ZMP
si:dkeyp-87a6.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
DNAH8
Human Description:
dynein, axonemal, heavy chain 8 [Source:HGNC Symbol;Acc:2952]
Mouse Orthologue:
Dnahc8
Mouse Description:
dynein, axonemal, heavy chain 8 Gene [Source:MGI Symbol;Acc:MGI:107714]
Alleles
There are 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30123 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa32492 | Nonsense | Available for shipment | Available now |
| sa13336 | Essential Splice Site | Available for shipment | Available now |
| sa11639 | Essential Splice Site | Available for shipment | Available now |
| sa9089 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa12494 | Nonsense | Available for shipment | Available now |
| sa16014 | Nonsense | Available for shipment | Available now |
| sa24530 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30123
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079342 | Essential Splice Site | 660 | 4667 | 15 | 79 |
| ENSDART00000142660 | None | None | 438 | None | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 34858902)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 33710351 |
| GRCz11 | 24 | 33596526 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGTCTGTTGATGCACTGATTGACACATGGCTTCAACGACCACTCACTG[T/C]AAGGGCATTTTGCAAATATACCATTAGTGAGCTGACACTTGAAAGACTGT
Long Flanking Sequence:
ATGAACGCCAATTAGAATTAAGGTCTGTCAATCACGGCTTTAAAGTCAAGTTGAAATTGAAGTGACCATATTTACTTTAGTAACTCAGCTCTTATGTGTTATGTCACTAGTGAAAACTACATCTTCGGAAAGTTTGACACATTCTGCAAACGTCTGGAGAAGATAACAGACATGGCAACGACTCTTGAAGATTTTTCAGTTCTGCAGTTTATGAAATTTGAAGGTGTTGAGAAAATATACATGCGCTACCAAAACATCGTGTCCACCATCAAATCCAAGACCTACAATGTGCTTGACCATCGCAAATTAGAGGTTAGAATGCGTATTAATTTTTATAGTTTATTTTGTATGTTTGACTTGAGCCATCTCTCATATGATTTATTTATTTAATGCTTTTTTTTAGTTTGACAATGATTACATCGAGTTCCGAAATCAAATCCAGGTGCTTTATCAGTCTGTTGATGCACTGATTGACACATGGCTTCAACGACCACTCACTG[T/C]AAGGGCATTTTGCAAATATACCATTAGTGAGCTGACACTTGAAAGACTGTTCTGTTCATTACAGGTCATGACTGATATAATAAACAAATATATTTCTCCTACACTGAAAAAGTCCATATTATTGATTTCACCCACAGACTGAACAGGTCCTTGAGCTGTTGTCCAGATTTGAGAACGGTGTGGGCAGACAAATGGACCTCAACCAGAAATACATGGTAGTTCTGCAACGCTACGAATGTGACCTTGAGTTTGTGCGCAAATGCTACCAAAAAGAAAAGGACAATCCCGTTTCACAACTAACCCCTGTAAGTTGCCTGTTATATAAACTATTCAGCTTTATTTTATCTACAAAGAAGAGAATATGGAACACAAATCAGGGTTCAACGCTAAGGATTTTTTCTACTGGTCCGATCGGGCAAGTGGTTTAGATTTTTACTTGCCCTGCCAAAATTTTCACTGGCCCCACCAAAAAAAAGGGAAGTTAATAGCTATTTTTAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32492
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079342 | Nonsense | 1455 | 4667 | 31 | 79 |
| ENSDART00000142660 | None | None | 438 | None | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 34878119)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 33729568 |
| GRCz11 | 24 | 33615743 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGATCTTCACAGAATCAAACGAGAGCTCAACCTCCTCTCCAAGCTCTA[C/A]AGTCTTTACAATTCTGTCATTGACAGCGTTTCAGGCTACTATGACATACT
Long Flanking Sequence:
ATTTTTATCCTGCAAAATGACAGAATAACAAATATATTGGTTTCTTATCTCTTAACAGTGTTTAAGTTAAAATATTGGTTTACAGTTGCCAAAAAAATCATGTCTAAAAACTTTGTTATGAAAAAAAATCGTTTTAAAATTTTGTTTTAAATTAGTTAGAAATTTCATCAGTAGTTTACAGAATAAAACCAAAATATATTTACCATAAAAAAATCCAGACAAACAGAATTTTCAATAGTTTTTTTTATGATTATTTTTACCAAAGAAGCAGTACTCTACTGACTTATGAGGTTCCCCTTCATTGGAACTACAATGGGTGTCTGGAACAGACGATTGAAGATCGCTAGACAACCATTGTCTGTTCCAGACACACGTCTCTGTTCCCTATTCTTTAGACTATATCTGTTCTTGTTTATTCTCTCATATTTTTCTTTTGTTTTTTCAGAATATCCTGATCTTCACAGAATCAAACGAGAGCTCAACCTCCTCTCCAAGCTCTA[C/A]AGTCTTTACAATTCTGTCATTGACAGCGTTTCAGGCTACTATGACATACTATGGGCCGACCTCAATATAGAGAAGATCAACAATGAGCTGCTGGATTTCCAGAACAGGTTTCTTATGATAGTCACATACTTAAAGGTCTCGTGAATCAATTTAAAATGCGCATTTATATTTAATGTTTGATGTAATCTTGACCGAAACACGAAGAGAGGGTGAGACATAGGTTAGCTCCTCCTCTTTTTAAAAAAAAACAGCCAATAGCGTTTTAAGTGGTTGAGCTCAAGTACATCAATTGAAAAGCAAACGAGAAGCGTCTTGAAAGCTTGGCATGTCAGATACTAGGGAGCATTTGATTGGTTATGATGTGATGAGAAATTGTAGGATAGGTTAGCGTGATTAAAAACATTGATCAATTCATGCAAAAGTCACAAACTACAAGCTTTACATGTTCATGTCAGTTTTATATCTTCTAAAGGTGAATTTTGTCAATGTTTTGGAACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13336
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079342 | Essential Splice Site | 1491 | 4667 | 31 | 79 |
| ENSDART00000142660 | None | None | 438 | None | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 34878228)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 33729677 |
| GRCz11 | 24 | 33615852 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTCAATATAGAGAAGATCAACAATGAGCTGCTGGATTTCCAGAACAGG[T/G]TTCTTATGATAGTCWCATACTTAAAGGTCTCGTGAATCAATTTAAAATGY
Long Flanking Sequence:
ACTTTGTTATGAAAAAAAATCGTTTTAAAATTTTGTTTTAAATTAGTTAGAAATTTCATCAGTAGTTTACAGAATAAAACCAAAATATATTTACCATAAAAAAATCCAGACAAACAGAATTTTCAATAGTTTTTTTTATGATTATTTTTACCAAAGAAGCAGTACTCTACTGACTTATGAGGTTCCCCTTCATTGGAACTACAATGGGTGTCTGGAACAGACGATTGAAGATCGCTAGACAACCATTGTCTGTTCCAGACACACGTCTCTGTTCCCTATTCTTTAGACTATATCTGTTCTTGTTTATTCTCTCATATTTTTCTTTTGTTTTTTCAGAATATCCTGATCTTCACAGAATCAAACGAGAGCTCAACCTCCTCTCCAAGCTCTACAGTCTTTACAATTCTGTCATTGACAGCGTTTCAGGCTACTATGACATACTATGGGCCGACCTCAATATAGAGAAGATCAACAATGAGCTGCTGGATTTCCAGAACAGG[T/G]TTCTTATGATAGTCACATACTTAAAGGTCTCGTGAATCAATTTAAAATGCGCATTTATATTTAATGTTTGATGTAATCTTGACCGAAACACGAAGAGAGGGTGAGACATAGGTTAGCTCCTCCTCTTTTTAAAAAAAAACAGCCAATAGCGTTTTAAGTGGTTGAGCTCAAGTACATCAATTGAAAAGCAAACGAGAAGCGTCTTGAAAGCTTGGCATGTCAGATACTAGGGAGCATTTGATTGGTTATGATGTGATGAGAAATTGTAGGATAGGTTAGCGTGATTAAAAACATTGATCAATTCATGCAAAAGTCACAAACTACAAGCTTTACATGTTCATGTCAGTTTTATATCTTCTAAAGGTGAATTTTGTCAATGTTTTGGAACACACTAGCTAATAAATATATAGAAAATTACCAATATTAATATTAACATTTAAAAAACTTTCTTTTAATTTTTATGGGACCTTTAAAATGGATCAAATACTATATGGGAATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11639
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 |
|---|---|---|---|---|---|
| ENSDART00000079342 | Essential Splice Site | 2295 | 4667 | 46 | 79 |
| ENSDART00000142660 | None | None | 438 | None | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 34894063)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 33745512 |
| GRCz11 | 24 | 33631687 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGATTCTYAAACTTGTGCARCTRTATGAGACTCAGAGAGTGAGACACG[G/A]TTAGTCATTCATTATTCATYTGWCAAATATATGTCACATGCTCAGAYTAC
Long Flanking Sequence:
TTTTATTTGTAGATGGTCATGACAGCTCTTGCTGATGCTTATTCAAACTTTTTGAATACTCAACAGGTCCATTATGACTTTGGCTTGAGGAACATCTTGTCTGTTTTAAGAACGTTGGGTGCTGTTAAGAGGTCCAATCCAACAGAGCCAGAAAAGACTGTGGTCATGAGAGTTCTGCGTGACATGAACCTCTCCAAACTGGTGAATTTAATCAAAATCTGATCAGAAATAACATCGTGAAGTAACAGTACAGATGTTTGTTTTTTCACAAATACTCTCAGCAAATAACCCTATTTTGATCTTCATTCAGGTTGATGAAGATGAGCCTCTGTTCATGAGCCTGATCAATGACCTGTTTCCGGGGATCATGCTGGATAAAGCTGGTTACCCTGACCTGGAAGCTGCTATCACCAAACAAGCTGAAGAAGCAGGACTGATTGCACACCCACCCTGGATTCTTAAACTTGTGCAACTGTATGAGACTCAGAGAGTGAGACACG[G/A]TTAGTCATTCATTATTCATTTGACAAATATATGTCACATGCTCAGACTACAGGAATACACAAAGTGGAGGCTGTAGTTATGTTTTTTCAACACATTTCTAAACATAATCGTTTTAATAACTGATTTCTAATAACTCATTTCTTTTATCTTTGCCATGATGACAGTTTATTATATTTCAGTAGATATTTTGTCAAGATACTAGTATTAAAGTGCAAGTTAAAGTGCAACTTAAAGGCTTAACTAGGATAATTAGGTTAATTAGGCAACTTAGGGTAATTAGGCAAATCATTTTATAACATAAAAAATATCGAAAAAAATACTTATTCTAGAAGAAAAAAATATAAGAAATACAGTAAAAAATTCATTGCTTTGTTAAACATCATTTTGTAAATATTTGAAAAGGAAAGAAAAATCACAGGAAGGCTTACTATTTGACTTCTACTGTAGGTATGATGACCCTTGGTCCCAGTGGAACAGGAAAAACCACGTGTATCCACACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9089
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079342 | Nonsense | 2990 | 4667 | 56 | 79 |
| ENSDART00000142660 | None | None | 438 | None | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 34921743)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 33773192 |
| GRCz11 | 24 | 33659367 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAAATATCCCGTATAATCCGGACGGCTCGTGGGAATGCWCTACTGGTT[G/T]GAGTCGGAGGTTCTGGGAAACAGAGTCTCACCAGACTTGCATCCTTYATA
Long Flanking Sequence:
ATTTCCCTAATTTAGAAAAAAGTACAATGATAAAAAATAAAAATAAAAAGCTTCAAAATGAAAAAAAAAATCTCTAAAAATTGACAATTTACAATAGATTTTGTTTGAATGTTTACTGTCATTAAATGCTATCTCACAGCAATTCATAACTTTTTGTTTTAGTGGCTAACTCTTAATTTAAATTCATGAATTTGTGCGATCTTATTCGTACAATTTTGTAGGATTTGCTGATCCCCAATGACATTTGGGTTTGGTGCCATGCTTCCTTATAAAAAGCATATATTTTCGTATGACTGAGGTTTCCTCATGAGATCAAGCTGGATTATTATATATTAGATTTTCTTTGACATATATTTATGATAATCATTAAGAATTTGATTTAACTTTAATGTTAATCTCCATTTGGTTAATGTTAATCTACTTTGTCACAGGATGCCATGATCCATTTGATGAAAATATCCCGTATAATCCGGACGGCTCGTGGGAATGCACTACTGGTT[G/T]GAGTCGGAGGTTCTGGGAAACAGAGTCTCACCAGACTTGCATCCTTCATAGCTGGATACCAGAGCTTTCAAATCACACTGACAAGGTAACAATACTGCTCAGAGTTCTCTTGATTGGTTTGGATTAAATAAAAAATAAAATCAATAGATTTCGTTTGGGTTTGCTTAGTGTGTATGCTATAATTTCTAAGACCTAAAATCTGAAGCAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGCAATCTCACAAAAGGTTTATTAGTCTAAAGTATTTTTATTTTATTTATTTATTTATTTATTTATTTTTAGATATTTTCTATTTAAATTGTTTCATTGTTCATTACTATACCCTGGATTCATTTTTCTAGTTGCATATTCTTGCAATATGTTTGGGATGAATACTAAGAAATACCTTGTACTTTCCTAAAGGGTCACACCTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12494
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 |
|---|---|---|---|---|---|
| ENSDART00000079342 | Nonsense | 3861 | 4667 | 68 | 79 |
| ENSDART00000142660 | None | None | 438 | None | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 34936043)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 33787492 |
| GRCz11 | 24 | 33673667 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACGCTCGAGAGGAGTACCGTCCAGTGGCCAYCAGRGGGAGCATCCTGTA[T/A]TTYCTGATTGTGGAGWKGAGTCTGGTCAAWGTGMTGTACCAAACCTCCCT
Long Flanking Sequence:
GAGCAACCTTCTGTACAGGCTGACCAGCATTCAAGGCTCTCTAGTCGAGGACGAGTCTCTTATCGAAGTGCTCAAAGTCACAAAGACTACTGCACAGGAGGTACGTCCTCTTTTTTATTTATTTATTTATTATTGTTATTATTTTTATATATACAATTTTAACAATGCAGATTAAAAACAGGAAAAAAATCATCTATAAACATCTATATATCATCTAAATATTCATCTCAGTGCATAAAATTTCGCAAACAAGAAAAATAGATAAAAAGAATAAGTAAATAGTTACATTTAGCATGTATCATCCTTCATTTTTAAACTGAGGCAGCTGTAATATTGTTATATCTTATCTAAAGTTTAGCCTCCACCTTTTATGAATGAAATGGAGTCTGTTTTAAACTCTAGGTGAGTCAAAAGCTGACAGTTGCTGCAGAGACAGAAATTAACATCAACCACGCTCGAGAGGAGTACCGTCCAGTGGCCACCAGAGGGAGCATCCTGTA[T/A]TTCCTGATTGTGGAGATGAGTCTGGTCAATGTGATGTACCAAACCTCCCTCCGCCAGTTCCTGGGCATCTTTGACATGTCGATGGAGAAGTCGCCGAAGTCTCAGGTTACAGCCAAAAGACTTGAAAACATCATGGAGTTCCTCACTTTCGAAGTGTTTCGCTACACAGCTCGAGGGCTCTATGAAGATCACAAGTTCCTTTTCACGCTGCTTCTGGCCTTGAAAATAGACCTGCAGACCAAAAATATTTCCCACAACGAGTTGCAGACATTCATCAAAGGTTTGGATCAAGTTTTTAGACTAATTTAAAGGGTGATATGTTAAATCAACTGCACAATTCCCATATAGAAATGTTGTGTATGACAGTATGCAGATTACATACAGTACACGACATTCAAGTTCTTATTGTCATATTTTCAACATATACTTCTTAATAATATGCAAAAATGCCAATTTATAAATATTTATATATACAGTACTGTGCAAAGGTTTAGTTCACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16014
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 |
|---|---|---|---|---|---|
| ENSDART00000079342 | Nonsense | 4199 | 4667 | 72 | 79 |
| ENSDART00000142660 | None | None | 438 | None | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 34945284)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 33796733 |
| GRCz11 | 24 | 33682908 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATGTGTGATCTGTAATGCAGGGGTGAAGGCTGGACTCAAGCGGACATA[T/G]AATAGTGTGACKCAAGAGCARTTGGAGATCACAAACATGCCTCAGTGGAG
Long Flanking Sequence:
TGGAATGCATCATTCTGATTGATCAGCTATTTAAACAGCCAAGGTTTGATACGATTTCTATTATGCAGGGCATTCCTTGCAGGCCGATCTCCATGGGACAGGGACAGGAAGTGCATGCAAGAAGGCTTCTGGCACAGAGCATGTCTGATGGAGGCTGGTTACTTCTGCAGAACTGCCATCTGGGATTGGACTTCCTGGATGAAGGTCTAGAGACAGTCACAACAACAGAGAACATCCATGACAATTTTAGGTTGTGGGTGACTACAGACGTGCATCCCAAATTCCCCATAAACTTCCTGCAGTCTTCTATTAAATTCACCAATGAGCCTCCGCAAGGTAGAAAAAGGGAAAGCTGTTTTTTTTTTTTTTTTTTTTTTTGAGGTGGGGGGGGGGGGGGGGGTACATATTTAATATTGTGACTAAATATAAATGATACAAGAGTAAAAGAGGAAATGTGTGATCTGTAATGCAGGGGTGAAGGCTGGACTCAAGCGGACATA[T/G]AATAGTGTGACTCAAGAGCAGTTGGAGATCACAAACATGCCTCAGTGGAGACCACTTTTCTATGCTGTGGCATTTCTGCACACCACGGTCCAGGTCAGGACAGCTGTTAAACCACGTCACTCACTGCTCATAGTGACACACTGCTTTAAATACTCACATCATCAGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATGCAGTGGGGGAAATAAGTATTCAACACATCACCATTTTTCTCAGAAAACATATTTCTAAAGTTGTTGTTGTTCTACAGCTTGATTTTCTTTCTCTGAAAGCATTTGAGAGTTTCCTTGGCTGTGTTTTGGATCATTGTCTTGCTGAAATGTCCACCCTAGTTTAATCTTCAGCATCCTGCTAATGTAGATGTTGGACTGAAGCAGCTGATATTCATTTACAATGATGAAGGGCAGAGGGTTGCTGAAGAACTACTGAGAGATTTTAGCTGCTGTCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24530
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 |
|---|---|---|---|---|---|
| ENSDART00000079342 | Nonsense | 4359 | 4667 | 75 | 79 |
| ENSDART00000142660 | Nonsense | 130 | 438 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 34947350)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 33798799 |
| GRCz11 | 24 | 33684974 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTTGTTCAACAGGTATTTGGCCTCCATCCCAACGCTGACATCACTTAC[C/T]AGACCAATTTGGCTAATGATACCCTGAGTACCATCCTCAACATCCAGCCC
Long Flanking Sequence:
CAACCAGGCTGATTTCACCTCCAGTGTCCAGTTTGTGCAGAACCACTTGGATGACATCGACATCAAGAGAGGAGTCAACTGGAATTGCCTGCGCTACATGTTGGGAGAGGTACAATTTGGACTTTCTACTGTGCTTTTGTTCATTGTTTATTTGACAAACCTGCTTATTAGTACTTTTGGTTGTGTAGGTTCAGTATGGTGGACGTGTCACAGACGATATGGACAAACGCCTGCTCAATACTTTTGCTCGCATCTGGTTTAGTGAGAGCATGTTTGCGGACAAATTCTGTTTCTACAAAGGATATACTATACCAAAGGCCAGAATGCTTCAGGATTACCATGCACATATTGATGCTCTGCCATTGGTTGATACACCTGAGGTAATACAGCCATTAATTATTCTTTTATTTATTTACTAGTGGTCACAAATTCAATAACCAATCGATTCTAACTTTGTTCAACAGGTATTTGGCCTCCATCCCAACGCTGACATCACTTAC[C/T]AGACCAATTTGGCTAATGATACCCTGAGTACCATCCTCAACATCCAGCCCAAAGACAGCAGCAGTGGAGAGGGCGAGACTAGAGAGTCGTCAGTCCAGAAAATGGCCAATGAGATGTTAGAAAAACTTCCAGCTGACTATGTGCCACATGAGGTGAAAATGTGGTTTTAGGGCCACCCCCATGAGCCACTTCTAATGCTCAAAGCATATTTGTGTCAAATTTAAATGTAGAACATAATTTTTTCAATAACTTTATACAGGTGAAAAGCAGCCTACAAAAAATGGGAGCATTCCAGCCCATGACAATATTTCTCCGTCAAGAGCTTGACAGAATGCAGCGTGTTATTGGTCGTGTTCGCAGTACCCTCACTGACCTTAAACTTGCAATTGATGGTAAGTTTAAGAAACTTTCACTCACAATGAAAAAAAGTGCTTTAATTGTTTTGCAGGGGGCATTACATGAAAAATGTGTAATGTCCTTCATTTGTACACACATTACAC
Associated Phenotype:
Not determined