ZMP
gpr98
Ensembl ID:
ZFIN ID:
Description:
G-protein coupled receptor 98 [Source:UniProtKB/Swiss-Prot;Acc:Q6JAN0]
Human Orthologue:
GPR98
Human Description:
G protein-coupled receptor 98 [Source:HGNC Symbol;Acc:17416]
Mouse Orthologue:
Gpr98
Mouse Description:
G protein-coupled receptor 98 Gene [Source:MGI Symbol;Acc:MGI:1274784]
Alleles
There are 21 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31473 | Essential Splice Site | Available for shipment | Available now |
| sa31474 | Nonsense | Available for shipment | Available now |
| sa18129 | Essential Splice Site | Available for shipment | Available now |
| sa14200 | Nonsense | Available for shipment | Available now |
| sa10539 | Nonsense | Available for shipment | Available now |
| sa20524 | Nonsense | Available for shipment | Available now |
| sa15969 | Nonsense | Available for shipment | Available now |
| sa20525 | Nonsense | Available for shipment | Available now |
| sa20526 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31473
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000008043 | Essential Splice Site | 405 | 6198 | 8 | 90 |
Genomic Location (Zv9):
Chromosome 5 (position 50518429)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 48084127 |
| GRCz11 | 5 | 48735638 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTAGTAAACGTTTTATCTGCGGTATCTCTAATCTCTGCTTATTTGTCTC[A/T]GATATGAAGGCATGATCATTGTAAGGAATGGAGGAACACACGGAGCTGTT
Long Flanking Sequence:
AAAAATAAATGAATGAATGAATCCTCATTAAATTTCTCACTTTAAAATACAGAATTTTACCCCAATTTTGTTCTCAACTTTTAAAACATTTGTTGTATTTGTCTAAATTTAACCATTTTGAATTTCCATTTTGGAAATAACCTTTCATTTAACATTTTTAAGGTGTATTTTGTTCTGACTAAATATAATGTGACAGTGAAGTCCTGGGCAAATTTACGTTACCTGACATTACCCAAGCAATACTATCTTTTCAACATTTGATTTATTGTAATTTTTACAGTGTTAAAGCTCTGCTATCGTTCATTTTTGATTGCCTGTTACTTTATGTTTCAGTGCATCGTATTACTCTTAATAAGGACAAATTCATTACACTGGAAGCTAGCCATTTTAGTCTTGTTTTAATGTTAATTAAAAAAAGAAACCTAAGTGCCAGTGGTGAGTGCAGTATACTGTAGTAAACGTTTTATCTGCGGTATCTCTAATCTCTGCTTATTTGTCTC[A/T]GATATGAAGGCATGATCATTGTAAGGAATGGAGGAACACACGGAGCTGTTTCTGTTCAGTGGAACATCACAAGGAACTCCACTGACAGATCTCCGGTCTCTGCCGATCTTAACCCTGCAGCAGGTACCTTGAGGTTTTCTGAGGGCCAGATGAGTGCTGTACTGCCTTTAAACATCACCCAGGACAGCCTCCCAGAAGAAGCCGAGGCTTTTCTCCTCAAACTGATCCCAGGATCTGTACAAGGAGGAGCTGAAGTGGATGAGCCGATGGAAGTAAGTGCTTCATTTTTTTTTAGAGAATGTATTCGGATTACAGCGGCGGCTCAATTCTGAGGTGGATTTGGTTTTGAAAGATGAGTGCGAGCTGACGTTGATGACAGCTTAAAGGAAAATGTTATTATTCATGATATGCCTGGGCACTGGTTGTCTTACATGTTGAAATGTCACCCGCTTTGATGGTATTCTAGACCTTTATGCTTAGTTTGGTTGCCGATCCTTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31474
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 |
|---|---|---|---|---|---|
| ENSDART00000008043 | Nonsense | 535 | 6198 | 9 | 90 |
Genomic Location (Zv9):
Chromosome 5 (position 50523668)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 48089366 |
| GRCz11 | 5 | 48740877 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGTATTCAGAGTCAGCCAGAGGGGCGATTCCTCTCCCTAAGCTTTCTC[A/T]GAGAAGGGGGGACTTTGGGAGAGGTACGACTTACACTGACTGCCCTCTAC
Long Flanking Sequence:
TGTACATTAATTGTTATTTTAAAGTGACAAGACGAAAACAGCCAATAAATATGTATTGTTTTTATTTACCCCTTTTGTTTTGTTCATTTGTTGATTATATGAACTTACAGAATGCGTAATAGATGCATTTATTTGAACCTATTAATGAATGAGATTTTAACAGAACTGAATTCAGCATTATATTTTTTTAGAATGCAATTGTTCACTTAGCCTACTGTAAAATCTTTCTTTGAACGTGAATATATATATATATATATATATGTTACGAATTGCTATTGCTATGATGTTTTGGATAAAAGAAGTTCTATCTGTCTTAAATGCTAGAAAAAATTGACATTGCAACAGCTGTAAGGAAACTAAACTATACTGTTTGTCCTTCACAGATGGTGTTCTTCATTCAGGACAGTGATGATGTCTATGGTCGATTTGGCTTTCATCCAAGAGAGAATCAGAGTATTCAGAGTCAGCCAGAGGGGCGATTCCTCTCCCTAAGCTTTCTC[A/T]GAGAAGGGGGGACTTTGGGAGAGGTACGACTTACACTGACTGCCCTCTACATACCTGCCCGTCCACTGGACCCTTCACGAGCCCGAGATGGGGTGCTGAATGGCACCAGTGTCAACACTGTGCTGTTCAGTTCCGGTCAATCAAGAGCTCAACTCATTCTGCCCATCCGTAATGATGCCTTCCTGCAAAACGGGGCTCATTTCCGCATACAGGTAGGATAAACTGTTCAAACCATAAGGACTGCATGTATATAATACAACCCCAAATCAGAAAAAAATAGGGACATTACAGTTGGGACAACACATTCTCTATTGGAGACAGGTTGGGACTGCAGGCAGGCCAGTCAAGAATACTGTATCTTGAGTCTTTTAATTATTATAGGCACTGTTGAAAGTGAATATCCAAATATTTTCCTATTTGTTTTTGAGGAACATTGTTTTTAAACATTTAAAAAAAAATTCTCCTGTATTTGTTGGCAAACTGGTGATCCTTTTCTCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18129
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 |
|---|---|---|---|---|---|
| ENSDART00000008043 | Essential Splice Site | 1632 | 6198 | 22 | 90 |
Genomic Location (Zv9):
Chromosome 5 (position 50552766)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 48118464 |
| GRCz11 | 5 | 48769975 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCCAATGCKACAGGCTTYATCCTCTTCCAGYCGGGTCAGCTATCTGAGR[T/C]AACAGGATCAACTTGTCAAGCAGTTATTATTCATGACCACWAGACCACYG
Long Flanking Sequence:
ATATTATTTATTTATTTATTTAGTGATTCTTAATGTGATAGATCTCTGATAGAACTCTGGAGGTATGGTGATAACCAATATTTATTTATTTATTTAGTTTGTTAGTTAGTTTGTTTGTTTATTTATTCATTTATTCATATTTTTAACCCAAATACAATGTACAATTTATGTTTTTATTTTTTTATTTTTTATTTTTTTTAGTTTGTTTGTTTTGTGTGTGTGTGTGTGTGTGTGTGTATTTGTGTGTTGCTTTTAAAGGACCTAGAGTTAATGTAATTCTACTGTACTTGGCTTTGAATAACCTTTATTCTTTTTTTATCAGATAGCTGAGGAGGGCTCTATGATCTCTTGTGTGGTGGAGCGCACACGTGGGGCTCTGGACTACGTCTATGTAAACTACACCGTCACTCAGCTTGATTCACCAGCAGACTTGTCAAATGCCTCAGACTTTGCCAATGCTACAGGCTTCATCCTCTTCCAGCCGGGTCAGCTATCTGAGG[T/C]AACAGGATCAACTTGTCAAGCAGTTATTATTCATGACCACAAGACCACTGCACTATTATATAGTATTTACTGTGAAATGACTAAGCAACTTCTCTTCAAGTGATGACAGTGTGAAATACAGAAACAAATTCACTTTGCGATTAAGATCCAAACATACTGTGCATCAGCCACAAGTAGTAGTTTTTTTATTAGGCACCAGCACTTGATTGTAGATACTAGTACTTATAGTAGCTTTATCATTCACTTAATTCTTTCATTCACTGTCCTTCGGCTTAGTCTCTTTATTTATCAGGGGTGGCCACAGTGGAATGAACTGCCAACTTATCCAGCATATGTTTTACACAGTGAATGCTCTTCCAGCTGCAACCCAGTACTGGGTAACACCCATACACTTGCACATTCACACACTTACACTACAGCCAAGCATCAGGAGGAAACCCAATTGAACACAGGGAGAACATGCAAACTCCACACAGAAATGCTAGCTTACCCAGCCGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14200
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 |
|---|---|---|---|---|---|
| ENSDART00000008043 | Nonsense | 1653 | 6198 | 23 | 90 |
| ENSDART00000008043 | Nonsense | 1653 | 6198 | 23 | 90 |
Genomic Location (Zv9):
Chromosome 5 (position 50556031)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 48121729 |
| GRCz11 | 5 | 48773240 |
KASP Assay ID:
2259-6455.1 (used for ordering genotyping assays)
KASP Sequence:
TGCTRGTTGTAAATGATGATCTTCCTGAAGTTKATGAGCACTTCCGGGTT[C/T]GAMTGGTGTCTGCAAAATCAGGCGATGGCAAACCAGGTTCCACTCCCACC
Long Flanking Sequence:
TATTTAATTATTGTTTATTTATAATGCTGTGTTTACAGCCAAATAGTTGATTTACAGCTCCATCTAGTGGAGGTTTAATACTTTGGTTTTGTTTAACTGACTGTGACCTCACTCATAGGCTCATAGTCCAATTTATTATGCCCTTCACTTACTAACGTCCCTCCAACATTGATTACGTTAGTAAGTATCCACTACTAGCAGAACATCTGAACCCTTGAAGTACTTGGGAACTATACTGTTTTGGCAACATAATCGCACTGCATTCTGGGACATATACTGTATACTGTACTTGCTCCCTCTGTCAAAATTGAGGGATCGAGGGTCTATGTACACTTTCCTCATTCACTTGATGAAGTGTAACGCAATTTAATTTGCAAGTGCTTGTCTAAAAGAGGACTGAAACACAGTGACCTACTTATTTGCTGTCTCTGGTCTCACAGGTTTTAAACCTGCTAGTTGTAAATGATGATCTTCCTGAAGTTGATGAGCACTTCCGGGTT[C/T]GACTGGTGTCTGCAAAATCAGGCGATGGCAAACCAGGTTCCACTCCCACCAGTGGAGCCAGCATTGATCCAGAAAAAGCTGTCAACAACATTACTGTCAAAGCCAGCGACCACCCATATGGTACAGTATAGCACTTTCAGAGATGTGCTTTCAGTTTTTATACAGCTAAATGACTGGTTGTTGTTATGATTTCAGGCCTGCTGCAGTTTCAGACGACTCCAGTGCCTGTGGGAATGATCAGACCTGCTCTGGAAGAGGCTCGGGTCACTGTTCAGGAGGAAGCTGGTGTGGTCAGACTGCTGGTGGCCAGAGCACAGGGGCTGTTGGGACGAGTGATGGTGGGCTATCGGACATCTCCATTCACAGCAGCTGGATCAGAGGACTATGAGGTATCAGCTGCAGCTGGATATCACTTTAAAGAGTTAAAACCATAGTTAAAATCAAAAAGTAAAGGGATTTTTTTTTCAATTGTGAGTAATTTTATTTTGGTTACTTTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10539
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 |
|---|---|---|---|---|---|
| ENSDART00000008043 | Nonsense | 1988 | 6198 | 28 | 90 |
Genomic Location (Zv9):
Chromosome 5 (position 50562221)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 48127919 |
| GRCz11 | 5 | 48779430 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTCCRTGTGGCMGAAGCAAATGCTCTTGTTGCCCTAACCATACAGAGR[A/T]GAAAGGGCTTAATGGGAAGGGTACGAGTGGCMTATCGGACACTAAGGGAC
Long Flanking Sequence:
ATTGATGTGTGATGTAATACAGATATTTAGCGACTTTTCAGGCAGAGCTTAGCACCTTTTAATTGAAAATAGTTAGGTACAATGGAGGTGCATGTCAGTGTTATAAAATAACAATAAAAATCAGCCTTAATGTGTAAGTGTTTTGTTTTTCCCAGGTAATCCGTACCTTTGGCGCTCTATCCAATGTGACAGTGTACTGGGAGGCGGATGCTGCTTCAGAAGGGGAACTCGTTTACAGATCTGGCAATGTGAGCTTTGAGGTGGGTCAGACTGTCAGAAGCATCTACCTACTGATTTCCCAAGATGATGTTCCAGAATTGGACAAGACCTTCAAAGTCCGTCTTACCAATGCTTCTCATGGTCGACTTGGGAAGGAAACCACTGCCACCTTGACTGTATTGGCCAGCGACGACCCATATGGACTTTTTGTATTCTCTGACAACACCAGGCCAGTCCATGTGGCAGAAGCAAATGCTCTTGTTGCCCTAACCATACAGAGG[A/T]GAAAGGGCTTAATGGGAAGGGTACGAGTGGCCTATCGGACACTAAGGGACACTGATACTGCCCCGTACAGCACACCAGGAGTGGGTCGGGCCAGCGAAGGGAATGATTTTATAGCTGTTGTGGACTCTGTGATTTTCTCAGCCAATCAAAGTGAAGTAAATGTGACCCTGAGGGTGCTTGATGATAATGAACCAGAGAGGGCCGAATCTGTTTTTCTGGAACTTGTCAGTGTCACTTTGATTGAAGGGTTGCAACCCAGACCAGGTAAATAATCACACAAAACAGTTAATTTATTTAATAAAAGTGTATTAAAAATAAATATACTGGTTATTTATTTATTAAAAATGTGTTTAAAAAAATGAATGTTTTAACATTAATTGTTGGTTTTCCAGTGGCGCTTTCCCCTCGACTTGGCCCACGGAATGTCACCATTGCTCAGGTCATTATAGAAGCCAGCGATGATGCTTTTGGGGTGCTACAACTCTCTTCTTCTGCAGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20524
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000008043 | Nonsense | 2578 | 6198 | 33 | 90 |
Genomic Location (Zv9):
Chromosome 5 (position 50568640)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 48134338 |
| GRCz11 | 5 | 48785849 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATTTTTGCTCTACAGTATTAACCCTAATGCCACTCAGGAGGGTCTGTA[T/A]CTGGAAGTGAGGGAAGAACCTAAAACTACAGTGCTGCTGGTGATTGAGAG
Long Flanking Sequence:
AACATCACCACAAACACAAACGTGCTCAATTTCTGTGCAGCTTTCTGCCTTCGAGAGCGAGCTTGCCAAGCTTTCAGCTTCACCAACACAACCACGCCAAGTTGCTTCTGGGTAACATCTGGGGTCAGTCAATTGAGTCCGTCCCCACAAACGTTCACCTATTTAAAAAACACCACAGCGACCGCGTCTCTGTTTAGCTCACAGGCTGTTGCTGGGAGTGACTTCATAACCATGACGGCTCAGACCACAACCATGCTGGATGGATCGGGAGTCGCTAACCTCACCGTACCCATCTTGACTGACTCTTTGCCAGAAATGGATGAGAGTTTCATCATTAAGATCCTGAAGGTTAGCTTGGTCAACGTGACAGCAACTGCCAGGAACTTGCCAACAATTAGGCAGCCGGACACAGCTTTAGTGACTATAGGTATGAATGGAGACGCATTTGGAATATTTTTGCTCTACAGTATTAACCCTAATGCCACTCAGGAGGGTCTGTA[T/A]CTGGAAGTGAGGGAAGAACCTAAAACTACAGTGCTGCTGGTGATTGAGAGAAGAGGAGGCAGTATGGGACAGGTTACAGTGGAGTGGAAGTATGTTGGTGGCAGCGCCACACCCAATGCTGACTTTAATGGCACAGGGGAAACCCTCATCTTTGCAGAGGGTAAGTCTTGTTTACCTTGTGTTTGTTAACATGTTGTTATCTCTCTACTTTGTTGACCTCTAAGAAGGTTATCCGAGTTACAAATGAGAGAGCGCGCAGGGGCGGGGTTGTTGAGGGGAAAAGTTCGGTTGAAGTTGTCTCGTGTGTGTGCGAGGAGGGAATGAACAAAATAAAGTGTGCTTACTAAATAAACGTCATGTTTATTCAACTTTACAGTGTTGTTGATGGGATTGGCAGTTTAGGCCATGAGAAGTCTAGAGAACTCCATTAGCAAATGTTTCATTTAATATTTAAGCTTTTAACTCTTAATCTAGTCTTGCAGTTTTCATATTTCAGTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15969
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 |
|---|---|---|---|---|---|
| ENSDART00000008043 | Nonsense | 4479 | 6198 | 67 | 90 |
Genomic Location (Zv9):
Chromosome 5 (position 50607957)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 48173655 |
| GRCz11 | 5 | 48825166 |
KASP Assay ID:
2259-6462.1 (used for ordering genotyping assays)
KASP Sequence:
ATGAGATTTTTGAGTTGCAACTCACYGGTGCCACAGGAGGTGCCATACTT[G/T]GAGCTCAGCTAATTGCACGAATAACGATTGCCAAGAGTGACTCGCCAAAY
Long Flanking Sequence:
TCTCTTATCGACTGTTGTCATTTTCCTCTCATCTTGACTCCTACTATTAGTATTTATGTTGTGCTCTGGGTTCACCTTTGGGCCACTTCAGCCAATAGTAGAACAGTAACTACAGTGGAGGTGGGGATAAAAATAGTAAAGCCCCATCTGACTGTTCAGATTACCAAAACAAACTTTTTTTTATAAATGTACATCCATTAATTGTTCAACTAAAGAATAACAATGTTTACTAGCAAAATAAACATGGTAAATGTTTATTTCACACAGACTTTAAATTATTTGTGAATGCCATAAATTGGTACATTTTGTTTTGTAGAGTTTTCTATTCAATGTATGATACGACTAAACAGTGGTCATGAGTAGCTATATAGAACGATATAGCATTTTAAATGAGTGGGAGTTTGGAAAATTGTGCTGAAAAGTGTGTTCATTTTGTCCACAGTGAATTTAATGAGATTTTTGAGTTGCAACTCACTGGTGCCACAGGAGGTGCCATACTT[G/T]GAGCTCAGCTAATTGCACGAATAACGATTGCCAAGAGTGACTCGCCAAACGGTGTGGTTCGATTCATCAACCAAAGCGCCATCACCATCCCAAACCCCAACAGTACCGTCAGACTGAGTCTGTTTGCAGAGAGAGCAGACGGGCTGCTGGGAGACGCCACGGTGAGCCCCTGTCTAGACTATGAGCTCACATTTCTGATGCACATAGCTATAAAATACCAGCTTCTTTACATGTGGGACTTACAGTAGAGCACTTAGAGGAAAGGTTGACGTCAGTGTCCAATGTATAAATCAATTACTCAGTCAATAAATTCATGCATAAGAATTGTTAAATTTGATCTCAAGTTCATTTTAAGCAACATACTTCCTGTAAAGACTAAAATCAAAGACCGGAGTTTTAAAATATTTAAAATGTGCTTGGAATGTTTCCTCCTCTTCAGGTAATGTGGCAGATTCAAGGCCCAAACTCAAATGAGGTTTTACCATCCATGAACACAGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20525
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 |
|---|---|---|---|---|---|
| ENSDART00000008043 | Nonsense | 4763 | 6198 | 70 | 90 |
Genomic Location (Zv9):
Chromosome 5 (position 50610703)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 48176401 |
| GRCz11 | 5 | 48827912 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTATTCCCAAAACCAGTCAGTGGTTGTCAACGCTGCAGACCGAAGCAGA[C/T]AACTCATTATCAGCGTCAACAGGCTGGCAGGAGCTTTCGGCAATGCCAGT
Long Flanking Sequence:
TCACTGTGGTGAACCCAGATTAATAAAGGGACTAAGCCGATAAGAAAATGATTGAATTAATGATTTACTTTTTCGTTTTACTGTACTTTTGATTGATAAATGCAGCCTTGGTCAGCAAAAAACATTTCTTTCAAAAACAACTTTGAAATATATATTTTTTAATTTAGCAAGAAACAACTTTTTTGTCCCCCTCACAGGTTTTCTGGCAAATTCTCAGTGATGCAGACACATCAGGAGACTTCGCTGCCCTGCGTGGTTCAGTCATCATCCTGGCAGGACAGCGTTTGGCAGAGATCATCCTCACCCTGCTGCCCGACTCTGTGCCTGAGCTGGAGGAAACATACACCCTCCGTCTGACCTCTGTAGAAGGTGGCGCAGAGCTGGACTTAAACCGCAGCATCACCCGTCTGAAGGTCCGTGCCAATGACGAACCCCATGGGGTGTTTGTCATGTATTCCCAAAACCAGTCAGTGGTTGTCAACGCTGCAGACCGAAGCAGA[C/T]AACTCATTATCAGCGTCAACAGGCTGGCAGGAGCTTTCGGCAATGCCAGTGTGGGATACAGGATAAGTTTTACCACTCCTGGGCAGAGTTTTACAGAGGACACGATCACTGGAAACATACTGGTGAAGGATGGAGAACATGAGGCCAGCATTAGAGTCCCAGTTAGTAGCCAGGTGAGTGATTTAAAGCCACAGTATGTCATTTTCAGCGCTACAGGGTGCAAATTCACAATAAAAAAAACATATTTTGGTGACACCGTGACTGAGTGTGGAATCGTGGGAGTTGTCATCTTCACTAAATCCTGTGGAACTCTTCATGTTCATGGATGAGCTAAAGCATTCAAAGCGCATGTAACGAAGGCCAGCTAGTAAGTGCTGTGCATGTAAACCTCACTTCTCTGACCTCTCAAAGTGCTCTAGTGACAGATGCTAGTGGCCATGGTCTTTAGCCTCCTTATTAGAGCAACCAACTCCCATGCAGAAGGTCGCCGGTTCTATACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20526
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 |
|---|---|---|---|---|---|
| ENSDART00000008043 | Nonsense | 6093 | 6198 | 88 | 90 |
Genomic Location (Zv9):
Chromosome 5 (position 50712066)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 48277764 |
| GRCz11 | 5 | 48929275 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCACCGGTGCAGCTACTGTCGGCGGAGGAGAAATCAGCAAGTCTACG[C/T]AAAACCTCATCAGTGCCATGGAAGAGGTGTGTTCATTACCAAGGATCCTG
Long Flanking Sequence:
TTTGTGTTCAAAAGAAGAAAGAAACTCAAACTGGTTTGGAACAGGTGAAAGATGAGTTACCAATGACGCTATTTTATTTTTGAGGGGTTCAACTACCCTTTTAAAATGAATGAAGTTTGCAGTTATCATCAGTATTGATGCTGGAAAAGAAATCTACTGATAAAAGTCACAGAAAGACACCATTATGGTAGATTATTGACAGATAGTTTTATCCTTAACGCGCATATGTGTAACTTTTAAATAAACAGATAGGGGTAATGCAAAATCATTATACTCATAATCCTCTTATGTGATAGCATGTTGAGCTCTCCTAACAAGTTTGTTTTTATCTCTTTTAGGGTCTCTATGTGTTTTCTGTGTACTTCGTCATGCATAATCAGCTCTTCTGGCCTGGTAAGGCAACCTACACGGTGGAGATGAACGGTCACAGCAGCCCAGACTCCATTTACCAGAGCACCGGTGCAGCTACTGTCGGCGGAGGAGAAATCAGCAAGTCTACG[C/T]AAAACCTCATCAGTGCCATGGAAGAGGTGTGTTCATTACCAAGGATCCTGATGCATGTTTCTTATAAATACTTATGCCTAATTTGGCAGTGGCATCTGGTCAGAGGTGTAAAGTAACAAATTACAAATACTCAAATTATTGTGTAACTGCTAATTAAGTAAGCAGTTTGAAAAATGTGTACATTTACTCTCTTTGAGTACTTTTTAGTGCTGTATCTGTTCTTTTACTCCACTATTTTCCTTCAACCCGCAGTCACTACTTTTACCTGCAGTCACAATTTTTTTTTTCTTATCAATGGGGATTGGTTAAAAAAAAAAACAGTCCTGCGATTCCATTCCAATCAAATCACATAGACAGTAAAATCGCATTACTCTAAGCAATTTTAAGATATGGGCACTTTATAAATGCAGCAAACCATTTGGACGCATAAAGAGTGTCCAAGAGGATGTCCAAAATCATCCAAACATCCAAAAGGTGACTGTTTTAATGAAGGATGCCTA
Associated Phenotype:
Not determined