ZMP
NP_571708.1
Ensembl ID:
Description:
roundabout homolog 2 [Source:RefSeq peptide;Acc:NP_571708]
Human Orthologue:
ROBO2
Human Description:
roundabout, axon guidance receptor, homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:10250]
Mouse Orthologue:
Robo2
Mouse Description:
roundabout homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1890110]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa42608 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa24995 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa14991 | Nonsense | Available for shipment | Available now |
| sa30686 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa10275 | Essential Splice Site | Available for shipment | Available now |
| sa35976 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa35975 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa35974 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa6395 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42608
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 |
|---|---|---|---|---|---|
| ENSDART00000014877 | Essential Splice Site | 56 | 1387 | 2 | 27 |
| ENSDART00000099344 | None | None | 111 | None | 3 |
| ENSDART00000099346 | Essential Splice Site | 56 | 736 | 2 | 15 |
| ENSDART00000129511 | Essential Splice Site | 56 | 1391 | 2 | 28 |
Genomic Location (Zv9):
Chromosome 15 (position 37974528)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 39251708 |
| GRCz11 | 15 | 39098469 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATATGAAGTGTCACAGAAGCTGTAAAGTTTCATTGTTTTTTCTCGTTTA[G/T]ATCCGTGGAGGGAAGCTGATGATCTCTAACACCAGGAAAAGCGACGCTGG
Long Flanking Sequence:
CTTGCTTTTGTTTAGTTTTTAGTTTAGTTTATTTGTTTTGCTTTAGTTTTGTCTTGTTTTTGTTTTAATTAATTTATTCTCTATTTTTTTTTTTTTTAGATTTTTGCTGTCTTCATTTAATTGTTGTGTTGTATTTGCTTATGTTATGCAATGTTTTTGCTCAGTTTGTTGAAGTCTAAATATTTACAGTCTCAGTGAAGTAATACTAATAATTGCCCTATGAAGTTTCCAGTTGATTACAAAGATGTTTTATTTCAGACTCATTCTAAATATTTCTAAACAAAGAGAGCTTTATTCAGGGTGTGGTGTAGCGGTTAATGATCTGGCCTTGAATCTAGAACATTACGGCTTCAAAACCAGCAATAGGTGAATCATAAACCACATCTATTTTGCCCTTGAGCAAGACACCTAATCTCAGGTAGCTCCATTGAGAGTGTTGCGGTATCTTATCATATGAAGTGTCACAGAAGCTGTAAAGTTTCATTGTTTTTTCTCGTTTA[G/T]ATCCGTGGAGGGAAGCTGATGATCTCTAACACCAGGAAAAGCGACGCTGGAATGTACATCTGCGTGGGCACCAACATGGTCGGCGAAAGAGACAGTGAAACAGCCCAGGTCACTGTGTTCGGTACGTTCATAGCCACAAAGTAAATGTAAAAATAAAATAAACTAAAATTACCAAAGAGGGTGACACGGTGGCTCAGTGGTTAACACTGTCTCCACACAGCAAAAAAGTTGATTGTTTGAGTCCGGGCCGGGCCAGTTGGCGTTTCTGTGTAGTTTGCATGTTCTCCCTGTGTTAGCTTGAGTTTCCTCTGCTCCAGTTTTCCCCACAGTCCAAAGACATGCACTACAGGTGAACTGGATAAACTAAATTTTCCATAGTGTATGAGTGTGGATGTGAGAGTGTATGGTTGTTTCCCAGTACTAGGTTGCAGCTGGAAGGGCATCCGCTGTGTAAAACATATGCTGGAATAGTTGGCGGTTTATTCCGGTGTGATGACCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24995
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 |
|---|---|---|---|---|---|
| ENSDART00000014877 | Essential Splice Site | 233 | 1387 | 6 | 27 |
| ENSDART00000099344 | None | None | 111 | None | 3 |
| ENSDART00000099346 | Essential Splice Site | 229 | 736 | 5 | 15 |
| ENSDART00000129511 | Essential Splice Site | 233 | 1391 | 6 | 28 |
Genomic Location (Zv9):
Chromosome 15 (position 37949720)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 39276459 |
| GRCz11 | 15 | 39123061 |
KASP Assay ID:
554-7348.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAAAGGGAACCCGCAGCCGGCAGTCTTCTGGCAGAAAGAAGGAAGTCAG[G/A]TAAGGACACATCTTTCTCTTTCATTATTCCCCTAACCTACAGTACTGCTC
Long Flanking Sequence:
TACTGTAGCGTGTCCTCTCCGTGTGTCCTGACCGGAATGACCCACCCCTCCCTCTGGTGTTGTGACTGCAGCACGGCCATGCCTGAAAGCTGCCCGTCATTCATTCGGTACCGCCATCTGCGGCCCCACCTGGATGAATGGCTTCCCGTGGTTACTGTTGCTGTCCTTGCTGTTTGTGGTCAAAGCAAACAGATAAACCCAAAGGCCGAATGCTGTCAAAAACGGGCTAATGCATGGAAGCTCTGTCTCAGTAACCTCGGCAGACCATGCTTGTGGATGCCTGATGTTCCCACTGATCAGCGTGTGTATGTTGGTGTGCATTTGTGTGTGTGCGAGGGCATGGTGTAATGTCCATGTGTTTGGTTCTTGGCTCAGCTGCACCGCAGTTCGTGATCAGGCCGCGGGATCAGATTGTGGCACAGGGACGCACCGCCAGCTTCCCCTGCGAGACTAAAGGGAACCCGCAGCCGGCAGTCTTCTGGCAGAAAGAAGGAAGTCAG[G/A]TAAGGACACATCTTTCTCTTTCATTATTCCCCTAACCTACAGTACTGCTCTCTTGGTTATGTTGAAGCTTTTGAGATAGTGGTTAATGTACTCTACATGCTTCAGGGATGTTTGCAATTGCAGGCAATACAGTTGGTAAATAAATTCTGGAACCCAGCAATGTTCAGTTTTGGGCATGCACAATATATCGGCTACCATACTAGTGATTGTTACGTGTTTATGATGTTCAATAATTAAAGGGATGATACGTAACAATCAGTGAGTCTATTGATGCTGGGTGAATGAGGAGGAGACACATACGCTTGATAAGTGAAAGAAAATATGATAAGTGAAAAAAGTAAGTATTTATTAATGGATAATGTCAAACAATGAATATAAGATGGAAGATAAATGTAATTTTAAATAATTGAATTAAATAAAGAAAAATAGAAGTGTTGCCAAAACAAAGAAATAAATATAACAAAACGAACTAACTAAACCCCAACCCACTAAACTGACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14991
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 |
|---|---|---|---|---|---|
| ENSDART00000014877 | Nonsense | 341 | 1387 | 8 | 27 |
| ENSDART00000099344 | None | None | 111 | None | 3 |
| ENSDART00000099346 | Nonsense | 337 | 736 | 7 | 15 |
| ENSDART00000129511 | Nonsense | 341 | 1391 | 8 | 28 |
Genomic Location (Zv9):
Chromosome 15 (position 37934557)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 39290918 |
| GRCz11 | 15 | 39137520 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCWGTCCCAACCAWCAGCTGGCTGAAGGACGGGGTCAGTCTGCTGGGC[A/T]AARACCCTCGGATGTCCCTGCAAGACCTCGGCAGCCTGCAGATCAAGGGT
Long Flanking Sequence:
ATTATTATTATTATTATTATTTATTTTTTATTTTATTTATTTATTTTATTTATTATTTTTTTTACCCAGATCTATATAAACAGGCATTGTACATAATTGTTTACAAATCCATTATGGAAAACCTTGTATATTTCAAGTATACTGCTGTTATGAAAATATACCCCACATCTGCACTTTCATGAATTTCCTCATCAATATGAGTAAGAGGTTCATTTCAGTCTGTAAGGATTTTTAGAAATATGGACGTATTTACACAATAACAGGGTATTAAAACTACACTGGGGTAAAGGCACACATGGGAAGATCTGGTCTTAATTCTTGTTCTTTCCCCTTTTTTTCTTTCTGGTTTAGTGTTGACCGATCGCCCTCCACCCATCATCCGGCAGGGTCCAGCTAACCAGACTCTTGGTGTAGACAGTGTGGCTCTTTTGAGGTGCCATGCATCCGGAGAACCAGTCCCAACCATCAGCTGGCTGAAGGACGGGGTCAGTCTGCTGGGC[A/T]AAGACCCTCGGATGTCCCTGCAAGACCTCGGCAGCCTGCAGATCAAGGGTTTACGGGTGAGCCTAAACACTTGTATTTCTTTATTTCTATATTATTTAACTTTATTTTACTTTACTTTGTTTTGTTTTATTTTATTTTATTTTATTTTGCCTTCTGCATTTGGCAAAGTTGGGTGCATTAAAATATACAAATGCAATTAAATATTTAATATAAAAAGTTGCAATACATGGTTTTAATCCCAGCTATTAATGACCAGTTTTTATTTTTGCCTACTCAGTACATCCCTTCTATGAATGTTCAGATATATATCTGTCATTGTGTATTTCTAAGACCATTTGTGTATGATTGCGTGACTATCCGCTGTCAGAAATGCCTTCGTCTAAGTGTGATGTATAAGCTCAGCAAAATTCAATCAGATATCGGTAAGACATAACAGAGACGGGCAGAGGGAATCATATTGCATTACGGGGATGAATGGGAAATATTGATTTTGGTAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30686
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 |
|---|---|---|---|---|---|
| ENSDART00000014877 | Nonsense | 348 | 1387 | 8 | 27 |
| ENSDART00000099344 | None | None | 111 | None | 3 |
| ENSDART00000099346 | Nonsense | 344 | 736 | 7 | 15 |
| ENSDART00000129511 | Nonsense | 348 | 1391 | 8 | 28 |
Genomic Location (Zv9):
Chromosome 15 (position 37934536)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 39290939 |
| GRCz11 | 15 | 39137541 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGAAGGACGGGGTCAGTCTGCTGGGCAAAGACCCTCGGATGTCCCTG[C/T]AAGACCTCGGCAGCCTGCAGATCAAGGGTTTACGGGTGAGCCTAAACACT
Long Flanking Sequence:
TATTTTTTATTTTATTTATTTATTTTATTTATTATTTTTTTTACCCAGATCTATATAAACAGGCATTGTACATAATTGTTTACAAATCCATTATGGAAAACCTTGTATATTTCAAGTATACTGCTGTTATGAAAATATACCCCACATCTGCACTTTCATGAATTTCCTCATCAATATGAGTAAGAGGTTCATTTCAGTCTGTAAGGATTTTTAGAAATATGGACGTATTTACACAATAACAGGGTATTAAAACTACACTGGGGTAAAGGCACACATGGGAAGATCTGGTCTTAATTCTTGTTCTTTCCCCTTTTTTTCTTTCTGGTTTAGTGTTGACCGATCGCCCTCCACCCATCATCCGGCAGGGTCCAGCTAACCAGACTCTTGGTGTAGACAGTGTGGCTCTTTTGAGGTGCCATGCATCCGGAGAACCAGTCCCAACCATCAGCTGGCTGAAGGACGGGGTCAGTCTGCTGGGCAAAGACCCTCGGATGTCCCTG[C/T]AAGACCTCGGCAGCCTGCAGATCAAGGGTTTACGGGTGAGCCTAAACACTTGTATTTCTTTATTTCTATATTATTTAACTTTATTTTACTTTACTTTGTTTTGTTTTATTTTATTTTATTTTATTTTGCCTTCTGCATTTGGCAAAGTTGGGTGCATTAAAATATACAAATGCAATTAAATATTTAATATAAAAAGTTGCAATACATGGTTTTAATCCCAGCTATTAATGACCAGTTTTTATTTTTGCCTACTCAGTACATCCCTTCTATGAATGTTCAGATATATATCTGTCATTGTGTATTTCTAAGACCATTTGTGTATGATTGCGTGACTATCCGCTGTCAGAAATGCCTTCGTCTAAGTGTGATGTATAAGCTCAGCAAAATTCAATCAGATATCGGTAAGACATAACAGAGACGGGCAGAGGGAATCATATTGCATTACGGGGATGAATGGGAAATATTGATTTTGGTAAATTGTTTGATACTATCACTTAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10275
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 |
|---|---|---|---|---|---|
| ENSDART00000014877 | Essential Splice Site | 387 | 1387 | 9 | 27 |
| ENSDART00000099344 | None | None | 111 | None | 3 |
| ENSDART00000099346 | Essential Splice Site | 383 | 736 | 8 | 15 |
| ENSDART00000129511 | Essential Splice Site | 387 | 1391 | 9 | 28 |
Genomic Location (Zv9):
Chromosome 15 (position 37932122)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 39293353 |
| GRCz11 | 15 | 39139955 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAAGTTCTAGTGGGGAAACAWCATGGAGTGCTTTCTTGGAGGTCAAAGG[T/C]ACTTGTTTGAAACTGTACACATTGTWAGTAATTTGGTTCTTCTAGAAACA
Long Flanking Sequence:
ACTTACATCAATGCAGATTAAGAGACCTATAAGTGCTAGGAACTTACACCAATCCAGGTTGGGAGACATCTTGGTTGGAGGGATTAACACCAAAGCAGGTTGGGAGACCTCTAAGTGGGAGATACTTACACCAGTGCAGGTTGGGAGAGTGGTAAGTGGGAGGGAATTACACCAAAGTATGTTGGAGTACATCTAGGAGGGAAAGACTTACACCAATCCAGGTTGAAAGACCTCTAAGTGGTAAGAACTTACACCAATGTTGGTTGGCAGGCCTCTATGTGGGGGAGACTCACACCAAAGCAGGTTGGGAGACATCTTAGGAGGAGGGACTTAGACCAAAGCATGTTGGAAGACCTCTAAGTGTGAGGGAATTACACAAAAGAAGGTAAATTCACCTGTTTTGTTTCTATTTTTCAGCTCTCTGATTCTGGCATTTATACTTGTGTGGCTGCAAGTTCTAGTGGGGAAACATCATGGAGTGCTTTCTTGGAGGTCAAAGG[T/C]ACTTGTTTGAAACTGTACACATTGTTAGTAATTTGGTTCTTCTAGAAACAGTTTGATTTCCTGATTATTTTGTCTTTCTTCAGAGGCTGGGAGTCTTGTTGTAGTTAAAGATCGGGATGAGAACGAGCTTCCAGGACCTCCTTCCAAACCTCAGGTCACAGATGTCACTAAAAACAGCGTGTCATTATCCTGGCAGCCAGGCCTTCCCGGAGCATCAGCCATTTCTACATATGTCATAGAAGCATTCAGGTACAAGTTGTGTATTAATTTAATTGGTTTTGCCTTTAGGGGAGTGTTCATAGTTTTACTGAAAGATCATTTGTTTAAGTACTCAACCAAACCAAAGTTCTCTCAAAGTAGATGACAATTTTAGTTGGCAACAAGGAGGATTTATGTTGAAAGAATCTTTTCAATCTATTTCCAGATGATTTAAAACATTGAAAATGTATCTCTAAACACATTTGGAGGGTACAAAAAACATGAACAGTATAGATTGTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35976
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 |
|---|---|---|---|---|---|
| ENSDART00000014877 | Nonsense | 552 | 1387 | 13 | 27 |
| ENSDART00000099344 | None | None | 111 | None | 3 |
| ENSDART00000099346 | Nonsense | 548 | 736 | 12 | 15 |
| ENSDART00000129511 | Nonsense | 552 | 1391 | 13 | 28 |
Genomic Location (Zv9):
Chromosome 15 (position 37926428)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 39299025 |
| GRCz11 | 15 | 39145627 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCCCTCAGGTTGACCGCCAGTCTCAGTTCATCCAGGGCTACAGGGTTT[T/A]GTACAGGCAGATGTCAGGCCTGTCTTCTCCAGGAGCCTGGCAAACTCAGG
Long Flanking Sequence:
CTCATGCGCAATTTGCAATTACACTAAATGCATGAGCCTAACTGAACCGCGATCTGGCTCACCTCTTCTATCTGGGCTAGTGCTGGCCAATTGAGCCGCACCTGGGCCCAATTCGGAGCACTCACACTTGTCTAGCAAACTGTGAAACACGCCCAGGCATGGTTCGGATAGCCTAGAGTGAGTAAGCCCTTACTCATTAATTAGTGTTACGGTTTCGGGCGAATGTAAGTAGGAAGGTAGTAAATATATAGCACAAAATTGATAGTATTTGAAGTGTTTGTTACTGTAGGTGCTTCATATAGTTTAAAAATGCTAAATATTACTTTTCTTATCTTTTGACATACTGTGTTTTCACATAGTTAATAATAGAGAAGCTTTTGATTTCATCTTTATATTTTGGGTGACTTTAATTCTACATACTCGTTTTGACTCCAGTTTTTGAAATGTCTCATCCCCTCAGGTTGACCGCCAGTCTCAGTTCATCCAGGGCTACAGGGTTT[T/A]GTACAGGCAGATGTCAGGCCTGTCTTCTCCAGGAGCCTGGCAAACTCAGGATGTGAAAGTCCCCTCAGAGAGGAGCATGGTGCTCTCGGCTCTAAAGAAAGGCATCGTCTACGAGATCAAAGTGCGTCCATATTTCAATGAGTTTCAGGGCATGGACAGCGAATCCCGAACCGCAAGAACAACAGAGGAAGGTATAAAATTTAACTTCTTTTATGTAATAAAACTGTGCTGTGTGCAATGGTGTAAAGTAACAAATTGCATATTCTCGACTGTAATTGAGTAGGTTTTTTTTCAGAAATTTAAGTAGTTTAGCAATAAAAAATGACTGCTTGACTGCTACCTTTTCAGTTTTTTGGTTTGAAGAACTTCCAATTATAAGAGCTGCGAGAAATCCCTTTATCACTTGCTTTATACATTAGGAAAATAACATTACACTTGGTGTTTTAGTGTGACATTAGTACCTTCAGCATATCTGTGGCCAAAATTGTTCCTCCTTGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35975
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 |
|---|---|---|---|---|---|
| ENSDART00000014877 | Nonsense | 649 | 1387 | 14 | 27 |
| ENSDART00000099344 | None | None | 111 | None | 3 |
| ENSDART00000099346 | Nonsense | 645 | 736 | 13 | 15 |
| ENSDART00000129511 | Nonsense | 650 | 1391 | 14 | 28 |
Genomic Location (Zv9):
Chromosome 15 (position 37915123)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 39310246 |
| GRCz11 | 15 | 39156848 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAACAGCACATCTATTAGCATCTCCTGGGACCCTCCGCCTGCAGAACAC[C/T]AGAACGGCATCATACAGGAGTACAAGGTGAACAACAATTAACACTTATTA
Long Flanking Sequence:
TGTCTCTCAGTAAATGTGTTTTTGGAGTAAATCCCTCCTTTCAAAGCCAGGATATGAAACGATAGTGAGATGTGAAGAAGCGTCAGTGTCAGGCTGAAGAAAATCCTCCTCTAATGAACTCGTGCACTAAAGCTCAACACACATACATGCACTGCTTAATGCCAACACAGTGACTCTTTCAGAGGAAGCAGGATGAGAGCGTGCCACGGCCATGTACATCAATCCTTTGCCAAACAATGCCAGACCCAGGCTGAAAGAAGCCTAATCTGTTCGGAAAAGTGCAGAATGTCAATATTTGCGGTGATGAAGCTCTGCTGCTTGATTTCATATTCATGTGGCTTGTATTATATTGAAGTACACCAGAGCCTTGAGGCTTTTTTTTTTGTGTGTATTTTTTTGCAGCGCCCAGTGCTCCTCCTCAGCAGGTGACTGTACTCACTGTGGGCAACCAGAACAGCACATCTATTAGCATCTCCTGGGACCCTCCGCCTGCAGAACAC[C/T]AGAACGGCATCATACAGGAGTACAAGGTGAACAACAATTAACACTTATTATTCATTTCATTTATTTCTTTAATCTGGAGAAATTTTGCATTATTCATAGTGCTAATGAAACATTTTAGTCTTACCTTAAACTTAACATTATATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTATTATATTATATTATATTATATTATGGGCGTCATGGTGGCACAGTGAGTAGCATGATCGCCTCACAGCTAGAAGGTCGCTGGTTCGAGCCTCGACTGGTTCAGTTGGCATTTCTATGTGGAGTGTGTATGTTCTACCATGTTCGTTTGTGCATGTTCGTGTGGGTTTCCTCCGGAACTTATTACTTATTACTATTTACTGTTATTTTTTCAGTATGAATGAAAAATCATAATAAAATCGCATTCTTAGTTATAATATAATATAATATAATATAATATAATATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35974
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000014877 | Essential Splice Site | 715 | 1387 | 15 | 27 |
| ENSDART00000099344 | None | None | 111 | None | 3 |
| ENSDART00000099346 | Essential Splice Site | 711 | 736 | 14 | 15 |
| ENSDART00000129511 | Essential Splice Site | 716 | 1391 | 15 | 28 |
Genomic Location (Zv9):
Chromosome 15 (position 37912972)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 39312531 |
| GRCz11 | 15 | 39159133 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGCGCCGGGGTCGGAGTGAAGAGCGAACCACAAACCATCATCATTGG[T/A]ACCAGAAATGTTTAATTCTCAGCTTTTTATCTGTCAAACTCAACACTGCA
Long Flanking Sequence:
TATGTTATGTTGTTTTACATTATATTACTTTACATTAAAAGAGATGATTACTGAAATATGCATTAAGGCTATTACATTACATTACGTTACATTATGTTATGTTATGGTTTGTTATGTTATGTTGTGGTATATTGTTTTACATTCTATTACTTTACATTGTAAGAGATTATTAATGAAATGTGCTTAGCAGATTTATTTATTTATTATAATTGTTTTAAATCCTCAATAGTTTTCAATAGTTTATTTTGTTTATTACATTTATTTATATTGTTCAAGTCACAAAGAGTTGTCATGTGCAGTTAGTTAACCCTCTTCTATCTCTCTCAGATCTGGTGTTTGGGGAATGAGACCCGTTTTCATGTGAATAAGACGGTGGACGCAGCGATCCGCTCAGTGGTGGTTGGGGGTCTCCAGGCGGGGGTCCAGTATCGGGTGGAGGTGGCCGCTAGCACCAGCGCCGGGGTCGGAGTGAAGAGCGAACCACAAACCATCATCATTGG[T/A]ACCAGAAATGTTTAATTCTCAGCTTTTTATCTGTCAAACTCAACACTGCATGCCTGTTTCCACAAATTTCCATGATCCATCATTGTAAAATAAGAATTGATTAATCAATTTATCTTAATAATGCGATAGATATGTTTACTTATGTGGAAAATTACCGCTCTAGGCAAAGGACGGTTATGCCACCCTCAACCCTAAAGTGAAACCGGGGGGGAGGGTGTCGAGCGACGCCGCCCTCCCTATTCTGCCGCCCTAGACGCAGACATAACTGAGTGAGGGTGCGGGTGGTGAGGGTAGTGTCGCAGACGCCACCCTAGACGCAGATATAACTGAGGGCGCGGGTGGTGAGGGTAGTGTCGCGGACGCCGCCCTAGACGCGGATATAACTGAGGGCGCGGGTGGTGAGGGTAATGTCGCGGACGCCACTCTCTCTATTCTGCTGCACTAGATGCAGATATAACTGAGGGCGGAAGAGGTGAGGGTTGTGTCGGGGACGCCGCCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6395
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 |
|---|---|---|---|---|---|
| ENSDART00000014877 | Essential Splice Site | 799 | 1387 | 18 | 27 |
| ENSDART00000099344 | None | None | 111 | None | 3 |
| ENSDART00000099346 | None | None | 736 | None | 15 |
| ENSDART00000129511 | Essential Splice Site | 800 | 1391 | 18 | 28 |
Genomic Location (Zv9):
Chromosome 15 (position 37898692)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 39327025 |
| GRCz11 | 15 | 39173627 |
KASP Assay ID:
554-4488.1 (used for ordering genotyping assays)
KASP Sequence:
ACCCCAGTGACGTTCCAGCGTGTTGATGGAGGCTTGATGAGCAACGGGAG[G/A]TAAGATTCCTGTCATCTGCTCTCTCGTTTCCCCTTGTTWTTCCTCAGCAT
Long Flanking Sequence:
GTTGAAATGATGTTTGTTAAGTAATCTTAAAGCGAAAATGTAAATTCTGATTTATTTACTCTTGCCATTTCAATCTGTACTTGAATGGAGTTCAACGTTGTTTTGCATCCCATTAACATTTGTCAAATGGAATTATTTTACACTACTTTTTCTCAATAATCCATTACTTCATTGTTTCTTTTTGAACACTATTTGTTTAAAATCACTTTCATTTGGCAAGAATGTGAAGGAATATAGACTAAATTGGAGTTGCCATGATTTCATTCATTCATTGCTGATTTATTTTGCAGTTTGAGAAGTTCTGAGCCATTTGTACAAACTTTCCAGCTGTGTAAATGTTCATGTTTCAAAACAATCATGAATTAGGACGAGAATAAGTGATTGATTTCTTGTTATAATGAATGTAATGATGACTCAGTCTTTTTCTCTCTGTTTTCTACCCTTTTTCTGACCCCAGTGACGTTCCAGCGTGTTGATGGAGGCTTGATGAGCAACGGGAG[G/A]TAAGATTCCTGTCATCTGCTCTCTCGTTTCCCCTTGTTATTCCTCAGCATGCCACAAAACAGCGCTGGTTATTATCTTTGTGCCAATCACCTGCCTTTAACCTTCAAAGACCAGCCCCTCAATTCCAAACCTCATTCATATTCTGTCCATCATCCTCTGGAAGGTCATCAAAACCATTATCCTCTACAAGGCAGTCGTCTTCCAGCCCGCACTCCGCTTTTAAGGGTTCGCGCCATCGCTGCACTGTTAGAAATTCATCTTAAGGGACGCTTCGGAAGAGAGAATTGAAAGGTTGTTTCTATAGGTTTCTGTGAGAGTTCTTGTGACACACAGCCGTTTCTCATGGGTCAGCAGCTTGATTAACCTTCTAAAAGTCACGCCAGAGTCCATCAATGCGGAACAATTCTTTGCATAACCAATAAAACAGGCTTCGTTCAGATATAAAGAAATAATTCAACCAAAAATATTCAAGATATTGGGCACTTTGCTGGTGTCAAACA
Associated Phenotype:
Not determined