ZMP
LOC100149107
Ensembl ID:
Human Orthologue:
HIVEP2
Human Description:
human immunodeficiency virus type I enhancer binding protein 2 [Source:HGNC Symbol;Acc:4921]
Mouse Orthologue:
Hivep2
Mouse Description:
human immunodeficiency virus type I enhancer binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:13380
Alleles
There are 11 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17118 | Nonsense | Available for shipment | Available now |
| sa36300 | Nonsense | Available for shipment | Available now |
| sa6459 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39140 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa42860 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36299 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa12410 | Nonsense | Available for shipment | Available now |
| sa13991 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17118
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 |
|---|---|---|---|---|---|
| ENSDART00000022010 | Nonsense | 60 | 1696 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 6162552)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 6241488 |
| GRCz11 | 17 | 6398718 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTATTCCTTGCGGATTCTCATTTAAAACTAAGAGCAACTTATACAAACAC[A/T]GAAAATCTCACACMCATGCTGYGAAAGCAGGATTGGTTTCAGTTTCAGAG
Long Flanking Sequence:
TCATGGAGGCTACTAAAACCTCAGGTGAAGTGGAAAGTTCCGAACAGATTATCAGTTTCAAAGATGACGAAAAACACTTGCCATCCGAGATGACCCAAAGAGGCCAATCCTCTGGCTCAGAGGACAAAATAAGACTTGCGGAGCAACCCCAGACCCCATCTGTAAGTCCATCTCCTGGTATAGAGCCGCAGGTCCTTGCTTCAGGAAATACACTTACCTCAAAATCTAAAGAACAGAGTCACGTCCAGCTCAGGAGGAAGAACGTTCCTCTTCCAAACAAAAGATATCTCCAGGCTGAGTATGAGATGCTTTCTGGGGGCCTTCACAAAAAGGAGCAGAAGTCTGTTAAAACTGGGAAATATGTCTGCCAGTATTGTGGAAGAGCTTGTGCCAAACCAAGTGTACTAAAGAAGCACATCCGCTCTCATACTGGCGAACGACCGTATCCATGTATTCCTTGCGGATTCTCATTTAAAACTAAGAGCAACTTATACAAACAC[A/T]GAAAATCTCACACCCATGCTGTGAAAGCAGGATTGGTTTCAGTTTCAGAGCAAGACTGCAAGAATACGGATGAGGTGGCGGAGGGTGAAATGCATTCGGATGCAGAACAAAGCAGCGATACCGATGAAGAGGTTGCGGAGGACTTGTCCTTGGATACAACAAGCCATATTAAAGAAACAGAGGGTTATGTGCAAGAAAAGGTCGGGAAATTGGCCAAAAAGGAAGCCCTTTTTCCATCGCAGACGCCACTCAAAAAGGAAACTGGACCATCAGGAAAAGTTTCTTTATGGCAGTTTCGGGAAATGACGGCACCTGTGGCTATTGCTCAGATAGACCAAATGGTTGAGTTTTCCACCATCAAGCAAAAACTAGCACTACGGCTATCAGAGAAGAAAAGTCAAGAATCCGATCAGTCCCTGTCCTTGCCCAGTTCATACAGTAAAGGCAGCACCGATTCCGGATACTTCTCTCGTTCTGAGAGTGCAGAGCAACAGATCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36300
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 |
|---|---|---|---|---|---|
| ENSDART00000022010 | Nonsense | 175 | 1696 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 6162207)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 6241143 |
| GRCz11 | 17 | 6398373 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGGGAAATGACGGCACCTGTGGCTATTGCTCAGATAGACCAAATGGTT[G/T]AGTTTTCCACCATCAAGCAAAAACTAGCACTACGGCTATCAGAGAAGAAA
Long Flanking Sequence:
TTAAAACTGGGAAATATGTCTGCCAGTATTGTGGAAGAGCTTGTGCCAAACCAAGTGTACTAAAGAAGCACATCCGCTCTCATACTGGCGAACGACCGTATCCATGTATTCCTTGCGGATTCTCATTTAAAACTAAGAGCAACTTATACAAACACAGAAAATCTCACACCCATGCTGTGAAAGCAGGATTGGTTTCAGTTTCAGAGCAAGACTGCAAGAATACGGATGAGGTGGCGGAGGGTGAAATGCATTCGGATGCAGAACAAAGCAGCGATACCGATGAAGAGGTTGCGGAGGACTTGTCCTTGGATACAACAAGCCATATTAAAGAAACAGAGGGTTATGTGCAAGAAAAGGTCGGGAAATTGGCCAAAAAGGAAGCCCTTTTTCCATCGCAGACGCCACTCAAAAAGGAAACTGGACCATCAGGAAAAGTTTCTTTATGGCAGTTTCGGGAAATGACGGCACCTGTGGCTATTGCTCAGATAGACCAAATGGTT[G/T]AGTTTTCCACCATCAAGCAAAAACTAGCACTACGGCTATCAGAGAAGAAAAGTCAAGAATCCGATCAGTCCCTGTCCTTGCCCAGTTCATACAGTAAAGGCAGCACCGATTCCGGATACTTCTCTCGTTCTGAGAGTGCAGAGCAACAGATCAATCAGTCGAGTGCAAGTGCCAAATCATATCAAGAAATTATGTTTGGCAAATGTTATAGACCAGCGACCAGGCCAAAGCAATCAATCACTGTACAAACCTGCATGACAGACATAAATGAAGCCACATCTAGCTTCATGATTACACTGAACAAAGGCATGATGCCTGGTGACACGGACTCCTCCATTCACAGAAGCAAAAAAGACCTAGTCCGATCAATAAAAATTGATTCAGAGTCGTTCCAAGAGGAAGATTACCAAGAATGTCAAATTCCCAGCTCTGACCTTCTGGAAACAGCATTGGAGAGTAGTGTATTCTTGCGCAGTAACTCTCTTCCAACCTCATCTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6459
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000022010 | Nonsense | 276 | 1696 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 6161904)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 6240840 |
| GRCz11 | 17 | 6398070 |
KASP Assay ID:
554-5442.1 (used for ordering genotyping assays)
KASP Sequence:
GCATGAYAGACATAAATGAAGCCACATCTAGCTTCATGATTACACTGAAC[A/T]AAGGCATGATGCCTGGTGACACGGACTCCTCCATTCACAGAAGCAAAAAA
Long Flanking Sequence:
CCTTGGATACAACAAGCCATATTAAAGAAACAGAGGGTTATGTGCAAGAAAAGGTCGGGAAATTGGCCAAAAAGGAAGCCCTTTTTCCATCGCAGACGCCACTCAAAAAGGAAACTGGACCATCAGGAAAAGTTTCTTTATGGCAGTTTCGGGAAATGACGGCACCTGTGGCTATTGCTCAGATAGACCAAATGGTTGAGTTTTCCACCATCAAGCAAAAACTAGCACTACGGCTATCAGAGAAGAAAAGTCAAGAATCCGATCAGTCCCTGTCCTTGCCCAGTTCATACAGTAAAGGCAGCACCGATTCCGGATACTTCTCTCGTTCTGAGAGTGCAGAGCAACAGATCAATCAGTCGAGTGCAAGTGCCAAATCATATCAAGAAATTATGTTTGGCAAATGTTATAGACCAGCGACCAGGCCAAAGCAATCAATCACTGTACAAACCTGCATGACAGACATAAATGAAGCCACATCTAGCTTCATGATTACACTGAAC[A/T]AAGGCATGATGCCTGGTGACACGGACTCCTCCATTCACAGAAGCAAAAAAGACCTAGTCCGATCAATAAAAATTGATTCAGAGTCGTTCCAAGAGGAAGATTACCAAGAATGTCAAATTCCCAGCTCTGACCTTCTGGAAACAGCATTGGAGAGTAGTGTATTCTTGCGCAGTAACTCTCTTCCAACCTCATCTAAGTCTAATCTGAATACACCACAAGGACTAAGAAGCAGTAATTCATTTGATGAGAGAATGACAGGTGCTGATGTCACCTACCGGGGTGCAATGGGTATGAGGAGGCTCATGCGGCAATCTGCGTTTGAACACTCTGCTAATGAAGGTCACGCAGAATCAGACTGCTATACTCATTTGGCTTGTAGCTTAAAATCCGACTTGAAAATTCACAGCATAGATGATTCCAAAATGGCTGCTGAAAACTTTCAAGAAACAGAGACATGTTCAGTTTGTCCAGGCCACTCGTCAGAATCTTCTACAAGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39140
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000022010 | Nonsense | 331 | 1696 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 6161738)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 6240674 |
| GRCz11 | 17 | 6397904 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTCCCAGCTCTGACCTTCTGGAAACAGCATTGGAGAGTAGTGTATTCT[T/A]GCGCAGTAACTCTCTTCCAACCTCATCTAAGTCTAATCTGAATACACCAC
Long Flanking Sequence:
TGTGGCTATTGCTCAGATAGACCAAATGGTTGAGTTTTCCACCATCAAGCAAAAACTAGCACTACGGCTATCAGAGAAGAAAAGTCAAGAATCCGATCAGTCCCTGTCCTTGCCCAGTTCATACAGTAAAGGCAGCACCGATTCCGGATACTTCTCTCGTTCTGAGAGTGCAGAGCAACAGATCAATCAGTCGAGTGCAAGTGCCAAATCATATCAAGAAATTATGTTTGGCAAATGTTATAGACCAGCGACCAGGCCAAAGCAATCAATCACTGTACAAACCTGCATGACAGACATAAATGAAGCCACATCTAGCTTCATGATTACACTGAACAAAGGCATGATGCCTGGTGACACGGACTCCTCCATTCACAGAAGCAAAAAAGACCTAGTCCGATCAATAAAAATTGATTCAGAGTCGTTCCAAGAGGAAGATTACCAAGAATGTCAAATTCCCAGCTCTGACCTTCTGGAAACAGCATTGGAGAGTAGTGTATTCT[T/A]GCGCAGTAACTCTCTTCCAACCTCATCTAAGTCTAATCTGAATACACCACAAGGACTAAGAAGCAGTAATTCATTTGATGAGAGAATGACAGGTGCTGATGTCACCTACCGGGGTGCAATGGGTATGAGGAGGCTCATGCGGCAATCTGCGTTTGAACACTCTGCTAATGAAGGTCACGCAGAATCAGACTGCTATACTCATTTGGCTTGTAGCTTAAAATCCGACTTGAAAATTCACAGCATAGATGATTCCAAAATGGCTGCTGAAAACTTTCAAGAAACAGAGACATGTTCAGTTTGTCCAGGCCACTCGTCAGAATCTTCTACAAGGAAACGAAGAAAAGACAAAACTGTCACGGAGGAGGAAGACTTTCATATTCAGGACAAGCCATCAAATGTGACTGGACTCTCAGAGGATCTTGAGACAAAGCAAATTTCTTCAGATAGTGTTGTTTCTGACACTGAGAGGAAGGCTGGCAGCAATGTTATTTCTGTCATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42860
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000022010 | Nonsense | 404 | 1696 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 6161520)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 6240456 |
| GRCz11 | 17 | 6397686 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAAGGTCACGCAGAATCAGACTGCTATACTCATTTGGCTTGTAGCTTA[A/T]AATCCGACTTGAAAATTCACAGCATAGATGATTCCAAAATGGCTGCTGAA
Long Flanking Sequence:
AAATTATGTTTGGCAAATGTTATAGACCAGCGACCAGGCCAAAGCAATCAATCACTGTACAAACCTGCATGACAGACATAAATGAAGCCACATCTAGCTTCATGATTACACTGAACAAAGGCATGATGCCTGGTGACACGGACTCCTCCATTCACAGAAGCAAAAAAGACCTAGTCCGATCAATAAAAATTGATTCAGAGTCGTTCCAAGAGGAAGATTACCAAGAATGTCAAATTCCCAGCTCTGACCTTCTGGAAACAGCATTGGAGAGTAGTGTATTCTTGCGCAGTAACTCTCTTCCAACCTCATCTAAGTCTAATCTGAATACACCACAAGGACTAAGAAGCAGTAATTCATTTGATGAGAGAATGACAGGTGCTGATGTCACCTACCGGGGTGCAATGGGTATGAGGAGGCTCATGCGGCAATCTGCGTTTGAACACTCTGCTAATGAAGGTCACGCAGAATCAGACTGCTATACTCATTTGGCTTGTAGCTTA[A/T]AATCCGACTTGAAAATTCACAGCATAGATGATTCCAAAATGGCTGCTGAAAACTTTCAAGAAACAGAGACATGTTCAGTTTGTCCAGGCCACTCGTCAGAATCTTCTACAAGGAAACGAAGAAAAGACAAAACTGTCACGGAGGAGGAAGACTTTCATATTCAGGACAAGCCATCAAATGTGACTGGACTCTCAGAGGATCTTGAGACAAAGCAAATTTCTTCAGATAGTGTTGTTTCTGACACTGAGAGGAAGGCTGGCAGCAATGTTATTTCTGTCATTCAGCACACAAATTCACTAAACAGACTGAACTCTGCAGAGAAGTTGAGTGAGGTTAGATCCCATCAGTTAGACAAAATTGGCAAATTCATGGAAAAGGGGCATAGCATGGAATGTCACAGAACAGGATCAGAGTGTCAATGGGGACCCTGTGGTTTTCTGCACCAGAAACTTCACATGCATAAACAGCCAACGTCTCAGCCTAATATCCAGGTCCCGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36299
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000022010 | Nonsense | 946 | 1696 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 6159893)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 6238829 |
| GRCz11 | 17 | 6396059 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACAGCCTACAAGCATCACCAGCAAAGCTTAAAACAGGTATACCTCTAT[C/A]ATTAACCTCCAAAACCATTTCAACTACTGAAGCCCCAAGTGGTGGTGCAA
Long Flanking Sequence:
TGAGGGATCCATTGAGAAAATGAGATACTCTTTGATTTCTGGTAGTTCTTTTCCACATCACAGACAATATAGCCCAGTGCAATCCTCTTCCCAGCATGTTAAACCAACTGTTTGCAATGTCCATGACATGGAAAATGTAATGCTTGTAATTAAGAAAGAACCCGAAGAGTCTAAATCACCTGAAACTTATGTTAACTTGAGAGAACCCCAAGAGGATTGTTCTCAGAGTTTGGGCAATGTTTTGTCAACAATAGCAGTGCTTTCACAAGCTCAGCAAGCATTAGCCAGTCAATGCTCATCTGGGTTGCTTGTTCCTGTCAGAATTCAGATGCAAGTACCATCTTACGGAAACATAACATATACTAGTATATCTCATATTCTGGATTCTCATATCCAGAAACCCATTTCTTGCCTAGAACACAAAAAATCCTCCTCTCAAAGTCAACAACTGCACAGCCTACAAGCATCACCAGCAAAGCTTAAAACAGGTATACCTCTAT[C/A]ATTAACCTCCAAAACCATTTCAACTACTGAAGCCCCAAGTGGTGGTGCAAACAAGCGTATGCTCTCACCTGCAAGTAGCATTGAACTCTTTATTGAGGCAAAGCAGCAAAAACGAGTCAAAGACGAGAACATTTATGGTCAGATTGTTGAAGAGCTTAGTGCTGTAGAGTTAGGAAATCTTGAAGTTGAAAAAGAAAGTCCCAAGTCAGAATTCACCTCCGAGCCCATTGATAAGATGGATATGGATGAGGCAACCCAAGAGTTTTACAGCAATGCAGAGTTGCAGTCTTCAGCCAGAATTTCTCAAGATGCTGCTATTATGGAGCAAAAGCCAACACCTGAAAGCATGATGGCTAGTCATCATTCTGCTTCTTGTATCAGTTTAATGCCCTCTGCAATAACTGGTACTTTACTGTTCTCAAAATTTCCTGGTCTTCACACTACTACTTGCATGAGCTGGTGCTATCTCAATACCACCAAACCAAATAGCACCCACACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12410
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 |
|---|---|---|---|---|---|
| ENSDART00000022010 | Nonsense | 984 | 1696 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 6159780)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 6238716 |
| GRCz11 | 17 | 6395946 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YCTCACCTGCAAGYAGCATTGAACTMTTTATTGAGGCAAAGCAGCAAAAA[C/T]GAGTCAAAGAYGAGAACATTTATGGTCAGATTGYTGAAGAGCTTAGTGCW
Long Flanking Sequence:
GCAATGTCCATGACATGGAAAATGTAATGCTTGTAATTAAGAAAGAACCCGAAGAGTCTAAATCACCTGAAACTTATGTTAACTTGAGAGAACCCCAAGAGGATTGTTCTCAGAGTTTGGGCAATGTTTTGTCAACAATAGCAGTGCTTTCACAAGCTCAGCAAGCATTAGCCAGTCAATGCTCATCTGGGTTGCTTGTTCCTGTCAGAATTCAGATGCAAGTACCATCTTACGGAAACATAACATATACTAGTATATCTCATATTCTGGATTCTCATATCCAGAAACCCATTTCTTGCCTAGAACACAAAAAATCCTCCTCTCAAAGTCAACAACTGCACAGCCTACAAGCATCACCAGCAAAGCTTAAAACAGGTATACCTCTATCATTAACCTCCAAAACCATTTCAACTACTGAAGCCCCAAGTGGTGGTGCAAACAAGCGTATGCTCTCACCTGCAAGTAGCATTGAACTCTTTATTGAGGCAAAGCAGCAAAAA[C/T]GAGTCAAAGACGAGAACATTTATGGTCAGATTGTTGAAGAGCTTAGTGCTGTAGAGTTAGGAAATCTTGAAGTTGAAAAAGAAAGTCCCAAGTCAGAATTCACCTCCGAGCCCATTGATAAGATGGATATGGATGAGGCAACCCAAGAGTTTTACAGCAATGCAGAGTTGCAGTCTTCAGCCAGAATTTCTCAAGATGCTGCTATTATGGAGCAAAAGCCAACACCTGAAAGCATGATGGCTAGTCATCATTCTGCTTCTTGTATCAGTTTAATGCCCTCTGCAATAACTGGTACTTTACTGTTCTCAAAATTTCCTGGTCTTCACACTACTACTTGCATGAGCTGGTGCTATCTCAATACCACCAAACCAAATAGCACCCACACAGTCGCACCATTCTCAGAATATGCCTCATGGTTTGTGAGATGCCATAACCCCAACCCACCAGATATTAGCACTGGGATGGTTCTTGCCCTTCTCCGATCTAAACAGCAAAGACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13991
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 |
|---|---|---|---|---|---|
| ENSDART00000022010 | Essential Splice Site | 1324 | 1696 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 6158504)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 6237440 |
| GRCz11 | 17 | 6394670 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCACCGACAGCTATGGACAATACAGAAGATGCTGGTAGGAGCCTGTTCT[G/A]TAAGAAGCTAGGCATTAGCCTAGCCAAAACAATTTCTGAGCCASTTATAA
Long Flanking Sequence:
GTTTCATCCATCATTCGGCAAACAGAACCAATGCGTGTAAAGATATTTGAAGGAGGGTATGAATGTGTATTGTAATAATATTAATGTTCATATGTCACTGAAGTAATGCATCCTTGTATAAGTGTTGTTTATTCCTTTCAGGTATAAGTCCAATGAGGAATATGTGTATGTAAGGGGCCGTGGTCGGGGAAAGTATATATGTGAAGAGTGTGGTATTCGTTGTAAGAAGCCAAGCATGCTTAGGAAACACATACGGACGCACACTGATGTGAGACCCTACATCTGCAAGTGCTGCAATTTTGCATTTAAAACTAAAGGTTGGTTTTACCACACATTTAAGCATGACTGCAATAGTTTGAGACAGAAAAATAATCCCTTTTTTCTTTTAGGGAATCTTACCAAGCATATGAAGTCAAAAGCTCACATGAAAAAATGCCTTGAACTTGGAGTTTCACCGACAGCTATGGACAATACAGAAGATGCTGGTAGGAGCCTGTTCT[G/A]TAAGAAGCTAGGCATTAGCCTAGCCAAAACAATTTCTGAGCCACTTATAAAACCCCAATGTTAAAAAAAATCTTATTTTTGTTTTATTCCCCTACGGCTTGTATAGATGACACCCAGAAATCCTTGGGCATCATGCCAGCGGAACAAACCATTAAACATCAATTCTCAGATGTGGAGGATTCTGATGGTGCCGATGAGGATGAACCAGACGAGGATGAAGATGATGAATGTGATGGTGATTCTACACCAAAAACGTTGTCTAGAAGCACAAGTCCTCAGTCCTATGCTGTCAACAAGCCATGTATGTCTGGCTGCCTCCCTAAACACTTTGACTCAGGCTGCAATCTACCAAAGGAGCAGCTTGAAGCGTCCTCTTTGACTATTGAGGATGACCTGAATTCTGATCAGTCAAGCTGCTCCTTTGAGCTCTGCCCACCTCAGCTGCTGTCACCTTGTTGGGACTCACCTCGACAGAGGTACATGTCCCCAAGAGGAGATCT
Associated Phenotype:
Not determined