ZMP
si:dkey-91m11.5
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC560226 [Source:RefSeq peptide;Acc:NP_001116725]
Human Orthologue:
BCR
Human Description:
breakpoint cluster region [Source:HGNC Symbol;Acc:1014]
Mouse Orthologue:
Bcr
Mouse Description:
breakpoint cluster region Gene [Source:MGI Symbol;Acc:MGI:88141]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34433 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41236 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41237 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31660 | Essential Splice Site | Available for shipment | Available now |
| sa41238 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21327 | Nonsense | Available for shipment | Available now |
| sa16588 | Essential Splice Site | Available for shipment | Available now |
| sa34434 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34433
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 |
|---|---|---|---|---|---|
| ENSDART00000062073 | Nonsense | 44 | 1291 | 1 | 23 |
| ENSDART00000137009 | Nonsense | 44 | 1290 | 1 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 31349341)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30492067 |
| GRCz11 | 8 | 30501299 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTCGGAGACATCGAGCTAGAACTGGAGAAATGCCGAAACTCCATTAGG[C/T]GACTGGAGATGGAAGTAAACAAGGAGCGATTTCGAATGATCTACCTGCAA
Long Flanking Sequence:
CTGAGAAAATAACAGCGCTATTTTCCTGATAACTTCTTAGGATACATTAGCAAACCTAATCTTTTTAAGCAGCTGATATGAATAATATGTGAATTTTGCACCCGAATCTGTTCACAAGGGATCATCATTTGCCATTTAAACGACATGGGATGTGAATAGGTGTTTGAAGTGCACATGGATGTTTCTGCTATGCTGCTTGTTTGTCTTTCCAAGATAAGCTGAGTAAGTGTTTATCAGATGTTGAGATGATGTTTTGCATGTACACTGGACAAATGTTGGATATAAACTTATGCTTTGGGTGTATACATAAAAACAAGTGAATTCTAATGTCACTTTTTTCCACTAGTAAGAAAAACCTGCTGTAAGCAATCATGGTAGAACCTGTCGGTTTTGTGGAAGCTTGGAAAGCTCAGTTCCCTGACTCAGACCCTCCTGAGATGTCTTTAAACTCTGTCGGAGACATCGAGCTAGAACTGGAGAAATGCCGAAACTCCATTAGG[C/T]GACTGGAGATGGAAGTAAACAAGGAGCGATTTCGAATGATCTACCTGCAAACACTTTTGGCCAAGGAGCGAAGAAGCCACGACTCTCAGCGATGGGGATTCAATAGGGTCTCACAAAGTGAGCGAAAGCCAGCATCTATGGATGGCCATCATCAAAAACCAGATGGAAGCAGGTGTCTCCCAGCCAAACTGAAGCATTCGACAGCAGTAGAGGAGAGTCGTGAGCCTCAGCAATGTGTTGAGGTGGTGGGAGGTGATATTTCAGACTTAGACAAACAGAAAAACAGAGACGGAGAGATTGATGGGATGTCTCCATACAAAAAGAGGAGTGTTGAAACATCCCCCAGAGCCATCACTGGACGTGGACCTGTGTCCCAAGATGCGGATGGTATTTCAGAGTCTCCACCGAAGGTCACCTCTGGGTTGGGAGTTGCAGCACTTCGCTCCAACTTTGAACGTATAAGAAGAGCCAATTCTCAGTCATCTGGCGAAGGAAAAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41236
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 |
|---|---|---|---|---|---|
| ENSDART00000062073 | Nonsense | 399 | 1291 | 1 | 23 |
| ENSDART00000137009 | Nonsense | 399 | 1290 | 1 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 31350406)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30493132 |
| GRCz11 | 8 | 30502364 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGCCCCACCGCCTACCGAATGTACAGAGAGAAGAGCCGCTCTCCATCC[C/T]AGCACTCCCAGCAGTCGTTCGAGAGTGGCAGCCCTCCCACACCACAGTCC
Long Flanking Sequence:
GAGACGTCTCAGAGAAGATAAGTAGTTTGGGCAGTCAGGCTATGCAAATGGAGCGCAAGAGGTCTTTGCATTCTGTCCCTGGAAATTTGTCCACCGCTTTTGGAGACATGCGAAAGCCAGAGCGATCTCACGAAAGAGCCATAGACAGTGGCTGCAACTGTGATTACGAGGACTCTGATTTGAACCCTGGGTTCCTCAAGGACAGTTCGGTAAGACTTAATGGAAGAAGAGCACCTCAGCAGAACTGGCAGCAGTCTGACTGTCAGCCCTACACGACTGTTTACGTTGGAGGCATAATGGGAGACGGGGAGGACCTGCACTTGACGTGGCCCAGGCGCTCTTACTCACCTGGGAGTTTCGAGGATGGATACACGCCAGATTGCAGCTCCAATGAAAACCTGACATCAAGTGAAGAAGACTTCTCCTCAGGACAGTCCAGCCACGTGTCTCCAAGCCCCACCGCCTACCGAATGTACAGAGAGAAGAGCCGCTCTCCATCC[C/T]AGCACTCCCAGCAGTCGTTCGAGAGTGGCAGCCCTCCCACACCACAGTCCCAAAAGCGTCTCAAGCAGCAGTTAGCACTCTCTGAAGCCAATAGCGGTGTCCGCAAGATCTGGCCCAGTGAGGGAAGCTCTAACAACTTCAGCAACAGTTTCCATGGAGATCTGGGTAAGACAGCATTCTTGCAGTGTTTACTTTTCTGTGTACTGTAGTGTTTGTTTGATGGGGTTTTCACAGGATTTCACTCTCCCACAGTAGGCAGGATAATGAAAAGAAAAGACACAAAGAACATAGACGTTTTATGAAAGGGTTTTTGTCTTTTTAGTGGATTTGCTGTTGTGCAGAGCTGCTAACATTTATCTGATTTGGATTGAGTTGAGAAAGTTTCACATTTTTAAATGCCTGCTAAACCAGTTAGGATGACTCTCTTATCAGAGAATTCATTCTCTAAAATAATATGTTACATATTATAAAAAAACATTTAAAGTGTGTGAAGGATCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41237
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 |
|---|---|---|---|---|---|
| ENSDART00000062073 | Nonsense | 416 | 1291 | 1 | 23 |
| ENSDART00000137009 | Nonsense | 416 | 1290 | 1 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 31350457)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30493183 |
| GRCz11 | 8 | 30502415 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCACTCCCAGCAGTCGTTCGAGAGTGGCAGCCCTCCCACACCACAGTCC[C/T]AAAAGCGTCTCAAGCAGCAGTTAGCACTCTCTGAAGCCAATAGCGGTGTC
Long Flanking Sequence:
AGCGCAAGAGGTCTTTGCATTCTGTCCCTGGAAATTTGTCCACCGCTTTTGGAGACATGCGAAAGCCAGAGCGATCTCACGAAAGAGCCATAGACAGTGGCTGCAACTGTGATTACGAGGACTCTGATTTGAACCCTGGGTTCCTCAAGGACAGTTCGGTAAGACTTAATGGAAGAAGAGCACCTCAGCAGAACTGGCAGCAGTCTGACTGTCAGCCCTACACGACTGTTTACGTTGGAGGCATAATGGGAGACGGGGAGGACCTGCACTTGACGTGGCCCAGGCGCTCTTACTCACCTGGGAGTTTCGAGGATGGATACACGCCAGATTGCAGCTCCAATGAAAACCTGACATCAAGTGAAGAAGACTTCTCCTCAGGACAGTCCAGCCACGTGTCTCCAAGCCCCACCGCCTACCGAATGTACAGAGAGAAGAGCCGCTCTCCATCCCAGCACTCCCAGCAGTCGTTCGAGAGTGGCAGCCCTCCCACACCACAGTCC[C/T]AAAAGCGTCTCAAGCAGCAGTTAGCACTCTCTGAAGCCAATAGCGGTGTCCGCAAGATCTGGCCCAGTGAGGGAAGCTCTAACAACTTCAGCAACAGTTTCCATGGAGATCTGGGTAAGACAGCATTCTTGCAGTGTTTACTTTTCTGTGTACTGTAGTGTTTGTTTGATGGGGTTTTCACAGGATTTCACTCTCCCACAGTAGGCAGGATAATGAAAAGAAAAGACACAAAGAACATAGACGTTTTATGAAAGGGTTTTTGTCTTTTTAGTGGATTTGCTGTTGTGCAGAGCTGCTAACATTTATCTGATTTGGATTGAGTTGAGAAAGTTTCACATTTTTAAATGCCTGCTAAACCAGTTAGGATGACTCTCTTATCAGAGAATTCATTCTCTAAAATAATATGTTACATATTATAAAAAAACATTTAAAGTGTGTGAAGGATCTGTTAAAGGCATGTTGCAACAGTCACGTTATGAAAGTTTAAACTTAATGTTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31660
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 |
|---|---|---|---|---|---|
| ENSDART00000062073 | Essential Splice Site | 771 | 1291 | 9 | 23 |
| ENSDART00000137009 | Essential Splice Site | 770 | 1290 | 9 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 31418326)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30561052 |
| GRCz11 | 8 | 30570284 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTACCGACATTCTGCTCTGCGCTAAATTGAAGAAACAAACTGGAGGG[T/C]AAGACATGATTTATTTTTCATTCCTATAGAATCATTGTTGTTTGTCTTTT
Long Flanking Sequence:
TGTCTTGTCTTGAGTCACAGGGTTTCACTAGAGACAAATTGCTGGACATTTGGACGCATACACCACCTAATCTACCCGCTATACACTTTTTATACACATATACACACTTATTTAACATACTTTACGTGCCAATTTGCACATAACAGTTGCACAAATAACGTTGTATATAGTAATATATCTGCACATACACTTGTAAGTTTGTATATTTGCATTCACTACTTACTTATATTTTTAAATATATTTATTATCTGTTTTTTTGTCCTGTCTCTGTAATTCTGTTGCACTTTAGGAGCTCTGTCATGTAAACAAATTCCTTGTATGTGTGAACATACCTAACAATAATGCTCTTTCTTTCTTTCTTATTCTTGTCTTTGAAGAATCGACAGCTTCTTCGAGACCAGTTTATGGTGGAGTTAGTAGAAGGTGCACGAAAACTGCGACACGTCTTCCTCTTTACCGACATTCTGCTCTGCGCTAAATTGAAGAAACAAACTGGAGGG[T/C]AAGACATGATTTATTTTTCATTCCTATAGAATCATTGTTGTTTGTCTTTTTTGCCATCTGCTGTTGATTGTCATGTATGTGAGCGCTGGTTTGGATGTCTATGTATGTGTGTGTGTGTGTGTTCAGGAAGGGGCAGCAGTATGACTGTAAGTGGTATATCCCGCTAGCGGACGTCACCTTCCAGACCATCGATGAGTCTGAGTCCTCGCCTGTTCCACAGATACCAGAAGAGGAGATTGATGCTTTGAAGGTCAAGATCTCTCAGATCAAAAACGAGATCCAGCGGGAAAAGGTGGATGAGATCATCAGAAATGCTCTTCTACTGCCAAAAAAATCAGCTTTTTGTTGACTGTTTTCAATCTGGTCTCTCTGTGTGTTCAGAGAGTGTGTAAAGGAGGAAAAGTGCTGGATCGCCTCAGGAAGAAACTGTGCGAACAGGAATCGCTGCTTCTCCTTATGTCTCCCTGCATGGCCTTCAGAGTCAGTAACAGGAACGGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41238
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 |
|---|---|---|---|---|---|
| ENSDART00000062073 | Nonsense | 798 | 1291 | 10 | 23 |
| ENSDART00000137009 | Nonsense | 797 | 1290 | 10 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 31418533)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30561259 |
| GRCz11 | 8 | 30570491 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCCCGCTAGCGGACGTCACCTTCCAGACCATCGATGAGTCTGAGTCCT[C/A]GCCTGTTCCACAGATACCAGAAGAGGAGATTGATGCTTTGAAGGTCAAGA
Long Flanking Sequence:
TGCATTCACTACTTACTTATATTTTTAAATATATTTATTATCTGTTTTTTTGTCCTGTCTCTGTAATTCTGTTGCACTTTAGGAGCTCTGTCATGTAAACAAATTCCTTGTATGTGTGAACATACCTAACAATAATGCTCTTTCTTTCTTTCTTATTCTTGTCTTTGAAGAATCGACAGCTTCTTCGAGACCAGTTTATGGTGGAGTTAGTAGAAGGTGCACGAAAACTGCGACACGTCTTCCTCTTTACCGACATTCTGCTCTGCGCTAAATTGAAGAAACAAACTGGAGGGTAAGACATGATTTATTTTTCATTCCTATAGAATCATTGTTGTTTGTCTTTTTTGCCATCTGCTGTTGATTGTCATGTATGTGAGCGCTGGTTTGGATGTCTATGTATGTGTGTGTGTGTGTGTTCAGGAAGGGGCAGCAGTATGACTGTAAGTGGTATATCCCGCTAGCGGACGTCACCTTCCAGACCATCGATGAGTCTGAGTCCT[C/A]GCCTGTTCCACAGATACCAGAAGAGGAGATTGATGCTTTGAAGGTCAAGATCTCTCAGATCAAAAACGAGATCCAGCGGGAAAAGGTGGATGAGATCATCAGAAATGCTCTTCTACTGCCAAAAAAATCAGCTTTTTGTTGACTGTTTTCAATCTGGTCTCTCTGTGTGTTCAGAGAGTGTGTAAAGGAGGAAAAGTGCTGGATCGCCTCAGGAAGAAACTGTGCGAACAGGAATCGCTGCTTCTCCTTATGTCTCCCTGCATGGCCTTCAGAGTCAGTAACAGGAACGGCAAGGTGAATCATTTACATATTACATTTACTCATTGAGCAGACGCTTTTATCCAAAACAACTTACAAGTGAGGATTAAAGAAGCACTTTAAATCATCAGAGAGTTGGTGTTTGTAAACGCTAAGACAAGTTTAGGTTATTTTTTGTTTACTTTTTTCTTTCTTTTCAGTAGCACAAAATCTTCTCAAACTGCGTGTTTGCTAAAAGGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21327
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 |
|---|---|---|---|---|---|
| ENSDART00000062073 | Nonsense | 881 | 1291 | 12 | 23 |
| ENSDART00000137009 | Nonsense | 880 | 1290 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 31419930)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30562656 |
| GRCz11 | 8 | 30571888 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCAGGGTTATACATTCCTGATTTCATCTGACTATGAACGAGAAGAATG[G/A]AGAGAAGTCATTCGGGAGCAGCAGAAAAAATGTAAGCACTTACAAGATGT
Long Flanking Sequence:
AGTAGATTTTAAATTAAATTATGTAGTTTCTTATGGCCTGTTAGGAGAAATTAGCTTGTTTTAATCATGAACTAGCTTAATGCTATAAATAATTTATAAATAATATAGAGGAGGCACAGCATTCTGCAAACCTTATTCAAAGCTTAAGCGTTTTTTGGGGGTAAAATTATTTAAAAAGTCATGAGAACAAAGTACAAAGATGTTTTTTTTCTTCAAACTTTTAATGTGTTGCTAATACAATGTTTAAAAAACATATTAGGTGTTTGTGTTACCTTTAAATTATTTATTAAATCATTAATTGGTATTAAATGCTTAGGTTATCCTTCATAAGTCCTGGGAAAAGCTCAGTACATTGTCAAAAGATGCAAATGTAACATGAATTTAGATATGTAAGTAAGCTGTTTTCAAAAGTTCTTATCTCTTGTGCCCTTCTTGTGTTTTATTTCTTTATTTCAGGGTTATACATTCCTGATTTCATCTGACTATGAACGAGAAGAATG[G/A]AGAGAAGTCATTCGGGAGCAGCAGAAAAAATGTAAGCACTTACAAGATGTTCCTCACAAAATCTTCCTAACTTCTTTACAGTCTCTTATTTCCAGTTAAAAGCAGATACAGCTGGCTCCAATGACTAAGTCGCTTGTGTTTGTTTCAGGTTTCAAGAGTTTTTCTTTGACTTCTCTGGAGTTGCAGATGCTTACAAACTCTTGCGTGAAGCTACAGACAGTTCACAGCATTCCTCTGACAGTCAATAAAGATGGTGCGTGTTTAATTTTTTTGTTTTGCTTTGCTTTGTTTTGCCCTCTGACAGTTAATAAAGATGGTGAGTGTTTGTTTGTTTTTTTTTGTTTTTTTTTTTGTTTTGATTTGTGTTTTGTTCTCTGAAAGTCAATAAAGATGGTGAGTTTTTTGTTTTGTTTTGTTTCCTGACAGTCAATAAACATGGTGAGTTTAGTTTTTTTTTTTTTTTTTAAGTTTCATTTTGTTTTGTTTAGTTTTGCTTTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16588
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 |
|---|---|---|---|---|---|
| ENSDART00000062073 | Essential Splice Site | 1024 | 1291 | 16 | 23 |
| ENSDART00000137009 | Essential Splice Site | 1023 | 1290 | 16 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 31424264)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30566990 |
| GRCz11 | 8 | 30576222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATGATGGCGAAAACATKGATCGCGTCATGGCCAAGGGGCAGATTCAGG[T/C]ACGGCTTTTTCAGTTTGGACYKTATCAGAATTACTTTMACTCTACGTTTT
Long Flanking Sequence:
TAGAAAAAGTGTTTAGTGTAATATTTGTACAAAATTTAACATGTAACCACAATGTTGTCTGTTCTCTCCCTGACCTCAGATCTGTACTGTACATTGGAGGTGGACTCGTTCGGCTACTTTGTGAACAAGGCAAAGACTCGTGTTTACAGAGACACTACAGAGCCAAACTGGAACGAGGTCAGAAATATAAACCGCCCACAACCACACAGTTGTCTACAATGAATGTTAATAAAAACACACACAGTAATGTTTATCTCAGTATGGTGCAGTTCCACTTTGTGCCACGAATTGACACTAGAAATGCAGCTGTAAATATGCAAACGGATGTAATGCTGGTTGAATGCTGTGATTGAATGAAGGTTGAATTTTGTGTTGACAGGAGTTTGAGATCGAGCTGGAGGGCTCACAGACCCTCAGACTGCTGTGTTATAGTAAAATCAAACAGTGCAGGGATGATGGCGAAAACATTGATCGCGTCATGGCCAAGGGGCAGATTCAGG[T/C]ACGGCTTTTTCAGTTTGGACTTTATCAGAATTACTTTCACTCTACGTTTTTAGTGCTTGAGTAGAGCTGCACATTTATTAAAAAACAAATTGTAACAAAATGTAATTAATTACTATTAATTATTTAACTTTATTAATAACTGACAAGTTAAATTTTAACTGACATATTAAATATTAATATTAACTTACATAAACTCACTTCTCTCTAGATTAATCTATTGCATGCTATTAATAAGGAAATTTTTACATTCATTTTTGTTTTGAATGTTTTTTATTAAGTTGAATGAATTTTATTAAGTCAGACCGTACATCCCAGGGTAAAAAACTAAAAATAAATAATAATAAAAAAAACTTCATAGTGTTTTGTTTATATTTTAACACAGAAAGATTCAATTAAATTAAATAATTCAATAATTCAATTCAATTAAAATGTTATAATATTTTTTTTTATTTAGTATTTTTAAAGTATTAAAGTTAAAAGTTAATTAATTAAAAACTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34434
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000062073 | Nonsense | 1066 | 1291 | 18 | 23 |
| ENSDART00000137009 | Nonsense | 1065 | 1290 | 18 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 31434948)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30577674 |
| GRCz11 | 8 | 30586906 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCTATGCGATTTACCAGCAGAGAGTTCAGTCTGAAGCGGATGCCCTCC[A/T]GAAAACAGTCTGGAGTGTTTGGAGTCAAAATCGGGGCCGTCACTAAGTAA
Long Flanking Sequence:
TGAAAACAGTTGTGCTGGTTCATATTTTTTGTGTAGACAGTAATACATTTATTTTCCAAGACTAATAAATTTAGCATATTTATTAAATTAGTCTTTCATAATAATGTGAAAATATTTATGATCGTTTAAAATATATAAAAGTGACATATCAGGTGTGAAAATATAGACATAAGTTCTTAAAATATGTCATATACCTCCATCAGTACATGAATCCATTAACATCCTCCAATCATTAGTTAACAATTATTTGTCTCCCATAATATGAAGCACACCGATGGATTAAATTCATGTGGCTTGATATTAAGCTGATGGACGAAGCTTACATTGATTTAATTCTTGATTATTTGATAGGTGAGATTGAGTACAGAGCTGTTTTGTTCTCATCAGTGAGTGTTTTTGTGGAAAAAAAACTTGTGCATATTCATCACTCTTTCCAGATTGAGGTCAAGCTGTCTATGCGATTTACCAGCAGAGAGTTCAGTCTGAAGCGGATGCCCTCC[A/T]GAAAACAGTCTGGAGTGTTTGGAGTCAAAATCGGGGCCGTCACTAAGTAAGTAAAGTTACAGATCAATCCATATATGACTGATTTAAATGCGCTATACACAGTACTAGTGCAAGTGGATTTTTGCTCAAATTGAAATATGAATAATTTCTTAGACAAAGACAGACTGTGATACATTTTATGTCAATTTTCATAACAAGAACATCTCAAACAATGTCACCTTTAAATTTATTAAGACAACTGAACGAATGACACGCGATAACAGTTATAATAAGCTCACAAAAAATTTATTTATTTTCATCACATGTAAAAACCTGTTTAAAAAGCATCTGGGAGACTCCCGAAACTTCCCGTCCTACTCATAATTCTCTCTTCATATAGCCGTATGCCTATTACATATCCATAAAACACTGTGTAATAACCGTGCTCAGATCATATCGATTTCTCACTGCAATCAATCCGCTCCAGAATTCGTTTCAATCGAGCCGAGGCCATCTCATTC
Associated Phenotype:
Not determined