ZMP
si:dkey-120e24.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
RICTOR
Human Description:
RPTOR independent companion of MTOR, complex 2 [Source:HGNC Symbol;Acc:28611]
Mouse Orthologue:
Rictor
Mouse Description:
RPTOR independent companion of MTOR, complex 2 Gene [Source:MGI Symbol;Acc:MGI:1926007]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18403 | Nonsense | Available for shipment | Available now |
sa14901 | Nonsense | Available for shipment | Available now |
sa23914 | Nonsense | Available for shipment | Available now |
sa3126 | Nonsense | F2 line generated | Not yet available |
sa37289 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1469 | Nonsense | Available for shipment | Available now |
sa23915 | Essential Splice Site | Available for shipment | Available now |
sa43626 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18403
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 |
---|---|---|---|---|---|
ENSDART00000058311 | Nonsense | 55 | 1724 | 3 | 38 |
ENSDART00000142961 | Nonsense | 19 | 1698 | 1 | 36 |
Genomic Location (Zv9):
Chromosome 21 (position 20029273)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21164762 |
GRCz11 | 21 | 21201398 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCCCTCCGAGAACATGCGAGAGATCCTGCAGAATGTGGCCAAACAACAA[G/T]GAGTCTCCAACATGCGGAAACTCGGCCATCTTAACAACTTTATCAAGGTT
Long Flanking Sequence:
CTATTTCAGAAAAAACATGTATAACAAATGTTTATGTATAAATAAAATCTAAAATGTAACTTCATAGTGTGTGTAATTTAAGTTGAGATGTCAGCTTTGATGATTCACTGTTGCAGTGTGGTAGAGATTTATCATTGGTTCCTGATGCATGCTGCAATAAAACTCAGCAGAGGGTGTTATTTATGAGATCGATTTTCTGAGATGACAGGAAGTTACATCGTGTTTAGGAAACGCACTAAATCTAAATAGCTTTTGTGTGCTTTCTAATGTAACTGTTCTCTTTATTTATTCAATCGTGAAAATTGATCTCTGCTTCTTGTGGTTTTGTCACACCAACAGTGGAAATGTTTTGGTCACTAATATCTTGTGGTTCTAGACCAAACATAATGTCTTTTTGATGACTTCACAACTCGCAGCTCTTGCTTCATTTGTCCTCCTGTTTTCTTCCAGAGCCCTCCGAGAACATGCGAGAGATCCTGCAGAATGTGGCCAAACAACAA[G/T]GAGTCTCCAACATGCGGAAACTCGGCCATCTTAACAACTTTATCAAGGTTTGTTAACTCAAAAGTTGGTCAGGAGTTGCAGAATGGGATATACAGCATATATGCATTGGCTCAAGATCGCAGACCGAGTGCCTTAGTGCCCTAGCAGTGCTGATATATAGCCATATTGCACTGCTACTTGTGTGATATTTCGTTTATGCAACAGTTCAACGGCATAATTGTATATAAACAAATTACAATTAAAAAGCAAAGCAAACACTAATAGATTACTTAGAAACTTAGAATGTCACTTACCTGTTTTATAATGATTTGTTCAGCTGTAGTTTGAAACTGACGCTGAGAAAACACTGAGTGTTTCTTTCCCTAAGGACTTATTATGCGGTCTTTGTCATCAACTTGTGGCGGAACGTCAAGCGTCAATTTCTTTGCTCTGTTCAATATGACAGATTAATGCCGCTGACGTGCAAAACATTTTTAAATAGGCAGTGTCTTTACAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14901
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 |
---|---|---|---|---|---|
ENSDART00000058311 | Nonsense | 132 | 1724 | 5 | 38 |
ENSDART00000142961 | Nonsense | 96 | 1698 | 3 | 36 |
Genomic Location (Zv9):
Chromosome 21 (position 20036045)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21171534 |
GRCz11 | 21 | 21208170 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCAGGGACAGTAATATCCTTCAGAAGGTGTTGCGTCTCCAGGTGGATTA[C/A]CTGATTTCCAGGTCTGTWMCACGTTTTATTGCACTAAATKGGGGTCAGCT
Long Flanking Sequence:
AATTCAGGTTTTCCTCAAACACGACTATGAATCATAAATTCAGAGAAATTCTGCATGTGGTGTTTAAATTTATTCAATTGCTGTGTTTTAAAAAATGTTTGAATCGTGGTAAAAATATGAGCCTAAATAATAATATTTTTATAATAAATATAAACTTAAATATAATATAAATAAGTAATTTAAATATAAATAAATATTCCTGTGGATGAGTAATGAGAGAGCATTAGATTTGATTTCATTACTGTGAATAAAAAAATGGATTAATTATGCACTTCTGAAATGATCCTGATCCAAAAAATAAATAAATGCATAAAACCATTAATTCTCAGTAAATATATGATGGGAATGATGTTAAATGCAGTGCGTTGTTATTTCCACAGCCTCAGGTTGGCTCTCCTCAATGAGGCTAAGGAGGTTCGGGCGGCTGGCTTGCGTTCTCTCCGCTACCTCATCAGGGACAGTAATATCCTTCAGAAGGTGTTGCGTCTCCAGGTGGATTA[C/A]CTGATTTCCAGGTCTGTTACACGTTTTATTGCACTAAATGGGGGTCAGCTATTTTAGCTGTTAAATTCATGTCTAAGTTTGAAATTGTGGGCTAGAAGCTAAGCGTTTTCATCAGAAGCTTGATTTGATGCTAATGTGTGCCGAGTTGTGGATCACCTCTTGTTAGCGTCTCATCCTATGTGTGTGTGAGAGAAGGGCTGTTCATATGATGAGCTAGTCAAGTCTGGTTAAGGTTATTTTAAAGCATTTTGAGCAGGATTTGCTACTTTTTTGTATCCTGCTGTAGGTGGATAACCATGTAGCTTTGGTTCTTTTTTTTGTCCTGTCTGAACATACACAACAAGTCAGGTCATTGAATTGGAAAATGAATAAATAAGAATGGCTGTAGAACACATGTGATTGAATCTTTTTTGTGGATCATTTTAGAAACTACATTGACTAGCTGTGTTGACTGGTTAGCGTAATGTTATCTAATGTGATCTTTTGACCTGTAGGTGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23914
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 |
---|---|---|---|---|---|
ENSDART00000058311 | Nonsense | 482 | 1724 | 17 | 38 |
ENSDART00000142961 | Nonsense | 446 | 1698 | 15 | 36 |
Genomic Location (Zv9):
Chromosome 21 (position 20045872)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21181361 |
GRCz11 | 21 | 21217997 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTTTGGTTGTGTTTTGTAGACGGGCGAGTGCTGCGGTTAATTACTTG[A/T]AGAGATTTCATGAGAAGAAGAAGCGAGGCCCCAAACCCAATAGTCTTTAC
Long Flanking Sequence:
TGACTGTTGAGGACATGCACATTGCGATATTGAGGCTTAAACGATATATTGTGCAGCCCTAATGATGATGCTGTTGTTTTTTTAGGGCTTGGTTGAAGTGATCACTAGCAGTGAAGATAGTGTTTCAGTTCGTGCAACTATCCTCTTAGGAGAACTCCTGCATATGGTAAAGTACTAAACTGAGGTCAACTGTTCATACAGCACACTCATGTAGTGTATATCCCAAATAACCTTGAGTTACCTTTATTTTATTTTCAGGCCAACACCATTCTCCCTCATTCTCATAGTCACCACCTGCACTGCCTGCCCACTCTAATGAACATGGCTGCTTCCTTTGACATTCCTCAGGGGAAAAGACTGTGAGTTAGCCATCCTGCCCTACATAGACGGCAGCACAAATAGCGCAGTGTCAGAGTATGAGACCAGTGATTATTTATTTTGATGGAGCTTTGTGTTTGGTTGTGTTTTGTAGACGGGCGAGTGCTGCGGTTAATTACTTG[A/T]AGAGATTTCATGAGAAGAAGAAGCGAGGCCCCAAACCCAATAGTCTTTACTTGGACCTCATTGTCCGTAAATCTCTGGCTGCTCATTATTGTCGGGACCAGCACCTCAGGCCTCAGAGGGACATTTTTGTCATTAAGGTAGTTGCTGTTAACTGTAGTAATGCTTTTATGGATGTCATTTCTGACATGATTGTTGTGTTGTTCAGGACACTGAGGAGGCCCTTATGATGAACCTCAGAGACAGTCAGATTCTCAATCATAAACAGAATTTGGAGTGGAACTGGGTCCTAATCAGCACCATACTCAAGGTAGAATTTTTTATTTTTATTGTGGTGTTTTTAAAGTGTTTAAGCACCATTGTTGATGGAACAGATGTCACACTCCTATTTTTTAATATTGCATTTTAAAATTATAATATACTTATATTATAATATCAATATACATACAGAGGGAAAAAATTATTAAACATGTCATGTTTTTTCCTGGGAATAATATTTTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3126
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000058311 | Nonsense | 1021 | 1724 | 30 | 38 |
ENSDART00000142961 | Nonsense | 985 | 1698 | 28 | 36 |
Genomic Location (Zv9):
Chromosome 21 (position 20057922)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21193411 |
GRCz11 | 21 | 21230047 |
KASP Assay ID:
554-3214.1 (used for ordering genotyping assays)
KASP Sequence:
AGCTTTGGCCTGTGGTCCCCGATGAGGTGGAGCAGCACCAGAACCTACAG[C/T]AGCAGCAGCAACAGCACCAGCAACCCCTCATTCACCTATCRTCAGCTCCC
Long Flanking Sequence:
GTAGTTCCAGTTTTCACAAACGAAATAACAAAAAAGACACTTCATTGGTTTCCCACTTGTCATAATGCAATAGTGTGAAGCAACTGCACCCAGAATAAACATAGGGTAATCGAAAGTTAACATTACCAGAACCTTACCAGACACTTCTGGTTTCAAACTTACTTTCTCGGAAACCGTAATCCCATTTTTTTTTTTTTTCTGAGTTTGCATGACTCAGTGAATTGTGTCAGTCCTCTTCTGCTACTCTTTGGCAATCTCACATTCCTTTATTTCAATGCACTCTGAGCTTTGCTTCTTTCCCACCCCCCATTTTAACTTGCTCTCTCAATCTTTCCCCTTACCCTTATTTCAGGACTTGTCTGTATGTTCTGGGACTCATTTCTAAAACCAAGCAGGGTTGTGAGGTGCTCAAGCTTCATGGCTGGGATGCAGTCAGGCACAATCGCAGACAGCTTTGGCCTGTGGTCCCCGATGAGGTGGAGCAGCACCAGAACCTACAG[C/T]AGCAGCAGCAACAGCACCAGCAACCCCTCATTCACCTATCGTCAGCTCCCAGCACCCTCAGCTTAACCTCAGAGTCCACCAGCTCTAGACACAACAGCGAGAGTGACTCCATTCAGCCAAGTGAGTGCTGCTCCCACAGACTCATCCATGACTAACAGCATATAGTGCAGAACTGTGGTTTAGGGTGGAGATGCTTATTACCAGCTGATGGTTAGCTGGGCTCCATATCTGTTCATTTCAAGCATGTTTATCTTGTCACTATCATTATTACCTTAGAATCTGACTATAGTATAGTGCTGTGAATGTGTCTTTTTAAAATGGCGTCATTTTTGTTTTCTATGTTGGTAAATCATTACAGTTTAGAATGATAGCATAGCACATATGGTACCAACTTAACATTACTGATGCTTTGCTATCATTTGTTCAATAAAGTATCCCTTTTTATTCCGGTTCTTGAATTAGAAGCATAGTCATTTCTTTAACATGCATTCAACTTGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37289
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 |
---|---|---|---|---|---|
ENSDART00000058311 | Nonsense | 1022 | 1724 | 30 | 38 |
ENSDART00000142961 | Nonsense | 986 | 1698 | 28 | 36 |
Genomic Location (Zv9):
Chromosome 21 (position 20057925)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21193414 |
GRCz11 | 21 | 21230050 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGGCCTGTGGTCCCCGATGAGGTGGAGCAGCACCAGAACCTACAGCAG[C/T]AGCAGCAACAGCACCAGCAACCCCTCATTCACCTATCGTCAGCTCCCAGC
Long Flanking Sequence:
GTTCCAGTTTTCACAAACGAAATAACAAAAAAGACACTTCATTGGTTTCCCACTTGTCATAATGCAATAGTGTGAAGCAACTGCACCCAGAATAAACATAGGGTAATCGAAAGTTAACATTACCAGAACCTTACCAGACACTTCTGGTTTCAAACTTACTTTCTCGGAAACCGTAATCCCATTTTTTTTTTTTTTCTGAGTTTGCATGACTCAGTGAATTGTGTCAGTCCTCTTCTGCTACTCTTTGGCAATCTCACATTCCTTTATTTCAATGCACTCTGAGCTTTGCTTCTTTCCCACCCCCCATTTTAACTTGCTCTCTCAATCTTTCCCCTTACCCTTATTTCAGGACTTGTCTGTATGTTCTGGGACTCATTTCTAAAACCAAGCAGGGTTGTGAGGTGCTCAAGCTTCATGGCTGGGATGCAGTCAGGCACAATCGCAGACAGCTTTGGCCTGTGGTCCCCGATGAGGTGGAGCAGCACCAGAACCTACAGCAG[C/T]AGCAGCAACAGCACCAGCAACCCCTCATTCACCTATCGTCAGCTCCCAGCACCCTCAGCTTAACCTCAGAGTCCACCAGCTCTAGACACAACAGCGAGAGTGACTCCATTCAGCCAAGTGAGTGCTGCTCCCACAGACTCATCCATGACTAACAGCATATAGTGCAGAACTGTGGTTTAGGGTGGAGATGCTTATTACCAGCTGATGGTTAGCTGGGCTCCATATCTGTTCATTTCAAGCATGTTTATCTTGTCACTATCATTATTACCTTAGAATCTGACTATAGTATAGTGCTGTGAATGTGTCTTTTTAAAATGGCGTCATTTTTGTTTTCTATGTTGGTAAATCATTACAGTTTAGAATGATAGCATAGCACATATGGTACCAACTTAACATTACTGATGCTTTGCTATCATTTGTTCAATAAAGTATCCCTTTTTATTCCGGTTCTTGAATTAGAAGCATAGTCATTTCTTTAACATGCATTCAACTTGGGACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1469
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 |
---|---|---|---|---|---|
ENSDART00000058311 | Nonsense | 1220 | 1724 | 31 | 38 |
ENSDART00000142961 | Nonsense | 1184 | 1698 | 29 | 36 |
Genomic Location (Zv9):
Chromosome 21 (position 20061106)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21196595 |
GRCz11 | 21 | 21233231 |
KASP Assay ID:
554-1394.1 (used for ordering genotyping assays)
KASP Sequence:
TRAACAGAACTGCAGAACGAAGCTCAGGGGTAGGAGATACCCACCGTGAA[C/T]AAACCAGTCGAGAAAGGCTTGCCGGTGATGGCTCAACCTCTGGAAGCGGG
Long Flanking Sequence:
CTGCCTAAATGACTTCTTTTTCAGCCATGTACATCCTGGATGATGAGAAGTTGGAAAGTTCTGAACTTTCAGAAGACCAGCCACTGTACTTTCGGCCTAAACTTCTAAAGGACCGCAGCCCCTTCACCATTTTGGCCTCCAGTCGACTTGTCCGGAACCGCTTCCTGATCTCCCTCTCCGGAAAGAAACTCCGCAGTACCAGTGACCCCAAAGGCACTGGCAGTAGCAGTAAACTTCAAGGCGAGCTCACTCTGGGAGGCCTCCGGAGGGTACGCACAGTCACAGAGCCCTCTATCTTCTCTTCTAGTCAGGGAGACGTTTTCAGTCCTGTATTTACAGATGGACATCTGCCAAAAAGCCCCAGTGTTAGTTTGGAGACTTCTTTTGTAGGCACTAAGACTTTGGATACTCAGGACAGCACATCTAGTATTGGAGAGCAAGAGGTACGTCTGAACAGAACTGCAGAACGAAGCTCAGGGGTAGGAGATACCCACCGTGAA[C/T]AAACCAGTCGAGAAAGGCTTGCCGGTGATGGCTCAACCTCTGGAAGCGGGGCTCAGTTTAAAAGCCGCAGCCAGAGTTTCAACACAGACACGACCACCAGCGGCATCAGCTCCATGAGTTCCAGCCCATCTAGAGAGACTGTAGGTTGTGTGGACTCTTCCACCATCGACACAGATTGTGTTAGCCTCAATACTGTCATTAGCACTCAAACTGTCAAAACCCTCCATTCTCTCACACCCCAGTCGAACCACTTGACTCTGTCCAAATCAAACTCAGTTTTGCTGATGCCGCCAGGTTCCTCTCACACTCTGCCCCGCAGAGCTCAGTCCCTTAAATCGCCTTCAGTCACAACCATCTCGAGCCTGACAGACTGTAGCTTCATGTACACCAGCCCTCGGGACGCACTGGGTTACGCTACCCTAAAAAGACTGCAGCAGCAACGTATCCACCCCTCCCTTTCTCATAGTGAGGCGCTTGCTTCACCTGCCAAAGACGTCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23915
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 |
---|---|---|---|---|---|
ENSDART00000058311 | None | None | 1724 | None | 38 |
ENSDART00000142961 | Essential Splice Site | 1462 | 1698 | 31 | 36 |
Genomic Location (Zv9):
Chromosome 21 (position 20064537)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21200026 |
GRCz11 | 21 | 21236662 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGGGCTGCAAAGTTCTTCTCGGGCGAGGCAGATGGTAAAGATAAAAATG[G/A]TTACTGAATATTGTATCAGTAGCTCGTTATTCTGCATACAAATCCAATAG
Long Flanking Sequence:
ATTGATTTAAATAGAGCCCTATAGCGGCAAAAAACAAAGAAATGTTTGTGAATATTTTTTCTAGACAAATACATAATACATTTGGATGTTCTTTGTTTTTAAATTTTTTTTTTTTTGGTAAGTGAAAAAATAGGGCTTAATTAGAGTGAAATAGTTCAAATATGTGAAAAATAGAGCTAATTAAAAATAAATTATTATTATTTCTAAAAATTAAAAAGCCATCTTAATATTGAAAGTACGTTCAATAATAAATTGTCCTATTGGAATGATATAAGATTTCTGGACTGAAAGAAAAAGTATTGAAACGTATTTCCTTGGGTTGACCAACACTGAAAACCAGTACAGAGAGGGAAGACTGAAGGTTTCACCTGAAATGTATCTTCTTTTGGTTGCTACCTAGATCAAGGACACGCCATACTTTCAAAAAAGGAAAAGTCCACCATCTGAAGACCGGGCTGCAAAGTTCTTCTCGGGCGAGGCAGATGGTAAAGATAAAAATG[G/A]TTACTGAATATTGTATCAGTAGCTCGTTATTCTGCATACAAATCCAATAGCAGTAGTGTCTCACCACTCAGTTTCAGTGACTGAAAGCTGTTCTTTTGTCAGGATCAAGCGAAGTGTCCAGACACTCTGTTCTGCGCTCTCAGCTTAGTATAACAGAGCTGATTGCAGTGAGTCGTATGGAGAAGCATCAAATGTTGGGTGCAGAGGAGACCGGCCTGCAGGAGCACACTGAGGAGAACTGTCTTTACTGTGCAGGGCTCTATGTACTTGGCTGCAATTCAAGCTCTGCCACGCAAAGCCGCACAGGTATGATCCAGGTTTTGTTGTTTATTTTCTGAACTATGCTTTGATAAAAGAGACGCCTTATACTGTATGTCAAGAAAATGAAGCAAGAATTTTGAACTTGATTTCATCCAACGGTGAAATGTTTGCCAAATAGGATGTTTAATTAAAATCATATTCATATATTATTAATCACATTTAAACATAGGGTTTTAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43626
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058311 | Nonsense | 1587 | 1724 | 35 | 38 |
ENSDART00000142961 | Nonsense | 1561 | 1698 | 33 | 36 |
Genomic Location (Zv9):
Chromosome 21 (position 20066030)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21201519 |
GRCz11 | 21 | 21238155 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGCAATCAGTCCATACACAACCTGGAAGTGATGCCTCAGTCTAAGTA[C/A]TCTGGAGTGTCAGGCTGCAGCGACGCCGTCTCTCAGGGCTCTGGTGGCAG
Long Flanking Sequence:
TGGGCGTACACCAGTGCACAGTGCTCTCCTGTATGTACGCAATGTACTGACAATGAGAATAAGAAACCATTGAGTAAAGCCATTATTTTTGTTCTGTGCACACACAAAAGTATTCTTATAGCTTAATATTCTGATTGAACCACTGAAGATATTTTTGGTACCTTTCTGGACTTTAAACAAGTCAGGAGCATTGCTGTCTTAGGAGAATGAGAGAGCTCTTGGATTTCATCCAAAATATCTTCATTTGTGTTCTGAAGATGATCAAAAATCTCTGTGGTTTTTAATGTCACAAGGAAGAATAATTATTGACTGAATTTGTTTTTTTGGAAAGGTAACATGGGATCAGACATCGTAAAAGTATTCCTCTTCTAGTCATCTATTTATTTACTCACTATAGATTCTTCATCTCTCAACTGTATTTCAGACTATCCTGACGCTACATTCTCGGAATGGTGCAATCAGTCCATACACAACCTGGAAGTGATGCCTCAGTCTAAGTA[C/A]TCTGGAGTGTCAGGCTGCAGCGACGCCGTCTCTCAGGGCTCTGGTGGCAGCACTCGCAGCACTGAGCTTGTTCTTGGTGAGCAATCCTTCAGGCTGCAAATTCGGACTCGATCATTTCCTATGCCTATAGTACAGGTTGAGTAAATTGTTTAGCTGTACATATTTTTTTTTCTGGCAGGGGTGAAAAACATTCCAGAAGATGCTCCGGCCTGTCGAGTTCTTCTGAGGAAGGAGGTGCTTCGTCTGGTCATCAACCTAAGCTCCTCAGTGGGCACTAAAGGGAACGAAACTGGACTCCTCACGTAAGCATTGATGATTATAATTCCCCTGTTTATTTCTTTATTCACGTTGATTTAGTTGAAAACCGCTTTAAATTATTATTACTTTAGTTTGACCTATTTGGTCATTTTCCTGAGGAACATTGAGGGTAAGTACTCCTTAAAGGGACTGTTCAGCTAAAAGTAAAAATTCACTCACCATTGTGAGTTTTCTTTGTTTAC
Associated Phenotype:
Not determined