ZMP
mtor
Ensembl ID:
ZFIN ID:
Description:
serine/threonine-protein kinase mTOR [Source:RefSeq peptide;Acc:NP_001070679]
Human Orthologue:
MTOR
Human Description:
mechanistic target of rapamycin (serine/threonine kinase) [Source:HGNC Symbol;Acc:3942]
Mouse Orthologue:
Mtor
Mouse Description:
mechanistic target of rapamycin (serine/threonine kinase) Gene [Source:MGI Symbol;Acc:MGI:1928394]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38710 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21374 | Essential Splice Site | Available for shipment | Available now |
sa16755 | Nonsense | Available for shipment | Available now |
sa34485 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31678 | Nonsense | Available for shipment | Available now |
sa30906 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41292 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11792 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38710
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 |
---|---|---|---|---|---|
ENSDART00000075189 | Nonsense | 420 | 2515 | 9 | 58 |
ENSDART00000122801 | Nonsense | 420 | 2563 | 9 | 58 |
Genomic Location (Zv9):
Chromosome 8 (position 48456484)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46294742 |
GRCz11 | 8 | 46302621 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCACCTGCTGGGCTGCCTAAAAAAAGAAAAGGAGCGGACGGCAGCATTT[C/T]AAGCGCTGGGGCTACTGGTGGTGGCTGTGAGGGCTGATATTCAGCCATAC
Long Flanking Sequence:
TGGCGTTGAATAAATGTACAATCTGTACATCCTGCATTTAGCATTATGACGAGCTGTTAGCTGATTGAATGCATAGCTGCCTTTTTCACAGAAAGCTCATTTACTTTTTCTGCATCTCTTCTTTTCAAAATAAGAGTCCCACATACACTAATCCAAACTTAGATGAGCTTAAAAATAAAGGAAACAAATACATTTGTTGTGATCTCAATAGGAAACATTTTGGCCAATGAAACATAGTGTGCAGTATCCGTAACAGTTGTTTTTTTGTTCAGATTGGCCTGCTTTTCACTGCAAATTCAGCATTTTCTAAGTATATCCAGATTTTCATTCTATGGCATCTTTAAGGACATCCTATGCACATTAAACAACATATTATTTTGTTTTGATTGTTTGATTTCATCCTATGTACATATTTTTAATCCTCAGATCAGTATTTGCAGGACACTATGGGGCACCTGCTGGGCTGCCTAAAAAAAGAAAAGGAGCGGACGGCAGCATTT[C/T]AAGCGCTGGGGCTACTGGTGGTGGCTGTGAGGGCTGATATTCAGCCATACCTAAGCAAGATCCTGGAGATTATCAAAGCTGCATTGCCACCGAAAGACTTTGCGCACAAGTAAGAACCAAGAACCATCTAAATTGGAAGACTGTCAGTACATACAGTAGCTCACTTCTAAACAGTAGCTGAAGTAATTCAAAGTGCTGACCTTGAGTGGGAAATTTTCTCTACTTGATCTTTTCTTTACTTTAAACAATGATGGAGTTATAACATTTTACGGGGGCATTTATATACATATCGGGGCATATGTAGCTCCTTAAAAAAAGAAATATATTTTATTGTAGTTATAAACTGTTACGTTCCCCTCAACTCTGTCTAAGGGGACACGGGTTTTGTGTGTGTGTTTTAGCATTAAGGTCCTATGAGCAACCTTATAAAGGACCAAACAAAAGAAATATGCAACCTGAATGAAGATTAACAAAATATTTATTGAAGGATTAAGGAAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21374
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075189 | Essential Splice Site | 910 | 2515 | 18 | 58 |
ENSDART00000122801 | Essential Splice Site | 910 | 2563 | 18 | 58 |
Genomic Location (Zv9):
Chromosome 8 (position 48429356)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46267614 |
GRCz11 | 8 | 46275493 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGCTTCTGCCGTCAGCCTCTCCGAGTCCAAGTCCAGCCAGGATTCAGG[T/C]AATCAGATGCACCCGCTAACGAAAGCTCGCATCAACACAATTACTCACAG
Long Flanking Sequence:
TAACCTAGTTAAGCCTTTAAATTGCACTGTCATTCTAGTATCTTGCACAATATTATGTACCACATCATGGAAAAGACAAAAGAAATTAGTTGTTAGAAATTATATATCTTATAAAAATATATTTTAACATTTTCTCTTCAAAAAACAGGTTGATGTTCTTGTTAAAAAACTAAATGTTCTTGGTACTTTGTAATATAAAACCATTTGCATTTTTGCCACTAGGTTGAAGCTTTTGCAGCTTTTTGCAACAACTTAATTGTTTCATGTTCAATCAACATAAGTCAACTTAATTCCTTCACGTTGTCCCAACACAGATTGATTGTGTTGAACCCAGTATTTTTAACAGTGTGCTCCTGTCCCTCTCCTCAGGCCATTCGTGTTCTAGGTCTGCTAGGAGCTCTGGATCCCTACAAACACAAAGTGAACATCGGAATGATCGACCAGTCTCGAGATGCTTCTGCCGTCAGCCTCTCCGAGTCCAAGTCCAGCCAGGATTCAGG[T/C]AATCAGATGCACCCGCTAACGAAAGCTCGCATCAACACAATTACTCACAGATGCATAGAAGTGTGTGTCCGCCCATCTGATACATACATTCTCCAGCGCAAACCGAGCACATCTTCATAGACCGATTTCCCTTTCCAGTGACACAGCCAGAATTTTTTTGTTTCGCCTTTCACAAAAAATTAGCACACACATTTCATCCTTTTAATCATTACATTTTTTGAGTCTCCATTCCTTGCTTTTGTACACCATGTTTTTTTTGTCAAGTAAAATGAAATTTGATCAAATTATGATTGCATTTTCTTAAGAGGCCTGTTTGCTTTCTACCCGTGTCATCCTTTTGCTTATTCCATGTGCATGTTCCTAAAAGTCAGAACAAATAGTTCTCCATTATCTGACGAAAACGGTTTGCCTCTCACTGGCTTGAACGCTGTGTTCAAGTACAACATGTCCACTATTTCTAAAAACAGTCCCTTGATAGAATGTTGAATAGGGTCAATTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16755
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 |
---|---|---|---|---|---|
ENSDART00000075189 | Nonsense | 930 | 2515 | 19 | 58 |
ENSDART00000122801 | Nonsense | 930 | 2563 | 19 | 58 |
Genomic Location (Zv9):
Chromosome 8 (position 48419091)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46257349 |
GRCz11 | 8 | 46265228 |
KASP Assay ID:
2260-1081.1 (used for ordering genotyping assays)
KASP Sequence:
ACCAGCGAGATGCTGGTCAACATGGGCAACCTGCCGCTAGACGARTTTTA[C/A]CCAGCAGTCGCCATAGTGACCCTGATGCGTATCCTGCGTGACCCGTCKCT
Long Flanking Sequence:
TTTGTACTCAATGTCAGAAGTGTCAATCTCAAGCACTAGATAAAAATCGGTATCATTATCAGCTCAAATAAATGCTAGTTGTGCATCTCTAGTATTTATGAAATTTACCAATATTGTATCGGTATCAGACTTGGTAAGACTTGTATACAGGAGGTATCAGACTTGGTTTTGGTTGCATGTTGTTGTTTTTTTGTTAAAATCTATAACACAATAAGGCCAAAAAATACTATTTCTAGTATTTATGAAATTGACCAAAATTGTATCGGTATTGTAATTGTTTGAATGTTTTTTTGTGTATCTGTATCGTTATTTGCCCAGTTATGGGTCGTTATCGGGCCCAAACGTATTATGCATACTTTTATTTATATACATCTCACATGAAAGCAATCACCACTCATATTTTGACATCTAACATGTTGAATATGATTGTTCTCAACAGCTGACTACAGCACCAGCGAGATGCTGGTCAACATGGGCAACCTGCCGCTAGACGAGTTTTA[C/A]CCAGCAGTCGCCATAGTGACCCTGATGCGTATCCTGCGTGACCCGTCGCTGTCCAATCACCACACCATGGTCGTTCAGGCCGTGACCTTCATTTTCAAATCTCTTGGCCTCAAATGTGTGCAGTTCCTGCCTCAGGTCATGCCCACCTTTCTCAACGTCATCAGAGTGTGTGATGCCAGCATCAGAGAGGTACAATACTGTCCCACTGCATTCTACGTTATCTAAAGTCACCTTAATAACTAAATGAATAATTTGGTACAATCCACTTATTATGTACATACCTGTTTTTACATTGTACTTATATTTGAAAAAAAGATTTGCATGTAATTTACATCTCTAATTCTTTTGTGTTTTTAAAGTACACTGTTGTACACCTTAATCAATCGTTAAACCTACCCACACCACTAAACATGTCTCTAACCTTACCTGTCTCACCTAAGTAGCACCCCAATTGTAGTGCATTACAATATGAAAAGTACATTGCACTTATTTTTTGAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34485
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 |
---|---|---|---|---|---|
ENSDART00000075189 | Essential Splice Site | 1170 | 2515 | 23 | 58 |
ENSDART00000122801 | Essential Splice Site | 1170 | 2563 | 23 | 58 |
Genomic Location (Zv9):
Chromosome 8 (position 48397798)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46236056 |
GRCz11 | 8 | 46243935 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCCTCCATGGACACACTGTCCTCGCTGGTCTTCCAGCTTGGTAAAAAG[G/A]TACAAGCTCTAAATCTACCCCAAGTCTGTCCAATAGTTATAGTTGCGTAT
Long Flanking Sequence:
CAGATGTGTTTTCTATTCTCTCTGTCCTGTTTTTTAAAAGCTTCAATGGTCAATATATACAAAGTAGGACGAATAATAATACATTCATAATTTATTGCAAATGAAGCAAATTAGGTGTGTACATTTGCCACATCAAATGAAGATAAAAAAACATAAAGATGGAAATATGCTCAGAAATTATAGCTGCTCGATTATGGGGAATACTGTAATCATGATTATTTTGGTCATAATTGTAATCATGATTATTTAAAACGATTATCAGTGGGCATATAGTCATATATTGACAGTTTAACTTAATGTTTTTAATTACTTTTGATCATTTCTTTTTGTTGTTTAGGGTTGCTTTGGAGACTTTAGATCGCCTGACTGAATCGTTGGACTTCACGGATTATGCCTCCAGAATTATCCACCCCATTGTTCGCACTCTTGATGTTACTCCAGAGCTGAGGAACTCCTCCATGGACACACTGTCCTCGCTGGTCTTCCAGCTTGGTAAAAAG[G/A]TACAAGCTCTAAATCTACCCCAAGTCTGTCCAATAGTTATAGTTGCGTATGTAATATTTCAGAGCATTATCTTTTTGGGTGCGGTGCCTCTAAAGATGTCTTAACGGTTTGAAAATAAACTTTTAAACCAATTCCCGGAGTTTTATGTGATGAAGTAGCTGTGTAATTATTTCCTAGTGTCTCGCTAATGCACAAAGAGGCTTTCAATCAGAGACAGGGATGAGGTCATGGCTTGAACCATTCTTCCAAAAACCCTTTTAAAATTACCAGTCAACATGTGGCCATCATGAACACCAGACGCATGTTCTGATCCCTTTGATCACTGCAGGCCACGATCCTCGGTTTCCTGTGTTAGAGGAGCAACGCTTTATTTGTGTACTTCCTACTTGATGGGCTTTTAGGCACATGCATACACATGTGCTCGCATTCATTCCCGACACCATTTTATTATACCGTATGGAATCAAAATAATCATTTCAGTATGCTTACCCTCCCATTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31678
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 |
---|---|---|---|---|---|
ENSDART00000075189 | Nonsense | 1266 | 2515 | 26 | 58 |
ENSDART00000122801 | Nonsense | 1266 | 2563 | 26 | 58 |
Genomic Location (Zv9):
Chromosome 8 (position 48387508)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46225766 |
GRCz11 | 8 | 46233645 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGCATGGGGTGCAGCCAGAAAGGTGTCCAAAGATGACTGGCTGGAGTG[G/A]TTGAGACGACTTAGTGTGGTCTTGCTAAAGGAATCCTCCTCACCAGCCCT
Long Flanking Sequence:
ATATTGAAATATGTTTTTTTCCCTTATAATTCAGGACTAGTATTTCTGATTTCAACTGTATATATTTTCATTTGAGCCACATCTGTCTTCAGAAGCACACTAGATCATCCTTTTCAGACAGAGATAGTGTACATATGTCCTCTGGGCGCACTATTGAAGGCATTGTCTGTTGTCTGCGATTCGTGAACGCATCATAATTACTCACAGGTGTTCCCTGAGAGCTTTTTCCACTGTCTTCCGAACCATCGCATTCAATTTCAAATATTGAACATTCACCCATGGATGGACTCAACAGCCTAGAGTGTCTTTTGTCTTCATTTAAAAAAAAAAAGAAGGCACACATACAAAGGTGCCTGAATGCTCTCTGTGTAGTAGCGTGCAAGGCAGATGACTAGATCAGAATTCATCACACATGTTTTGTCTGTGTATTAGTTCTCTTTCTGCTGTTTGCAGGCATGGGGTGCAGCCAGAAAGGTGTCCAAAGATGACTGGCTGGAGTG[G/A]TTGAGACGACTTAGTGTGGTCTTGCTAAAGGAATCCTCCTCACCAGCCCTGCGCTCCTGCTGGTCTCTAGCACAGACGTATATACCACTGGCTAGGTAAACTTTACCTTCTTTGTCTGTTTTTCTACTGAGGTACCATTTCAGTAACAGGCCCAGTGTTCATATGAAAGCTTGTGAAAATATATATTCAAGCCCTGGAAATCTAGAGTGCATAGATACAGTTTCTTGAATTTATTTTGTTCAAGACGTTTTTGCGACGGATACAAATCTTTATTTTTTTTTACTGGTCCATTAATATGTTATTTTTACAACATGTTAGTTATGCACATTTCCATATTATGTTAAAGGAACCCTCTATTTTATTTGGAATTCTGGTGGGAGAATCAGATCATTAAATCGGATTAAACCATTAGCATCTCAACAAATGTTTCAATAATTTTGCTATTGAATGCTTGACTATTTTGTAGTTTGTGTAGAAAATAGAAAATGTATATATTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30906
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 |
---|---|---|---|---|---|
ENSDART00000075189 | Essential Splice Site | 2038 | 2515 | 44 | 58 |
ENSDART00000122801 | Essential Splice Site | 2038 | 2563 | 44 | 58 |
Genomic Location (Zv9):
Chromosome 8 (position 48268031)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46106289 |
GRCz11 | 8 | 46114168 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGATGGAGAGAGGACCACAAACCCTAAAAGAAACATCATTTAATCAG[G/A]TAAAAACGCTCATAACTCACTGTAAAGTCGAATTCCGTATGTAAGAGACT
Long Flanking Sequence:
CACACAGAAACGCCAACTGACCCAGCCGAGGCTCGAACCAGCAGCCTTCTTGCTGTGAGGCGAGAGCACTACCTACTGGACCACCGCGTCACCCCAATACAACCACAAAAATACAAATAATAATTTAAGCCACGGAACAAAAAACAACCCAAGTAGTTAAAAGTAATCCAACTCGAGGACTTGGCAGCCATGATGGTGGGTATGGTAGCAGCTTTGGTAATTGCTATTTTTAAGCTTAGCCAAGGATAAAAACACAATCCGAAACATCTGCCAAAAATCCAAATCCCCACATGAGCACTGTTTCTACCCATGTTTAGGTGAGCGAGGAGCTTATCAGGGTCGCTATTCTCTGGCATGAAATGTGGCACGAGGGGCTGGAGGAAGCGTCACGTCTATATTTTGGAGAGAGGAACGTCAAGGGAATGTTTGCCGTTCTGGAGCCCCTCCATGCCATGATGGAGAGAGGACCACAAACCCTAAAAGAAACATCATTTAATCAG[G/A]TAAAAACGCTCATAACTCACTGTAAAGTCGAATTCCGTATGTAAGAGACTTTTATAAGCTAATAATGTCATGTTACAGTTAAATCACCACTGTTAAGGAGTATTTTGAGTCCAGTAAAATCACTTCACCACATGATTTATTGTGTATATTCTGTTTGTATATCAGGTAATAGTTCATTTTACAGTGTTGATCTTATATACAGTAGATGGAAGGCGTAATCATTATTACAGTAGGAATAAGGATGTTTCCAATAGTAACTTTTCACGTTAGTTCATAATACATTAGGATTACACTTTATCCATTATTTTTGGTGTCTTTTTAAATGCAAAAACAATAATAACAAAAGATTGGCTTTTGTTATAACAAATATTTTTGGATCTTTGACATTTTTAAAAATTCATCTTTGCACATTTGAATTAAGACTTGGAGAACTTTTGTTTTATACCCAAGTTTTAGAAAGCAGATTCCCACCTGAAGTTTGTATTCCATGAGCTCTCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41292
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 |
---|---|---|---|---|---|
ENSDART00000075189 | Nonsense | 2221 | 2515 | 48 | 58 |
ENSDART00000122801 | Nonsense | 2245 | 2563 | 48 | 58 |
Genomic Location (Zv9):
Chromosome 8 (position 48253069)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46091327 |
GRCz11 | 8 | 46099206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGGTTCCTCACTGTGACACGCTGCACGCACTGATTCGAGACTACAGA[G/T]AGAAGAAGAAGATCCTGCTCAACATTGAACATCGCATCATGCTCAGGGTA
Long Flanking Sequence:
TAGCGTCAACGCTTGACTGAGGGCGTGTCTGAAGATGGGGCTGACATGATTATCCTAACAGCGTCAAATGAAATTTGTCCCCAATTGGCTACTGTCATAGCTGGGGTATTTGCATGAAGCAATCTGATTGGCTGGCAATTTCGTTGGCACTTGAAAAGTTGAGAAATCCCCAATTTCTGCAGCGAGCAATGAGCAATGAACGTCATTGATTCAAAGGGAATGGAAAGCGCTGACGCCCTGTGTGAATGAGGCGTTACAAGTCTTGAGACTAGTGGATTTGTCCTATTTCTAAATATCACTAAGCTTATGGTGTAGTTACATTTTGATGTTGTCATTTTTGTGGCTCATGTTTTGATTTTTTTCTCTCTCTCTATCTCTGATAAATGTTTCTTTTGAGCAGTATTCAGCGCTATGCTGTGATCCCGCTTTCCACCAACTCTGGCCTGATTGGCTGGGTTCCTCACTGTGACACGCTGCACGCACTGATTCGAGACTACAGA[G/T]AGAAGAAGAAGATCCTGCTCAACATTGAACATCGCATCATGCTCAGGGTAATGTGTCAAACCCTAAAATTATTTTTTTACTGTAAAATTACTGTACGGTTTCTTGCTGTATTACTGAAAATTACTGTATCCTACTGTATTCATTTTGACCGGAAGTTGCTGCAACTTTTATTTCACGACTTCCACATGAAGTTGAATGTTGTTAAGGGGGCGGAGCTTTTTGTGCATCATTTCCTCATACTAATGGTAATAGAGGCGTGGTTAAGAATATTGTGGCTGAAGCCACCAAACTGACATCAGCAGTGAAAGACCACCACTCCAAAGTTTCAAACGGTTGGACGTTGACACTAAACGTAGACCTTATTAGACCTTAAAAACTTAGGAAAATGACTGTATTGTGGAATATCAATGGAAAGACATTTTAAAGTTAGTCCACTCCTCCTTTATATGCGCCAGACATGACCTAATGCAATGTGAGGTGCTCCACAGAGCTCACTTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11792
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075189 | Nonsense | 2435 | 2515 | 55 | 58 |
ENSDART00000122801 | Nonsense | 2483 | 2563 | 55 | 58 |
Genomic Location (Zv9):
Chromosome 8 (position 48242917)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46081175 |
GRCz11 | 8 | 46089054 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTCGTGTAGAAGCCATGGAGGGTATTGACCTGGGAGAAACAACGCAC[A/T]ARAAGCCTGGAACTACMGTGCCTGAGTCCATTCACTCTTTCAGTAAGTCT
Long Flanking Sequence:
ACAGTGAGTACACAACCTTTACTTGTTCAAAACCATATCAGAGTCATGCAACTGATGCTTCTCCGTCTTACAGCAAACACTAAAGGAAATAAGCGATCCCGGACCAGAACTGACTCCTATACTGCAGGACAGTCTGTTGGTAAGCCTTGGACTTCATCTCCATTCCAATTATCAGCAGCAAACTAAATTAAACTCTGTGATGAAATGAAAATTGACAGTTTTATTTGGTGTGTTTTTCATGTCAAAACTTGTTGTCAACTATGATATGCTGTTACTAGTCCTTCTGTACAGTACAGAGATTTACTAGAAATCCCATATACTTTGCTTTCATTTTTTAGAATGCCTCATAATGGCAGTGGCATACATATTTAAGTGCTCATGTTCATATAGAATTTCCATCAAAACTAACGTTCCTGGAAATCGATACATTTTTGTGGTATGTTTTTGGTATGTTTCGTGTAGAAGCCATGGAGGGTATTGACCTGGGAGAAACAACGCAC[A/T]AAAAGCCTGGAACTACCGTGCCTGAGTCCATTCACTCTTTCAGTAAGTCTTTAAAGTGTCTTTGTTTGTTGTCTTTGTTGTTGTTTAATTATTGATATTATTGATTTCTTGTAATGGAGGGTTTGTAAGAAAGGCCCAATCCCAATTCTATTTTGTACCCCTTCCCCTTGGCCCTTAAAATCGAGGGTGAAGGGGAAGGGCTTCAAAATTTACTCGTAAGAATTGGGACAGCGCTACAGCACCTGCACACGTCATCACATGTCGTTGCGATCTCTTGCTTCATATGAGATCAGACGATCTCGACTGCTGTAGTTATTCCAGTTGGGTTATTTTTTGGTATTTATGTTCAGGAAATCTCTGAACGATCTAATGCGGCAATAAGATCGTAACTATACTGTGCATTTACTCTATGGTCATATTCAGCAATGTAAACACACGAACCCAACATTAACATTATTGCAGACACTGTAAAAAGCTCATTCACAGCCACTAGACATTAC
Associated Phenotype:
Not determined