ZMP
ryr1a
Ensembl ID:
ZFIN ID:
Description:
Ryanodine receptor 1a [Source:UniProtKB/TrEMBL;Acc:A7M793]
Human Orthologue:
RYR1
Human Description:
ryanodine receptor 1 (skeletal) [Source:HGNC Symbol;Acc:10483]
Mouse Orthologue:
Ryr1
Mouse Description:
ryanodine receptor 1, skeletal muscle Gene [Source:MGI Symbol;Acc:MGI:99659]
Alleles
There are 19 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21768 | Nonsense | Available for shipment | Available now |
sa21769 | Essential Splice Site | Available for shipment | Available now |
sa16264 | Nonsense | Available for shipment | Available now |
sa12583 | Nonsense | Available for shipment | Available now |
sa17197 | Nonsense | Available for shipment | Available now |
sa34942 | Essential Splice Site | Available for shipment | Available now |
sa18239 | Nonsense | Available for shipment | Available now |
sa13565 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21768
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 |
---|---|---|---|---|---|
ENSDART00000014749 | Nonsense | 365 | 5056 | 12 | 105 |
ENSDART00000137089 | Nonsense | 331 | 5028 | 11 | 104 |
Genomic Location (Zv9):
Chromosome 10 (position 34450135)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33478100 |
GRCz11 | 10 | 33421960 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGTATGGCGAGTCCATGTGCTTTGTGCAGCACGTCGCTACAAGTCTGT[G/A]GCTCACATATGCCTCGGTGGATGCCAAGTCTGCTCGGCTGGGACCACTGA
Long Flanking Sequence:
TGCTATAAAATAAACACTTATTTGAGTGTTATTTTTCCATTATTCTAAAAAACCAAAAAGCCCAAATTCTCAAAACTGACTGGTGCATGAAAAAACATTACCCAACCCCCCTGTAGTCCCGTGCCCCAATAAGCTAATGTTCAATATCATTGTACACAGATGGAGTGGTAGCCACATGAAGTGGGGTCAGTCATTCAGGGTGCGCCACATCACAACAGGCAGGTATCTGTGTCTGGACGAAGAGAAAGGACTCCTGATTGTGGACCCAGAAAAGGCAAATACGAAGCAGTCAGCTTTCTGCTTTCGTGCATCAAAGGTCTGTTCTAACTTGCTGTCTTTGGGATGTTGCTGTTTTAAGAGAGTCTTTTTAAACTAATGTCATGTGACTGAGCAGGAGAAGACAGAAGTAGCTCAGAAACGTGATGTGGAGGGAATGGGGATCCCAGAGATCAAGTATGGCGAGTCCATGTGCTTTGTGCAGCACGTCGCTACAAGTCTGT[G/A]GCTCACATATGCCTCGGTGGATGCCAAGTCTGCTCGGCTGGGACCACTGAAGAGGAAGGTATGAGTACTAGCCTAATGTACACTAAAGTTAGTAGACAGTATGGTATTTTTGGGGATTGTATTAAATATACAGTACAAATGTTTTGTTAAAGGGGGAAATTACACAGGTGTACACACTCTCTCCTTATTAAGACTCTAAGCTTTTTAAAACACCAGTTAAAAAGTAAAATCATAGCTTACTGGTGTATATTCAAACATAAAATATCACAGGTCACAGACTGTTAATGTGAATACGGTTTTCTTATCTTCAGGCTATCCTGCATCAGGAGGGTCACATGGATGATGCTTTGACTGTGGCTCGCTCTCAGACAGCTGAATCGCAGGCTGCCAGGATGATCTACAACACGGCAGGACTTTTCACTCAGTTCATTAAGTATGTCTGCACACAGCTAAAGTCATTTTACACAAAATGATACAACTTGAAGGGGAGTGTAGGATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21769
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 |
---|---|---|---|---|---|
ENSDART00000014749 | Essential Splice Site | 534 | 5056 | 15 | 105 |
ENSDART00000137089 | Essential Splice Site | 500 | 5028 | 14 | 104 |
Genomic Location (Zv9):
Chromosome 10 (position 34452527)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33480492 |
GRCz11 | 10 | 33424352 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGCCGAGTCGTGGAAAGAGATCGTCAACTTATTTTATGAGCTGCTGGG[T/C]TTGTCTCTGTTTACTCATGATTGTATGATGCAATTTAAAATGATGTACTG
Long Flanking Sequence:
TGTGTATGATTGTATGGTATGGAAAACATTTACTTGCTGTTGCAGGGGTTTGGACTCTCTAAGTGGGAAGAGTAAATCTCCAGGACCTTCCCCTTCTCTGCCTCTAGACGCCATAGTTCTGTCATTGCAGGATCTCATCTTCTATTTCCGACCTCCAGAAGAGGAGCTGGAACATGAGGAGAAGCAGACCAAACTGCGCTCCTTAAGAAACCGCCAGAATCTCTTCCAAGAGGAGGTTAGACATCCTCAAAAATACATATGAATACAAAGAAAAAAATCCAATCTTTCATTCAGTGTATGTAGCAAAAAAATAAATACATTTTAATGCACAAACACAAATCCAGCTTCTGCTTTGTCGCACAGGGCATGATCACTCTTGTATTGGACTGTGTTGATCGGTTGAATGTCTACAACACTTCAGCCCACTTCTCAGAATTTGCTGGAGAGGACGCAGCCGAGTCGTGGAAAGAGATCGTCAACTTATTTTATGAGCTGCTGGG[T/C]TTGTCTCTGTTTACTCATGATTGTATGATGCAATTTAAAATGATGTACTGTTGTTAGGAAAATGGAATTCGCTTGTAAAATGTTTTTTTTTTCTCGTTCAGCATCTCTGATCAGAGGAAACAGGGCAAACTGTGCTTTGTTCTGTGATAATCTTGACTGGTTGGTCAGCAAACTGGATCGTCTGGAGGCATCCTCGGGTAGGAAGCAATCATTTATTTAGACTCCAAATAAAGGCTTTTGGGATTGATTGTTTTGCATAAAGTGTATGCAAAATTTATGTTTGCTGACTGATACTTACAGCACATTTTTGACATAAATGACCAGTCAGAAGCTTAAAAAAATGAAGAATAATAATTCAAATTATTATTAATTATTAAATAATTGAGCATGGCGAGACGGAATCTGCGGACGTTTTTTGCTATTTCTGCAGAGAATTTTGGTAAAAATCTGCGGATTTCTGCGGAATTATTTTGGGAGTATCATAACAAAAACCTTAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16264
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 |
---|---|---|---|---|---|
ENSDART00000014749 | Nonsense | 1884 | 5056 | 37 | 105 |
ENSDART00000137089 | Nonsense | 1850 | 5028 | 36 | 104 |
Genomic Location (Zv9):
Chromosome 10 (position 34479394)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33507359 |
GRCz11 | 10 | 33451219 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCCTGAACAGCAGCTGGTCTGCAAAGAGGAAGGAGCGGAGGTAAAAGAG[C/T]AAGAGGAACCAGCAGACGGTGGAAATGATGGAGAGYTGCTGGATGAAGGG
Long Flanking Sequence:
ATTATATTTTATTTTTATATTAGCAATTAATAAAATAAAGAACTGTAAATATAAAAATGTTTACTGATAAAAAGGACAAAAAAACAACAGAATTACCAACAATTAAAAAAAAATATATATATATAATAACTAATATCAATTATTAATAAAAGTTCCTAAAACAGCACTTAAATTATCTAGATTGACTGTTCTAATCCTTTTGTTCTGTGCTGTAGATGCTTAAAGATCATGCCCTCAGCATGCTTACAGAAGCTGTGCAGGACGGTGGCCAAGCCATTCGAGATCCTGTAGGGGGCAGCGTTGAGTACCACTTTGTGCCCATCCTGAAGCTCATCAGCACCCTTCTCATTATGGGTGTATTTGATGACGACGATGTCAAGCACATCCTGAAACTGATCGAACCATCCGTCTTCAGCAGCAACAGTGAGACTCCAGCTGAAGAAACTGGAGATCCTGAACAGCAGCTGGTCTGCAAAGAGGAAGGAGCGGAGGTAAAAGAG[C/T]AAGAGGAACCAGCAGACGGTGGAAATGATGGAGAGCTGCTGGATGAAGGGATGGGAGAGGAAGAAGAGCTTGAGGAAGAGGAGGAGGAGGAAGATGAAGAGTATGAGGAGGAGGTGAAAAAAGAGGAGGATGAACATGCTGCTGAAAAAACAGACAGAGAGAAAACTACAGATGGAGAAACTGAGAAGGAAACTGGTGCAGCAGAGGCTGAAGTAAGGGAGGAGGAGGATGTTGGAGAAGGACTGCTGCACATGAAGCTTCCAGAGTCTGTCAAACTCCAGGTGAAGTACTGCTGATGGCGTTTTAGTATTTCTTTTTAGTATTTTACAAGCAAATTGCATGAATTCTATTTCCATTTTTTCTTTTCAATTTCATTGTTTTTTTTTTATTAAAGGACTCCATCTTTTAAAAAATAGACTTATTCTACAAGTCCTCTAAAGCAGGGGTTCTCAACCTTTTTCACTTCAAGGCCCACTTTTTTCTCCAAAAATTTTTTGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12583
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 |
---|---|---|---|---|---|
ENSDART00000014749 | Nonsense | 2054 | 5056 | 39 | 105 |
ENSDART00000137089 | Nonsense | 2020 | 5028 | 38 | 104 |
Genomic Location (Zv9):
Chromosome 10 (position 34481948)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33509913 |
GRCz11 | 10 | 33453773 |
KASP Assay ID:
2260-3439.1 (used for ordering genotyping assays)
KASP Sequence:
TAAACTATATTTTATATACAGGTGAACATGTTGATGAACTTTAAGAACTG[T/A]CCAGAGGAAGAAGATTGCCCCGTTCCWGAGGATGTCCGGAATGGCCTCCT
Long Flanking Sequence:
AAATGTTCAAAGTGACATTAAAGACAATTTTAATGTTTCAAAGATTTTGATTTTAAATTTTAAATGCAGTTCTTGCTATTCACCAGGGAAAAACAATCTATAAAAATATTTAACAACAACTTGAAAATATTTCTTGAGCAGCAAATCATTATATTAAAATGTTTTCAGATGGGTCATGTGACACTAAATCTGCTTTGCCATCCCATCACACAATAAGTTAAATGTAAAAAAAATGTATAGACAATTTTAAAATAAATTAGTATTATACAATATTAAGTTTTTACTGTATTTTTTACTTTTATTATAGATCAAAATAATTTAACAGTATTATTGTTATATTGTATTTTTGATAAAAAAATTGCAGCCTCTGTGTTTAGAAGAAACTTTTTAATATGTTTTTTACTATTTTTAATAACCAGAATAAATGTTATCTTTAGAAGCTACAATTTTTAAACTATATTTTATATACAGGTGAACATGTTGATGAACTTTAAGAACTG[T/A]CCAGAGGAAGAAGATTGCCCCGTTCCAGAGGATGTCCGGAATGGCCTCCTGACATTTCACCATGACCTTTTAGCTCACTGTGGTCAGTTTTAACAAACAAACTAATCTTGTTTCAATGATCATGCTGTCACAGTTTAACATTAGTACTTGTATCATTAAAGCCTAGTTCACACTAGAGGATTTTAAGCCTGATTTCAGCCCGATTTGGAAGTTAACGAGGTCGCCGACAGATCGGGCTGTGATCCGGAAGAAATCTGTGAGTGCACGGCACTCGCCGGTCTTTATGTGTGAACTACTGAACAACGCATCAACGAGGCTCGCTGACGCGTCGCCGACACCTCGCAGACGGAAATCCAACATTTAGCATGCTGAATATTCCAGAGCAGTCGGCCGACTCAACCCCACGTGTGGTCCGATGTAGTGACGAGCTGCAGCCAATGAGAGAGCATATCAGTATGAGCTGAATGCCTGTGTTCTCAGGAGCTCAGCAGAAACATCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17197
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014749 | Nonsense | 2368 | 5056 | 45 | 105 |
ENSDART00000137089 | Nonsense | 2334 | 5028 | 44 | 104 |
Genomic Location (Zv9):
Chromosome 10 (position 34493105)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33520963 |
GRCz11 | 10 | 33464823 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAAGGGTTACCCGGATATTGGATGGAACCCAGTTGGAGGAGAAAAGTA[T/G]CTGGAYTTCCTGCGCTTTGCTGTGTTTGTGAATGGTTTGTAAAATATATG
Long Flanking Sequence:
CATTTTTGAATACTTTAGCTTACACATGAACATGATTTCTGTAGGTTTCCCATTGAATGATGACCACAACTCCCATGATTCCACACATTGTCATCAAAATATGCTTTTATTTGTTGTGAATACACACCCTCTAGCAGCGAAACTTACACGCTGTATCTTTAAATTGTATTATATTAAACTATAAGTAAATATTTTAATGGTTGTATTATATAACCAGTGATCACTCTTTCAGGAATGCGTGGCTCCACTCCTCTTGATGTTGCTGCTGCTTCCTGTATCGATAATAATGAGCTTGCCCTGGCTCTCCAAGAGCAAGACCTGGAGATGGTGCGTTAGGCTAAATTACATATTAAAAAAAGTTTGTGAGCAGTTTTTCATTTTGTCTTTCTCTTCGTGCAGGTAGTAAAGTACCTGGCAGGCTGTGGTCTGCAGAGCTGCCCTATGCTTTTGTCAAAGGGTTACCCGGATATTGGATGGAACCCAGTTGGAGGAGAAAAGTA[T/G]CTGGATTTCCTGCGCTTTGCTGTGTTTGTGAATGGTTTGTAAAATATATGGTTGTATCTCTCTTTAAAAAAGTGTTTAGTTTACATATGTTTAGAGTATAGCTTTTTAGTTTGTTAGAGTGAGAGGTGTGATGGGGGATGGCATAAAAATAATAATTGATGGTATACCTATAACAAACAAAAATACAATCCATTACTCCGTTTAATTAATTTTCTCATAATTGTGAAATTAAATGTTGACTTTTGCTCCAGATAGCGTCACCCCAATAATAAGGCAAGTTTTTGGGGGTTTGTCATCTTTCAATTCCAGTGCAAAAAAAAGCATGTGTTTTAGGATATAACTCAGGTTTTTGAGCACATTTTGCTATTATTATTCATTTATTCGTTTGCTGGAAATTAGAACTGAATTTAGAAATAGTTTTGAAACGAATATTTGCGCTTAACAAACAAAAGTATTTATTTATAGGCTAATTGATGTCTGTGCGTAAAGGTTTCCCTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34942
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 |
---|---|---|---|---|---|
ENSDART00000014749 | Essential Splice Site | 2380 | 5056 | 45 | 105 |
ENSDART00000137089 | Essential Splice Site | 2346 | 5028 | 44 | 104 |
Genomic Location (Zv9):
Chromosome 10 (position 34493141)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33520999 |
GRCz11 | 10 | 33464859 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGGAGAAAAGTATCTGGATTTCCTGCGCTTTGCTGTGTTTGTGAATGG[T/C]TTGTAAAATATATGGTTGTATCTCTCTTTAAAAAAGTGTTTAGTTTACAT
Long Flanking Sequence:
TTCTGTAGGTTTCCCATTGAATGATGACCACAACTCCCATGATTCCACACATTGTCATCAAAATATGCTTTTATTTGTTGTGAATACACACCCTCTAGCAGCGAAACTTACACGCTGTATCTTTAAATTGTATTATATTAAACTATAAGTAAATATTTTAATGGTTGTATTATATAACCAGTGATCACTCTTTCAGGAATGCGTGGCTCCACTCCTCTTGATGTTGCTGCTGCTTCCTGTATCGATAATAATGAGCTTGCCCTGGCTCTCCAAGAGCAAGACCTGGAGATGGTGCGTTAGGCTAAATTACATATTAAAAAAAGTTTGTGAGCAGTTTTTCATTTTGTCTTTCTCTTCGTGCAGGTAGTAAAGTACCTGGCAGGCTGTGGTCTGCAGAGCTGCCCTATGCTTTTGTCAAAGGGTTACCCGGATATTGGATGGAACCCAGTTGGAGGAGAAAAGTATCTGGATTTCCTGCGCTTTGCTGTGTTTGTGAATGG[T/C]TTGTAAAATATATGGTTGTATCTCTCTTTAAAAAAGTGTTTAGTTTACATATGTTTAGAGTATAGCTTTTTAGTTTGTTAGAGTGAGAGGTGTGATGGGGGATGGCATAAAAATAATAATTGATGGTATACCTATAACAAACAAAAATACAATCCATTACTCCGTTTAATTAATTTTCTCATAATTGTGAAATTAAATGTTGACTTTTGCTCCAGATAGCGTCACCCCAATAATAAGGCAAGTTTTTGGGGGTTTGTCATCTTTCAATTCCAGTGCAAAAAAAAGCATGTGTTTTAGGATATAACTCAGGTTTTTGAGCACATTTTGCTATTATTATTCATTTATTCGTTTGCTGGAAATTAGAACTGAATTTAGAAATAGTTTTGAAACGAATATTTGCGCTTAACAAACAAAAGTATTTATTTATAGGCTAATTGATGTCTGTGCGTAAAGGTTTCCCTATCCAAGAGGGAAAGTGAAAGTGATCCATTATCTTTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18239
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014749 | Nonsense | 2894 | 5056 | 57 | 105 |
ENSDART00000137089 | Nonsense | 2860 | 5028 | 56 | 104 |
Genomic Location (Zv9):
Chromosome 10 (position 34499012)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33526870 |
GRCz11 | 10 | 33470730 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTGTTYTCTTACTTTCTTAAWAGGCAACCTATGACCCCAGTCATGGCTA[T/G]AGCCCCCAACCTATTGATATCTCAGGCAKGACACTGTCCAGAGAGCTACA
Long Flanking Sequence:
ATGCCAAGACTCATCCCATGCTCAGACCTTACAAAACATTCTCTGAAAAGGCAACCGAGTTTATTTTTACTCGATCTCTTTAAGACTACAGTGTTTGTTTTTGTTATCGTGTGTTCCTTACATCAAATGTTTTGCATTAGGATAAAGAAATCTACCGCTGGCCTATTAAAGAGTCCATCAAGGCCATGATTGCCTGGGAGTGGACACTGGACAAAGCCAGAGATGGAGAGGATGAGAAAGTTGAGAAGAAAACAGCCCGTAAGATCTCACAGACTGCACAGGTGAGAAAAGACAAGTATATAGACATATTTATCAATACATAACATGCATATGTAACTAAATACAGGCTACATACAGCTCAGCCATGATTTGTGTTTTTGTGTCTAACATTAAACGACAAATTGCATACATTATTGGTGCTCTTAATAAGGGTATAATATCATAACTCATGTTGTTCTCTTACTTTCTTAATAGGCAACCTATGACCCCAGTCATGGCTA[T/G]AGCCCCCAACCTATTGATATCTCAGGCATGACACTGTCCAGAGAGCTACAGGTACACAATACAACATCAACTTAGAATTAAAGAGCCCCTATTATGCATTAAAAAATATAATATTTTGGTTTTGGGGGTCTCCAACAAGAGGCTGATATGCATGCAAGGTCAAAAAACACGTTAATTGTCTTAAAATATGCATTTATTTTAACCTAATTTTCTCAATGACGTCCTTATGATTTGTTTAGTTTATTCATTCTTCCAAGCTGTGGTGATTGGTCCAACATATGGAAATGTTTTATGTTGATGTCAATACAGAACAGCAAAAGATTTGAACTCAAGACGATTCATATAAACGACTCTATACTTTTTTTTTTTTTTTTTTTTTGAGAATCAATAGTTTTAAAGATGGTGCACTTTCAGATTTAGACCTCAGCTGGATGTACAAATGATAACAAATAATCTATTTAAATAAATAAGAAAAATAATTAAAAAGACTATTAAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13565
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 |
---|---|---|---|---|---|
ENSDART00000014749 | Essential Splice Site | 2911 | 5056 | 57 | 105 |
ENSDART00000137089 | Essential Splice Site | 2877 | 5028 | 56 | 104 |
Genomic Location (Zv9):
Chromosome 10 (position 34499064)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33526922 |
GRCz11 | 10 | 33470782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCCCCAACCTATTGATATCTCAGGCAKGACACTGTCCAGAGAGCTACAG[G/A]TACACAATACAACATCAACTTAGAMTTAAAGAGCCCCTATTATGCATTNA
Long Flanking Sequence:
AACCGAGTTTATTTTTACTCGATCTCTTTAAGACTACAGTGTTTGTTTTTGTTATCGTGTGTTCCTTACATCAAATGTTTTGCATTAGGATAAAGAAATCTACCGCTGGCCTATTAAAGAGTCCATCAAGGCCATGATTGCCTGGGAGTGGACACTGGACAAAGCCAGAGATGGAGAGGATGAGAAAGTTGAGAAGAAAACAGCCCGTAAGATCTCACAGACTGCACAGGTGAGAAAAGACAAGTATATAGACATATTTATCAATACATAACATGCATATGTAACTAAATACAGGCTACATACAGCTCAGCCATGATTTGTGTTTTTGTGTCTAACATTAAACGACAAATTGCATACATTATTGGTGCTCTTAATAAGGGTATAATATCATAACTCATGTTGTTCTCTTACTTTCTTAATAGGCAACCTATGACCCCAGTCATGGCTATAGCCCCCAACCTATTGATATCTCAGGCATGACACTGTCCAGAGAGCTACAG[G/A]TACACAATACAACATCAACTTAGAATTAAAGAGCCCCTATTATGCATTAAAAAATATAATATTTTGGTTTTGGGGGTCTCCAACAAGAGGCTGATATGCATGCAAGGTCAAAAAACACGTTAATTGTCTTAAAATATGCATTTATTTTAACCTAATTTTCTCAATGACGTCCTTATGATTTGTTTAGTTTATTCATTCTTCCAAGCTGTGGTGATTGGTCCAACATATGGAAATGTTTTATGTTGATGTCAATACAGAACAGCAAAAGATTTGAACTCAAGACGATTCATATAAACGACTCTATACTTTTTTTTTTTTTTTTTTTTTGAGAATCAATAGTTTTAAAGATGGTGCACTTTCAGATTTAGACCTCAGCTGGATGTACAAATGATAACAAATAATCTATTTAAATAAATAAGAAAAATAATTAAAAAGACTATTAAAATAATTGGCGGCGCAGTGGGTAGCACGTTTGCCTCACAGCAAGAAGGTCGCTGGTT
Associated Phenotype:
Not determined