ZMP
lrrc6
Ensembl ID:
ZFIN ID:
Description:
leucine-rich repeat-containing protein 6 [Source:RefSeq peptide;Acc:NP_001002311]
Human Orthologue:
LRRC6
Human Description:
leucine rich repeat containing 6 [Source:HGNC Symbol;Acc:16725]
Mouse Orthologue:
Lrrc6
Mouse Description:
leucine rich repeat containing 6 (testis) Gene [Source:MGI Symbol;Acc:MGI:1859553]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39914 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19850 | Nonsense | Available for shipment | Available now |
sa14388 | Essential Splice Site | Available for shipment | Available now |
sa19849 | Nonsense | Available for shipment | Available now |
sa14481 | Nonsense | Available for shipment | Available now |
sa25885 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19848 | Nonsense | Available for shipment | Available now |
sa33003 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39914
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 |
---|---|---|---|---|---|
ENSDART00000075347 | Nonsense | 34 | 440 | 2 | 12 |
ENSDART00000132346 | Nonsense | 34 | 440 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 43224653)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43274117 |
GRCz11 | 2 | 43123535 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGAGAGATCTTCTCCCTTGAGGAGCTTTCCCTTCATCAGCAGGACATC[C/T]AGAGAATCGAGCACATCCACAAGTGGTGCAGAGACCTCAAAATCCTTTAT
Long Flanking Sequence:
GGGCGGGATTGCTACTTGAATGTAAACCGAACAACCACAATAAAACTTGCCTCTTTCCTTCATTAAAAGCGGTTAAAGTTGTTTTACAGATAGTTGCCAGGAATACATGACATTGGATGCGATTTTAAGGTAATTCCTGATGAAATTTATTCTAAGTGAATATTTCTTGTGTTTATTGCACCGCTGAAATTTTCAACAGGAGCGTCTGAAGTGAGTCTGTTTCTGTAGCAACGTCTAACAAACTAGACCAGCAAGTCATGGTCCGCAGTAAGTGCTTCATGTATTTTAAACATTATTTGCTTTAAGCTAAATGTTATTTTACAACATTGATCGTATTTTCCTCACCCGTAAACATTTGACCTTTCGCGGTTAAGCTGTTTGTAAACGAATCGCCCCTCTTCCTCCGTTCAGTCAGTGAGGATCTGATCCGCCGCAGAGCAGAGCACAATAACGGAGAGATCTTCTCCCTTGAGGAGCTTTCCCTTCATCAGCAGGACATC[C/T]AGAGAATCGAGCACATCCACAAGTGGTGCAGAGACCTCAAAATCCTTTATTTACAAAACAACCTCATCCCTAAAATAGGTAAATACTGGACAGTGGTATTGTGGTATTGCAGCAACTCAAACGCATGGCTGTTTATGTAAACTCTTGTAACTTTGTTTTTGCAGAAAATGTCGGCAGGCTAAAGAAGCTGGAATATTTAAATCTGGCACTGAACAACATTGAGGTCATTGAGAATTTGGAAGGTGACTTCATACAGTGTGTGTGTGTGTGTGTGTAACTGGGTCAAAAATAGATTGGTTTCTGCATCAAATTAAATGTAAAAAAAATAAATTAAATGCAAGTGTATGCTTTAGTGCTTTAAATGCAAAAACAAAATATCATAATATGGGTGAAATGATCCTCCAATCATTATTTAGCATAACAGATTTATTTATAAAAAAATGAAACTATATATATATATATATATATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19850
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 |
---|---|---|---|---|---|
ENSDART00000075347 | Nonsense | 50 | 440 | 2 | 12 |
ENSDART00000132346 | Nonsense | 50 | 440 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 43224603)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43274067 |
GRCz11 | 2 | 43123485 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAGAATCGAGCACATCCACAAGTGGTGCAGAGACCTCAAAATCCTTTA[T/A]TTACAAAACAACCTCATCCCTAAAATAGGTAAATACTGGACAGTGGTATT
Long Flanking Sequence:
CTCTTTCCTTCATTAAAAGCGGTTAAAGTTGTTTTACAGATAGTTGCCAGGAATACATGACATTGGATGCGATTTTAAGGTAATTCCTGATGAAATTTATTCTAAGTGAATATTTCTTGTGTTTATTGCACCGCTGAAATTTTCAACAGGAGCGTCTGAAGTGAGTCTGTTTCTGTAGCAACGTCTAACAAACTAGACCAGCAAGTCATGGTCCGCAGTAAGTGCTTCATGTATTTTAAACATTATTTGCTTTAAGCTAAATGTTATTTTACAACATTGATCGTATTTTCCTCACCCGTAAACATTTGACCTTTCGCGGTTAAGCTGTTTGTAAACGAATCGCCCCTCTTCCTCCGTTCAGTCAGTGAGGATCTGATCCGCCGCAGAGCAGAGCACAATAACGGAGAGATCTTCTCCCTTGAGGAGCTTTCCCTTCATCAGCAGGACATCCAGAGAATCGAGCACATCCACAAGTGGTGCAGAGACCTCAAAATCCTTTA[T/A]TTACAAAACAACCTCATCCCTAAAATAGGTAAATACTGGACAGTGGTATTGTGGTATTGCAGCAACTCAAACGCATGGCTGTTTATGTAAACTCTTGTAACTTTGTTTTTGCAGAAAATGTCGGCAGGCTAAAGAAGCTGGAATATTTAAATCTGGCACTGAACAACATTGAGGTCATTGAGAATTTGGAAGGTGACTTCATACAGTGTGTGTGTGTGTGTGTGTAACTGGGTCAAAAATAGATTGGTTTCTGCATCAAATTAAATGTAAAAAAAATAAATTAAATGCAAGTGTATGCTTTAGTGCTTTAAATGCAAAAACAAAATATCATAATATGGGTGAAATGATCCTCCAATCATTATTTAGCATAACAGATTTATTTATAAAAAAATGAAACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATAGGGATGCTCCGATCAGGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14388
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 |
---|---|---|---|---|---|
ENSDART00000075347 | Essential Splice Site | 60 | 440 | 2 | 12 |
ENSDART00000132346 | Essential Splice Site | 60 | 440 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 43224573)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43274037 |
GRCz11 | 2 | 43123455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGACCTCAAAATCCTTTATTTACAAAACAACCTCATCCCTAAAATAGG[T/G]AAATACTGGACNNNNNNNNTGTGGTATTGYAGCAACYCAAACGCATGGYT
Long Flanking Sequence:
GTTTTACAGATAGTTGCCAGGAATACATGACATTGGATGCGATTTTAAGGTAATTCCTGATGAAATTTATTCTAAGTGAATATTTCTTGTGTTTATTGCACCGCTGAAATTTTCAACAGGAGCGTCTGAAGTGAGTCTGTTTCTGTAGCAACGTCTAACAAACTAGACCAGCAAGTCATGGTCCGCAGTAAGTGCTTCATGTATTTTAAACATTATTTGCTTTAAGCTAAATGTTATTTTACAACATTGATCGTATTTTCCTCACCCGTAAACATTTGACCTTTCGCGGTTAAGCTGTTTGTAAACGAATCGCCCCTCTTCCTCCGTTCAGTCAGTGAGGATCTGATCCGCCGCAGAGCAGAGCACAATAACGGAGAGATCTTCTCCCTTGAGGAGCTTTCCCTTCATCAGCAGGACATCCAGAGAATCGAGCACATCCACAAGTGGTGCAGAGACCTCAAAATCCTTTATTTACAAAACAACCTCATCCCTAAAATAGG[T/G]AAATACTGGACAGTGGTATTGTGGTATTGCAGCAACTCAAACGCATGGCTGTTTATGTAAACTCTTGTAACTTTGTTTTTGCAGAAAATGTCGGCAGGCTAAAGAAGCTGGAATATTTAAATCTGGCACTGAACAACATTGAGGTCATTGAGAATTTGGAAGGTGACTTCATACAGTGTGTGTGTGTGTGTGTGTAACTGGGTCAAAAATAGATTGGTTTCTGCATCAAATTAAATGTAAAAAAAATAAATTAAATGCAAGTGTATGCTTTAGTGCTTTAAATGCAAAAACAAAATATCATAATATGGGTGAAATGATCCTCCAATCATTATTTAGCATAACAGATTTATTTATAAAAAAATGAAACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATAGGGATGCTCCGATCAGGATTTTTGCAGCCGATACCAAGTCATGGTGATCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19849
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 |
---|---|---|---|---|---|
ENSDART00000075347 | Nonsense | 69 | 440 | 3 | 12 |
ENSDART00000132346 | Nonsense | 69 | 440 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 43224462)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43273926 |
GRCz11 | 2 | 43123344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCTTGTAACTTTGTTTTTGCAGAAAATGTCGGCAGGCTAAAGAAGCTG[G/T]AATATTTAAATCTGGCACTGAACAACATTGAGGTCATTGAGAATTTGGAA
Long Flanking Sequence:
TTCAACAGGAGCGTCTGAAGTGAGTCTGTTTCTGTAGCAACGTCTAACAAACTAGACCAGCAAGTCATGGTCCGCAGTAAGTGCTTCATGTATTTTAAACATTATTTGCTTTAAGCTAAATGTTATTTTACAACATTGATCGTATTTTCCTCACCCGTAAACATTTGACCTTTCGCGGTTAAGCTGTTTGTAAACGAATCGCCCCTCTTCCTCCGTTCAGTCAGTGAGGATCTGATCCGCCGCAGAGCAGAGCACAATAACGGAGAGATCTTCTCCCTTGAGGAGCTTTCCCTTCATCAGCAGGACATCCAGAGAATCGAGCACATCCACAAGTGGTGCAGAGACCTCAAAATCCTTTATTTACAAAACAACCTCATCCCTAAAATAGGTAAATACTGGACAGTGGTATTGTGGTATTGCAGCAACTCAAACGCATGGCTGTTTATGTAAACTCTTGTAACTTTGTTTTTGCAGAAAATGTCGGCAGGCTAAAGAAGCTG[G/T]AATATTTAAATCTGGCACTGAACAACATTGAGGTCATTGAGAATTTGGAAGGTGACTTCATACAGTGTGTGTGTGTGTGTGTGTAACTGGGTCAAAAATAGATTGGTTTCTGCATCAAATTAAATGTAAAAAAAATAAATTAAATGCAAGTGTATGCTTTAGTGCTTTAAATGCAAAAACAAAATATCATAATATGGGTGAAATGATCCTCCAATCATTATTTAGCATAACAGATTTATTTATAAAAAAATGAAACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATAGGGATGCTCCGATCAGGATTTTTGCAGCCGATACCAAGTCATGGTGATCGGTCGATATCGATTCTGATGCTTCAAGCTTTATATTGCACATTAAGTAAAATACTTAAGTGGAGCTCTCTCCTTACCTAAGTGAATAAATGAAGGATGCTGCATGTAATCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14481
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 |
---|---|---|---|---|---|
ENSDART00000075347 | Nonsense | 84 | 440 | 3 | 12 |
ENSDART00000132346 | Nonsense | 84 | 440 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 43224416)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43273880 |
GRCz11 | 2 | 43123298 |
KASP Assay ID:
2259-2512.1 (used for ordering genotyping assays)
KASP Sequence:
GCTGGAATATTTAAATCTGGCACTGAACAACATTGAGGTCATTGAGAATT[T/A]GGAAGGTGACTTCATACAGTGTGTNNNNNNGTGTGTGTGTNNNNNNNNNNGTNNNNNNNNNNNNGTAACTGGGTCAAA
Long Flanking Sequence:
ACAAACTAGACCAGCAAGTCATGGTCCGCAGTAAGTGCTTCATGTATTTTAAACATTATTTGCTTTAAGCTAAATGTTATTTTACAACATTGATCGTATTTTCCTCACCCGTAAACATTTGACCTTTCGCGGTTAAGCTGTTTGTAAACGAATCGCCCCTCTTCCTCCGTTCAGTCAGTGAGGATCTGATCCGCCGCAGAGCAGAGCACAATAACGGAGAGATCTTCTCCCTTGAGGAGCTTTCCCTTCATCAGCAGGACATCCAGAGAATCGAGCACATCCACAAGTGGTGCAGAGACCTCAAAATCCTTTATTTACAAAACAACCTCATCCCTAAAATAGGTAAATACTGGACAGTGGTATTGTGGTATTGCAGCAACTCAAACGCATGGCTGTTTATGTAAACTCTTGTAACTTTGTTTTTGCAGAAAATGTCGGCAGGCTAAAGAAGCTGGAATATTTAAATCTGGCACTGAACAACATTGAGGTCATTGAGAATT[T/A]GGAAGGTGACTTCATACAGTGTGTGTGTGTGTGTGTGTAACTGGGTCAAAAATAGATTGGTTTCTGCATCAAATTAAATGTAAAAAAAATAAATTAAATGCAAGTGTATGCTTTAGTGCTTTAAATGCAAAAACAAAATATCATAATATGGGTGAAATGATCCTCCAATCATTATTTAGCATAACAGATTTATTTATAAAAAAATGAAACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATAGGGATGCTCCGATCAGGATTTTTGCAGCCGATACCAAGTCATGGTGATCGGTCGATATCGATTCTGATGCTTCAAGCTTTATATTGCACATTAAGTAAAATACTTAAGTGGAGCTCTCTCCTTACCTAAGTGAATAAATGAAGGATGCTGCATGTAATCCCTTAAACATGTCTCTTATAACCATTTAGAGTGGACAGGTCATGGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25885
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 |
---|---|---|---|---|---|
ENSDART00000075347 | Nonsense | 90 | 440 | 4 | 12 |
ENSDART00000132346 | Nonsense | 90 | 440 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 43221748)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43271212 |
GRCz11 | 2 | 43120630 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAATTACAAACTCTAATATACGTTTGGTTGTGCGTAGGTTGCGAGAGCT[T/A]ACAGAAACTAGACCTGACAGTGAATTTTGTGGGTAGGCTGAGCAGTGTGG
Long Flanking Sequence:
GAATTCAAATGACACATTTTAATCTAGATTAATCTAGTTTATTTCCAAGATTAATCTAGATAAAAAAAATAATGCCTACCTATAAAATATTTTAATATATATAGTAGAATAGAATGTTTTGGAATTTTTTGTTTGTTGCTTATGTTGTTATGATGTAAGAGATGTTAAAAGATGTGTAAAATCAGTGTTAATTTAGATTATTGAGTTATTAATCTCTTCATTAACATTTAGAATTTTGATATTTTTTATTTTCACTTAATAAGTAAAGTCTTAGCAATTTTGTTGTGATTTTTCATTTGAGTTTACATACCTTTATACCTAATATACCAACACACAATTTGGTTTTGTTACATTTTTATATAATTTTAAATATTAACAAAATCTTTTTTAAATGTTTTGCTTGAAAAGTGTGATGTGAAAGTCTATGTTTATTTATTTTTTACAATGACTGTAATTACAAACTCTAATATACGTTTGGTTGTGCGTAGGTTGCGAGAGCT[T/A]ACAGAAACTAGACCTGACAGTGAATTTTGTGGGTAGGCTGAGCAGTGTGGAGACGCTGAAGCACAACCTTCATCTCAAAGAGCTCTATCTGGTGGGAAACCCCTGTGCTGAATACCACGGGTACAGACAGTATGTGGTGGCAACAGTGCCTCAACTACAGGTACAGCACTGATACACACACTCACTGAAGAGACACATTTAAGACCTGTTTATACCAAGAATAATAATTATAAAGATAACCATGATGATAACTACATTAGCATCCTCACCACACGTGGTATGTTTATTTATTATAAGCACTCTCTTCAGTTTTGTCATCTACTAGTTTAAATACTCACTTTTTTACCAGGATTTATTCTAACTGCATGTCAATGTTTTCATAGTTCATCAGCTGGAAAATAAATGTAGTTTGTTTTTCTGTTTATAATTTGTGGGCCGACACAGTGGCTCAGTGGTTAGCATTGTCGCCTGACAGCAAGTAGGTCACTGGTTTGAGCCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19848
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 |
---|---|---|---|---|---|
ENSDART00000075347 | Nonsense | 91 | 440 | 4 | 12 |
ENSDART00000132346 | Nonsense | 91 | 440 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 43221746)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43271210 |
GRCz11 | 2 | 43120628 |
KASP Assay ID:
2259-2510.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTACAAACTCTAATATACGTTTGGTTGTGCGTAGGTTGCGAGAGCTTA[C/T]AGAAACTAGACCTGACAGTGAATTTTGTGGGTAGGCTGAGCAGTGTGGAG
Long Flanking Sequence:
ATTCAAATGACACATTTTAATCTAGATTAATCTAGTTTATTTCCAAGATTAATCTAGATAAAAAAAATAATGCCTACCTATAAAATATTTTAATATATATAGTAGAATAGAATGTTTTGGAATTTTTTGTTTGTTGCTTATGTTGTTATGATGTAAGAGATGTTAAAAGATGTGTAAAATCAGTGTTAATTTAGATTATTGAGTTATTAATCTCTTCATTAACATTTAGAATTTTGATATTTTTTATTTTCACTTAATAAGTAAAGTCTTAGCAATTTTGTTGTGATTTTTCATTTGAGTTTACATACCTTTATACCTAATATACCAACACACAATTTGGTTTTGTTACATTTTTATATAATTTTAAATATTAACAAAATCTTTTTTAAATGTTTTGCTTGAAAAGTGTGATGTGAAAGTCTATGTTTATTTATTTTTTACAATGACTGTAATTACAAACTCTAATATACGTTTGGTTGTGCGTAGGTTGCGAGAGCTTA[C/T]AGAAACTAGACCTGACAGTGAATTTTGTGGGTAGGCTGAGCAGTGTGGAGACGCTGAAGCACAACCTTCATCTCAAAGAGCTCTATCTGGTGGGAAACCCCTGTGCTGAATACCACGGGTACAGACAGTATGTGGTGGCAACAGTGCCTCAACTACAGGTACAGCACTGATACACACACTCACTGAAGAGACACATTTAAGACCTGTTTATACCAAGAATAATAATTATAAAGATAACCATGATGATAACTACATTAGCATCCTCACCACACGTGGTATGTTTATTTATTATAAGCACTCTCTTCAGTTTTGTCATCTACTAGTTTAAATACTCACTTTTTTACCAGGATTTATTCTAACTGCATGTCAATGTTTTCATAGTTCATCAGCTGGAAAATAAATGTAGTTTGTTTTTCTGTTTATAATTTGTGGGCCGACACAGTGGCTCAGTGGTTAGCATTGTCGCCTGACAGCAAGTAGGTCACTGGTTTGAGCCCCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33003
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 |
---|---|---|---|---|---|
ENSDART00000075347 | Nonsense | 134 | 440 | 4 | 12 |
ENSDART00000132346 | Nonsense | 134 | 440 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 43221615)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43271079 |
GRCz11 | 2 | 43120497 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTATCTGGTGGGAAACCCCTGTGCTGAATACCACGGGTACAGACAGTA[T/A]GTGGTGGCAACAGTGCCTCAACTACAGGTACAGCACTGATACACACACTC
Long Flanking Sequence:
TGTTGCTTATGTTGTTATGATGTAAGAGATGTTAAAAGATGTGTAAAATCAGTGTTAATTTAGATTATTGAGTTATTAATCTCTTCATTAACATTTAGAATTTTGATATTTTTTATTTTCACTTAATAAGTAAAGTCTTAGCAATTTTGTTGTGATTTTTCATTTGAGTTTACATACCTTTATACCTAATATACCAACACACAATTTGGTTTTGTTACATTTTTATATAATTTTAAATATTAACAAAATCTTTTTTAAATGTTTTGCTTGAAAAGTGTGATGTGAAAGTCTATGTTTATTTATTTTTTACAATGACTGTAATTACAAACTCTAATATACGTTTGGTTGTGCGTAGGTTGCGAGAGCTTACAGAAACTAGACCTGACAGTGAATTTTGTGGGTAGGCTGAGCAGTGTGGAGACGCTGAAGCACAACCTTCATCTCAAAGAGCTCTATCTGGTGGGAAACCCCTGTGCTGAATACCACGGGTACAGACAGTA[T/A]GTGGTGGCAACAGTGCCTCAACTACAGGTACAGCACTGATACACACACTCACTGAAGAGACACATTTAAGACCTGTTTATACCAAGAATAATAATTATAAAGATAACCATGATGATAACTACATTAGCATCCTCACCACACGTGGTATGTTTATTTATTATAAGCACTCTCTTCAGTTTTGTCATCTACTAGTTTAAATACTCACTTTTTTACCAGGATTTATTCTAACTGCATGTCAATGTTTTCATAGTTCATCAGCTGGAAAATAAATGTAGTTTGTTTTTCTGTTTATAATTTGTGGGCCGACACAGTGGCTCAGTGGTTAGCATTGTCGCCTGACAGCAAGTAGGTCACTGGTTTGAGCCCCGGCTGGGCCAGTTTGTGTGAAGTTTGCATGTTCTCCCCGTATTGGCGTGGGTTTCTTCCAGGTGCTCTGGTTTCCCCCAGACATGTGGTATAGGTGAATTAAATAAACTAAATTGGCCATAGTGAGTGCGTGT
Associated Phenotype:
Not determined