ZMP
OTOG
Ensembl ID:
Description:
otogelin [Source:HGNC Symbol;Acc:8516]
Human Orthologue:
OTOG
Human Description:
otogelin [Source:HGNC Symbol;Acc:8516]
Mouse Orthologue:
Otog
Mouse Description:
otogelin Gene [Source:MGI Symbol;Acc:MGI:1202064]
Alleles
There are 11 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16704 | Nonsense | Available for shipment | Available now |
| sa40967 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34131 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21034 | Essential Splice Site | Available for shipment | Available now |
| sa10228 | Nonsense | Available for shipment | Available now |
| sa18441 | Essential Splice Site | Available for shipment | Available now |
| sa21033 | Essential Splice Site | Available for shipment | Available now |
| sa18470 | Essential Splice Site | Available for shipment | Available now |
| sa17990 | Essential Splice Site | Available for shipment | Available now |
| sa44672 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40966 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16704
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 |
|---|---|---|---|---|---|
| ENSDART00000083804 | Nonsense | 110 | 2794 | 4 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 40919957)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39256214 |
| GRCz11 | 7 | 39527231 |
KASP Assay ID:
2259-9256.1 (used for ordering genotyping assays)
KASP Sequence:
GCACTCGTTCAATCAGCCTCTTCCTGCCATGGGAGGGCGAGATTAGGTTA[C/T]AGCACTTCAGTGTTACTTTCAAGGGTCAAAGGTAATGAACATTGACAMTC
Long Flanking Sequence:
CACATTGTTATCAAAGAAGAAAATCTAATATTCTGAAATGTATAATAAATAATCTGATGAAGGTTTTGAGCTGAAACTTTACAGACATATCCTGGAGACACAAAAGACTTCTCTTAAACCTTGAAAAAGGGGGAAAATAGGTGATCTTTAACTGTGGAAGTGAGACAATAAGTTGGGTTCCACACACTCAAATTGTTTTAAGACAACATGAAGAAATTAAATTTACTTCCATAATAATTTTTTTATAAATTTATGTGGATTGAACATGAAACAGCTACGTTGTCCCAAAATAACCTCAAGAATTGTGTTGTGGTAGATGATTGTAGTTAGCAAATACCCTGTTCACCTGCAGTCTGTTTTATAACAGCTTTATCTTATGCCATGCTTCATTGCTAATTGTTGATCTGCAGGTGCATAATGACCCAGAATGCAGTTCTTCTCCTTACTCCTGCACTCGTTCAATCAGCCTCTTCCTGCCATGGGAGGGCGAGATTAGGTTA[C/T]AGCACTTCAGTGTTACTTTCAAGGGTCAAAGGTAATGAACATTGACAATCAAACACATCCTGTCACTTAACCTGACCTGCATGATATCTATAAATCCCCTCTCTGTAGCATGTGGCATGTTCTCTCTTTAGTGTGCAGCTATAAGTTAAATATGTTCTCTCTGTAGTGTGCTGCTGCCCCATCACATCCATGATGTTGAGCTGGAGCGAATCTCTGACTACATTGTAGTTTCTCAGCCGCATGTCTTCACACTGGCCTGGCAGGGTCTCACCAGCTCTGTGTACATCAAAATGAGCCCTGAGTTTGTAGGACACACCTGTGGACTTTGTGGGAATTTCAATGCTGACACTCAAGATGACCTGAAGACCAGCTATGGCAAGTGTTGCTTTATTTGTTGCATTTGTTACATTGTCAGTATACTTTTTTGTCAAGTGTTCTCTTTAGACAGTTAGTTTGTTAGATCACACTCTCCATGCCAATCTAGCCCCGGTCTCCAGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40967
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083804 | Nonsense | 203 | 2794 | 6 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 40917485)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39253742 |
| GRCz11 | 7 | 39524759 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTGCTCAGGTGTTTTCACACAGGATTTGGCCATGTTTGGAAACAGCT[G/A]GGCTGAGGAGGAGCCGGAGTTAGCCAGATGTACTGTCGTTCCCTCACTCT
Long Flanking Sequence:
GCCAAAGGAAAATGAATGAATGAATGAATGATTGAATGTATAAAACATGTCATGATAAGGATTGTTCTGAAATGTTTATTTGTTTGTTTGTTTGTTTTGTTTATTGACATAATAATTCTTAACTGCATTATTTCACACCATGTCAATACATTTCTGTAAAATATACATGCATATATGAATATACACGATATAAAGATCATTAAAATTAAATAAGACAGATGTTTCACCTCTACTTTTTGTGACAGTTGGACAAGTAATGTTTGATGAAGCTGTTAATTGTTGACATGCTGTATACTCCATCTAAAAGTATTTTATACAACATTTTATATCCATGTTAAACATTTTTTAAATAGTTTATAATAATGAAACCGGAAACAAATTTGTAAACTTTTGTCATAAAACATTTACAGAAAAAATGAACACATTTACTTACTAATATGCATGTATTGTTGTTTGCTCAGGTGTTTTCACACAGGATTTGGCCATGTTTGGAAACAGCT[G/A]GGCTGAGGAGGAGCCGGAGTTAGCCAGATGTACTGTCGTTCCCTCACTCTACCCCTCACCATGTGCCACGCTGGATCCTCATGTCTTATTGGTACCTAACACAAAACACTCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATATATTCTTGTCCAACACCAACCAAAGTGTCATAATCAATGAAATGGGTCATTTACACCCAAACACATGGTTGATAAGGAAACTTGTTCTTCACTGCAGAAAGTGGAGGAAGTTTGTTCCACTCTTCTGAGGGAACCGTTCCAGTCCTGCCATGAGTTTGTCAGTCCATATTCATACATGGCAAGTTGCTCCAATGACCTGTGCTTGTAAGTACTGGCATAAGACGCATCTACTGAAATTGATCACACTTCCTGGGAAGTTATAAGCTTGAATTGCAATACTGCTTTACTTTCCAAAGGTGTATACTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34131
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 |
|---|---|---|---|---|---|
| ENSDART00000083804 | Nonsense | 252 | 2794 | 7 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 40917141)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39253398 |
| GRCz11 | 7 | 39524415 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGGAAGTTTGTTCCACTCTTCTGAGGGAACCGTTCCAGTCCTGCCAT[G/T]AGTTTGTCAGTCCATATTCATACATGGCAAGTTGCTCCAATGACCTGTGC
Long Flanking Sequence:
TTTAAATAGTTTATAATAATGAAACCGGAAACAAATTTGTAAACTTTTGTCATAAAACATTTACAGAAAAAATGAACACATTTACTTACTAATATGCATGTATTGTTGTTTGCTCAGGTGTTTTCACACAGGATTTGGCCATGTTTGGAAACAGCTGGGCTGAGGAGGAGCCGGAGTTAGCCAGATGTACTGTCGTTCCCTCACTCTACCCCTCACCATGTGCCACGCTGGATCCTCATGTCTTATTGGTACCTAACACAAAACACTCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATATATTCTTGTCCAACACCAACCAAAGTGTCATAATCAATGAAATGGGTCATTTACACCCAAACACATGGTTGATAAGGAAACTTGTTCTTCACTGCAGAAAGTGGAGGAAGTTTGTTCCACTCTTCTGAGGGAACCGTTCCAGTCCTGCCAT[G/T]AGTTTGTCAGTCCATATTCATACATGGCAAGTTGCTCCAATGACCTGTGCTTGTAAGTACTGGCATAAGACGCATCTACTGAAATTGATCACACTTCCTGGGAAGTTATAAGCTTGAATTGCAATACTGCTTTACTTTCCAAAGGTGTATACTAGATGCTCATTAGAATAATGCACTTTTTAGCTGTTGTGTATGTGTAATTGTTTCATCTGGTACAGGTCCGGTCCTAATGGTGCAGTTGTGTGCCAGGTGTTCACAGAGTATGCCAGAGCATGCGCCCATGCTGATCATCCGCTGCATGACTGGAGAACACACTTTCCTGTTTGCAGTAGGTCACATGATATCGCACAAATATTTGAATATATGTTGCAGATGTTGTTGCAGATGTTGCATATAGGTTGCATGTTGATTCTTTTCTCATATGAGTTTGTTATAAATTAATACATGGGTGGCACGGTGGCTCAGTGGTTAACACTGTTGCCTAAAAGCAAGAAGGTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21034
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 |
|---|---|---|---|---|---|
| ENSDART00000083804 | Essential Splice Site | 851 | 2794 | 21 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 40886257)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39222514 |
| GRCz11 | 7 | 39493531 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAAGAATATTATCCAGGAGACAAAGTATCTTCCCCATGTCATCAGTGG[T/A]GAGATTATGTTCACTTACATTCAGGTCTTCACACAGAGCTTTAGGAAAAC
Long Flanking Sequence:
GTTAACGCCTGTCTATCTGGGGTGTAAGTTTACTCAGTTCTAACGGACAGTGTGCTGGGAACTCTCTGAGACCCTCAGGCCAATGGAAATGATTCACAGCAATATTACAAGATCTTTATCAGCAAGAGAGAGAGAGACAGAGAGAAAGAAGCTCTTTGGATCTGTGAGAATCAGAATCGGCTGCTTTTCTCATGTGACAATTGAGATTTTTCTTTCATCTGTTCATCTATCCAAATATTCTTATCTCAGGTACTGTAGAATCCTCAGAAATCGTATTGGCATGGCTTCTGGACTCACACATGTGTGCTCACATGCATAAATGCACTTACATACTGTACATGCCATCCATCATGTTTCTGTTTTCTTTACACTGTGCTTATGTGTGTTTCAGGCTCCTGAAGCATGGCGATGAGTGTTTTAAGCCACGTGCTTGCCCATGTTTGTGGAAAGGAAAAGAATATTATCCAGGAGACAAAGTATCTTCCCCATGTCATCAGTGG[T/A]GAGATTATGTTCACTTACATTCAGGTCTTCACACAGAGCTTTAGGAAAACATTTGGAAAACATCATGGAATAACATTTATGTTCTAGTCTGCAGTTTTCAATCCTGGTCCTCATGACTCTCCGCTCTGCATATTTTGTGTGTCTCTCTTGTTTTAATATGCATATTTGGATTAGCAGATTGTTAGAAGAAATATCTACTGTATGAAGGAACTGTGTATAGACAAATATGCATATAAATACATATAATGCGTATAAAGCTTTATGAAGAAACTGTCTATAGACTGTGTGTTCCCTACCTACTGCTCTATACCTCCTGGACATTAGCTGAACTTGAAGAGCGCTTAATTGAAAAACAAAGATTTTTGCTAAACTGTTTGCAGCATCTTCAGACAAAAATGATTGTGTGAAGTATGAAGAGATATTTAACCGTAACCATGCTATTTGAATAAAAACTTTATTTCCCTTTGAATTGAATATGCTTTTTTCTAACTGGAATCTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10228
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 |
|---|---|---|---|---|---|
| ENSDART00000083804 | Nonsense | 956 | 2794 | 24 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 40882860)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39219117 |
| GRCz11 | 7 | 39490134 |
KASP Assay ID:
2259-9253.1 (used for ordering genotyping assays)
KASP Sequence:
CATGTGCAGAAYCCATCCAGTGTGATTGACAGGCAGAGAGYATATATCTG[G/A]CAGGCAGGATATTACACCATTGTACATCTGCTTGGGGAAGACCTCACAGT
Long Flanking Sequence:
TCTGTTATTCAGATATTTTGCATATTAGCCTGATTTTTCAACTAGATTGGACATGCTTAAGGAACAATTAAATTAGAAATGTGTCCATATATGGTATGAAATATGGTGTCATTGATATGAAATGATTTTATACAAATATTGTTTTACATTTTAAATGTTAATTAAAAAGAAATAAAAAAGAGTCCTGTTTGACTTAAATTTAAATAAATAAAAGTTTAATTTCTACTATATGTGCATCGAGATTTATATGGACTTTAAATGGTAACAGGTTGAGTAGTTAAAGTACTTAAGTTTAATTAAGTTACTGTTCAAAAAAAGTATTTGGTAAACCCTTACACCTTTAGCTTATTCCTATACACCACTGGGTATGAGTAAATACACTTTTTAATGCAAGTCATGATGATGTTTGACCTGTTTCTCTGAACACTGAATTAATTTGTGGCTATTGGTCATGTGCAGAACCCATCCAGTGTGATTGACAGGCAGAGAGCATATATCTG[G/A]CAGGCAGGATATTACACCATTGTACATCTGCTTGGGGAAGACCTCACAGTGCTGTGGGACAGAAAGACCACCATACACATACAAGCTGGACCACGCTGGCAGGTAAAAACACAATGGTGAATGTGTTACTAAATGTAAACATGTGAATTAGTTTTTCCAATTAACCATTTTCTTTTAGAGTTTTGATTACCGTACAAGACTGCATTTTTATTTTTTCAATTCTTAGGGCAGGCTTACTGGTCTTTGTGGGAACTTCGATCAGAAGACAGCGAATGAGATGAGAACACCAGAGAACATTGACTCGTCAACACCACAGGAATTTGGCAACAGCTGGACAGCAGCAGAGGCACGACAAACAGATAAATATACATGCAACAGCAATCACTTTTTTATAGTTGTTGGTGTGGATAGATCTTTCCCAACAAATAATTTGTCTTTTTAAGTGCCAGTGATTATGTAATGATAATACACAAGCAAAACGCAGTGTCTTAACTACATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18441
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 |
|---|---|---|---|---|---|
| ENSDART00000083804 | Essential Splice Site | 1069 | 2794 | 26 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 40880308)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39216565 |
| GRCz11 | 7 | 39487582 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGTGTGGGATTTTGCKCAGTGAAGTRTTTCMAGTCTGCCACCCTGTGG[T/A]AAGTCGATCACCTCTGAGTGGTTATCATTCCCACTGAGAGAAAATGTGCA
Long Flanking Sequence:
AATATAGCACAGATGTGGTCACCATGACCTGGGTTTAATAATTGAGGCAGTGTTGTTTTGCATTACAAATGGTTTTTAATTTAACCAAAGTTCAGGCAAGCAAGTGACATTATTTGTCTGATTTGCCATTTTTGGAGGTAAACAGCTGCCTATCTGAGGATGCAAACATTCTGATTCAAAACCAAGAAGAAAAAAAACACAATATGAACACATTTTAATTGGGAGCTGAAGGGGGAGAACAATTTAAATCAGGATTGGACCAGGCAATTACAGTACAGTAGATGAAGTTTGAAAGCACCCTGAGCACTTGTTTTGACCACACTGTGTGTCAGAAATCTGATGGTAGTAACACTTAAGAATGTTTTTGTGAATGTCTCATCAGTGTGTGAACAGTCCTGATATAAGGCACCCCTGCAATCTGAATCCACTTCGAGAACCCTTTGCAAAACGGCAGTGTGGGATTTTGCTCAGTGAAGTGTTTCAAGTCTGCCACCCTGTGG[T/A]AAGTCGATCACCTCTGAGTGGTTATCATTCCCACTGAGAGAAAATGTGCATGTGAGTGAGAAAGGGTCTCTGTGTTTAAAAGTGTTTGATGCTCTGTAGGTAGATGTCACATGGTTCTACATGAACTGCTTGGTGGACACATGTGGCTGTAACCGTGGAGGAGACTGTGAGTGCTTCTGCACAAGTGTTGCAGCATATGCTCACCGCTGCTGTCAGAAGGGCATACCTATTGACTGGCGCTCTCCATCTATCTGCCGTGAGTGACACCTCTCAATGACTAAATTCATAACAAATAAATATGCTTTAATGAAGAAACACTCTTCTAAAACTAACTGATAGATAACAGTAATAAGCAACTGAACATCTAATGGTTGGTTGATTCCTATGAAACAATGAGTAATACTTGCTTCTTCCTCCTACAGCTTATGACTGTGAATACTACAACAAAGGTGCATCTGCAATATTTGATAATAATATTTATTATTGTCTGAGATCTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21033
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083804 | Essential Splice Site | 1070 | 2794 | 27 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 40880209)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39216466 |
| GRCz11 | 7 | 39487483 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGTGAGTGAGAAAGGGTCTCTGTGTTTAAAAGTGTTTGATGCTCTGTA[G/T]GTAGATGTCACATGGTTCTACATGAACTGCTTGGTGGACACATGTGGCTG
Long Flanking Sequence:
GCAAGTGACATTATTTGTCTGATTTGCCATTTTTGGAGGTAAACAGCTGCCTATCTGAGGATGCAAACATTCTGATTCAAAACCAAGAAGAAAAAAAACACAATATGAACACATTTTAATTGGGAGCTGAAGGGGGAGAACAATTTAAATCAGGATTGGACCAGGCAATTACAGTACAGTAGATGAAGTTTGAAAGCACCCTGAGCACTTGTTTTGACCACACTGTGTGTCAGAAATCTGATGGTAGTAACACTTAAGAATGTTTTTGTGAATGTCTCATCAGTGTGTGAACAGTCCTGATATAAGGCACCCCTGCAATCTGAATCCACTTCGAGAACCCTTTGCAAAACGGCAGTGTGGGATTTTGCTCAGTGAAGTGTTTCAAGTCTGCCACCCTGTGGTAAGTCGATCACCTCTGAGTGGTTATCATTCCCACTGAGAGAAAATGTGCATGTGAGTGAGAAAGGGTCTCTGTGTTTAAAAGTGTTTGATGCTCTGTA[G/T]GTAGATGTCACATGGTTCTACATGAACTGCTTGGTGGACACATGTGGCTGTAACCGTGGAGGAGACTGTGAGTGCTTCTGCACAAGTGTTGCAGCATATGCTCACCGCTGCTGTCAGAAGGGCATACCTATTGACTGGCGCTCTCCATCTATCTGCCGTGAGTGACACCTCTCAATGACTAAATTCATAACAAATAAATATGCTTTAATGAAGAAACACTCTTCTAAAACTAACTGATAGATAACAGTAATAAGCAACTGAACATCTAATGGTTGGTTGATTCCTATGAAACAATGAGTAATACTTGCTTCTTCCTCCTACAGCTTATGACTGTGAATACTACAACAAAGGTGCATCTGCAATATTTGATAATAATATTTATTATTGTCTGAGATCTATTTCATTTTTACAACTGTGCATGTTTTTTTTTTTTTTTGTAATCCACATAGCTTTAGGGAAAGGGCCGCTGAAGCTGTTGACCTACAGAGAAAGGGGAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18470
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 |
|---|---|---|---|---|---|
| ENSDART00000083804 | Essential Splice Site | 1701 | 2794 | 34 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 40875009)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39211266 |
| GRCz11 | 7 | 39482283 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTCACTTCTGAGAAACCTCTGCTAACATCTACTGCAGCTGAAGAGGAG[G/A]TTGTTTCCACCACTCAAACAWCCACAACTACACATTTGACAATACAKCTT
Long Flanking Sequence:
GTCCAACTACTGATAGGGCTTTACAGACAGATTGGAGAGTAATCCAAACAACTTCAACTCAATTAGAATTAACAGAAACATCTCAAATCAGTGTCAGGACAGCAGAAACCCCGCTTACCACCTATACTACAATGCCACCCACCTGGGCACCTACAGAAGAAACAACAACACTGCTTACATCGCAAATGTCGCCCACTGACAAAACAACTTCTAGAGTTCCCTCCACTTCTACTACACTCGGCTATACAGAGTCCTCCTGGAGTTTATCTTCCACCACTTCTCTTTATACAGAGAAAGTCAGCACATCACCAATTCATCCTCATTATACTACAACTGTGGCCACCACTCCTGCACTGTCTGAGATTTCTTCAGCCTCACCATCCATACTTACATCATCAGTATCTCAAACGACATCAATATCTCAAACCCCAACAATAACCACAGAAACAGCTGTCACTTCTGAGAAACCTCTGCTAACATCTACTGCAGCTGAAGAGGAG[G/A]TTGTTTCCACCACTCAAACATCCACAACTACACATTTGACAATACATCTTGATACAGAGACAACTAAGGCTTCTCTTGACACAGATAGGGCTGTGATTACAACTGCTGCGACCGCCCAGACACCAACTTTGGTGCATGAAACCTCCAGTACCATTCCTTCCACAATGGCTCCAAGACTTACAACTCGTATCACACCGGTCTTAACCTCACGGGTAGGTGTAGATACCATTCGACAGACTCCACAAGATGTGGCCACAACTAGCATTTCACCTCCTACTAGGATTGAGACAACAATGACAACATCTACTACAGTTTCGACAGAAAAAGAGACCTCTGTTTCCACAACTATTCCAAGTACAGCTGCTGCTTCTAGCACACTTACAACACCCATACCTGAAATCCCAGAATTCACCTCTGGGTTTACAGAGTACACTGCTGTATCTGGTTCAACCACAACACTGCCTTCATTTACTGGAACAACTCCAACTCGAACTGGAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17990
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083804 | Essential Splice Site | 1702 | 2794 | 35 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 40874813)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39211070 |
| GRCz11 | 7 | 39482087 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTACCATTCCTTCCACAATGGCTCCAAGACYTACAACTCGTATCACAC[C/T]GGTCTTAACCTCACGGGTAGGTGTAGATAYCATTCGACAGACTCCACAAG
Long Flanking Sequence:
TGACAAAACAACTTCTAGAGTTCCCTCCACTTCTACTACACTCGGCTATACAGAGTCCTCCTGGAGTTTATCTTCCACCACTTCTCTTTATACAGAGAAAGTCAGCACATCACCAATTCATCCTCATTATACTACAACTGTGGCCACCACTCCTGCACTGTCTGAGATTTCTTCAGCCTCACCATCCATACTTACATCATCAGTATCTCAAACGACATCAATATCTCAAACCCCAACAATAACCACAGAAACAGCTGTCACTTCTGAGAAACCTCTGCTAACATCTACTGCAGCTGAAGAGGAGGTTGTTTCCACCACTCAAACATCCACAACTACACATTTGACAATACATCTTGATACAGAGACAACTAAGGCTTCTCTTGACACAGATAGGGCTGTGATTACAACTGCTGCGACCGCCCAGACACCAACTTTGGTGCATGAAACCTCCAGTACCATTCCTTCCACAATGGCTCCAAGACTTACAACTCGTATCACAC[C/T]GGTCTTAACCTCACGGGTAGGTGTAGATACCATTCGACAGACTCCACAAGATGTGGCCACAACTAGCATTTCACCTCCTACTAGGATTGAGACAACAATGACAACATCTACTACAGTTTCGACAGAAAAAGAGACCTCTGTTTCCACAACTATTCCAAGTACAGCTGCTGCTTCTAGCACACTTACAACACCCATACCTGAAATCCCAGAATTCACCTCTGGGTTTACAGAGTACACTGCTGTATCTGGTTCAACCACAACACTGCCTTCATTTACTGGAACAACTCCAACTCGAACTGGAACAACTACAACTCCTGTGGCGTCAGTTCTTACCCAGACTACTATTTCAACACATCTACCTACTTCCTCTATTGTCACTACAAGTAGTCCCATAACCAGCTCAAGTACCTCTACAGAACACCATCTGGTGGATGAAAGTCCCATGGTCACAACTCTGCCACCTACTCCAGACACTGCCCAAACAACACGAAGTACATCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44672
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083804 | Essential Splice Site | 2123 | 2794 | 40 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 40871652)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39207909 |
| GRCz11 | 7 | 39478926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACATTCCTCACTCTTCACATCTTTCATCTTTCTCTTTGTCACCCTGTCC[A/T]GGTAGTTGTGATGGTAATCCATTAAATGATCTGACTCTGTCTAACGGTAC
Long Flanking Sequence:
TTCCAGCTTGTGTGGAACTTTACTAATTTGTGTCTGGCAGCTTTAAACATCACTCACAAATCTAACGAAGTTCTTGTGAATCGTCTTCAGAGACGTGTGAGTATCTATCAGTTTGCTTTTTTTGAAAAAAGATTTTTAAATGGCTTAAATAAAACCTATTAATGAGTGGAAGAGATTCAAAGGTTCACTGTGTTGTTTTTTCAGCTGTATGTGAACTCTAGGTATGCAAAGCCACGTTTTAAGAAGTATGGTTTTGAGATTCTGGACACAGGAAACATGTACCTTATACGGAGTCCAGCTGGTTTGAAGATCCAGTGGTTCCACACTACAGGCATGATGGTGATTGAGATGGACAGCTATAACAATAGACTGCCCACGATGGGATTGTGTGGTATGAAACCAATAACTGCACATCTTATCCACTCTCAAGAGAATAAAATCATCTGCTTCCACATTCCTCACTCTTCACATCTTTCATCTTTCTCTTTGTCACCCTGTCC[A/T]GGTAGTTGTGATGGTAATCCATTAAATGATCTGACTCTGTCTAACGGTACAGTTGTGCCTGAGCAAGAGGATCCAGCCGTATTCATCGATAGCTGGCAGATTCCCAACACCACCAGCTACGTCAGCAACAGCAGGCGGCGAGAAGTCAACTGCACCACCAGTGACTGCTCTCAGTGCTTTAACATGCTGAACAACAACACCTTCACCCTCTGCCATGCTTATGTATGACACACCAAATGCACCTGCCTCAGGTATCAACCACATCTTCAGAACACTTACTGGAGTTTGTGTTGCAGGTTCCTCCAGGAGTGTTCTGTGAGATGTGGGTGAGAGATGTGGAGTATGTCAATAATCCGTGTATCGCTTTGGCTGCTTATGCTGCTTCCTGCCACAAATTCAACATCTGCATGGAATGGAGGAGCTCTGATTTTTGCCGTATGTATGCTCAGGCATTTTAACACTGCTTTAACTAGCCGTTTGTTTTATGGCTGTATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40966
Status:
Mutation detected in F1 DNA
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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 |
|---|---|---|---|---|---|
| ENSDART00000083804 | Nonsense | 2248 | 2794 | 42 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 40871036)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39207293 |
| GRCz11 | 7 | 39478310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTCTAGAATAATGCTTGGGTGTTTTTCTGTGTAGCATTCGTGTGCCCA[G/T]GAAACCTTCGGTACCAAGCATGTCTGCCTGCCTGCACTGCCCCATCCTGT
Long Flanking Sequence:
GCTACGTCAGCAACAGCAGGCGGCGAGAAGTCAACTGCACCACCAGTGACTGCTCTCAGTGCTTTAACATGCTGAACAACAACACCTTCACCCTCTGCCATGCTTATGTATGACACACCAAATGCACCTGCCTCAGGTATCAACCACATCTTCAGAACACTTACTGGAGTTTGTGTTGCAGGTTCCTCCAGGAGTGTTCTGTGAGATGTGGGTGAGAGATGTGGAGTATGTCAATAATCCGTGTATCGCTTTGGCTGCTTATGCTGCTTCCTGCCACAAATTCAACATCTGCATGGAATGGAGGAGCTCTGATTTTTGCCGTATGTATGCTCAGGCATTTTAACACTGCTTTAACTAGCCGTTTGTTTTATGGCTGTATATATATATATATATATATATATATATATATATATATATATATATATCATTTAAATGCAACATGTAGTGTTTTTTTCTAGAATAATGCTTGGGTGTTTTTCTGTGTAGCATTCGTGTGCCCA[G/T]GAAACCTTCGGTACCAAGCATGTCTGCCTGCCTGCACTGCCCCATCCTGTCCAAACCAAGAGTTTGAGTTTGTCCCAGAGCAATGCACAGGCCTTTCAGAGGGCTGTGTGTGTCCTGAGGGGACTCTATTACACCGGCCCTATTCAGCCCTCTGCATTCCACCCAGCAAGTGTGGTATGACCCTAGTCTTTTTCTTTCTTTTTCTTTATTCAAAAGTGCAGTGATTACTGAGAAACGCCTTTGATATTTGAAATCAACACCAAAACAAATAGCTCAACCAGAATGAAATGCATCTCTCCCTCTGTTTTGTTTACATAAGTTAAGATAATGAATGGTGAAGGAAATTGTTTTTGTGCATGTTTGAAGTATTTCTATTGCTCAGAAAATTCTCTTACTGCACCTTAACTTAAAAGTTCACCCCAAAATAAAAATTCACTCACTATTAACCCAACCTTGTGTGCTTCCAAACCTTTCTGTTGATCTCAAAAGAAGATATTGGT
Associated Phenotype:
Not determined