ZMP
loxl1
Ensembl ID:
ZFIN ID:
Description:
lysyl oxidase homolog 1 [Source:RefSeq peptide;Acc:NP_001036790]
Human Orthologue:
LOXL1
Human Description:
lysyl oxidase-like 1 [Source:HGNC Symbol;Acc:6665]
Mouse Orthologue:
Loxl1
Mouse Description:
lysyl oxidase-like 1 Gene [Source:MGI Symbol;Acc:MGI:106096]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23390 | Nonsense | Available for shipment | Available now |
sa16620 | Nonsense | Available for shipment | Available now |
sa5916 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6538 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1005 | Nonsense | Available for shipment | Available now |
sa36736 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44900 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36735 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23390
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 |
---|---|---|---|---|---|
ENSDART00000006078 | Nonsense | 26 | 527 | 1 | 7 |
ENSDART00000127496 | Nonsense | 22 | 526 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 49006133)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 50155339 |
GRCz11 | 18 | 50151904 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGATGAGCTTGTGGGTATTAGGAAGTGTAACGGGACAGTCCCAATCT[C/T]AACCCGACGACACAAACCCATGGAGGCAGATGATCCAGTGGGAGAATAAT
Long Flanking Sequence:
CATTAGTCTTCTCAATATGACACTGCGAGACTCAATGCATTGCCTTTTTTAACTTGCTGGACTAACAATTCAGAGCTTTCACTTTGTTTATAAGTCTTCTCAATATCTTGCCTGTTGCTTTTAGTCTGATTTGACACTGTAAGTCTTTAATGCATTGCCATCCTTAACTTGCTGGATCAACAATTCAGAGCTTTAATTATTTTATTAGTCTTCTGAATATCTAGCCTGTTGCTTTTAGTCTGATTTGACATTGTGAGTCCTCATTTTTAACTTGCTGGATCAACAGTTCAGAGCTTCGCCTTCTTTTATTAGTCTTCTGGATATCTTACCTGTTGCTCTTAGTCTGATTTGACACTGTTAGTCTTCAATGCATTGCCATCTTTAACTTGCTGGATCAACAATTCAGAGCTTTAACTTCGTTCTTTAGTCTTCTCAATATGCTGCATGTACTTTTGATGAGCTTGTGGGTATTAGGAAGTGTAACGGGACAGTCCCAATCT[C/T]AACCCGACGACACAAACCCATGGAGGCAGATGATCCAGTGGGAGAATAATGGACGTGTTTATAGTCTACTCAACAGCGGAGCCGAATACGTCCCGGCTCGGAACCAGGAACGGGATAGGAACCATCGAGTGCTTCTTGCTGACGCTCCAAATCGTAGGTCACAGGGTGGAAATGTGCGAAGACAAGCACCCTCAAGAGGGAGCTCGGAGACGGTGAGGGGTCAAGCCAGACACCCGTTTGGATTCGGACAGGTGCCGGAAAACTGGCGGCAGCAGCAAGGTGCGGTGGGAAGAAGCGAAACAAGTCGATTTCAGTCACAAACCGGCTCTCGTTATAGACCGTCATCTGGAGCATCATCATCAGCATCATCATCATATCCTCAATATCCAATCCCGCAACAGCCTCCGTTCGGTGCTCCGTATGACCAAGGTTACATTTACATTTACTCATTTAGCAGACACTTTTATCCAACGCTATACTCTTCTATGCTCTTTTCACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16620
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 |
---|---|---|---|---|---|
ENSDART00000006078 | Nonsense | 128 | 527 | 1 | 7 |
ENSDART00000127496 | Nonsense | 124 | 526 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 49005827)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 50155033 |
GRCz11 | 18 | 50151598 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGAAAACTGGCGGCAGCAGCAAGGTGCGGTKGGAAGAAGCGAAACAAGT[C/T]GATTTCAGTCACAAACCGGCTCTCGTTATAGACCGTCATCNNNNNNNNNA
Long Flanking Sequence:
TATTAGTCTTCTGGATATCTTACCTGTTGCTCTTAGTCTGATTTGACACTGTTAGTCTTCAATGCATTGCCATCTTTAACTTGCTGGATCAACAATTCAGAGCTTTAACTTCGTTCTTTAGTCTTCTCAATATGCTGCATGTACTTTTGATGAGCTTGTGGGTATTAGGAAGTGTAACGGGACAGTCCCAATCTCAACCCGACGACACAAACCCATGGAGGCAGATGATCCAGTGGGAGAATAATGGACGTGTTTATAGTCTACTCAACAGCGGAGCCGAATACGTCCCGGCTCGGAACCAGGAACGGGATAGGAACCATCGAGTGCTTCTTGCTGACGCTCCAAATCGTAGGTCACAGGGTGGAAATGTGCGAAGACAAGCACCCTCAAGAGGGAGCTCGGAGACGGTGAGGGGTCAAGCCAGACACCCGTTTGGATTCGGACAGGTGCCGGAAAACTGGCGGCAGCAGCAAGGTGCGGTGGGAAGAAGCGAAACAAGT[C/T]GATTTCAGTCACAAACCGGCTCTCGTTATAGACCGTCATCTGGAGCATCATCATCAGCATCATCATCATATCCTCAATATCCAATCCCGCAACAGCCTCCGTTCGGTGCTCCGTATGACCAAGGTTACATTTACATTTACTCATTTAGCAGACACTTTTATCCAACGCTATACTCTTCTATGCTCTTTTCACATTTGCTGTGCGTTTCAGTTTAGCTATGGTTTTGTTTGTGGAGCCATTTCTATAGATTTCTTGACAGATATGTTGTCTGAGTAATTCTGTAGGTCAGCAGAGTTGCTTAACTAAACATATTCATATCAAGCAACTTACAAGTAAAGGTAAAAGAAGCACTTCAAATCATCAGAGAGTAGCTGTATATAATTAATAAGTCTTTAAGTCTTGAGTATATTAAAAAAGTGCTCAGTTAAGTTTTTAAGTTGAACCGATTTAAATTTACAAGTCATTTTAACTTGCATCGATAGGGTCTATGCAAATGAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5916
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006078 | Essential Splice Site | 169 | 527 | None | 7 |
ENSDART00000127496 | None | 166 | 526 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 49004300)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 50153506 |
GRCz11 | 18 | 50150071 |
KASP Assay ID:
554-3805.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTTNNCAACAATTGTCACTAAAATAACCTTGTTTATGAYCCAGTTTC[A/T]GACAGGTCATATGAACCTCCATTCCKTGGGACGGGGTRTTCGGCAGGCAC
Long Flanking Sequence:
AAGTAACATAATCATGACTTTTTATTATTTTAGTCATTTTTACAGTGTATATTTACACATGTATAGTTTTGCACCTTTAAATTAGTTATTTCGATACTATTTGTGCATTTGTTGTGCATCTCAGTTTTTGTTTGTTTCAATAATGGTTTTGTTTCTATGTTGGTGAACACATTTCTATTGAGTTTTTTTCAACGCAATCTCACGGCAATTCGTAACTTTTTTTCAGCATATCTAGAGGGCTAATGCTGACAACTGATGATCGACAATAAAAATGACACATTTTAACACTTTCCAACAGTGAAAACCAGCAACAATCAAGAATGCATGATTATATGGTGTTTGCCTTTGCAATCAATAGATGTGATTATAATGGAAGTCAATGGGGCAAAAACAGCACTAATATAACCTAAGCGGAGTCAATTTAAACAACACACAAGGGTTAATTTGTGATTTTTTTTCAACAATTGTCACTAAAATAACCTTGTTTATGACCCAGTTTC[A/T]GACAGGTCATATGAACCTCCATTCCTTGGGACGGGGTATTCGGCAGGCACGGGTGGAGGTTTAGGTGGAGGTGGTTATGGAGGATATTCTACAGGCAGTTTCGGTGGAGGAAATCCTGCAAATGATGATCGATATCGATTTTATCCACCGTACGGTCAACAATACCAGGCTGTTCCAGCCCAACCTGCACAGCCACCGTTCTCTGACGGTCTGGACCACAGATACACACACAGTCTGTTCAATGAGGATAATCCTGCAGTTCCTAACGGTGCTTCAAGCAATACGGGCTCATCCTTTCAGCCTGCGGTGCAAAGTCCACAATATGAACAGTTTCCGCCGTACGGAAGGCCTCAGCCGCAGCCTCCATTTCTACAACCAGCGCCACGAAACCCGCTGGTCTCCAACACTGCAGAAAACCCCAACATCAATGTAGGCAGCGTTTATCGCCCTCAACAAAGAGGTAGGATGCTTCTGAAATACACTGAAAAAAATGGGTTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6538
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 |
---|---|---|---|---|---|
ENSDART00000006078 | Nonsense | 171 | 527 | 2 | 7 |
ENSDART00000127496 | Nonsense | 169 | 526 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 49004292)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 50153498 |
GRCz11 | 18 | 50150063 |
KASP Assay ID:
554-5151.1 (used for ordering genotyping assays)
KASP Sequence:
CAACAATTGTCACTAAAATAACCTTGTTTATGAYCCAGTTTCWGACAGGT[C/A]ATATGAACCTCCATTCCKTGGGACGGGGTRTTCGGCAGGCACGGGTGGAG
Long Flanking Sequence:
TAATCATGACTTTTTATTATTTTAGTCATTTTTACAGTGTATATTTACACATGTATAGTTTTGCACCTTTAAATTAGTTATTTCGATACTATTTGTGCATTTGTTGTGCATCTCAGTTTTTGTTTGTTTCAATAATGGTTTTGTTTCTATGTTGGTGAACACATTTCTATTGAGTTTTTTTCAACGCAATCTCACGGCAATTCGTAACTTTTTTTCAGCATATCTAGAGGGCTAATGCTGACAACTGATGATCGACAATAAAAATGACACATTTTAACACTTTCCAACAGTGAAAACCAGCAACAATCAAGAATGCATGATTATATGGTGTTTGCCTTTGCAATCAATAGATGTGATTATAATGGAAGTCAATGGGGCAAAAACAGCACTAATATAACCTAAGCGGAGTCAATTTAAACAACACACAAGGGTTAATTTGTGATTTTTTTTCAACAATTGTCACTAAAATAACCTTGTTTATGACCCAGTTTCAGACAGGT[C/A]ATATGAACCTCCATTCCTTGGGACGGGGTATTCGGCAGGCACGGGTGGAGGTTTAGGTGGAGGTGGTTATGGAGGATATTCTACAGGCAGTTTCGGTGGAGGAAATCCTGCAAATGATGATCGATATCGATTTTATCCACCGTACGGTCAACAATACCAGGCTGTTCCAGCCCAACCTGCACAGCCACCGTTCTCTGACGGTCTGGACCACAGATACACACACAGTCTGTTCAATGAGGATAATCCTGCAGTTCCTAACGGTGCTTCAAGCAATACGGGCTCATCCTTTCAGCCTGCGGTGCAAAGTCCACAATATGAACAGTTTCCGCCGTACGGAAGGCCTCAGCCGCAGCCTCCATTTCTACAACCAGCGCCACGAAACCCGCTGGTCTCCAACACTGCAGAAAACCCCAACATCAATGTAGGCAGCGTTTATCGCCCTCAACAAAGAGGTAGGATGCTTCTGAAATACACTGAAAAAAATGGGTTTGCATGTAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1005
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 |
---|---|---|---|---|---|
ENSDART00000006078 | Nonsense | 216 | 527 | 2 | 7 |
ENSDART00000127496 | Nonsense | 214 | 526 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 49004156)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 50153362 |
GRCz11 | 18 | 50149927 |
KASP Assay ID:
554-0909.1 (used for ordering genotyping assays)
KASP Sequence:
GGCAGTTTCGGTGGAGGAAATCCTGCAAATGATGATCGATATCGATWTTA[T/A]CCACCGTWCGGTCAACAATACCAGGCTGTTCCMGCCCAACCTGCACAGCC
Long Flanking Sequence:
GGTTTTGTTTCTATGTTGGTGAACACATTTCTATTGAGTTTTTTTCAACGCAATCTCACGGCAATTCGTAACTTTTTTTCAGCATATCTAGAGGGCTAATGCTGACAACTGATGATCGACAATAAAAATGACACATTTTAACACTTTCCAACAGTGAAAACCAGCAACAATCAAGAATGCATGATTATATGGTGTTTGCCTTTGCAATCAATAGATGTGATTATAATGGAAGTCAATGGGGCAAAAACAGCACTAATATAACCTAAGCGGAGTCAATTTAAACAACACACAAGGGTTAATTTGTGATTTTTTTTCAACAATTGTCACTAAAATAACCTTGTTTATGACCCAGTTTCAGACAGGTCATATGAACCTCCATTCCTTGGGACGGGGTATTCGGCAGGCACGGGTGGAGGTTTAGGTGGAGGTGGTTATGGAGGATATTCTACAGGCAGTTTCGGTGGAGGAAATCCTGCAAATGATGATCGATATCGATTTTA[T/A]CCACCGTACGGTCAACAATACCAGGCTGTTCCAGCCCAACCTGCACAGCCACCGTTCTCTGACGGTCTGGACCACAGATACACACACAGTCTGTTCAATGAGGATAATCCTGCAGTTCCTAACGGTGCTTCAAGCAATACGGGCTCATCCTTTCAGCCTGCGGTGCAAAGTCCACAATATGAACAGTTTCCGCCGTACGGAAGGCCTCAGCCGCAGCCTCCATTTCTACAACCAGCGCCACGAAACCCGCTGGTCTCCAACACTGCAGAAAACCCCAACATCAATGTAGGCAGCGTTTATCGCCCTCAACAAAGAGGTAGGATGCTTCTGAAATACACTGAAAAAAATGGGTTTGCATGTAGATACTGTCTTGTTTCTTGTTCAAATATCTAAACATTCCTGAATCAAGAAGCATTTTCTAGACAAGCAAAACTTATTGTCTTGTTTTGTCAGAAATAATAAGCCAAAATCAAACTATAACACACCATCCAGACTCTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36736
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 |
---|---|---|---|---|---|
ENSDART00000006078 | Nonsense | 316 | 527 | 2 | 7 |
ENSDART00000127496 | Nonsense | 314 | 526 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 49003856)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 50153062 |
GRCz11 | 18 | 50149627 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGTCTCCAACACTGCAGAAAACCCCAACATCAATGTAGGCAGCGTTTA[T/A]CGCCCTCAACAAAGAGGTAGGATGCTTCTGAAATACACTGAAAAAAATGG
Long Flanking Sequence:
TTGTGATTTTTTTTCAACAATTGTCACTAAAATAACCTTGTTTATGACCCAGTTTCAGACAGGTCATATGAACCTCCATTCCTTGGGACGGGGTATTCGGCAGGCACGGGTGGAGGTTTAGGTGGAGGTGGTTATGGAGGATATTCTACAGGCAGTTTCGGTGGAGGAAATCCTGCAAATGATGATCGATATCGATTTTATCCACCGTACGGTCAACAATACCAGGCTGTTCCAGCCCAACCTGCACAGCCACCGTTCTCTGACGGTCTGGACCACAGATACACACACAGTCTGTTCAATGAGGATAATCCTGCAGTTCCTAACGGTGCTTCAAGCAATACGGGCTCATCCTTTCAGCCTGCGGTGCAAAGTCCACAATATGAACAGTTTCCGCCGTACGGAAGGCCTCAGCCGCAGCCTCCATTTCTACAACCAGCGCCACGAAACCCGCTGGTCTCCAACACTGCAGAAAACCCCAACATCAATGTAGGCAGCGTTTA[T/A]CGCCCTCAACAAAGAGGTAGGATGCTTCTGAAATACACTGAAAAAAATGGGTTTGCATGTAGATACTGTCTTGTTTCTTGTTCAAATATCTAAACATTCCTGAATCAAGAAGCATTTTCTAGACAAGCAAAACTTATTGTCTTGTTTTGTCAGAAATAATAAGCCAAAATCAAACTATAACACACCATCCAGACTCTATAGGATGGGACTAGCTGGAAATAATCAGTGTTGGAAATACAATAAAGAAGAGGGTACTTATTTGCACATGATCTGGGAATGTTGTCTAGTTCAGTGGTTCTCAAAGTGGGGGTCGGGACCCCCCAAGGGGTCGCGGGACAATAAAGGGGGGTCGCCTGGTGATTTCCAAAAATCTATTTATTTATATTAAACCATAAAAATTACCAATAAACTACTGAAGAGAAAAATTGTTGTTCATAGTTAATATATACTATATAGTTACTACAGTAGCTTATAGTTACTAGTTCTATTGGATTGCGACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44900
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 |
---|---|---|---|---|---|
ENSDART00000006078 | Nonsense | 456 | 527 | 5 | 7 |
ENSDART00000127496 | Nonsense | 454 | 526 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 48986354)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 50135560 |
GRCz11 | 18 | 50132125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGACCTGCGACTTCGGCCATCTGAAGAGATACGCCTGCACTGCACACACA[C/T]AGGTCAATATCATCTGCTGCTACTCGCAATGACGTTATTTATAGCAGGGT
Long Flanking Sequence:
AAAAATTTTATTTGAAAATTAGGCAAGTCATTGTATAACAGTGGTTTTTTCTGGAGACAACCCAACACTAATATTGCTGAAGGGGCCAATAATATTGAGCTTAACATGACTTTAACACAATTAAAAACTGCTTTTATTCTAGCCCAAATAAAACAAATAAGACTTTCTCCAGAAGAACAAATATTATAGAAAATACTGTGGAAAAATCCTTGATCTGGTAAACATCATTAGGGAAATATTAGCAAGAAAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATGACAAGAGGGCGAATAATTCTGACCTCAACTGCATGTCTCTTGTCTCCATCAGGCATTACCACAGTATGGACGAGTTCAGTCACTATGATCTGCTGGAGGTCAGCAGTGGCCGAAAAGTGGCGGAGGGACACAAAGCCAGCTTCTGTCTGGAGGACACGACCTGCGACTTCGGCCATCTGAAGAGATACGCCTGCACTGCACACACA[C/T]AGGTCAATATCATCTGCTGCTACTCGCAATGACGTTATTTATAGCAGGGTTCTGCAACTTTTGTCATAGCACAGACTAAGATAAATAAGGGACTAAGCCGAAGGAAAATGAATGAATGAATGAATGAATGAATGAATGCACCAATTTAGATATATTTTTGAAGGGGAAACTCACACCAAAGTGGGATCTCATATGGAGTCATTTTGCGTTCTTGCGGTGCAATAGAAACTCTGAAGACCTTTGATTTTCATGCTTAACTATGCAACTGTGGTTTGCTATGTGTTTATGTTTTAGTTTTTTTAATCCAAGAATTATTAGCCATTGTATTTGTATTATACTGAACGTTTTCATTTGTTTTAATTCTCCAGGGTCTCAGTCCGGGTTGCTTCGACACATACAATGCAGATATCGACTGCCAATGGATTGACATCACTGATGTTCAGCCAGGAAACTACATACTGAAGGTAACATTCTCAAAGGAGAACAAAACACTTACACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36735
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 |
---|---|---|---|---|---|
ENSDART00000006078 | Essential Splice Site | 456 | 527 | 5 | 7 |
ENSDART00000127496 | Essential Splice Site | 454 | 526 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 48986351)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 50135557 |
GRCz11 | 18 | 50132122 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGCGACTTCGGCCATCTGAAGAGATACGCCTGCACTGCACACACACAG[G/A]TCAATATCATCTGCTGCTACTCGCAATGACGTTATTTATAGCAGGGTTCT
Long Flanking Sequence:
AATTTTATTTGAAAATTAGGCAAGTCATTGTATAACAGTGGTTTTTTCTGGAGACAACCCAACACTAATATTGCTGAAGGGGCCAATAATATTGAGCTTAACATGACTTTAACACAATTAAAAACTGCTTTTATTCTAGCCCAAATAAAACAAATAAGACTTTCTCCAGAAGAACAAATATTATAGAAAATACTGTGGAAAAATCCTTGATCTGGTAAACATCATTAGGGAAATATTAGCAAGAAAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATGACAAGAGGGCGAATAATTCTGACCTCAACTGCATGTCTCTTGTCTCCATCAGGCATTACCACAGTATGGACGAGTTCAGTCACTATGATCTGCTGGAGGTCAGCAGTGGCCGAAAAGTGGCGGAGGGACACAAAGCCAGCTTCTGTCTGGAGGACACGACCTGCGACTTCGGCCATCTGAAGAGATACGCCTGCACTGCACACACACAG[G/A]TCAATATCATCTGCTGCTACTCGCAATGACGTTATTTATAGCAGGGTTCTGCAACTTTTGTCATAGCACAGACTAAGATAAATAAGGGACTAAGCCGAAGGAAAATGAATGAATGAATGAATGAATGAATGAATGCACCAATTTAGATATATTTTTGAAGGGGAAACTCACACCAAAGTGGGATCTCATATGGAGTCATTTTGCGTTCTTGCGGTGCAATAGAAACTCTGAAGACCTTTGATTTTCATGCTTAACTATGCAACTGTGGTTTGCTATGTGTTTATGTTTTAGTTTTTTTAATCCAAGAATTATTAGCCATTGTATTTGTATTATACTGAACGTTTTCATTTGTTTTAATTCTCCAGGGTCTCAGTCCGGGTTGCTTCGACACATACAATGCAGATATCGACTGCCAATGGATTGACATCACTGATGTTCAGCCAGGAAACTACATACTGAAGGTAACATTCTCAAAGGAGAACAAAACACTTACACACAGT
Associated Phenotype:
Not determined