGAGAGGATCACGTGCTTATGATTTATCACGGCCGGTCTCACATTTACTAATCAATATCTTCCAATCATACAAGCCCTAAGCTACTATAAATAACCACAGTTTTCAGTCCATTTTATCTTCGTTTGGAAGAAACCCCCCTCCTCCCCTTTTCTCCTCTTTTACCTCTGACTGGGCGACACGGCGGCCCAGTGGTTAGCACTGCGAGCCCCACAGCAAGAACACTGCCGGCCCTGGTTTCACAGGACCGGTGGGTGTTTCTGTGAGGAGTTTCCATGTTCTCCCCGTGTCTGGGTGGGTTTTCCCCGGGTTCTCCGGTTTCCTCCCACCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15692
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 |
---|---|---|---|---|---|
ENSDART00000041142 | Essential Splice Site | 684 | 1974 | 16 | 41 |
ENSDART00000138858 | None | None | 133 | None | 3 |
Genomic Location (Zv9):
Chromosome 6 (position 9263120)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8297544 |
GRCz11 | 6 | 8533083 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACACAGCCAAACTTTGTCCGCTGTATTATCCCCAACCATGAGAAACGG[G/A]TATATTGCCATCRTATTAGAWACCAAAAGTGGTGGTACAAANTCTTTTTGG
Long Flanking Sequence:
TTTCCACCCTTTCTGAATTAGGTGGATTACAATGCCGTAGCATGGTTGACCAAAAACATGGACCCTCTAAATGACAACGTTACAGCACTGCTGAATAATTCCTCCAATCCATTTGTGCAAGATCTGTGGAAAGATGGTCAGTATTACATTCTCTCTTTTATTACACTGTCTAAAAACAAAGCTGCCCTGCCGACACTGAATGTTTGTTCGTAATTGGTGTCACACAAAAACATGATTTACAGTTTTTTTGTTTTGATTAGTCACTGAGAATAAAGGCTAAAGATCTCCATTTGTTTTTTTTCATAGCTGATCGTGTGGTTGGATTGGAAACCATTGCTAAGATGTCGGACAGCCTTGCACCTAGTGCCTCTAAGACCAAGAAGGGCATGTTCCGTACTGTGGGCCAACTTTACAAAGAGTCCCTGGCCAAGCTGATGACCACACTGCACAACACACAGCCAAACTTTGTCCGCTGTATTATCCCCAACCATGAGAAACGG[G/A]TATATTGCCATCATATTAGATACCAAAAGTGGTGGTACAAATCTTTTTGGGCATTTAGTTATTTAATTGTTATATCGATGTTTTTTTTTTGGCCTTCAGGCAGGGAAGCTGGATGCCCACCTGGTGCTAGAGCAGTTGAGATGTAATGGTGTGCTAGAGGGCATTCGCATCTGCCGCCAAGGATTTCCAAACAGAATTGTCTTCCAGGAGTTCAGACAGCGGTGGGTAACTGTATTGAGTTGGTCATTTAGTGAGATTTATTTATCTTATTGGCTTCATCTAACTGTATATAGCCTGAAATTATTGATACCCCTGGATTTAGATTTAGATATGGTCTTATACCACTTTCCTGACTCATGAGTAGACCCACACGGAATCTGCACGCGCAGAATTCCGCAGATTTTCTGCAGATTTCTGCAGACTTTCTGCCCATTCTGTTTATTTACTTGAGTAAATGTGTAAATCTGAATTTATTCAGTTTTTATTCAGTAATTTATCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7029
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 |
---|---|---|---|---|---|
ENSDART00000041142 | Nonsense | 726 | 1974 | 18 | 41 |
ENSDART00000138858 | None | None | 133 | None | 3 |
Genomic Location (Zv9):
Chromosome 6 (position 9264573)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8296091 |
GRCz11 | 6 | 8531630 |
KASP Assay ID:
554-4668.1 (used for ordering genotyping assays)
KASP Sequence:
AAAATAGTAAGGTTAAAAACNAKTTTGCATTTACATATTGACATACAGATA[T/A]GAGATCCTGGCAGCGAATGCTATTCCAAAAGGCTTCATGGATGGCAAGCA
Long Flanking Sequence:
AACTTAAACACTAAAAACTGAACTACTCTGTTCCAATTACTATGGCCATTTATGTAAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCTATAGAAATAAAGCTGAATTGAATTGATTAAAGCAGCTGTTCCAAATGAATCAGGGTAGCTAGGATGCTTAAGAACAGCTTGGACTATTTGGAATGGAACTTTGGATTTTTCTATAGACGGCGACAATTTGCAATCATTTTTGACATCCTACCTAACCAAATGTGAATAAAAGCTGAGAAATTTATATTTTTTCCACAAGGATGTCTCTTTTATATCGTCTTATTCTTTTTTTAGGATAATTCTGTCAAAAAAAAAAAAAAAAAAAAAAAACTTGGTTTGAATAAAAGTAACTTTAAAAAAGAATTTGCCAGGGGTATGAATAGTTTTGGCCTTGGTTGTATATATATATAGTAAGGTTAAAATAGTAAGGTTAAAAACATTTTGCATTTACATATTGACATACAGATA[T/A]GAGATCCTGGCAGCGAATGCTATTCCAAAAGGCTTCATGGATGGCAAGCAGGCCTGCTGTCTGATGGTAAGACATTATCTAATGAACCCTTGATAAAGAAAATCATCTGACAGTTATAATGTAAATATGTCGTCCTTTTACTCAACTCTCCGTAGATTAAGCACCTGGACATTGATCCAAACCTGTACCGAATTGGTCAGAGCAAAATCTTCTTCCGCACTGGAGTCCTGGCTCAGCTTGAAGAGGAGCGAGACCTTAAGATCACAGTCATCATCATTGCCTTCCAGTCACAGGCCAGGGGATTCCTAGCCAGAAAGTGGGTAGAGTTTATTAATACAGAATCCTTTTTATGATAGCAAAGTGTAATTTTAATTAATCTCATTCATTTAAAACCACGTGTAGGGCCTTTGCCAAGAGGCAGCAACAGCTAACAGCTATGAAGGTGATCCAGAGGAACTGCGCTGCTTATCTGAAACTCAGGAACTGGCAGTGGTGGAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20641
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 |
---|---|---|---|---|---|
ENSDART00000041142 | Nonsense | 1197 | 1974 | 27 | 41 |
ENSDART00000138858 | None | None | 133 | None | 3 |
Genomic Location (Zv9):
Chromosome 6 (position 9272369)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8288295 |
GRCz11 | 6 | 8523834 |
KASP Assay ID:
2259-7167.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATAGAGGACGAGAGCCGCGTCCATGAGGCTCAGGTGCAGGAGATGAGA[C/T]AGAAACACACCCAAGCTTTGGAGGAGCTCACAGAGCAACTGGAGCAGTCC
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATAGATATATATATATATATATAAATTTTTTTTTCATGTTTTCAGAAATAATATGTCAAAGTTAAGTGAGTTTTCCCCTTATAACTAACTAAATAATTGGCCAAAGGGACAAACCAAAATTCACTTCGAAGTAAGATTATTTTACATGTTATTATACATATTTTTATACTTTATTTTACATATTGGATTAATAAATTCACTTTTAATTTTGACATTATTTCTGAAAATAAGACTTTTTTTTTTTTTGCTTGTCAAGCAAATGCTTCTTAATTAAAGAATTTTTAAATATTTGGACTATAAACAAGACAAAAAATCTAAATAAGAAAATCATTGTACCATTACCTTATTCATAAGGCTGCATATACCATATTTTCAGGGCCAAACGTGAGCAGGAAGTGACTCTTTTGAAGAGAGCTATAGAGGACGAGAGCCGCGTCCATGAGGCTCAGGTGCAGGAGATGAGA[C/T]AGAAACACACCCAAGCTTTGGAGGAGCTCACAGAGCAACTGGAGCAGTCCAAGAGGGTAGGCAACCATATCCAGAACTAAATGATGTTGGTTTGATTGACTTTCTGAATCTGAAGTGCTGATGTAAAATGATTTTTAGGTGAAGGTAAACCTGGAGAAAGCCAAGCAAGCTCTGGAGAAGGAGACGTCAGAACTCCACGTGGAGCTCCGTTCTCTTACTCAGGGCAAACAGGATGTGGAGCACAAGAAGAAGAAGCTGGAAGGACAGCTGGCTGATCTGCAGTCTCGATTTAATGACAGCGAGAGGCACAAAGCTGAGCTGGGAGATCGGGTCTCTAAAATCACTGTGAGTGATGGAGGGTATATTCATACACAGTTTTAGTCAGAATTATTAGCCCCCCTGTATAATTATTCCCCAATATATGTTTAATGGAAAGAAGACTTTTTTTCAACACATTTCTAAACATAATAGTTTTACTAACTCATTTCTAATAACTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16962
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 |
---|---|---|---|---|---|
ENSDART00000041142 | Nonsense | 1316 | 1974 | 29 | 41 |
ENSDART00000138858 | None | None | 133 | None | 3 |
Genomic Location (Zv9):
Chromosome 6 (position 9274360)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8286304 |
GRCz11 | 6 | 8521843 |
KASP Assay ID:
2259-7168.1 (used for ordering genotyping assays)
KASP Sequence:
GAAAGAACATAAAGCTTAGYAAGGATGTGGCTAGCTTGAGTTCTCAAGTT[C/T]AAGACACWCAGGTATGAGGGTCAAAAACGAGACATCTTATTTTGGTGTCW
Long Flanking Sequence:
CCCATGGCCAAACCAGTTCAGAACCACTGCTTTAGACTATCGAAAAAATATTAAGCTTAAAGGGGCTAATAATTTGACCTTAAAAATGGATTTTTTAAAAAAAAAAAACTGCTTTTATTCTAGCCGAAATAAAACAAATATGACTTTTTCCTGAAGAAAAAATATTATCAGACATACTGTGAAAATTTCCTTGCTCTGTTAAACATCATTTGAGAAATATTTAAAAAAGAAAAAAAAATTATAATATATATATATATATATATATATATATATATAAATGCTGATAAATAAGGGATAAGCCGAAGAAACAATTTACGAATGGACAAATAAAATCCGAGAAACACCCTTGTTTTTGACATTCATTTTGTGCAAATGGTGTATTTAACATGTGGCCTTTGTTATTGCAGGTGGAGCTGGAGAGCGTTACCAACCTTCTCAATGAAGCTGAGGGAAAGAACATAAAGCTTAGCAAGGATGTGGCTAGCTTGAGTTCTCAAGTT[C/T]AAGACACACAGGTATGAGGGTCAAAAACGAGACATCTTATTTTGGTGTCTTCATCAAATTAAATTTAGCAATTTAATTATTTATTTATACATAGCATATTCATCTTTAATGCAAGTAAAGTGTCTACATGCATGTTTCAAATAGCAATTGAAAAAAATAAAATAACGGACCACCATCATTCAACATAAAATTTAGATTTATTAAATTTGTATGGTACTTTCATTTATAGTGACAAAACTGAAGCTTCACTGTAAAAAGCAATTAGCTGGCTTTACTTTAAAGAAGTGAGTAAACTCATTGCATTAAAAATGATAAGAAAATGAACCATCTGCATAATTTTAAAAATTACATTAAGGGGATAGTTCACCCAAAAAATGAAAATTTACTTACTATTTACTCTCTCTCAAGTGGTTATAAAACATTATGAGTTTCTTTATGCTATTGAACTCTAAAAATTTTATTTTGAAGAAGGCTGAAAACCTGTAAACATTGACCTCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40634
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 |
---|---|---|---|---|---|
ENSDART00000041142 | Nonsense | 1434 | 1974 | 31 | 41 |
ENSDART00000138858 | None | None | 133 | None | 3 |
Genomic Location (Zv9):
Chromosome 6 (position 9276121)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8284543 |
GRCz11 | 6 | 8520082 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGACCAAGAACAGACTGCAGCAGGAGCTTGAGGACACGCTGATGGATT[T/A]GGACAACCAGAGACAGCTGGTGTCCAACCTTGAGAAGAAACAGAAGAAGT
Long Flanking Sequence:
TAGATCAGCTATGGCATTTGTAATTCTCAACATAGTTGGAGTTGTTGCTTTACAGTTTCTGTCTTTTTTAGGAGTTGCTAGCCGAAGAAACAAGACAGAAGCTGCAATTGTCTACCAAGCTACGCCAAATAGAGGATGACCGCAACGCCCTTCAGGAGCAGCTTGACGAGGAAGCAGAAGCCAAGAGAAATGTGGAGAGACATGTCTCAACACTTAACATTCAGGTTAACATTGTATTCTGAAGTAGTCTTGCTCTATTCATCTAGAAAAGCATCAATGTTTCACTCGTGATTATCCTTTATGGCCACAGCTCTCTGACTTCAAGAAGAAGCTGGAAGAAATGACGGGTAACGTGGAGCTTTTAGAGGAGGGTAAGAAGCGTCTGCAGAGAGACCTGGAGGCAGCGAATACTCAGTTTGAGGAGAAGGCCGCAGCCTATGATAAGCTTGAGAAGACCAAGAACAGACTGCAGCAGGAGCTTGAGGACACGCTGATGGATT[T/A]GGACAACCAGAGACAGCTGGTGTCCAACCTTGAGAAGAAACAGAAGAAGTTTGATCAGGTTTCTGTTTGTTTTTGTTTTTTTCTCATTGGATGTTGACATACAGCTGAAAAAATATTCACTATTTATCTCGGAAAGCATATTTGTAAGGGTGCTGTTGACTTGAAATGTTCGCCAGATGTTTATAGCAACAAAAGTGATCTATACAAACAAGGAAAACAAAACGAATTAGTTTAGAAATTGAGTTATATGTAATAAGATGAGATGAAACAGGGAAAAAAGTATTGAACACATGAAGAAAGGAAGGTGTAAAAAGGCATGGAAGGACCAGACAGCAGCTGAAATCTTTCAGCAGATATTTAGCAGTCCTGCACATTGGATGATGAAGATGAAACCAGGGTGGACATTTCAGCAAGACAATAATCACAAACACAGCCAAACAAACTCTTAACTGGTTTCAGAAAAAAAATGCTAGAATGGAGCAACTAGTTACCTGACCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16661
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041142 | Essential Splice Site | 1524 | 1974 | 32 | 41 |
ENSDART00000138858 | None | None | 133 | None | 3 |
Genomic Location (Zv9):
Chromosome 6 (position 9277233)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8283431 |
GRCz11 | 6 | 8518970 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCTGAAATGGAGGATCTAGTCAGCTCCAAAGACGAYGTRGGCAAAAACG[T/G]AAGTTCAGYAGTGTAARGGAAAATTTGAAACATTCCTTGCATTGGAATAT
Long Flanking Sequence:
ACAATCTGCATACAAGAGGCCACTTAAAGCTGTCCTTACCTAAAAAAAAGCCTTTTATACACAGTTTTAAATTCATTTTAGTAGTTCAGTACTTTCTCCTTGAGTCATTCCATTTTCATAACACATTTTTGAGATTTTTCTATGTTTGGATTGTTTGGGTTTTATCCAAACTCTGGGTCAATTTCATGTCAACAGCTTATTTAGAAATACATTTATCAGGAAAAATCGTGAAGTGTTCAATAGTTATTTTACCCGCTCTATGTTCATTTCTGCTGTTTCCTTTCAGATGCTTGCTGAAGAGAAGAGCATCTCTAGTAAGTATGCAGATGAGCGAGATCGCGCAGAGGCCGAGGCTAGAGAGAAGGAGACCAAGGCTCTGTCTTTGGCCAGAGCTCTGGAGGAAGCTCAAGAAGCCCGCGAGGAGTTCGAGAGAGCCAATAAAGCCCTTCGTGCTGAAATGGAGGATCTAGTCAGCTCCAAAGACGACGTGGGCAAAAACG[T/G]AAGTTCAGCAGTGTAAAGGAAAATTTGAAACATTCCTTGCATTGGAATATTTCAATCAAACTTATACCTAATTTCAGGTGCATGAGCTTGAGAAGTCAAAACGTGGCTTGGAGGCTCAAGTCGAAGAGATGAAGACACAGCTGGAAGAGCTGGAAGATGAGCTACAGGCTGCGGAAGATGCCAAACTGCGTCTGGAAGTGAACATGCAGGCTCTGAAGGCTCAATTTGAGCGAGACCTCCAGGGCAGAGATGAGCAAGGAGAGGAAAAGAAGAGGCAGCTGGTCAAGCAGGTGCAGTAGCTCTTCATTACCCATACTGGGATATCCAATTATATAAGTGTTTAAATGTATTTCCTCACCAACAGGTGCGTGAGCTGGAAACCGAACTTGAAGATGAGCGCAAGCAAAGGACTGCACTTGCTGCTTCCAAGAAGAAGCTGGAGGGAGACCTAAAGGACCTTGAGGGACAGATTGAGACGTCTAACAAGGGACGAGACGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20642
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 |
---|---|---|---|---|---|
ENSDART00000041142 | Nonsense | 1762 | 1974 | 37 | 41 |
ENSDART00000138858 | None | None | 133 | None | 3 |
Genomic Location (Zv9):
Chromosome 6 (position 9282272)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8278392 |
GRCz11 | 6 | 8513931 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGCAAGGCAACATGGAGATGCTCAATGACAGGCTGAGAAAGAGCGCA[C/T]AGCAGGTACATGCGTTACAGTACATCAAATAGACATTAATATTAGGGATG
Long Flanking Sequence:
CCTGGCCGCAGCTGAGAGGGCTAAAAAGCAAGTTGAAGCTGAGAGAGATGAACTGGCTGATGAGTTGGCCAGCAATGCATCTGGAAAGTGAGTATGACAACAAAATATCACTGAAATAGTTTTATCCCATGGAATTCATTATAAACCTCTGATATATTGACTTCCATTGAAAAACATGTGGTTCACTGTTACAATTAATAGTAGGCATATTTAGTTTAACTGTTTGTACAGGAACAGAGAGTAGTTCTAGACTTCAGTTATGTGAAATATTGCACTTTTTAGACATACCAGAAGCATTTATGTACTAAAATATTACCACAGAAATGTGCTCCGTGCATATATTCGGATTGAAACTAATATGTGTCTTGACTGAACCTCAAAGGTCTGCACTGTCTGATGAGAAGAGACGGCTTGAAGCCAAGATTCAGCAGCTGGAGGAGGAACTGGAGGAGGAGCAAGGCAACATGGAGATGCTCAATGACAGGCTGAGAAAGAGCGCA[C/T]AGCAGGTACATGCGTTACAGTACATCAAATAGACATTAATATTAGGGATGGACCCATTTGGAAATATTGACCTGTTGTGAATTGAAAAAGCGACAGGCTAGGAGACTTTTCGGGTATCTTCAAAGCACAATCCTTTAATGAGAACTTACGGTTGCTGTATTCATCATTTAAAAATCTAAACTAGTGCTGCTTTGCACTCAATTCAAATCACATTTTAGGGGGCAGTGATACATAGAGGTTGACACAAATCTAAACAAAGTATGCAAATGAAGTACAGGAGTCAGCCAAGTACACTTAAAAATAATATTTGCTGTTTGTAAGAGCTACTACTTAATTGCTATCTTAACTATCTTAATTGTTTCATTTTCAATCCAGGACCCTGCCTGATGGTCAGGAAATGCATAAAGACCATAGGTTAAATGTCAACTTGGCCTGCTAGTTTTGAATATTATATTGTTAAAAAAATACTCTTTAGATTTGGAGACCAATATATTGGCCGA
Associated Phenotype:
Not determined