ZMP
rttn
Ensembl ID:
ZFIN ID:
Human Orthologue:
RTTN
Human Description:
rotatin [Source:HGNC Symbol;Acc:18654]
Mouse Orthologue:
Rttn
Mouse Description:
rotatin Gene [Source:MGI Symbol;Acc:MGI:2179288]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44111 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8719 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32481 | Nonsense | Available for shipment | Available now |
sa25211 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa801 | Nonsense | Available for shipment | Available now |
sa30066 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44110 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37847 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44109 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44111
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 |
---|---|---|---|---|---|
ENSDART00000006930 | Nonsense | 203 | 2234 | 6 | 49 |
ENSDART00000142473 | None | None | 318 | None | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 15156304)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 15107752 |
GRCz11 | 24 | 15252171 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCATTAGTTCCCTTAGAAGCGACAACCACAACTTAGTGCGAACCACCTG[T/A]GAGCTGCTTCGTGATGTCATCATGCAAGACTTCCCAGCTGAAATATTCCT
Long Flanking Sequence:
GTAAATCTATTCCTACAATGCTATAATAAATTTTGCCTGTTTCACAGTAGGCTCAAAAGTATCCCAAAGCACCTCAAAAAAAACTCAAAAAGGACCTAAATGTTCTTTTGAATCTTTTTGTAAGACGTTTGTAACAACATAAACCGATTATTGATTAGGTGTTCTGTCATCTAGCCCAAAAATCTTTCCAATAGGCCCCGAACCACCCTTATTGTTAAAATCTGACCTCCACACTACACAGGACTTTATTATACTTTATGTTCCTTTTTTGTTTCTTTACCCTGCAGTCAGTACTAGGTGCTTGAAGTTCTCTGTTTTTCCATGGCTGTCTTTGAACACAACAGATCGACATATATTGTCATCAAATGAAAGGTACCCTCTGTTTGCTGTTATTTTACCTCATTTACCCTCTAATTTACATCCTACTGACAAAATAACATCATTTACTCGATCATTAGTTCCCTTAGAAGCGACAACCACAACTTAGTGCGAACCACCTG[T/A]GAGCTGCTTCGTGATGTCATCATGCAAGACTTCCCAGCTGAAATATTCCTGCAAAGGCCAAGTACAGTTCAAGTAAGACTTGAATTTCATTTCTGTCTTCAATCTGTCTGTTGTTTTAACCCCTGATGAGAGATTCATAAGTTGAGTGACAGCGATGAAAGTGATATCGCGGGGCTCCATAATCCCCGTTTCGTTCTATAATTGAAATTCCACAGAATCTGATTGGCTGTCCAATGCCTTCAACTCCGGAAAGTATTGGAATGACAGCGACAAATCTTGTCTTATGTCTAGAACTGTACCGTGATGATTAGCTGGCAAGCTGACACATGCCGTTTTAGTACAAGCGTTTAAAACCAAGTGACAAGCATTGTTGTTTATCTGTCAAAAATGTGTTGGCGCAGATGCATTGGAGATTATCTGAGATATGCAGTCTCAGTGCTCTCAATGAAAATTATTTATCAGGCTGGGATAAAGTGGTTTGGAAGCGCTCTCTTCAGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8719
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006930 | Essential Splice Site | 227 | 2234 | 6 | 49 |
ENSDART00000142473 | None | None | 318 | None | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 15156230)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 15107678 |
GRCz11 | 24 | 15252097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAAGACTTCCCAGCTGAAATATTCCTGCAAAGGCCAAGTACAGTTCAAG[T/G]AAGACTTNNNNTTCATTTCTGTCTTCAATCTGTCTGTTGTTTTAACCCCT
Long Flanking Sequence:
CAAAAAAAACTCAAAAAGGACCTAAATGTTCTTTTGAATCTTTTTGTAAGACGTTTGTAACAACATAAACCGATTATTGATTAGGTGTTCTGTCATCTAGCCCAAAAATCTTTCCAATAGGCCCCGAACCACCCTTATTGTTAAAATCTGACCTCCACACTACACAGGACTTTATTATACTTTATGTTCCTTTTTTGTTTCTTTACCCTGCAGTCAGTACTAGGTGCTTGAAGTTCTCTGTTTTTCCATGGCTGTCTTTGAACACAACAGATCGACATATATTGTCATCAAATGAAAGGTACCCTCTGTTTGCTGTTATTTTACCTCATTTACCCTCTAATTTACATCCTACTGACAAAATAACATCATTTACTCGATCATTAGTTCCCTTAGAAGCGACAACCACAACTTAGTGCGAACCACCTGTGAGCTGCTTCGTGATGTCATCATGCAAGACTTCCCAGCTGAAATATTCCTGCAAAGGCCAAGTACAGTTCAAG[T/G]AAGACTTGAATTTCATTTCTGTCTTCAATCTGTCTGTTGTTTTAACCCCTGATGAGAGATTCATAAGTTGAGTGACAGCGATGAAAGTGATATCGCGGGGCTCCATAATCCCCGTTTCGTTCTATAATTGAAATTCCACAGAATCTGATTGGCTGTCCAATGCCTTCAACTCCGGAAAGTATTGGAATGACAGCGACAAATCTTGTCTTATGTCTAGAACTGTACCGTGATGATTAGCTGGCAAGCTGACACATGCCGTTTTAGTACAAGCGTTTAAAACCAAGTGACAAGCATTGTTGTTTATCTGTCAAAAATGTGTTGGCGCAGATGCATTGGAGATTATCTGAGATATGCAGTCTCAGTGCTCTCAATGAAAATTATTTATCAGGCTGGGATAAAGTGGTTTGGAAGCGCTCTCTTCAGCTAATGCTCTTGAACTTTTGTGTAATTGTTTAAAAATTGAATGTGCCAGCGATTCCGACTCGGAGTGATCAGTTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32481
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 |
---|---|---|---|---|---|
ENSDART00000006930 | Nonsense | 264 | 2234 | 7 | 49 |
ENSDART00000142473 | None | None | 318 | None | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 15155351)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 15106799 |
GRCz11 | 24 | 15251218 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCATTGGCCTGTCTGCAACAGCTTTGCAGGAACTTGAAGAGCCGCCTA[C/T]GATTTTACAGAGATCCAAGCTTCTTCTCAGCCAAACAAGGTACCCCACAA
Long Flanking Sequence:
TATTTATCAGGCTGGGATAAAGTGGTTTGGAAGCGCTCTCTTCAGCTAATGCTCTTGAACTTTTGTGTAATTGTTTAAAAATTGAATGTGCCAGCGATTCCGACTCGGAGTGATCAGTTCAATTAGGTTTATTGAATCACTTTCATTCATTTGCATTGCTTTGGTACCACTGGAGGGGTAGTGCGTTTTAAATTGGTACAAATTACACAACTTAAAAGTCAGTATCAGGTGGCCTTTTATTTAGTGTCTAATTGAATGCAGAATCAGCTCTCCTGAAAGGCTTGCACCATTTAGATCAGTTGTTTTTGTTATAACAGGTCTGCACTTGTCCTCGTGGGTTTACAAGACAACATCAGCTTCTGTTTTCATGTATTGCTGTTTTCCCCCTCTAGAGTCTGCTGTCACTTCTCGGTCTGAATGTTGATGGTGATGTCAGCTACCTGACGTTCCAGGCATTGGCCTGTCTGCAACAGCTTTGCAGGAACTTGAAGAGCCGCCTA[C/T]GATTTTACAGAGATCCAAGCTTCTTCTCAGCCAAACAAGGTACCCCACAACATCTATTATGAATATGTAAACTTTTCCTAATGTGGGGGTTCGCTCCTAGCAGTTGAACTTTTTTATTCGAATTTTGCAGCACTCAAAAACTCAGATGCTCCATTTATACTTGGTATTAACTCTTTCCCAGTCATTGTTTTTTTTTTTTTTTTTTTTCAGTCACCAGCATTTTAAAGATTTTTACCTAAATTTGTTTATATATATATATATATATATATATATATATATATTAGGGATGGGAAGATTAACCGATATGTATCGATACGCGGTCATGCGCGTGCACGATGCGAGTGCATCGGTTGAGCAGCAGAGGATGAATGAAATTTTGGAAGCAAATCGAGATGCATCGGTTTTTGCGAGATGCATCGGTTTTTCCAAGATACAGCTTATATTTTTAATATAGAATGTATTTTTTATTTATTAACAAGTGTTGTCAACCTGTTTTGGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25211
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 |
---|---|---|---|---|---|
ENSDART00000006930 | Essential Splice Site | 435 | 2234 | 11 | 49 |
ENSDART00000142473 | None | None | 318 | None | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 15135811)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 15087259 |
GRCz11 | 24 | 15231678 |
KASP Assay ID:
554-7645.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACATGCTCTTACTAACATCAGTCTTTTTGTACATGTGTTTTTTTTAA[G/A]AGAGAGAAATTACAGGCATGTATAGAGATTTTGGGAGATGTTATTTGCTA
Long Flanking Sequence:
TCATAATGCATAAACTAATGTGAACACATGCCAGTAGCTACAATAAGTGCAGATATTTAGCCATGCTTCAGAAATGTTAACCATCTCAACCTAGAGTTTAATTGTGGTCATTATGCAAAGTTTACTTTGTTTCATTCAGCTTATGAGTGTTTTACATAAAATGGCATCAACGTATGATTGTATACCATGGATTATGTAGGTCGCACGGCACCAAATAGGCCTCGTCCAATGATGTTCATTGCCTCTAGAAATCTTTTTAAACGAACTCATTGTGTGTGCACCTATGAGAACATTCCCCAGCGCATATGATTATGTATATTTCACGGCGTGCCTCTCTCCCTCATTGATCTTTAATGCACGCTCATGGCGTTTTTATCTTGAAAAACTGCTGTCATCTGAAAACTTTCTTTGAAATGCACAGGACTCTTGCTGCCCCCTGCTGGCGGTAACATGACATGCTCTTACTAACATCAGTCTTTTTGTACATGTGTTTTTTTTAA[G/A]AGAGAGAAATTACAGGCATGTATAGAGATTTTGGGAGATGTTATTTGCTACCACCATGGCATGACTTCCTCAGAACATCCAGAATCGTCTCTGATCCACCACAGAATGGTCTTCACAGGCACTGCCGTTTTCACAATACGTCTCCTGCAAACCTTGTTACCTGTGGAGAAGGTGAGTGAGCATATGGCCGTGCCATTCTTAGACATTAATAAGCCGTGCCACCACTGTCGCTGAATGGACATATGGCCGTGTCCTTCATGGTCATTATTAAAACAAATGAGAGTGCGAAACACACCAGAAGTTCACAGTGAAAGGGTCAATTGTTCAGTTAAGCTCCAGACCTAAGGACAACACTATAATTGCAGACAAATCTATTAGCGTTTCATTTTTTGTGTGTGTTTTATTACCTTGTGTGTGTTGTCTTTACAAACAGGCTGCGGATAATCTTCCGGAAAGTACCGTGGCTGCCATTTTCCTGTTGTGTCTTGATATATCCTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa801
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 |
---|---|---|---|---|---|
ENSDART00000006930 | Nonsense | 1037 | 2234 | 24 | 49 |
ENSDART00000142473 | None | None | 318 | None | 9 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 15109137)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 15060585 |
GRCz11 | 24 | 15205004 |
KASP Assay ID:
554-0706.1 (used for ordering genotyping assays)
KASP Sequence:
TGCAGATCACCTGGAACACAGCATGGCATTCTGGGATTGATGGATTGCTA[G/T]AGCACCTGAGGGGTTTTAGAAGTGATGTGCCAGAGTAAGTTGGATTCATC
Long Flanking Sequence:
ACACTAATGTCAAATCCACCAGAGTTACAGACCACTCCTTTCTTTCTTTCATTTTATTAATGGTAAACATGCTATCAGCAAGAACGCTTCGGCTCACGTTCATTTCATTATCTTTGTTCTCTCATCAGGACTGACGAAGCTGGCTCAGACACAGGCCTGTCTTCCTTCTCACTTCCTGCAGCCATTATACGGAGGTAAATTACATCCCTTTACAAGTGCATTAACGGCCATTTAATTTCTCCATAACCTGGCTTTCAGAGTTGTCATTGGTCATTAAAGCAAGGGTTTAACTATTATTTGACAGATTGATTGCAGAACTGTTATATCTGATCTTTTTTCACAGGTACAATTTGCCGTTTCAAGCTCCTTCACATCATGCAGTGAGTCCATACTGTTCAGTTCTTCCTCCATACTCAGATCTCCTGAGTCTGAAGCCCGCCTGGGAAGCTCTGCAGATCACCTGGAACACAGCATGGCATTCTGGGATTGATGGATTGCTA[G/T]AGCACCTGAGGGGTTTTAGAAGTGATGTGCCAGAGTAAGTTGGATTCATCCGTTTAGATGTTTGTAAAAGTTCATGTTGGAGAGGACTTTCAGGAAATTTAATTTAATTTGATTTGATGTGATTTGATTTGATTTGATTTGATTTGATTTGATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTGTTACATTTGGTTACATTCAGTTAAAGTCAGTTACATTCAGTTATATTCAATTATGTCCCGTTTCATCCAATTACATCCACTTACATTCAATTACACCCAATTACAGCCATATACATTTAGTTACATTCAAATACATTACATTCATGTACATTGTCACACCCAATTACATCCAGTTACATCCAATTAAAGCCACTCACATCCAGTTACATTCAATTACATTACATTTAGTTACATTCAATTACATCGTATTGACTTGCATT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa30066
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 |
---|---|---|---|---|---|
ENSDART00000006930 | Nonsense | 1170 | 2234 | 26 | 49 |
ENSDART00000142473 | None | None | 318 | None | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 15102048)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 15053496 |
GRCz11 | 24 | 15197915 |
KASP Assay ID:
2261-8553.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCAAGCAGAATCAATCTGAACTGGACCAGCAGGACCTTAAATGGTTGT[T/A]GGAATTACTCCTAAACCAGGTATTTCTGAATAAACAGCCATCTAGAATCT
Long Flanking Sequence:
TTGACAGTCTTCATCTTCGGAGTAGAATTGCACCATGACACCTGTACTGCGACTGTTTGGGATGAATACATGTACCGTTACATCCATAATATTAATATTGTACATGCATACAGTATATATGCTTAGTTTAATATGTAATGCAATGTGCACATCTACTTGATATATACATTTACACTTTTATTTGTTTCTTATTTCACTTTTATCACAACAACCGTTTTATTTTAAGTGCTGTATGTAGAATGATTTTTTGATCCTTTTAACTTTGTAGGTTGACTTTGTTTGGTGACAAAAGTGCACTTTAATTTCTGACTCTGCTTTGAACTTCTTTTTTTTGTGTTTATATATGCATTTATTTATTGTTTAATTATCCCACAGATTTCTGGTTGTACGTCCAGCTTGCCATCAAGATGAGAGGCTCCTGGTGGACATTCTGTCCTTCCTCAACACGTTCTTCAAGCAGAATCAATCTGAACTGGACCAGCAGGACCTTAAATGGTTGT[T/A]GGAATTACTCCTAAACCAGGTATTTCTGAATAAACAGCCATCTAGAATCTGTTATGGATCAGTGCCTGCATTTCCTTTAGATTACTTTGGAGCCCTCATAAAACAATAAAGAGGCTTATTGTACCTCTGTAATTAAATTAACTTGCCCTCCTGCCTCAGATGAACACAGTGTGGTGTATTTATTAAGACGCTCTGAAATAAATCACACCGCAGAGCAATGCAAATACATTAATATCATAATAAAGCTTGTAAGGGAGAGCTGTTCATCAGCTGTCACTGTTTTTGTTTGTCACACTGAGGATGAATGGCTTTATTTCCTAAAATTCTCATCTCGCCTTGCTGCGCATTAATGTGTATGTATGCAAACAAAGCTGCCTTGCCGTTCGACGGAGAACGCTGGGTTTGATGAAACGCCTGGTGGGGGAGGTGGTGAAATGCAGAGAGCATCTACAGTCGCTGGAGTGTTGCTCAAACATCTGTGCTGTCTAAATGAAACACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44110
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 |
---|---|---|---|---|---|
ENSDART00000006930 | Nonsense | 1236 | 2234 | 28 | 49 |
ENSDART00000142473 | None | None | 318 | None | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 15085065)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 15036513 |
GRCz11 | 24 | 15180932 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACACTTTTACTCATTCTTTTGAATTTGCCTTTTTGTTTTTCAGGATGTG[T/A]GAGGTTTTGTCTGGACCGTTTGCCTCTGAACTGTCTCTGCGTCTGCTGCA
Long Flanking Sequence:
AAAAATTTTGGACAGAGTTGAAAAGCTTGTGCGAGCAAGACAGCCTACAATTCTGACTCAGTTACACCAATTCTGTCAGCAGGAATGAAAAAAACGTAAACAATACATTTGTATTTGTTCATGTTAGTTAACCTTAGTTAATGAAAATAGATTGATTCATTGCTAGTTCTTGTTAACAAGCATGAATTTGGAATTTAATAAGGTACTAGTAAATGTTAAAATGTAAATGTAAACCTATCATTAATAAATGCTGTGTTGTGTTGTTCATACTTAGTTCATGTTAGTAAATACATTGACATGAACTAATTCACCTTATTGTAAAGTGTGACCATGTCATTTCATTTCAGTGTCAATTACTTCAGCATTAAGTATTGTTCATAGTTATTACTGTAGTCTGCAATGAATAAAAGTATTCCTCACATGATATCATCACCCTTAGTGTCAAATAATAACACTTTTACTCATTCTTTTGAATTTGCCTTTTTGTTTTTCAGGATGTG[T/A]GAGGTTTTGTCTGGACCGTTTGCCTCTGAACTGTCTCTGCGTCTGCTGCAGTGTCTGCGCCTGTCTGATGCTCCGTGCTTTTACGGCCTGCCGTCTCTAGAGCGCACACTCAGGACCATGGCCCACGTGACTGCCCTGCCCGGCTGGAGCACCCACACTCCTAGCGTAGAGCCAAACACGCTCTGTCTCAAGTACCTCAGCGGCCTTCTGGAAGTATGTACACACACATGTGCTCAAGTGCCTCGGTTACACACAGAAATATACTTTGCACAGATTACATGCACACTCACTGCTCCTCACACATTAAACGCACACTCATAAGCAGAGTCCACGATGTTCCCAAACACTTAGACATGAACCACTCCAGAACCAACAAGCTCGAGTCTCAGCTGCTTTTCATCTGCTGTGCTTTGCAAGGCAGGTTTATTTGTATAGCACATTTCATACACAATGGTGGTTCAAAGTGTTTTACATAAACAAAAAAAAAAAAAGAAACATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37847
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 |
---|---|---|---|---|---|
ENSDART00000006930 | Nonsense | 1762 | 2234 | 39 | 49 |
ENSDART00000142473 | None | None | 318 | None | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 15066761)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 15018209 |
GRCz11 | 24 | 15162628 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACCTGGTCGGATGTGTTGACGCTTCTGGCTACTCTGCTGCGCAGGAAC[C/T]AAGCTGCGGTCGGCCCATCTGTCGCTGTGGCACTGGGGAAACACTGGCAG
Long Flanking Sequence:
GGCCCACAGTCAATTAGTCAACTGTTTGTTGTCCCTTATAGTTTTGTGACTCCCAAAGTGCTGTATTTGTGTTTTCTGATTGACTCTCCCAACTGACTCTCCCTCATTTTCTCTCTCTTCCTCCTCCCACACCTTGTTTTTTCTCTTAGGTGCTGAGTAGCTTGTATTATGTGCAAAGTTTCTGTAAGCTCCTGCAGTCAGCAACGATACACAGTGAGGATGTGCCGCTCCACAGAGAGTACTTCAAACTCCTGCTGAACAACCTCATTTCCATCCTCACGCTGCCTGTCGCTGACTTGGGTAACACAAAACATCTTGTGCAAATCCACAACCCAGCTGAAATCTCCCCAAAAAAGTCCTTTAAATAAAAGAAGTGTGTTTTTATATAAATGTGTATGTGTGTGTGGTTGTTTTGGTCCTCAGATGCGCAGACCCAGGGTGCAGTGCTCAACACCTGGTCGGATGTGTTGACGCTTCTGGCTACTCTGCTGCGCAGGAAC[C/T]AAGCTGCGGTCGGCCCATCTGTCGCTGTGGCACTGGGGAAACACTGGCAGCGTTTTTCAGGTGACAAACACACACACACACACTAACATACACACCAAAAAAAGTGTTACAAAGAGTGGAGACAGGTGAGAGGAAAGGGAAGGCAGAATGAAACAGAAGAGTACAGAGAGAAAATGATGGCAAACATGATGAAAGCGCAAAGGGACGGAGGGGAGAGAAGGATTGAGGAGTTTAGATGGAAGAGGATGTGCTAGAAAGATGTTGAGGAGATGGAGATAGAGACAGATGCAGTGGGAGGCCGGCTCATTATGCCTGTATATGTGGATGGGTGTCCCTGCTGCATATGACAGTCTGGGACAGAGACAGGAAGAACAATCAGCCTGCTTTAGATCTGATGGATGTGGTAGAAAATCCTGAAACAGGTGGGTGGGCAGTCGACTCGCTGACTTGCCTGCAGGTATCCAGGCTTTGGAAGCATTTTTTATTATTTTTTTAAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44109
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 |
---|---|---|---|---|---|
ENSDART00000006930 | Nonsense | 1978 | 2234 | 44 | 49 |
ENSDART00000142473 | Nonsense | 117 | 318 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 15054806)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 15006254 |
GRCz11 | 24 | 15150673 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCTTGATGATCTCACCATGGCAGCGGCTCTGGAACTGCTCTGCGTCTA[C/A]ACAGCGAACTGCACAGCGGGTAACTTTTCTGAAAGATGGAGAAATGAGAG
Long Flanking Sequence:
TTCGTTCTTCTGTTAAAACAAACAAACATATTTTGAAGCTGAAAAGCGTTGTTGACTTCCATAGTATTGTTTTTTTCCTTCTACGAATGTCAATAAACATCAGTTTTCAGCTTTCTTAAAGAAACCCATAAAGGTTTGGAATGAACTGATGGAGAGTAAATAGTGAGTAAATAATGTTTTTTGGGTAAACTACACATTTAATTTAAGACATGCTTTTTTTGGATGTTACATCATTTTTTTTATGTGTTTAGTAAATCCTGACAGTATTTTTTTCCAGTGCCAAGATAGGGTTTGTGTTGGCACAAGCTTTTAATAAATCTGCCCGAAGATGACTAATATTGAATGTTAGCAACAAATATTGTCTCATTTGTTGAATTAATTTTCTCCTCACAGGCTGTGGCTACAGATTTGCGTCTGGCTGTCGTGCTGTTGGCTTTTTGGCCCTGGCTCCTGCTTGATGATCTCACCATGGCAGCGGCTCTGGAACTGCTCTGCGTCTA[C/A]ACAGCGAACTGCACAGCGGGTAACTTTTCTGAAAGATGGAGAAATGAGAGCTAGAAATGGGGAATGACAGAGGGATAGAGCATTAGACAGGGATAACAGTGTGCTGAGATGATAATATATGAGCTTTTTGCTCACTGTAACCCTCTCATGAGTCATGTTACTGTACAGTAAGTGCCATTGTGTGTCAAATGCCAGGCTGACGTGAGCATGACACTTACAGAAGGGATTGTGTCATAGTCTAAGTGTGCTGCCAGATTACTGGAAAGCTAGGATGAAGCGTTTGTGTTAAGATGAGGTACTTTAGGGTAAAGATTATTTGGGCAAATTGATATATTCAGTGACTGTTAATACATTATACAATAGAGATCTAAATTAGAGAATCATATTTTGGATAATGTAGTCCACATTCAATATTTAAAGGAATTGTAGTTGTGGCTACTATAAAACATGTGAATTGGACTGTGTTTTTTTTTTACAAAAATAACCAATGTGCTTCAATC
Associated Phenotype:
Not determined