ZMP
myo18l2
Ensembl ID:
ZFIN ID:
Human Orthologue:
MYO18A
Human Description:
myosin XVIIIA [Source:HGNC Symbol;Acc:31104]
Mouse Orthologue:
Myo18a
Mouse Description:
myosin XVIIIA Gene [Source:MGI Symbol;Acc:MGI:2667185]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14885 | Nonsense | Available for shipment | Available now |
sa21785 | Essential Splice Site, Missense | Available for shipment | Available now |
sa16330 | Essential Splice Site | Available for shipment | Available now |
sa34958 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12353 | Nonsense | Available for shipment | Available now |
sa41712 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34957 | Nonsense | Available for shipment | Available now |
sa13591 | Nonsense | Available for shipment | Available now |
sa34956 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14885
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 |
---|---|---|---|---|---|
ENSDART00000110835 | Nonsense | 52 | 2454 | 1 | 43 |
ENSDART00000132023 | Nonsense | 41 | 1848 | 1 | 39 |
ENSDART00000145855 | None | None | 239 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 38405850)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 37128865 |
GRCz11 | 10 | 37072623 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAGAGTCTGGAGGAAATGAGCGTGAGGAGAGGTTTCTTTCATCTTCAT[C/T]GAAGCAACTCTAAACGGGAGACGAAAGGGAAGCTGGAGATTTCCAGTCCC
Long Flanking Sequence:
ATGTCAACTGACCCAGCCAGGGTTTGAACCAGCAACCTTCTTGCTTTGAGGCCACAGTGCTAACCACTGGGCCACCGTTGCGCCCTATTATTACATTATTATTGTTATTTTATTTATTATTTTTCAGTCCTTTTAACATGTGCATGCCTCCTGTATGCAGTGAGAAAGAGAGAAGGCACTAAAACAGCATTCTGTTCATCAATCTGTTGTTATAGAGGAGGGATTCACCAGTTGCTAAGGTGACCTTGGTGCTCTGGAGCTGGAGCAGGTCATGACTGAACGCCAACACTGATCTGTATGCCGTGAAGAGATCGACGTCTGCTGAATTCTACATTTAGGCCCCAATCATGTTTCACCTGATCAAGAAAGATAAAGACAAGGAAAAAGATGGGGCGAAAAAAGAGAAAAAGGAGAAGAAGGAGAAAAAAGAGCGAATGTCCCAGGCCGAGCTGAAGAGTCTGGAGGAAATGAGCGTGAGGAGAGGTTTCTTTCATCTTCAT[C/T]GAAGCAACTCTAAACGGGAGACGAAAGGGAAGCTGGAGATTTCCAGTCCCATTCCCATTAAGGTGGTCCGAAACACAGAACTCAGTCTGGCAGATGTAGACCTCAGGAAACTCTACTCTCAGGTAAAATATTTCCCAATCAAATTTTCTTGTTGTAATTAATTGCTGAAGCATTTATCATGTATATGGTATTATCATGATATTGATCTAACTTGCAAAAAAATTACTTTACGGGTATAAAAAAAAAAAACAATTGATGTTTTGCAGTGTTGTACACTCACCGGCCACTTTATTAGGTACACCTGTCCAACTGCTCGTTAATGCAAATGTCTAATCAGCCAATCACATGGCAGCAACTCAATGCATTTAAGCATGTAGGCATGGTCAAGACGATCTGCTGCAGTTCAAAATGAGCAAAAGAATAGGGAAGAAAGCGTATTTAAGTGACTTTGAAAGTGGCATGGTTATTGGTGCCAGACGGGTAGGTCTGATTATTTCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21785
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 > C
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110835 | Missense | 330 | 2454 | 2 | 43 |
ENSDART00000132023 | Essential Splice Site | 318 | 1848 | None | 39 |
ENSDART00000145855 | None | None | 239 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 38403179)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 37126194 |
GRCz11 | 10 | 37069952 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAACTGAGCCGCTGCTGGCTGAGGAACACCAAAGGCCCATATCGCGAGG[T/C]CTATGAGGTGAGATGCAAGTTTGTGTCATGGTTGTGATGTGTTTAACTAA
Long Flanking Sequence:
TGCTTCACCCCAAATAGAGGTCAAGGTATTCAATCAGTCGACACTACATTCTTTCCACCAAACCAGCCCCGCAAAAATCGTCCAGATTCCAGAAATAGTGGACCGAACATTCCCGGCAGATTTGCGATTACCGGCTGTGGCACCTCCACAGGTTCCTGCACCAAGAGAGCTGGAAATTCAACGTCGCAACACAGGCGATTTTGGCTTTTCTCTTCGGCGCACCACTATGGTTGACCAGCGGACCGATGGGTCGCTCTACAGAAAGGTCGTCCACTTTGCTGAGCCTGGTGCTGGGAGCAAAGACCCGACCTTAGGGCTGGTGCCGGGCGACCGTCTGGTGGAGATCAATGGGAGGAATGTGGAAAATAAAAGCAGAGATGAGATTGTGGAGATGATACGGCAATCTGGAGACACGGTGCGTCTGAAGGTGCAGCCCATCGTGGAGTTGAGCGAACTGAGCCGCTGCTGGCTGAGGAACACCAAAGGCCCATATCGCGAGG[T/C]CTATGAGGTGAGATGCAAGTTTGTGTCATGGTTGTGATGTGTTTAACTAACCAGTGAGGATGGTGGATTCGATGGAGAGTTTCATTTTACTTTTTTTGACAGCGTTTATCATCGTTGTTTAATGCCTTGGGACTAACAAAGGGTGACAATGTGAGCCTTCACAAAAACACACAAAATTACAGGTGTAACTGCACAATTAAAACAAAAAATGCCTTGGGTTTGTTTTTTGGTATGATGCACCCCGTTATAAGATGGCTGACCAATGATATGCATTTGTTTACAAGCATGTGTCAGAAGCATAAAGTTGCTCAGCACCACGTTGTGTCTTTGTGTGCCAGCGTATTTCTGCTTTTTCATTAATTGTCATCTATTGTCAGGTTAGTGGTTTGGCATGTTCACTCAGATCAACACAGGTAGCAAAGAACAATGGCCCAGATTTGCCATAAATCAGGCACAGCAGGCATTCATCCAGCACTGGCCCGGGTTTGGCAGAGGTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16330
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 |
---|---|---|---|---|---|
ENSDART00000110835 | Essential Splice Site | 332 | 2454 | 2 | 43 |
ENSDART00000132023 | None | None | 1848 | None | 39 |
ENSDART00000145855 | None | None | 239 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 38403171)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 37126186 |
GRCz11 | 10 | 37069944 |
KASP Assay ID:
2260-3546.1 (used for ordering genotyping assays)
KASP Sequence:
GCCGCTGCTGGCTGAGRMACACCAAAGRCCCATATCGYGAGGTCTATGAG[G/A]TGAGATGCAAGTTTGTGTCATGGTTGTGATGTGTTTAACTAACCAGTGAG
Long Flanking Sequence:
CCCAAATAGAGGTCAAGGTATTCAATCAGTCGACACTACATTCTTTCCACCAAACCAGCCCCGCAAAAATCGTCCAGATTCCAGAAATAGTGGACCGAACATTCCCGGCAGATTTGCGATTACCGGCTGTGGCACCTCCACAGGTTCCTGCACCAAGAGAGCTGGAAATTCAACGTCGCAACACAGGCGATTTTGGCTTTTCTCTTCGGCGCACCACTATGGTTGACCAGCGGACCGATGGGTCGCTCTACAGAAAGGTCGTCCACTTTGCTGAGCCTGGTGCTGGGAGCAAAGACCCGACCTTAGGGCTGGTGCCGGGCGACCGTCTGGTGGAGATCAATGGGAGGAATGTGGAAAATAAAAGCAGAGATGAGATTGTGGAGATGATACGGCAATCTGGAGACACGGTGCGTCTGAAGGTGCAGCCCATCGTGGAGTTGAGCGAACTGAGCCGCTGCTGGCTGAGGAACACCAAAGGCCCATATCGCGAGGTCTATGAG[G/A]TGAGATGCAAGTTTGTGTCATGGTTGTGATGTGTTTAACTAACCAGTGAGGATGGTGGATTCGATGGAGAGTTTCATTTTACTTTTTTTGACAGCGTTTATCATCGTTGTTTAATGCCTTGGGACTAACAAAGGGTGACAATGTGAGCCTTCACAAAAACACACAAAATTACAGGTGTAACTGCACAATTAAAACAAAAAATGCCTTGGGTTTGTTTTTTGGTATGATGCACCCCGTTATAAGATGGCTGACCAATGATATGCATTTGTTTACAAGCATGTGTCAGAAGCATAAAGTTGCTCAGCACCACGTTGTGTCTTTGTGTGCCAGCGTATTTCTGCTTTTTCATTAATTGTCATCTATTGTCAGGTTAGTGGTTTGGCATGTTCACTCAGATCAACACAGGTAGCAAAGAACAATGGCCCAGATTTGCCATAAATCAGGCACAGCAGGCATTCATCCAGCACTGGCCCGGGTTTGGCAGAGGTAAAACCGTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34958
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110835 | Essential Splice Site | 678 | 2454 | 10 | 43 |
ENSDART00000132023 | Essential Splice Site | 662 | 1848 | 10 | 39 |
ENSDART00000145855 | None | None | 239 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 38355612)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 37078627 |
GRCz11 | 10 | 37022385 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATCTTAGGGGCCATTTACCATCTCGGTGCTGCCGGGGCCACTAAAGG[T/C]AAAGCTACCAGTGTCTAAACTAATACAAATATTTAAATGTAGGAAGAGAA
Long Flanking Sequence:
ATCATTCATTCAAGAGACTGATTCAGAAGACTGATTAATTTGTTAAGTAATTCAAATTTCTTCAGATTAGTTCAATATTTTAAACAGACTGCAACAATATCAAGAATTGTGCAGATAAATGATTAAAACAGTATGCAAGTGAATGTTCCTCCACAACAGCAACTTGTTCAGATTAAAGCTGATCAGCTGAAGGAACTTTGTCTGCCTTTCAGGACTGAACTTCATTTCAATCACTTGGCTGAGAACAGCACTTTTGGACTCCATCCTCCCTCAAAGGTAAGAAAAGCCACACAGATCTTCATAATGCATAACTATTTTATCAGTAAACCTTATATCATACGCCCTTTTCTGTAGCTCGATGACAAGCAGAAAGCCACTCAGCAGTTCACCAAGCTACAGGCTGCCATGAAAGTGCTGGGAGTCTCTCCTGAAGAACTGAAGACTGTCTGGCTGATCTTAGGGGCCATTTACCATCTCGGTGCTGCCGGGGCCACTAAAGG[T/C]AAAGCTACCAGTGTCTAAACTAATACAAATATTTAAATGTAGGAAGAGAACTACAATAAAGGAATGTCTGACTGCAAAGAGTGTATTTTAACATCTGTCCACTGAGAGTCAGTAGTGGCACTTTACAGTCATGCTTCTGTTTCCATTGACTGGTACAGTACGGTATGGTACGGGTCGGTACAGGTCACCTTTATCATCCTTTTAGTGGGTGTGGTGTACAAGTTGACGTCATTCTCACTGTAGGAAATCGCGCTCAAAGTAAAGCTGCACGGGTCGTTCACATATCATGTGAGAAGCACTTCTCACAAAACAGATGCTTTATACACATAAATACTTGTGTATAAATGTTCATGACTAACTTTTCTATGAACATGATTTGATTATAACTGCAGGTCAATGACAGTGCGAAATAGACTACGGTAACGTCGCATGTTATTATCATCAGTTCAGAAAGTTCGATATTTCAAATATAGATGCGCACGCGAGCGATCACAAGCTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12353
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 |
---|---|---|---|---|---|
ENSDART00000110835 | Nonsense | 1029 | 2454 | 19 | 43 |
ENSDART00000132023 | None | None | 1848 | None | 39 |
ENSDART00000145855 | None | None | 239 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 38343210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 37066225 |
GRCz11 | 10 | 37009983 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTCTTATGCTAATTTATAAATTTGGTCCTTTCAATCAGGAWGCACTGY[T/A]GGACACCATCCGCAGATCCAAAGTTCACTTTGTCCACTGTCTGTTACCCC
Long Flanking Sequence:
AACAAGTATGTTCACTTAACATGTTTTTTCAATACCTGCAAACATATTGTGGTATTTTTATGTTTTAGAAGAGTTAAAAACTTAAATGCAGCACCTTTTAAGGTAATAAGTTTACTGTACTTGTTGACTTTAGTTAAAGTGACTAAACATGTTGTAACTTGGAACTGTTAAGCTGGCTTAACTTTAAAGGAAATGGGTTTAATAGCATTTTTAAGGAAATTTACAGTTTAAGATGAGAAACAACAAAAAGAAAAAGATGATGTTATCCAACTCATCTTATTTTTGACATGTTAACGACACAAGCATGGGCGAATATGTTTGATTACACTGATGTTTAAGACTTAACAGTTCCTCTTGATAGATTATATTGGTTTTGATGCAAATGAGCTGCTGTGTCTGGATTCTTTATTTTGCAGGTTGTCTAAATCACCAACAGAGTTTTATTTATCACACTCTTATGCTAATTTATAAATTTGGTCCTTTCAATCAGGATGCACTGT[T/A]GGACACCATCCGCAGATCCAAAGTTCACTTTGTCCACTGTCTGTTACCCCGAGCGGAGGTTCTGAGGGCCGCAGGGTCTCCAGATGAGAGCTGTGATCCTGGACTTATGCAGATCGATGTGGCTTTGCTCAGGGCTCAAATCCACGGCTTTAAACTGCTGGACAGCTTAAGGATTTACAGACAAGGTGAGAAAATATGAGAATATCCAATCAAACATGTAGACATTTGATATATTGAATATTCATTCAATATATCAAGATAATGAACATGCACAATATTGATATTGTAGGAAAATACAGTTCATAATTATTGGTTTACACTTTTAGAGTGCTTTTTAAGAATAGTTCATCATCGTCACAGCATTTGATCTATTTTCAAACACTAATACTTACAGTTAATCCTTCCTACGACACCTTTTCTATGACAAATTCTGTGACTATAGGCCTTTTGTTTGTTAACTCTGTACAGTAAGGCTCTATTTGTTACCATCAGTTAATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41712
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 |
---|---|---|---|---|---|
ENSDART00000110835 | Nonsense | 1090 | 2454 | 19 | 43 |
ENSDART00000132023 | None | None | 1848 | None | 39 |
ENSDART00000145855 | None | None | 239 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 38343028)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 37066043 |
GRCz11 | 10 | 37009801 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGCTCAAATCCACGGCTTTAAACTGCTGGACAGCTTAAGGATTTACAGA[C/T]AAGGTGAGAAAATATGAGAATATCCAATCAAACATGTAGACATTTGATAT
Long Flanking Sequence:
TTTAAAGGAAATGGGTTTAATAGCATTTTTAAGGAAATTTACAGTTTAAGATGAGAAACAACAAAAAGAAAAAGATGATGTTATCCAACTCATCTTATTTTTGACATGTTAACGACACAAGCATGGGCGAATATGTTTGATTACACTGATGTTTAAGACTTAACAGTTCCTCTTGATAGATTATATTGGTTTTGATGCAAATGAGCTGCTGTGTCTGGATTCTTTATTTTGCAGGTTGTCTAAATCACCAACAGAGTTTTATTTATCACACTCTTATGCTAATTTATAAATTTGGTCCTTTCAATCAGGATGCACTGTTGGACACCATCCGCAGATCCAAAGTTCACTTTGTCCACTGTCTGTTACCCCGAGCGGAGGTTCTGAGGGCCGCAGGGTCTCCAGATGAGAGCTGTGATCCTGGACTTATGCAGATCGATGTGGCTTTGCTCAGGGCTCAAATCCACGGCTTTAAACTGCTGGACAGCTTAAGGATTTACAGA[C/T]AAGGTGAGAAAATATGAGAATATCCAATCAAACATGTAGACATTTGATATATTGAATATTCATTCAATATATCAAGATAATGAACATGCACAATATTGATATTGTAGGAAAATACAGTTCATAATTATTGGTTTACACTTTTAGAGTGCTTTTTAAGAATAGTTCATCATCGTCACAGCATTTGATCTATTTTCAAACACTAATACTTACAGTTAATCCTTCCTACGACACCTTTTCTATGACAAATTCTGTGACTATAGGCCTTTTGTTTGTTAACTCTGTACAGTAAGGCTCTATTTGTTACCATCAGTTAATATAACTAAAGTCTGATGTTAATTTCTTAGTCAATTCCTAATAATGCATTAAAATCAAAAGTTTGAATCGTTTTATTAAAATTCACTTAAAAAACTTCAATAGGGCTATTTCTCATTGTTGATTTTTATGCATTAACTATTTTTTACTAATGAGACTTTCTTGTAAAGTGTACTTTATCATTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34957
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 |
---|---|---|---|---|---|
ENSDART00000110835 | Nonsense | 1357 | 2454 | 27 | 43 |
ENSDART00000132023 | Nonsense | 1216 | 1848 | 24 | 39 |
ENSDART00000145855 | None | None | 239 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 38318338)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 37041353 |
GRCz11 | 10 | 36985111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAACTTTGGAAACTCTGTGTTTGTCAGGAGGTGAATGGAGGCTGAAATA[T/G]GAACGCGCCATCAGAGACACAGAATTCACAAAGAAGAAACTCCAGCAGGA
Long Flanking Sequence:
ACAAGTTTTGCTGCTACACAACTGTAAACGTGCTAAATAAAATACAGTTTTTCTTTAAGAATTGTAGTATTATAATGTTATGAAGTTTTCTAACTGGCGAATGACCTAATGATCTAATGGGTTGTCTACTGTCATCTTTAATGTGCCGGTTTGTGTTTCACGAGGCGTGGCTTTGGACAGTAGGGGAGGGACTGTGATTAAAAAAATATTATGCTAACAAATAGCATTCTGGCAGGTTCTGGTGCACTCAGTGCTAAAAATCACTCACTTGTTTTTATTCACTCCTCCAAGCAGACTATATTAGTGGACTAGACTTAAAGTAGATGAGCAGTTAATCCATAGTCTATTGTACATTTTGATAGTATTACACTTTTTTTTATAAAGGAGTGTTGACGGCTTTCAGGGGTTCGAAACTTCTTAACATGCTAAAAACAAGCTCAACAAAACAATCCAACTTTGGAAACTCTGTGTTTGTCAGGAGGTGAATGGAGGCTGAAATA[T/G]GAACGCGCCATCAGAGACACAGAATTCACAAAGAAGAAACTCCAGCAGGAGATGGATGACAAGCTGGAGACAGAACAACAGAACAAGAGACACCTAGAGAGAAAAGTTAGTAAAGCACAACACACACAGACACACACACACACAGACACACACACACACAGACACACACACACACAGACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACGCCTAGTGATGTAATGCTGTTTCTAAGAGCAGGAAAAATAACTTTTCTCTTTACAAAACTTGGGATCCTTTAATAACCTCTACTGAGATAAATGTACTTCTCCAACCATCACCCCCACACCCACCCCTATAAGCTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13591
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110835 | Nonsense | 1731 | 2454 | 35 | 43 |
ENSDART00000132023 | Nonsense | 1569 | 1848 | 32 | 39 |
ENSDART00000145855 | None | None | 239 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 38304710)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 37027725 |
GRCz11 | 10 | 36971483 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGCTCMGTCGTCTGCAGAGAGAGAAGAATGACCTGCAGTCTCGCTTC[G/T]AGGAGGATCAGGAGGACATGAACGAACTCATGAAGAAACACAAAGCTGCA
Long Flanking Sequence:
AGTCAAAAACGCAAAGCAAACAGAAACAAAAACAGCTGAAGGAGTATACACTAACCTGCAGATTATTCAGTCACAAGATGGCACCAAACAGTCAAAAACGCAAAGCAAACAGAAACAAAAACAGCTGAAGGAGTATACACTAACCTGCAGATTATTCAGTCACAAGATGGCGCCAAACAGTCAAAAACTCAACGCGAACAGAAACAAAAACAGTTCATGCAGTATACACTAACCTGTGCAACATTTAGTCACAAGTGTGTCTTATCTTTGCAGTATTTTGGTATGTTTTGTCACATCATCTGTGAATGGTATTATGGTATAAGCTAGTACAGTATAAGCTGAAATCTGCCTGATGCCAAGATGGCCAGGTTGCAGGAGGTTTCGTCATCCTGGAAACATGTCAGAAAGTAGCTCACTCAAGCGGTCTGTTGTGTCTCTTTCAGCTGGAGGAGCAGCTCAGTCGTCTGCAGAGAGAGAAGAATGACCTGCAGTCTCGCTTC[G/T]AGGAGGATCAGGAGGACATGAACGAACTCATGAAGAAACACAAAGCTGCAGTGGCTCAGGTCAATTTATACACTGTTCACTTTTATTTACAGTTGAAGTCAAAATTATTCGCCCTCCTGTGAGTTTTTTTTCCAATATATTTCCCAAATGAGGTTTAGTAGCAAGGAGATTTTCACAGTATTTTCTAGAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCAGCTAGATTAAAAACAGTTTTTCATTTTTAAAAACCATTTTAAGGTCAATATTATTAGCCCCTTTAAGCAATATTTGTTTTCGACTGCCTACAGAACAAACCATCATTATACAATAATGCCGAGTTCAGACTGCATGATTTTCAAAGTAGTCGTGTCACATGACGCATGACTATCTGGGCTAGCGTTTCGTCGCTGCTTTGTTTACACTGCAAGATGGATCGCCGACAGGGACTTTCACATTGCATGACTTTACTATTGGAAGAATCGCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34956
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110835 | Essential Splice Site | 1989 | 2454 | 42 | 43 |
ENSDART00000132023 | None | None | 1848 | None | 39 |
ENSDART00000145855 | None | None | 239 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 38288245)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 37011260 |
GRCz11 | 10 | 36955018 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGATCATTTGCAGTTCTGCTGTTTTTAACGTGTTTTCTGTCCATCTTA[G/T]ACACCCCAATTCTGCTAATGCAGACGTGAAAGATGTAAAAGAAGGAAAGG
Long Flanking Sequence:
AATAAACAGTTCTTTGTGAATTACCAATTAGAAAGTTTAATTAAAAAAATTAGCAAACCTTGAGGAATAAATAAAGGATCCTGCCTTTTCTTTGCTGAGATGACTGGTTTTGTAGATACATTTACAGGATTAAAATATTTAGGCACTATCGATGTGGTTCACCAGAGTAACCGCCAAAACATACATGTCTTCTCCATCTGGGAGAGGTAATAAGAAGCTGAAGACAGTGTTTGATGACTTAAGATTCACGACTCGCACTGAGAGCTGCTGCTACTGTTCTGATCCTCAGTAGTATTAGTATGGAGCTGTTACGTAACGGCCATTAGGGGTTTAATCGCTTTACATTTATTCCTGGAGTTGGTGTAAAATATGCTCCTAATTTACCACTCAAATCTCTTGGTTCTTTCAATTCATGTTTATCTCAGTCATGGGTATCATCCTGTTATATTCACAGATCATTTGCAGTTCTGCTGTTTTTAACGTGTTTTCTGTCCATCTTA[G/T]ACACCCCAATTCTGCTAATGCAGACGTGAAAGATGTAAAAGAAGGAAAGGAGGGGAAAGAGGATGTTAAAAAAGACTCAGATGAGAGCCGTTCGGTGTCTGTGATAAGTTCGCTTAGCTACAGGAAGCGTGCACATCAGAAGGACTGGAACGGAGGTGCAGGGGATGAAACTTCGCTTTTCAGTGCCTTACGGGAGCAGCCGGAGATGCCTGACCGATTGTCACTGCGCAAAGCTAAAACCAAATCCACAGACAGGCCTGGAGATGACCTGGATGACCGAGGTTCGGTGATCTCCCAGGCTTACTCGGAGGCTGCTATTAGGGCCAGGAAGGGCCTTGATCGTCGCTGGACCAAGAGTAGTCCAGAATTTGACAAGGAGTCCATGGTATCCTCAGTGGCCCCAAGCCGAGCTTCTACCCGGCGTGGGATTGACGAAGATGAAGATGCGCGCTCTGGGGTGAGCAGCTTCAGCTTGCGGCGTAGTACTTCTTGGATTGATG
Associated Phenotype:
Not determined