ZMP
LOC556026
Ensembl ID:
Human Orthologue:
SSX2IP
Human Description:
synovial sarcoma, X breakpoint 2 interacting protein [Source:HGNC Symbol;Acc:16509]
Mouse Orthologue:
Ssx2ip
Mouse Description:
synovial sarcoma, X breakpoint 2 interacting protein Gene [Source:MGI Symbol;Acc:MGI:2139150]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39712 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa19617 | Nonsense | Available for shipment | Available now |
| sa10423 | Nonsense | Available for shipment | Available now |
| sa31240 | Nonsense | Available for shipment | Available now |
| sa39711 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa30808 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa4872 | Nonsense | F2 line generated | Not yet available |
| sa16918 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39712
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000131015 | Essential Splice Site | 20 | 427 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 55801318)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 54583864 |
| GRCz11 | 1 | 55261515 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGATCGCAAAATCACCAGAATCTCACATGAGAGCTCAAGACTCCACAG[G/A]TACACAATCACATTCAGATTTATTAAGCGGCTCTAAGGAATACTTTATTC
Long Flanking Sequence:
GTTACACAATTCATTTATTTTGCCCCAACACAAATCGATTAAGTTAATAATGAAGTGTTTAATAATTAAATTGTCCCAAAACATCTTAAGAATTGTTTCAGCTCATTAAAAAAATAATTTGAGTAACATATTTTGATTTGTTTTTTATGTAACAAATCATTTAACGATGCAAAGCTTATTAATTCAGCTTTGAAATGGTAGATATATCTCAATTAAAAGAAACATTGAAAGTTAAATAAGTTTGTATTGTTTCTCCCAAAACACTGTCTGGTTATTTTTGTCAATAGCATTTGTGGTTTTGAGACTTTAATAATTCCTACAAAAGTTTTTCCTTCAAATAATGAAGATATTCATTAGATATTATAATAGATTATAAATTGCATAAGATATTAGTGCTTCATTCATGATGTGATGCTGTTGTTCCAGTGACTGCAGGACTATGACGCACAAACAGATCGCAAAATCACCAGAATCTCACATGAGAGCTCAAGACTCCACAG[G/A]TACACAATCACATTCAGATTTATTAAGCGGCTCTAAGGAATACTTTATTCCTAGTTATTGTAAATTGTGACATTTTAGCGTATGTTCACACATATGACAAAATTAAACTAAAGAATACTACAAATAATGTTGAAATACAGCCTACGTGTTCTTTCATGTGTTTGGCGCCATCTTGTGACTGAATAATAATAATAGGCTAGTATAGTTCTTTCTTCAAAAACTTTACGTTTAATGAAAGAGCTAATAAACTATTACAGCTCAATTCAGTGTTTTGTGTCTAATAAGTTAGTTTTTGTGCTACTAATTCGTGTAATAATTGTATAATATGGCGCCTGTTGTTTTCACGGATTAAAGCCAACCCAACAAACACATTTACGTTGTAGCGATGTCTGCACAACGTTGTATTTTTTCAAAGGCAACGTTGCCGCTTACGTGCTCGCTACATTGTCACAACGTAGAAATGTAAGACGTGAGAAGGCTGTAGCAACGTTGTCGTGCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19617
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 |
|---|---|---|---|---|---|
| ENSDART00000131015 | Nonsense | 131 | 427 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 55797287)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 54579833 |
| GRCz11 | 1 | 55257484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTATCCAAAGCTATAGAGATATTAAACGTGTTGCCGAAGTGGACAGGA[C/T]GAAGAGAGGCTGGATTCAAGACGGCAAAGGCTGATGGGAGGTACATGCAG
Long Flanking Sequence:
GTCTCCTGTAAAACTCTCAGAATACCGCCCCCCCCCACCCTTCCTCAGCTTTTTGGAACAGTCCACGGATTGTCGTCCGATCTTGGTAGTACAGACAAGGGTCCCCACTCGTCAGTTTGTGCGACAATTCCAATACAACGAACCCCCCCCCCACCCCCCACCCCCCGCCAAACTCTGCGCACTTCAGTTCCGAATCACACCCCCCCCCCCTTATTTATGGGAGAAATACGGATGAATACCTTGATGGGATTATAGCGAGATAGAACTTTATAATAAAAAAAAGGAAGAGGGTTGACTGGTATGCAAGGTTACAATATACACAAACTTCCCTTAGTGCAATATGACATCATCAACAAAAATTTTGGGGTAAATATTGAATTTGTAAATATGGGCATTACATATAAATGCAAAAAAAAAAAAATCCATATACAGCACAGTTACAGTGATATTTCCTATCCAAAGCTATAGAGATATTAAACGTGTTGCCGAAGTGGACAGGA[C/T]GAAGAGAGGCTGGATTCAAGACGGCAAAGGCTGATGGGAGGTACATGCAGTGACCTGATGTCCTTTTCAAGTCTATCAAAAGCATTTAATTTCCGATAATGTGCATTAATGTTGACTTGAAGCATTTGTGTGTGCGATTTGTCTCCCCCTGCAGGATAGAAGAGGCATTGCGTCTGCTGTTAGACCGAAGAGAAGCTGAGCTCAGAGAAGCCATGAAACTAAGACACGGCCTTACGACGCTACTGCACATGCTCAGAAACAACATGGCACAGGTGAGAAAGACAACTGCACTTTCACTGTGTTTAATACGAAATCATTGTATGCGGAATTTAAATATGGAGTAAAGGCACAGTATGTACTTTTGGCCACTAGAGGGCCTGTATTCACAACAAACAAAGGTATATTTTGCTTATAAGTGTGGAATAATGGTAGTTGTAGTATTCACTATCCTACGGGACGATTTTAGAAATCATGTTGATGATGAGTAAAGTATTATTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10423
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 |
|---|---|---|---|---|---|
| ENSDART00000131015 | Nonsense | 222 | 427 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 55796185)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 54578731 |
| GRCz11 | 1 | 55256382 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGAGTCTGGGTGATCATGTGACGGGAGGYGTGGTCCAGGAGTGGATG[C/T]AAGTTCAGAAAACACTGCGGGAKCTCATGGCACAGAGTATAACCTRTTTA
Long Flanking Sequence:
TTATTAGAGCTTTTTAGAATTATTGAGGGTTCTGTTGTAATGGTGTCTAATAGAACACACTTATTAAACATATTAAAGCCTCACTGTTGTCTCCATAATCTAGAAAACCAAACCAGAAATTGAGAATTTGTGACATCATTAGCGTTAACACCAAACACACAGACACACACACACATTGCACATTCTCTGCATTTGAACAAACATCTTACAAACATTTGGGATAATGTACGTACATAAATCAGCAAAATATATAACTGTTATAATGTTTTTTGGATATTTCAATGAAAAAAATTGTTCCCCTGAAAAAGTCTAGGCTTCACTGTTGTATTTTTGAGTGTGCAAAAACATTAAGTAGATGCATCATCTATTTCAATCTGTTTAATTAGGCAATTCAGGACTCCAGCAACACAGGTGTGGAGGAAACTGAAGATAATGTGCTGGTCCAATCAGAGCAGAGTCTGGGTGATCATGTGACGGGAGGTGTGGTCCAGGAGTGGATG[C/T]AAGTTCAGAAAACACTGCGGGAGCTCATGGCACAGAGTATAACCTGTTTACTCTGTAACTGACAGCTTAAATAAGGCTTTAGAGACTTTAATTCATAAAAATAGAGTTGGTCTAAATTATAAGCCCTGATTTAAAATGTCAATTATTTTTCAAATGTTTTTCAGCTAACAAAGCTAGGACATTTTTCACAGTATTTCCCATTTATATTTTTTTTCTGGAGAAATTATTCTTTCGTTTAGCTGGAATAACTAAAACATTTTTAAAAATGTGGTCAATACTATTAGCCCCCTAAAGAAATGGTAATGCATTGGCTACAGAACAATCACAGTTGTCCAATGACTTGCTTAATTAACCTAACTTGCCAAGTTTCCCTAATTAACCTAGTTAAGGATTTAAATCACACTTTAAGGGCCTGAATACCCAAACAAAAGTATTTTCAAAATCACACTATTTTTCCATGCATATTAGCTACACTACAACCTTGATATCAATATCAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31240
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 |
|---|---|---|---|---|---|
| ENSDART00000131015 | Nonsense | 233 | 427 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 55796152)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 54578698 |
| GRCz11 | 1 | 55256349 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTCCAGGAGTGGATGCAAGTTCAGAAAACACTGCGGGAGCTCATGGCA[C/T]AGAGTATAACCTGTTTACTCTGTAACTGACAGCTTAAATAAGGCTTTAGA
Long Flanking Sequence:
GTTGTAATGGTGTCTAATAGAACACACTTATTAAACATATTAAAGCCTCACTGTTGTCTCCATAATCTAGAAAACCAAACCAGAAATTGAGAATTTGTGACATCATTAGCGTTAACACCAAACACACAGACACACACACACATTGCACATTCTCTGCATTTGAACAAACATCTTACAAACATTTGGGATAATGTACGTACATAAATCAGCAAAATATATAACTGTTATAATGTTTTTTGGATATTTCAATGAAAAAAATTGTTCCCCTGAAAAAGTCTAGGCTTCACTGTTGTATTTTTGAGTGTGCAAAAACATTAAGTAGATGCATCATCTATTTCAATCTGTTTAATTAGGCAATTCAGGACTCCAGCAACACAGGTGTGGAGGAAACTGAAGATAATGTGCTGGTCCAATCAGAGCAGAGTCTGGGTGATCATGTGACGGGAGGTGTGGTCCAGGAGTGGATGCAAGTTCAGAAAACACTGCGGGAGCTCATGGCA[C/T]AGAGTATAACCTGTTTACTCTGTAACTGACAGCTTAAATAAGGCTTTAGAGACTTTAATTCATAAAAATAGAGTTGGTCTAAATTATAAGCCCTGATTTAAAATGTCAATTATTTTTCAAATGTTTTTCAGCTAACAAAGCTAGGACATTTTTCACAGTATTTCCCATTTATATTTTTTTTCTGGAGAAATTATTCTTTCGTTTAGCTGGAATAACTAAAACATTTTTAAAAATGTGGTCAATACTATTAGCCCCCTAAAGAAATGGTAATGCATTGGCTACAGAACAATCACAGTTGTCCAATGACTTGCTTAATTAACCTAACTTGCCAAGTTTCCCTAATTAACCTAGTTAAGGATTTAAATCACACTTTAAGGGCCTGAATACCCAAACAAAAGTATTTTCAAAATCACACTATTTTTCCATGCATATTAGCTACACTACAACCTTGATATCAATATCAAGATGGCGTTGAGCATGGCTGCTGTATTGCGAGCTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39711
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 |
|---|---|---|---|---|---|
| ENSDART00000131015 | Nonsense | 258 | 427 | 8 | 12 |
| ENSDART00000131015 | Nonsense | 258 | 427 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 55794299)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 54576845 |
| GRCz11 | 1 | 55254496 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGGAGAAGCTGCTGGTTCATCTGGAGGAAGAGCTGGAGCAGAGCCGA[C/T]AGCTGATCCGAGCGCAGCAGCAGTTGCTACAGGTCAGACATACAAGACAA
Long Flanking Sequence:
ATAGCGCAGGTGTTTAGACCAGGGGTGGCCAACCCTGTTCCTGGAGAGCCACCTTCCTGCAAATTTCAGTTGCTATCCATATCAAACACACCTGAACCAATTAATTAGGACCTGAACACCACGTGATAATTACAGGCAGGTGTGTTTGATATGGGTAGCAACTGAAATCTGCAGGAAGGTAGATCTCCAGGAACAGGGTTGACCACCCCTGCTTTAGACTATGGGGGAAACCGGAGCACCCGGAGGAAATTCGCACCAACACGGGGAGAACATGCAAACTCCACTCAGAAATGCCAACTAGCCCAGCCGAGGCCCTGCAACCTTCTTGCTGTGAGGCCACAGCGCTACCCACTGCGCCACCGCGCCACTCCATTAAACATCACTAAAAGTCACAGGATGGCTAATAATGTTGTCATTAACTGCGTTCAGGTCCCATTGCTCCAGAAACAGACCAGGAGAAGCTGCTGGTTCATCTGGAGGAAGAGCTGGAGCAGAGCCGA[C/T]AGCTGATCCGAGCGCAGCAGCAGTTGCTACAGGTCAGACATACAAGACAAACTGTAATGCGTGATGTTATTTACCACAGTAACTGAGGTGTTTTCTCTCAGGAGAGTGTAAATCCTCCCCTCCCTGCTGTGCTGATGGACTGCTACTATATTGAGGAGTGGGAGCGGCTTCAGGACCACTGGGAGGAGTTTAAGAGGCAGAGGCGGAGCTTCCAGCGGGAGAGGCAGGCCTTCACTGAGGCTGCCATCCGATTGGGCCGTGAGGTAATTTATGCATGTGCATGTTTTTCTATCTTTAATGAAGCAACTGCAATGTTTAACTCTCGAAGCCTAGGGCTGTGTTTCCCAAACCTGCTCCTGAAGTCACACCAACTGTACACTTTTGTTTACCTCTCCCTAGAACATTAGAAGAAACTCCAAAACTTGAAGTTAATAGCTTAGATAGGGGAGACATCCAAAACATGTACTGTTGGTGTGCCTTCAGGAACAGAGTTGGGAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30808
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 |
|---|---|---|---|---|---|
| ENSDART00000131015 | Nonsense | 258 | 427 | 8 | 12 |
| ENSDART00000131015 | Nonsense | 258 | 427 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 55794299)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 54576845 |
| GRCz11 | 1 | 55254496 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGGAGAAGCTGCTGGTTCATCTGGAGGAAGAGCTGGAGCAGAGCCGA[C/T]AGCTGATCCGAGCGCAGCAGCAGTTGCTACAGGTCAGACATACAAGACAA
Long Flanking Sequence:
ATAGCGCAGGTGTTTAGACCAGGGGTGGCCAACCCTGTTCCTGGAGAGCCACCTTCCTGCAAATTTCAGTTGCTATCCATATCAAACACACCTGAACCAATTAATTAGGACCTGAACACCACGTGATAATTACAGGCAGGTGTGTTTGATATGGGTAGCAACTGAAATCTGCAGGAAGGTAGATCTCCAGGAACAGGGTTGACCACCCCTGCTTTAGACTATGGGGGAAACCGGAGCACCCGGAGGAAATTCGCACCAACACGGGGAGAACATGCAAACTCCACTCAGAAATGCCAACTAGCCCAGCCGAGGCCCTGCAACCTTCTTGCTGTGAGGCCACAGCGCTACCCACTGCGCCACCGCGCCACTCCATTAAACATCACTAAAAGTCACAGGATGGCTAATAATGTTGTCATTAACTGCGTTCAGGTCCCATTGCTCCAGAAACAGACCAGGAGAAGCTGCTGGTTCATCTGGAGGAAGAGCTGGAGCAGAGCCGA[C/T]AGCTGATCCGAGCGCAGCAGCAGTTGCTACAGGTCAGACATACAAGACAAACTGTAATGCGTGATGTTATTTACCACAGTAACTGAGGTGTTTTCTCTCAGGAGAGTGTAAATCCTCCCCTCCCTGCTGTGCTGATGGACTGCTACTATATTGAGGAGTGGGAGCGGCTTCAGGACCACTGGGAGGAGTTTAAGAGGCAGAGGCGGAGCTTCCAGCGGGAGAGGCAGGCCTTCACTGAGGCTGCCATCCGATTGGGCCGTGAGGTAATTTATGCATGTGCATGTTTTTCTATCTTTAATGAAGCAACTGCAATGTTTAACTCTCGAAGCCTAGGGCTGTGTTTCCCAAACCTGCTCCTGAAGTCACACCAACTGTACACTTTTGTTTACCTCTCCCTAGAACATTAGAAGAAACTCCAAAACTTGAAGTTAATAGCTTAGATAGGGGAGACATCCAAAACATGTACTGTTGGTGTGCCTTCAGGAACAGAGTTGGGAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa4872
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000131015 | Nonsense | 314 | 427 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 55794062)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 54576608 |
| GRCz11 | 1 | 55254259 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTTTAAGAGGCAGAGGCGGAGCTTCCAGCGGRAGAGGCAGGCCTTCACT[G/T]AGGCTGCCATCCGATTGGGCCGTGAGGTAATTTATGCATGTGCATGTTTT
Long Flanking Sequence:
ACCCGGAGGAAATTCGCACCAACACGGGGAGAACATGCAAACTCCACTCAGAAATGCCAACTAGCCCAGCCGAGGCCCTGCAACCTTCTTGCTGTGAGGCCACAGCGCTACCCACTGCGCCACCGCGCCACTCCATTAAACATCACTAAAAGTCACAGGATGGCTAATAATGTTGTCATTAACTGCGTTCAGGTCCCATTGCTCCAGAAACAGACCAGGAGAAGCTGCTGGTTCATCTGGAGGAAGAGCTGGAGCAGAGCCGACAGCTGATCCGAGCGCAGCAGCAGTTGCTACAGGTCAGACATACAAGACAAACTGTAATGCGTGATGTTATTTACCACAGTAACTGAGGTGTTTTCTCTCAGGAGAGTGTAAATCCTCCCCTCCCTGCTGTGCTGATGGACTGCTACTATATTGAGGAGTGGGAGCGGCTTCAGGACCACTGGGAGGAGTTTAAGAGGCAGAGGCGGAGCTTCCAGCGGGAGAGGCAGGCCTTCACT[G/T]AGGCTGCCATCCGATTGGGCCGTGAGGTAATTTATGCATGTGCATGTTTTTCTATCTTTAATGAAGCAACTGCAATGTTTAACTCTCGAAGCCTAGGGCTGTGTTTCCCAAACCTGCTCCTGAAGTCACACCAACTGTACACTTTTGTTTACCTCTCCCTAGAACATTAGAAGAAACTCCAAAACTTGAAGTTAATAGCTTAGATAGGGGAGACATCCAAAACATGTACTGTTGGTGTGCCTTCAGGAACAGAGTTGGGAAACACTGCTCTAGGAGACACCAGTTTACTTACAAGAGAACAAAAATGACTTTAAATGACAGTGATATTCATGTAAAAAGAAACCCTAAAGCAACCAAAAATGAAGATTTGACCCTTTAAAGGGCATCTATTTTACTGTTTTCAAGCTGTAAGATAAGTATTTTGTGTCTCCAGAATGTGTCTGTAAAGTTTCAGCTTAAAACACCCCTCAGATTATTTGTTACACCTTTTAAAGATTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16918
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 |
|---|---|---|---|---|---|
| ENSDART00000131015 | Essential Splice Site | 322 | 427 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 55794035)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 54576581 |
| GRCz11 | 1 | 55254232 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCGGRAGAGGCAGGCCTTCACTKAGGCTGCCATCCGATTGGGCCGTGAG[G/A]TAATTTATGCATGTGCRTGTTKTTCTATCTTWRATGAAGYAACTGCAATG
Long Flanking Sequence:
GGAGAACATGCAAACTCCACTCAGAAATGCCAACTAGCCCAGCCGAGGCCCTGCAACCTTCTTGCTGTGAGGCCACAGCGCTACCCACTGCGCCACCGCGCCACTCCATTAAACATCACTAAAAGTCACAGGATGGCTAATAATGTTGTCATTAACTGCGTTCAGGTCCCATTGCTCCAGAAACAGACCAGGAGAAGCTGCTGGTTCATCTGGAGGAAGAGCTGGAGCAGAGCCGACAGCTGATCCGAGCGCAGCAGCAGTTGCTACAGGTCAGACATACAAGACAAACTGTAATGCGTGATGTTATTTACCACAGTAACTGAGGTGTTTTCTCTCAGGAGAGTGTAAATCCTCCCCTCCCTGCTGTGCTGATGGACTGCTACTATATTGAGGAGTGGGAGCGGCTTCAGGACCACTGGGAGGAGTTTAAGAGGCAGAGGCGGAGCTTCCAGCGGGAGAGGCAGGCCTTCACTGAGGCTGCCATCCGATTGGGCCGTGAG[G/A]TAATTTATGCATGTGCATGTTTTTCTATCTTTAATGAAGCAACTGCAATGTTTAACTCTCGAAGCCTAGGGCTGTGTTTCCCAAACCTGCTCCTGAAGTCACACCAACTGTACACTTTTGTTTACCTCTCCCTAGAACATTAGAAGAAACTCCAAAACTTGAAGTTAATAGCTTAGATAGGGGAGACATCCAAAACATGTACTGTTGGTGTGCCTTCAGGAACAGAGTTGGGAAACACTGCTCTAGGAGACACCAGTTTACTTACAAGAGAACAAAAATGACTTTAAATGACAGTGATATTCATGTAAAAAGAAACCCTAAAGCAACCAAAAATGAAGATTTGACCCTTTAAAGGGCATCTATTTTACTGTTTTCAAGCTGTAAGATAAGTATTTTGTGTCTCCAGAATGTGTCTGTAAAGTTTCAGCTTAAAACACCCCTCAGATTATTTGTTACACCTTTTAAAGATTGTGATTTTCTGCTTTAAACACAATATAGCC
Associated Phenotype:
Not determined