ZMP
im:7147241
Ensembl ID:
ZFIN ID:
Description:
Im:7147241 protein [Source:UniProtKB/TrEMBL;Acc:Q56A51]
Human Orthologue:
SEC16B
Human Description:
SEC16 homolog B (S. cerevisiae) [Source:HGNC Symbol;Acc:30301]
Mouse Orthologue:
Sec16b
Mouse Description:
SEC16 homolog B (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:2148802]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa25333 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa15923 | Nonsense | Available for shipment | Available now |
| sa18286 | Nonsense | Available for shipment | Available now |
| sa20682 | Essential Splice Site | Available for shipment | Available now |
| sa145 | Nonsense | Available for shipment | Available now |
| sa33845 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa33844 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa26728 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25333
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 |
|---|---|---|---|---|---|
| ENSDART00000073789 | Essential Splice Site | 156 | 935 | 3 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 20071218)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 23827957 |
| GRCz11 | 6 | 23927766 |
KASP Assay ID:
554-7339.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGACTGACGCAGGAGTCTGCAAGAGCTTCATACTCCGATCAGCAGGGG[T/A]CTGTCAATGACTTGTTCTCATACGCTAATACTGTCAATCTAATGATTTAC
Long Flanking Sequence:
TTTATTCAGCAAGGAAAGGAAAGAAAGGTGTATTTCTTTTTTTGAATATTTATCTAAATACAATATAAGCATATTTAACTGTTTGCTCATCAGAAAATCCTCAAATCTTTCACAAGATATAAGACAATAGAAAACAGTTATTTTAAACGGTATTCATATTTTTTTTTATAATGTATCATTTGTCAATAAATCACAGTGCAACTGCTAATGCATTCAGGCAGGAATATGACTACTCCACTTCCAGCTACTGGCCCTACAGGGAAGACTATGGCTATTATGATTATCACGGTTATCACAGAACACAATACAGCTCTCCAGGTACATGATATTCAGTCTGAGCCTGCAGTTTTTAATTATCACAAAAACTCAATCTCAAGTCTCATTTTGGTTTTATAGATGGCGGCGGCTGGAGCCAGACAGATGGCTGGAGGACAGAGGGTCATCAGGGCCGAGGACTGACGCAGGAGTCTGCAAGAGCTTCATACTCCGATCAGCAGGGG[T/A]CTGTCAATGACTTGTTCTCATACGCTAATACTGTCAATCTAATGATTTACTGTTTATTTTAAATTAAGGGTCCTTGCCTTTCTTTAACAGCTATAGCTTTAAAACAGACAGTCAGCATGACCATGGTGTATCAGAGAGACACAGAGAAAGCATGGACAACGGAAATAGAACTGGAGAGGTATGTTTTCAGAAATTACTTTTCATACATTGTAATAAAGTTTACACTTTATTCTATGCATTGGTGTTCAATGGTGTAGGGGGGATTGATTAAAATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGAAAAGACTCATATTTTAAAAGTCACCTATGGTGAAAACCAACTTTTGAAAGCTGTTTGGACAGAATTATGTGTAGGTATAGTGTGTCCACAGTCAAATTGAAGTAATATAAACACAATAAGTCTCTTTTTTTAATTTCCTGATGTTAAAATAGGATCCAAATACAATACAATACAATACTGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15923
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 |
|---|---|---|---|---|---|
| ENSDART00000073789 | Nonsense | 216 | 935 | 5 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 20067527)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 23824266 |
| GRCz11 | 6 | 23924075 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCTGTCTTCAAGCAGCTATGAGCTCAGTCAGTATATGAATGGAGCTGAA[C/T]AGAGTGAGCTWGAGCTCAKTTCTCACACAGGTTTGTCAGAACCACAGTTC
Long Flanking Sequence:
TCCTGTTAGCTCATCATATTGCCAGTTTTGTGGTGAACAATTCATCTGTGCATGTCATTAAGAAAAAAATGAAATCTGAAAGTGCACTTCCTGTTTGTTTTCAGTTAAATTATCAGATTACGTGATTTTGAGTTAATGGGTGTGGCTAACATACTTAATCATGTTGGTTTAACTGTGAATTTTGACAACAAATAGAAATTGTGAACAGGAGTCTATTAGGTTGTAATAACTCTTCTAAAACCCCTTTCCTGATCTTTATGAATGAAATGCCTATTTTACTACATCCATTCATCCCGCAGTAGAAAAAGCCACTGTCAATTATTATTCCATTAGAAACTACGTCACAATTCAAAAAAAAATTATCACAGCTTCCGGTTCATTGGCACTTAAAGCTTTTTTTTCATTTTCAGGTGTATGATAATAGTGCTCTTGCCAACTCTAAAGCATCGGGTCTGTCTTCAAGCAGCTATGAGCTCAGTCAGTATATGAATGGAGCTGAA[C/T]AGAGTGAGCTTGAGCTCATTTCTCACACAGGTTTGTCAGAACCACAGTTCAGACACAGTACCTATCTAATCTTACTAACGCGTAACTATTTTTTGATTGGTCATTGGATTCAGAATTTCTGTGGTTGGTCATCTTATTTAGGTGTTGTGCCCGTTGAGGTCGCTCCACTCAAGTTCAGCATCCCTCATGTGGCAGTGAGTTTTGGGCCGGCAGGTCAGCTTGTGTGGGTCAGTCCAGCCCTGGCCTCTGAGGGTGAGCCTGCTCAAGTGGAACTCCACAGCCTGGAGGTTAGAAAAACATGATACAAACTTAAGTTTTAAGGCATAGTATGAGATGTTGGGTTGGATTACAGTTTTTTACAGATGCTAGTACACATTTCTCAATACTTTGGTCACTTTTGCAGGACTCTTCACACAACTGAAGTCCATGTGGGCTAAACTGAGGATCAATTATTATTGTTTTGGCACAAAGTCCATTCAATGGCTACATCTCTCAAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18286
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 |
|---|---|---|---|---|---|
| ENSDART00000073789 | Nonsense | 492 | 935 | 12 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 20052755)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 23809494 |
| GRCz11 | 6 | 23909303 |
KASP Assay ID:
2259-7425.1 (used for ordering genotyping assays)
KASP Sequence:
ATATTWCYGTATTTCTTWGCAGTCCTGGAGTAGTGAGAAGTGGGGAGACT[G/A]GCGAYCACACYTGGCTGTTATGCTGTCCAATGAGACAACRGACCCTGTCA
Long Flanking Sequence:
TTCCCTTATGAAGAAGAACGTCCTGGTTAAGTACGTTACCCACGTTCCCCGAATAGGGAACGGAGACGTGTGTCTCCACAGCCACAACACCTGAGTCTCCAGCTGGGAGCTGAGCGATCGGCTCTTCAGCAGGCAAAATTCTGACGAGCTAACTCACAGAGCCGACTGATATAGCCCTAATTGGCTCATCAGTTTCAGCTGTGGAGCTAGACTCCGCCAATTCAATTGCCATTTCACTGGCCCGTTTTCATATCTTCAGAAGTGATTGGTCATCTAAAGCACTCCCAAAGTCTGTTTATACAGACACACGTCTCAGTTCCCTATTCAGGGAATGTGGGTTACGTACGTAACCTGGAGGTTTTTACACTGTGATAACAGTGTGAAGTGTAATCCAGAGCTTCTGTCATATTTGATTTCCAAATATTTCTTTTATCATCTTTTTTGACCTAAATATTTCTGTATTTCTTTGCAGTCCTGGAGTAGTGAGAAGTGGGGAGACT[G/A]GCGACCACACCTGGCTGTTATGCTGTCCAATGAGACAACAGACCCTGTCATACATCACAGGTCCATCATCGCCATGGGCGATACACTAGGTGATGTCCAATCCAGTGTTATGTCACATTTATATCTTAAATTAAATAATTAATGAAGAGTTTTTTACTCTAATGTTTTCATCTCAGCCTCCAGGGATATGCTGTTTGCTTCACACATTTGCTACCTCACGGCTCAATGTCCTTTTGGCTGGTACAGAAATAGATCAGAACGTCTGGTTCTTTTGGGTAGTAAGCAAAGGTGAGGGTACAGTGTGAAGGCTGCAATGTCTGAATGGCTAAGTTCCCAAACTCAGATTGCTTTCCCTTTTAATCCTTTGATTGCAGTGTAATGTTTTCCAAGTTCTGTCACAACTCTGCCATTCGCTGTACTGAACTGTTTGAGTACTGCCAGCGGCTTGGAAATGCTGAGTTCGTCATTCCTGCTTTTCAGGTAACATTTCAGGAATCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20682
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 |
|---|---|---|---|---|---|
| ENSDART00000073789 | Essential Splice Site | 522 | 935 | 13 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 20052579)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 23809318 |
| GRCz11 | 6 | 23909127 |
KASP Assay ID:
2259-7424.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAATTAAATAATTAATGAAGAGTTTTTTACTCTAATGTTTTCATCTCA[G/A]CCTCCAGGGATATGCTGTTTGCTTCACACATTTGCTACCTCACGGCTCAA
Long Flanking Sequence:
CTAATTGGCTCATCAGTTTCAGCTGTGGAGCTAGACTCCGCCAATTCAATTGCCATTTCACTGGCCCGTTTTCATATCTTCAGAAGTGATTGGTCATCTAAAGCACTCCCAAAGTCTGTTTATACAGACACACGTCTCAGTTCCCTATTCAGGGAATGTGGGTTACGTACGTAACCTGGAGGTTTTTACACTGTGATAACAGTGTGAAGTGTAATCCAGAGCTTCTGTCATATTTGATTTCCAAATATTTCTTTTATCATCTTTTTTGACCTAAATATTTCTGTATTTCTTTGCAGTCCTGGAGTAGTGAGAAGTGGGGAGACTGGCGACCACACCTGGCTGTTATGCTGTCCAATGAGACAACAGACCCTGTCATACATCACAGGTCCATCATCGCCATGGGCGATACACTAGGTGATGTCCAATCCAGTGTTATGTCACATTTATATCTTAAATTAAATAATTAATGAAGAGTTTTTTACTCTAATGTTTTCATCTCA[G/A]CCTCCAGGGATATGCTGTTTGCTTCACACATTTGCTACCTCACGGCTCAATGTCCTTTTGGCTGGTACAGAAATAGATCAGAACGTCTGGTTCTTTTGGGTAGTAAGCAAAGGTGAGGGTACAGTGTGAAGGCTGCAATGTCTGAATGGCTAAGTTCCCAAACTCAGATTGCTTTCCCTTTTAATCCTTTGATTGCAGTGTAATGTTTTCCAAGTTCTGTCACAACTCTGCCATTCGCTGTACTGAACTGTTTGAGTACTGCCAGCGGCTTGGAAATGCTGAGTTCGTCATTCCTGCTTTTCAGGTAACATTTCAGGAATCTGAAAAGAGTCATTTATATGTGTTAAAAAAACGAAATAAATGAATAATAAATAAATAAAAAATAAATAAATAAATAATAACTAATAACTACAAATGATGTCACCATTTTTATTATTTTGTATTTTATTCCATTTACTTTTTATTTTACATAAATAATTAATATAAAAACTACAAAAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa145
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 |
|---|---|---|---|---|---|
| ENSDART00000073789 | Nonsense | 596 | 935 | 15 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 20047686)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 23804425 |
| GRCz11 | 6 | 23904234 |
KASP Assay ID:
554-0037.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGTTATCTATTGCATATTTATTCATCTGTTGTTTTCCATKTAGGTGTA[T/A]AAATTCCTGTATGCATGCCGGCTGCTGGACTGTGGGCTCGTTTCTCAGGC
Long Flanking Sequence:
CCCCACAAATCTATCTTTTAAAATTGATATTTTTAATAGAAAGCTATACAATATTATGTCTGCCCATATACATTAGATTAGTCAGTACTGAAGCCAAATCTGGAGCTTATCTAACAAAATAACTTGCGATAATGGTCTAAAAACTAGTACACCCCAATGCATATGTTGTAAAAAAATATTACATCCACATTTAAAAATGAGAAAAAATCAAAAGCAAAAAAAAATTTAAATTAAGTAGAAATTTTGTAGGTTGTAACTTTTTTTTTTATTTTGCTTTAATTTCTAAATATTTTTTATGACAATATTGTTTTACTAAATATTTAATAATGCTGTTTTGTTTAAATGCACCAAAATATATTACCTATATCCACCGAGAAATTAGTAAAAATTTTCAAAATAGGGTGTACTCAATTATGCTGAGCACTGTATGTTGTTGAGTCTGTACTTATGTCTGTTATCTATTGCATATTTATTCATCTGTTGTTTTCCATGTAGGTGTA[T/A]AAATTCCTGTATGCATGCCGGCTGCTGGACTGTGGGCTCGTTTCTCAGGCCTTCCACTACTGTGAAGTGGTGGGGAAAGCTCTGCTTAGAATAGACCAACCCCATGTGGTGCTATTGGGAGAGCTTATAAAAGTAACGCCCCTCTGTGCATGCTACACTGACACTGATCCTGCAGTTTTGTTCTGTTTGTGCATGCATTGCTCATGTAATGCCACTTCCAGCATGTTCAGTCTGTCTGTTTTGTTTGCTACAACAGTTGGTGGATAGACTGAAGTTCTCCGAAGCACAGCTCAATGACACGTGTGACGGTCAGCTTTTCCTGGACCCCGATTGGTTGGTGCAGATCCGCTGCAAACACCAGACCCTGCTGGTAATAAGTTTGCGCAGCATATATATGTTAGCTGTTAGTCCAATTTAAGATTAGCAGGACTGTTTATAGGAAGAATGAATGCCATCCATATGTAACTCTATGTACAGTCCACACTATCAATTTACTTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33845
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 |
|---|---|---|---|---|---|
| ENSDART00000073789 | Essential Splice Site | 641 | 935 | 16 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 20047430)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 23804169 |
| GRCz11 | 6 | 23903978 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAATGCCACTTCCAGCATGTTCAGTCTGTCTGTTTTGTTTGCTACAACA[G/T]TTGGTGGATAGACTGAAGTTCTCCGAAGCACAGCTCAATGACACGTGTGA
Long Flanking Sequence:
CTTTTTTTTTTATTTTGCTTTAATTTCTAAATATTTTTTATGACAATATTGTTTTACTAAATATTTAATAATGCTGTTTTGTTTAAATGCACCAAAATATATTACCTATATCCACCGAGAAATTAGTAAAAATTTTCAAAATAGGGTGTACTCAATTATGCTGAGCACTGTATGTTGTTGAGTCTGTACTTATGTCTGTTATCTATTGCATATTTATTCATCTGTTGTTTTCCATGTAGGTGTATAAATTCCTGTATGCATGCCGGCTGCTGGACTGTGGGCTCGTTTCTCAGGCCTTCCACTACTGTGAAGTGGTGGGGAAAGCTCTGCTTAGAATAGACCAACCCCATGTGGTGCTATTGGGAGAGCTTATAAAAGTAACGCCCCTCTGTGCATGCTACACTGACACTGATCCTGCAGTTTTGTTCTGTTTGTGCATGCATTGCTCATGTAATGCCACTTCCAGCATGTTCAGTCTGTCTGTTTTGTTTGCTACAACA[G/T]TTGGTGGATAGACTGAAGTTCTCCGAAGCACAGCTCAATGACACGTGTGACGGTCAGCTTTTCCTGGACCCCGATTGGTTGGTGCAGATCCGCTGCAAACACCAGACCCTGCTGGTAATAAGTTTGCGCAGCATATATATGTTAGCTGTTAGTCCAATTTAAGATTAGCAGGACTGTTTATAGGAAGAATGAATGCCATCCATATGTAACTCTATGTACAGTCCACACTATCAATTTACTTTTGCATACCCCAAAGTGCTCAATCATCATAAGGTCCTGTTTAGATCTTGGGTGTCGGGTGAAACGGTCAGAAGTGATCAGCAAAGACAGATTTACACCTCAGTTTAACGTGTCTCTAGTGACCACTTGTTACTGGAGTTAAAGAGAGCATGAATATGTGTATGTTTATAACTTTGTACATATATATTTTTACAAAACATTTTTTATGTTAAAGTTGTTAATCTTTTACTTTTATTTGTTTCTATCAATACAGTTATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33844
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 |
|---|---|---|---|---|---|
| ENSDART00000073789 | Nonsense | 649 | 935 | 16 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 20047405)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 23804144 |
| GRCz11 | 6 | 23903953 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTCTGTTTTGTTTGCTACAACAGTTGGTGGATAGACTGAAGTTCTCC[G/T]AAGCACAGCTCAATGACACGTGTGACGGTCAGCTTTTCCTGGACCCCGAT
Long Flanking Sequence:
TCTAAATATTTTTTATGACAATATTGTTTTACTAAATATTTAATAATGCTGTTTTGTTTAAATGCACCAAAATATATTACCTATATCCACCGAGAAATTAGTAAAAATTTTCAAAATAGGGTGTACTCAATTATGCTGAGCACTGTATGTTGTTGAGTCTGTACTTATGTCTGTTATCTATTGCATATTTATTCATCTGTTGTTTTCCATGTAGGTGTATAAATTCCTGTATGCATGCCGGCTGCTGGACTGTGGGCTCGTTTCTCAGGCCTTCCACTACTGTGAAGTGGTGGGGAAAGCTCTGCTTAGAATAGACCAACCCCATGTGGTGCTATTGGGAGAGCTTATAAAAGTAACGCCCCTCTGTGCATGCTACACTGACACTGATCCTGCAGTTTTGTTCTGTTTGTGCATGCATTGCTCATGTAATGCCACTTCCAGCATGTTCAGTCTGTCTGTTTTGTTTGCTACAACAGTTGGTGGATAGACTGAAGTTCTCC[G/T]AAGCACAGCTCAATGACACGTGTGACGGTCAGCTTTTCCTGGACCCCGATTGGTTGGTGCAGATCCGCTGCAAACACCAGACCCTGCTGGTAATAAGTTTGCGCAGCATATATATGTTAGCTGTTAGTCCAATTTAAGATTAGCAGGACTGTTTATAGGAAGAATGAATGCCATCCATATGTAACTCTATGTACAGTCCACACTATCAATTTACTTTTGCATACCCCAAAGTGCTCAATCATCATAAGGTCCTGTTTAGATCTTGGGTGTCGGGTGAAACGGTCAGAAGTGATCAGCAAAGACAGATTTACACCTCAGTTTAACGTGTCTCTAGTGACCACTTGTTACTGGAGTTAAAGAGAGCATGAATATGTGTATGTTTATAACTTTGTACATATATATTTTTACAAAACATTTTTTATGTTAAAGTTGTTAATCTTTTACTTTTATTTGTTTCTATCAATACAGTTATTATGACATATATTCTAATGGTTACAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26728
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000073789 | Nonsense | 869 | 935 | 21 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 20043792)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 23800531 |
| GRCz11 | 6 | 23900340 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTATATTGTTTCATGAACAGGCCTCAAAGCCCGGATGGTTCAGTGGCTG[G/A]TTCAAATCTAAGCCTAAAGAGGAACCAAAAGAAGACATCCCAGACCCTGA
Long Flanking Sequence:
TTTTTTATAACTGTTTATTAGTTGTAATATCACTAATAGGACATGTATTTATTTTTTAAGGTGGTGACTTTTCTGCTGAGGCACTGGTGAGAAAAACAAATAGATCTATTTCAGTTCCTTTTTAGTTTAAGCCTGAGAGTCCCGGAAGTTGTTTTTGCATGTAGAATTGAAATGAGTATATATTTAAACTGAAATTCATTTAAATTACAATTGCTAGTATGTAATTGTCAAATGTCTTATTCTCACAGATTGCTAGTGAAAATGATGCCACAGTTGGAAAGGTTAATCAGTTAGGGACATTTCCAAGCGAGGACAACAAGACCAAAACACAATCTGCAAAGGTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATATTATATTATATTATATTATGTTATATTATATTGTTTCATGAACAGGCCTCAAAGCCCGGATGGTTCAGTGGCTG[G/A]TTCAAATCTAAGCCTAAAGAGGAACCAAAAGAAGACATCCCAGACCCTGATTCTCCCACAGAGGTATATAACACTTCCTGTGACGTGATTTTTGGGAGGTGTTTAGATTTTAATGTTCTACATTTGGAACATCATTCATTATGACCTTTTTAAAATACATCTCTACACTTATTTTATACAGCAATCAACTATTTAGTAGACACGTTCATGCAACTTTCAAATAAGGAGAACAACAGAAGCAATCAGATCAACAAATCATAAACAGTTTGTGAGTGATATGATAATCAACAGTTAATCTAAAACAATTCACAATGTGTTTTTGGAATTAATAAATCAGAAAATAGGTAGTATTCATGGGCCAAGAGTTAATGAAAATTTTATTTATTTTTTCTAAGGAAAGTCACTTTAAGCAACACTATCTATTCTACCGGGAACTCTATCTTTGGCTGTTTAATGAAAATGGCCAAAGGCTCAGCTGCTGGTGTTAAGTTAGGATCTTT
Associated Phenotype:
Not determined