ZMP
megf6a
Ensembl ID:
ZFIN ID:
Human Orthologue:
MEGF6
Human Description:
multiple EGF-like-domains 6 [Source:HGNC Symbol;Acc:3232]
Mouse Orthologue:
Megf6
Mouse Description:
multiple EGF-like-domains 6 Gene [Source:MGI Symbol;Acc:MGI:1919351]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37685 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37684 | Essential Splice Site | Available for shipment | Available now |
sa37683 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15011 | Nonsense | Available for shipment | Available now |
sa18274 | Nonsense | Available for shipment | Available now |
sa16632 | Nonsense | Available for shipment | Available now |
sa11308 | Essential Splice Site | Available for shipment | Available now |
sa9745 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37685
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 |
---|---|---|---|---|---|
ENSDART00000112424 | Nonsense | 101 | 1513 | 3 | 36 |
ENSDART00000143206 | None | None | 1446 | None | 34 |
Genomic Location (Zv9):
Chromosome 23 (position 21549360)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 21328667 |
GRCz11 | 23 | 21255218 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTACAGGCAGGACTTCAAGATGGCATACAAATGCTGTCCTGGATGGTCC[C/T]AGAACAATTCAAAGATGGGCTGCCTTTATCGTAAGTGTTTCCACTATCAT
Long Flanking Sequence:
TCTGTCCTGATTTGGTATCAATAGTCCTTTTTAACACTGACAGCCATTTCTCAATAGCACACCTTTCAGTGTCAGCCAACTTCTAGCTGCTTTTGAGAATGGGCAGAGGGTTAGAGAAAGACAGCAGTTAGAAACCGATCCTTTTGTTGAGAGACGATGGTTATTAAGAGTCTCGGATGCTCCGGGAATCAAAAGGAAGCTCATGACTCTCACAGCCATCAAACCCCTCGGCAATTATGGCAGAACACTGAACAGCCCTCAAGAAACTGGCACCGAGATTGATAAATGTTGCCACTGCGTTGAACAAATGCTGAACTAATTGGGGTTTAGGGGTTTATTATTATTACATGACTCTTTGAAGTACTTCATTATTTTTGACGAAATTCTATGGTAAATAAATAATCTAGTCATTTTTTTATAGGACTACCTACTACATAGGATATAAACAAGTCTACAGGCAGGACTTCAAGATGGCATACAAATGCTGTCCTGGATGGTCC[C/T]AGAACAATTCAAAGATGGGCTGCCTTTATCGTAAGTGTTTCCACTATCATTTCTGTCTGATCAAGCATCCAAATGGCATGAAAATACAAAAATGTTGGGCAAATTCATACTGTAGGGCAATTTATCTCAATCTCATGAAACTGTGGATGGGAGTGGAAGAATTTGTATTTAAATGTGACCCTGGTATATCTGTAGGGATAGTTAACAATACTCAAAAAAATTAACTATTATTATTTTATTAACAATATACTTTATTTAAATTATTATATTTTTTGTTAAAGTAAAAAATTAAGTAAATTTCATTAACCATGTAGATATTTTGTAAATTTTTTTCCTACCGCAAAAACTTAAAAATGCTATTTGTCACCTTAGAATTATAAGGTTCTATCTGACATTTTTGTCAAAATTGAGTTATTAACATTCTTATTAAATGACAACTTATTTACATTATGGGATGTTTTTAAATAAGTTGTTTACATTTTAAGACTTTTTATTTACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37684
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112424 | Essential Splice Site | 322 | 1513 | 9 | 36 |
ENSDART00000143206 | Essential Splice Site | 265 | 1446 | 7 | 34 |
Genomic Location (Zv9):
Chromosome 23 (position 21458387)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 21237694 |
GRCz11 | 23 | 21164245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGCTAGTTTTTATTTTTAATCCTTTTTCATTTATTGCCTTTGCTTTGT[A/T]GATCTGGAGGAATGTGAGGAAGGAACGTCATGCTGTGAGCAGGATTGCAC
Long Flanking Sequence:
GCATCGTTACTACAGTATTCTTTGTGTCACATTATTCTTCAGAAATCATTTTAAATTGTTGATTTGCTGATATATGGCTATATATGAACATATATATGTAATTATAGATTATTTATTTGAACAAATATAGGTACATATTTTTGCAATATTTTAAAATATATGTTGCATATATGACATATAGTTAATGTGAAATACAAACAATAACTTACAGTATATGTCATTCATGTCTTTTGCATTTTTGCCATATATCAGATTTCTATATGGACAATTATTAATTCTCAGTCAATCAATATTTGTAATAATCAAACATGTTTATTAAGTCTTAAATCATCATATTAGACTTATTTTTGAAGGATCCTGTGACACTGAAAACTGGAATAATGATGCTAAAAATCTCCTTTAAATCACAGGAATAAATGAAATACTAAAATGGCATGTTATATGATTCCCTGTGCTAGTTTTTATTTTTAATCCTTTTTCATTTATTGCCTTTGCTTTGT[A/T]GATCTGGAGGAATGTGAGGAAGGAACGTCATGCTGTGAGCAGGATTGCACAAACTACCCTGGAGGGTATGAATGCTACTGCAGGGCAGGTTACAGACTCAATGCAGATGGATGCGGATGTGACGGTACTTCACAACCTGTTTACTGATGACCAACATTAAAGGAGAGCGAGGAGACATACAGTATTGTTCACTTTGTGTTGTGTTTGTGTAGATGTGGACGAGTGTGCGTCTGATAGAGGAGGCTGTGAACACACTTGTCAGAATACGGCTGGCTCATATCACTGCTTCTGTCGGTTTGGATATCGACTTGGTGAGGACAGACACTCCTGCATTTGTGAGTACATCATGGGGATGTCAGTTATGCGCTGTCTTTTGGGTTTGATTTAGTCACTGTTCTCGTGAATGATATATATATATATATACATACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37683
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 |
---|---|---|---|---|---|
ENSDART00000112424 | Essential Splice Site | 547 | 1513 | 13 | 36 |
ENSDART00000143206 | Essential Splice Site | 490 | 1446 | 11 | 34 |
Genomic Location (Zv9):
Chromosome 23 (position 21454099)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 21233406 |
GRCz11 | 23 | 21159957 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAAGTGCCGCTGCCCACCTGGAGTCAATGGAGACCTGTGCCAGGACGG[T/C]GAGTGACTGAATAAAATGAACACCTATCTGTGCCAAATCTGATGTTCAAA
Long Flanking Sequence:
GTTCTAATTAACACCTCGAATTGATATATTAGAAACAGCTTCTATTTCTCACAGCTGAACAACAGAAAACTAAATAAAATTGGCTAAACTAGCATTAAGCAGGTCAAAACTAACAAAACAAAAAAAAAAATTTAACGCAGAATATCTGACTTTATACTGTATTTCAGATAAACAGGTACGTTCACTTGACATGTTATTGAAATATCTGCAAACATTGTGGTATTTTTATGCTTTAGAAGAGTCAAAAACTTACATACAGCACATTTAACTAATGAAACCATATTGTAAAGTGGGAGCGAACAAACAGAAGTGTACTATGGGTAAAAAGTTATCATTAACACTTTAAGAAACTTTCTTTTATCTATTTTAGCCTGTCCAGAGGGAACATTTGGTAAAAACTGCTCCTTCACTTGCAAGTGCAGAAACGGGGGCACCTGTGACCCGATTAGTGGGAAGTGCCGCTGCCCACCTGGAGTCAATGGAGACCTGTGCCAGGACGG[T/C]GAGTGACTGAATAAAATGAACACCTATCTGTGCCAAATCTGATGTTCAAATCACTGTTGGTATGTTAATATGAAATAGTTAACGTTAAAATGCCCTTGATATGTTTTTTTTTTTCTTCTAAATGTTATGTTTCATGCAGTGTGCTATTTAGCAGTTTTATGAATGTAAATGTTCTGCAATGTTTCAAAGATCTAAGCATGTTAAATGAAGTGTTTGTATTTAAAAGAAAGAACCATTTCTGAACTGTGTGTAATGAGTCATCAGTAGTTTGAGTTTTACTTTAAAGTAAACCTACAGCATATAGGTTTTTATAACATTTCAAGCTTTGGTTTGGAACTCTCAAACAGTGTTGCTGAGACCTGATTGAGTTTGGTTTGTATTGTCAACGTGTTGAGAAGTTTCTGTTTTCTGTTTGTATGCACTCAGTAAAGGAAAATCGATAAGGTAAAACTGACACCATTCTGTCTTTATGTTTTTGGAAATTTGGGTTAGACACATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15011
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 |
---|---|---|---|---|---|
ENSDART00000112424 | Nonsense | 548 | 1513 | 14 | 36 |
ENSDART00000143206 | Nonsense | 491 | 1446 | 12 | 34 |
Genomic Location (Zv9):
Chromosome 23 (position 21453216)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 21232523 |
GRCz11 | 23 | 21159074 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCTTCAYATAAAAGCWGAAAGTAATCTGTACACTTTGTTCTTTAGGCTG[T/A]CCGAAGGGAATGTATGGAAAGCACTGCAACAAGAAATGTAACTGTGCTAA
Long Flanking Sequence:
TCAACGTGTTGAGAAGTTTCTGTTTTCTGTTTGTATGCACTCAGTAAAGGAAAATCGATAAGGTAAAACTGACACCATTCTGTCTTTATGTTTTTGGAAATTTGGGTTAGACACATGCTGTAAGTCGTAGACCAATCACAACTTACTGGGCCATTTATTTGTCCTCATTTGTAAGTCGTTTTGGATAAAAGCATCTGCTAAATGACTAAATGTAAATGTTATGTTGACCAATGACAGCAAAGTAGAGTGTCAAAAAAGGTTAAAAGAGACCGGATCCTTGAATGAACCATTTCAGAGACTGAGAAAAAAAAGAGCAAATACTACGATTTTTATTATGAGAAAATCAAAGCTATTCTAGTTATACAGTAGATTCATGTAAACCTATTATAAGTGTCCAACCAAAAAAAAAAAAAATTAAAACTATTAAAAGACTATAATAGGGGCACTTCAATCTTCACATAAAAGCTGAAAGTAATCTGTACACTTTGTTCTTTAGGCTG[T/A]CCGAAGGGAATGTATGGAAAGCACTGCAACAAGAAATGTAACTGTGCTAATAACGGCCGCTGCCATCGCACATATGGAGCCTGTCTGTGTGATCCAGGACTCTACGGCAGGTTCTGTCACCTCCGTAAGTCAGTAGTATTTCAGTGACTACAGAAGATGCTCCCACATTATGTGTTTACCCAGGTAGGGCAGGTTCCAGGTCTAACATCATTCTCTGGACCTGAAACAACATTCCTAGCAGTCAAAGCTTTAATCCTGTTCCAAACCATAACCAGAGATCAGAGTGAAAGTTATTGTGGGGTTTAAAGGTCTGAGACCAAACATGAAAATGCTTCTTGTTTTTCGTCTTTAAGTATTTTATTTCTACTTATTAACAGTTTTTTTCAGTGGCTTTGGTGCATTTCTCACAACACTTTACATTTGCACAACAGTTTTCTCAAAACAATTAGTACAAACTGCAAAACCTCGTTGATAACCTGCAAAAGCGTGTCACTTGTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18274
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 |
---|---|---|---|---|---|
ENSDART00000112424 | Nonsense | 604 | 1513 | 15 | 36 |
ENSDART00000143206 | Nonsense | 547 | 1446 | 13 | 34 |
Genomic Location (Zv9):
Chromosome 23 (position 21448614)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 21227921 |
GRCz11 | 23 | 21154472 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCCAGCTTGCCCCAAGTGGTCRTATGGATCTGGCTGCTCATCCGAGTG[T/A]CAGTGTKTGCAACAAAACAYGCTTGAGTGCCATCGACGTCATGGAACGTG
Long Flanking Sequence:
TTTTCATCTTTAGTAGCAACAATATATTGCAAAAGAAATATTAAATGAACGAAAAAGTACTAATGCCATGTTTGTACTTTAGTTTATATGACTAACCCAGACAACAATTCATTTGAAACTTTTAATTTTGTCATCTGAATGTGATTCCAATATTTGAAATAAAACAACTGACCAATAAAAATAACAATAATAAAGCTAATATTGTTCCTCTTTACAATTAATGTTGTGGTGTGCCTTTAATTACAATTAGAAGAGAACTTGTTTAATGGATGGATGGATTGATGGATGGATGGATGGATGGATGGATGGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATGATAATAATAATAATAATAATAATAATAATAATAATAATGTTATCTTTTTAACATCTGATGTTCCTCCTGATTGTTACAGAATGTCCAACACAATGTCTTTTCCAGCTTGCCCCAAGTGGTCGTATGGATCTGGCTGCTCATCCGAGTG[T/A]CAGTGTGTGCAACAAAACACGCTTGAGTGCCATCGACGTCATGGAACGTGTGTGTGCAAACCTGGCTATCAGGGGAAAACCTGCAACCGCGGTCAGTGCAAGAAGCACTAATCACTTGTTTAACAGCATGTGTGTATGAATTACAGTAAATATGCAAGAAGGAAATACTGTATGTAGGAGGTATGTATCACTGTACTGTATGTATGTAAACTCAAAAATGACCTTTGCTGCATATTCTTGTTTTAAATTAGTTGAAACAACACAATAATTAAGTTTTTTTTTTTTTTTTTGTAAAAATGATTAGGTTAACTCGAAGGACATAAAGGAATTGTATGAAACCCAGCATTTTTTACAGTGTCAGAAGTAAATATGTTCACAATAATTTGTCTTATGTTGTATCATTTGTGTTATCATTGCTTTTCAGAGTGTGATAGTGGATTTTATGGTCCAGGATGTAGATTAAAATGCCAGTGTCCAGCGGGAGTCTCTTGCCATCCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16632
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 |
---|---|---|---|---|---|
ENSDART00000112424 | Nonsense | 906 | 1513 | 22 | 36 |
ENSDART00000143206 | Nonsense | 849 | 1446 | 20 | 34 |
Genomic Location (Zv9):
Chromosome 23 (position 21436279)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 21215586 |
GRCz11 | 23 | 21142137 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATATTCATCTCAAACAGCWTGTCCTGAGGGCTTTCATGGCTTGGAGTG[C/A]CAGCAGAAGTGYCAGTGCTTGAATGGTGRCCRTTGTCATCCCGTGACTGG
Long Flanking Sequence:
ATCTGGGGTCGCCACAGCAGAATCAACCACCAACTTCCAGCTGCAACCCATTACTGGAAAACACACATACACTCTCATTCACACACATACACTACGGACAATTTAGTTTACCCAATTCACCTGTACCACGTCTTTGAACTTGTGGGGGAAACCAGAGCACCTGGAGGAAACCCACAAGAAAAAGGGGAGGACTGTGTGAGAACTGTCCAAGCTTCTCACTGAAATGCCAACTGACCCAGCTGAGGCTCAAAACAGCAATCTTCTTGCTGTGAGCCGATCGTTCTACCCACTATGCTATTGTGACGCCCAAAACTGTTCATTTACAGATATATTTTCTTCAGAATATGCTACTCATATAATATGTTTATAAAACAGCTCTTTTACTCCTGTAAGCAAACTAAACAATGACCTCAAATATAGGAAATTGTGAGCAAATCTGATCTCCTCTATATATATTCATCTCAAACAGCTTGTCCTGAGGGCTTTCATGGCTTGGAGTG[C/A]CAGCAGAAGTGCCAGTGCTTGAATGGTGGCCGTTGTCATCCCGTGACTGGAGGCTGCCAGTGTCCATCTGGTTGGGTCGGGCCAGTTTGCAATGCCAGTGAGTAATTTTACTGCGGTCAACATCCCATGACAGTCAACGGTAACAAGAAGCATGTTCAAAGCACTCCCTGTGTCTGTTGTGTAAGGTGAAAGGAAAGCACTAGAGCAGATGCTCTGAGTTTGTGTGGTGGTTTGCATGTGAAGTTACGAGATGTCCTAATGTGTGTCTGCAGTCTACATTTCAGTCTTTCATATGAAAACCTGGTGGCGTTGTGTTTCAGGATGTTTTAGTTCTTTCCATATATCTCAGAATAAATGCATGTTGTGTTGATTATATTTTTCTGTTTTTATATGCGTCTCATCATAGCGTGTGAAGCTGGCACCTTTGGGCCGGCCTGCAGTCAAACCTGTAGATGCCACAATAATGGCACCTGTGACCCTGCTGATGGGCGATGTGAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11308
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 |
---|---|---|---|---|---|
ENSDART00000112424 | Essential Splice Site | 1025 | 1513 | 24 | 36 |
ENSDART00000143206 | Essential Splice Site | 968 | 1446 | 22 | 34 |
Genomic Location (Zv9):
Chromosome 23 (position 21433173)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 21212480 |
GRCz11 | 23 | 21139031 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCCACTGCACATGTGTCAGTGGGTGGACAGGAGTGGCCTGTGAATTGGG[T/G]AAAGCACAGACCCAACACACTGTAGTAACTCCAACAGCTGCTGGCAATCT
Long Flanking Sequence:
AAGGCAGATATTTTTTTTTTTTTAAAAACATTTTTGGGACAAAATTATTAGCTCCTTTAAGCTATTTTTTTTCCGATAATCTACAGAACAAACCATTGTTATACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTGACCTTATTAACCCAGTTAAGCCTTTAAATGTCACTTTACACTGTATAGAAGTGTCTTGAAAAATATCTTGTAAAATATTATTTACTGTTATCATGGCAAAGATAAAATAAAATAAATTGAATCGAACCAGTTAGCAGCTTTCCTCACATAATCACACTCAGCTAAATGTATGTACAGTATACATCTCATTGTAGGTATTATAGGTAAGAAAGGTTTGTTTATTGTTTCCAGAGTGCTCAGCTGGATTGTATGGTGTGGGCTGCAACCAGCATTGCCTGTGTCAGAATGGAGGGTCGTGTGACCGAATCAGTGGCCACTGCACATGTGTCAGTGGGTGGACAGGAGTGGCCTGTGAATTGGG[T/G]AAAGCACAGACCCAACACACTGTAGTAACTCCAACAGCTGCTGGCAATCTTAAGATAAAACCTTTTGACAGATGCAAAGGTCACAGATCTCATTTATCTTCTGTTGTGTGTTCAGAATGTGCTGCGGGACACTTTGGCATGGACTGTCAGCACAAGTGTGAGTGTGTAAATGGCGGCGTGTGTGACCGTCACAGTGGCAGGTGTTTGTGCCCAGCAGGTTGGACAGGCACGCACTGTGAGACAGGTAAAAGACATTGGAATGATCTGATCTGGCCATATAAATATATCACATACTGTATAATATATGCTTATTTATAATTTATACTCTTTATGTTTTGGTCAGCATGCACTCAAGGTTTTTATGGTCCGGGCTGTAAGGAGCGATGCCGGTGTGATCATAACGCCGCATGCCACCACATCACTGGCACCTGCTTGTGTCCCGCTGGCTGGAGAGGGACTCACTGCGAAAAGGGTAGTTATTTGTTTTTATTTTTTGTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9745
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 |
---|---|---|---|---|---|
ENSDART00000112424 | Nonsense | 1356 | 1513 | 32 | 36 |
ENSDART00000143206 | Nonsense | 1299 | 1446 | 30 | 34 |
Genomic Location (Zv9):
Chromosome 23 (position 21418520)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 21197827 |
GRCz11 | 23 | 21124378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGTGACTGTARGAATAACAGCACATGCGACCGAGTGACKGGCGTCTG[T/A]CTCTGCTCTCCAKGTTTCTACGGACATCTATGTCAACATGGTGAATGATA
Long Flanking Sequence:
TAATGTAGGTTAGGTTTATGTCACCTAAATTAAAGTGTTACTAGTACTACTACATTTTGTATGTATGTAATTCATTTCTGTCATGTCAAAGCTTGCTTTAATGTCACATGATACTTCAGAAATGATTTTTTATATGCTGATTTGCTGCTTTATCATGAAATATTATTTTTGATGCTGGCTAAATAAATGATTTTATGCTGTATTATACAAACAAATAAAATGACAATAGAACTTTATTAATAAATATATTTTAGAGTTATGTTATTATATTATAATTATATTATTTTATTCCATAGATTTTATTCCAAAACGATCTATTTAAAAAGTGCAGTGTGGCATCAAAAGATTGTGTATACTAGAAAAAAGAAGGAAAGAGAAAAAATGAATTAACAGTCTCTGTTGTGTTGATCAGTGTGTCCCAGAGGACGGTATGGTTCAGACTGCAGTGAAGTGTGTGACTGTAAGAATAACAGCACATGCGACCGAGTGACTGGCGTCTG[T/A]CTCTGCTCTCCAGGTTTCTACGGACATCTATGTCAACATGGTGAATGATAATAATTACAAAAACTCACTGACTGTTTCAATGATTTTTTGTCATACCCATAACTTTAGTACATTTTTATAAAAACTGTACTTATTTATTGTATTGTATTTATTTATTTATTTATTTATATTTTTATCCAAAGCATGTCCTGTTGGCTTCCATGGTCATCGTTGCCAGCTTCTGTGTGACTGTGGTGCAAATGCACCTTGTGACCCTGAAACTGGCCGATGCCTCTGTCCTGCAGGATACCAGGGACTCCGCTGTGAGAGAGGTGCAGATGAGCTCTCAGACAACCTTTTTACTTGATATATATGTGTTTTATAAAGCAGTGAATTAAAACAGTTATTCACCATTAATTAAATATAAAATAATTATGTGTTTTTGTGTTTTAGAGGGCTGTATTAATTTTAAAATGTTATAATTGTGTGATAATTTTACATTTTTATAGATTTGAAAGCTT
Associated Phenotype:
Not determined