ZMP
LOXL2 (2 of 3)
Ensembl ID:
Description:
lysyl oxidase-like 2 [Source:HGNC Symbol;Acc:6666]
Human Orthologue:
LOXL2
Human Description:
lysyl oxidase-like 2 [Source:HGNC Symbol;Acc:6666]
Mouse Orthologue:
Loxl2
Mouse Description:
lysyl oxidase-like 2 Gene [Source:MGI Symbol;Acc:MGI:2137913]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34883 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa34882 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31777 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45401 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34883
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 |
---|---|---|---|---|---|
ENSDART00000127848 | Essential Splice Site | 262 | 648 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 20457861)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 20466644 |
GRCz11 | 10 | 20424025 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGATTCGGAAGCGCCAAAGAGGCTCTCACTGGAGCCAAGTTAGGACAAG[G/A]TTTGTGTGGCTTTTCATGCATGATATGTTTTATCAGTGCTTGTAAAACTG
Long Flanking Sequence:
TGGAAGGAATTGTTTTCCTGGAAATAACGTTTTCCTGTAGATCATCATGTTCTCTCAGGCTGGATGTCAGGGTGACACTTGAAAAAATCATGTAGTACATTAAATCATGCTTCCTTTTGGATAAAAAGAAGATTGCATAATATTTAAACATGGCCTCAGAGAGCTGAAGTGAGATTGTTTATACAGGCAAATGGGGGGAAAAAATCATCTGAATCACCTGGATCCAGAGACCGAGAGAGCTAGACTGTACAAACATGGGTCACCGAGGGTGTGTGAATTGATCATCCTGCTAATTTTTCCCTCTCTGATTCCTTAGCAACCCCTGGTGCGTCTGCGGGGTGGTGCAAATGTTGGCGAAGGCAGAGTGGAGGTGCTGAAGAATGGTGTTTGGGGAACAGTGTGTGATGATAACTGGAATCTAAAGGCTGCAACTGTAGTGTGTCGAGAGCTGGGATTCGGAAGCGCCAAAGAGGCTCTCACTGGAGCCAAGTTAGGACAAG[G/A]TTTGTGTGGCTTTTCATGCATGATATGTTTTATCAGTGCTTGTAAAACTGAAATGATTTGGAGGCACTGAGAATCAAGACTGAACACTCTTACCTTAGTTACCAAACTACTACATGTCCTAAAAGTTGGTGTTGGAGTTGGTGACTTTTTTTATCTTTAGCTTATTTTTATCTTTTGTCCGTAGTGATTCATAAAGTGCAAGTCAGGGGATTTTGACACTCACTCACTATCCACAGTGGAATGAACGGCCAATTACTCTGAAAAAGGTTTTGTGCAGGGGGTGCCCCTCCAGCTGCAACCCAACACTGGAAAATACCCAAACACTCACATTCACACGCACGCTCATACACTATGGCCAATTATGTTATTATGTCTACCACATACCTTTGGACTGTTGGGGAAACCCACGCGAACACAGGGAACACATACAAATTCCACACAGGATTGCTCCTAGCCCAGCCGGGACAAAAAAAAAAACAGCAACCTTCTTGCTGTGTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34882
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127848 | Essential Splice Site | 314 | 648 | 6 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 20453517)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTCATGAATCGGTATGATTGTGAAACACTGTTTGCTTTTGACTACAAC[A/C]GATACGACTAAGTGGAGGAAGAAACCCATTTGAAGGACGTGTGGAAGTTC
Long Flanking Sequence:
GAAAATTTCAGATGGCACAGAGGTTTTTGCATCTGAACTCTTCAAATAGACACATCCTTTGGTACCTTTTGGTGCCTGAAGCATTAACAAGAATTCAGTATCAACCACATGTCAAACACAGATATCTTCTACCAGGGTAATTTCTTTTTTTTGCATCAGAACTCAGAATTTCTTATTCATGAACACTATTTTGGATAATAATGCCCCATTTAATGTACACAATGTATTTAATGTGTACTTTTTTTGTCAGGAATGGGTCCGGTCCACATGAATGAGGTGGAGTGCTCTGGATTTGAGAAATCTCTCACTGACTGCTACTTTAATAATGATGCGCTGGGATGCAGTCATGAGGAGGACGCAGCTGTTCGCTGTAATGTACCTGCTATGGGCTTTCAGAAAAGGGTGAGGATTTTTAAAATATAATTTACATATTAATTAGCAATAGTTTTACGCTCATGAATCGGTATGATTGTGAAACACTGTTTGCTTTTGACTACAAC[A/C]GATACGACTAAGTGGAGGAAGAAACCCATTTGAAGGACGTGTGGAAGTTCTCGCTGAGAAGAACGGTTCTCTCGTTTGGGGAACAGTTTGTAGTGAAAACTGGGGGATTATAGAGGCTATGGTGGTCTGCAGACAGCTGGGATTAGGCTTTGCCAGCCATGCGTTCCAGGTAAGACTACTTACTAAATGTGAAAGTCCTTCAAAATTGAAAATCGAATGGGTTTAAACAGTCACAAAATACAAGCTACTATTCTACTGAACACATGATCACTATGAAAAAGTGCATTTAAACAATAAATTCATATTTCATAGTATTGTACTTGCCATTTAAATTCACCTTTTCATTCATTTTCTTTCACACACACTCTAAAGCAAGTAGTATTTATGCATCACACTAAGCTCTTCTGCTAAAATGATGTAGAGGGAAACAAAATAACAGTGAAGGGTCTTGATTCAATCTAAACATAAGTGGTCACAAGAGTCACATTTGAATTCATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31777
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 |
---|---|---|---|---|---|
ENSDART00000127848 | Essential Splice Site | 314 | 648 | 6 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 20453516)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCATGAATCGGTATGATTGTGAAACACTGTTTGCTTTTGACTACAACA[G/A]ATACGACTAAGTGGAGGAAGAAACCCATTTGAAGGACGTGTGGAAGTTCT
Long Flanking Sequence:
AAAATTTCAGATGGCACAGAGGTTTTTGCATCTGAACTCTTCAAATAGACACATCCTTTGGTACCTTTTGGTGCCTGAAGCATTAACAAGAATTCAGTATCAACCACATGTCAAACACAGATATCTTCTACCAGGGTAATTTCTTTTTTTTGCATCAGAACTCAGAATTTCTTATTCATGAACACTATTTTGGATAATAATGCCCCATTTAATGTACACAATGTATTTAATGTGTACTTTTTTTGTCAGGAATGGGTCCGGTCCACATGAATGAGGTGGAGTGCTCTGGATTTGAGAAATCTCTCACTGACTGCTACTTTAATAATGATGCGCTGGGATGCAGTCATGAGGAGGACGCAGCTGTTCGCTGTAATGTACCTGCTATGGGCTTTCAGAAAAGGGTGAGGATTTTTAAAATATAATTTACATATTAATTAGCAATAGTTTTACGCTCATGAATCGGTATGATTGTGAAACACTGTTTGCTTTTGACTACAACA[G/A]ATACGACTAAGTGGAGGAAGAAACCCATTTGAAGGACGTGTGGAAGTTCTCGCTGAGAAGAACGGTTCTCTCGTTTGGGGAACAGTTTGTAGTGAAAACTGGGGGATTATAGAGGCTATGGTGGTCTGCAGACAGCTGGGATTAGGCTTTGCCAGCCATGCGTTCCAGGTAAGACTACTTACTAAATGTGAAAGTCCTTCAAAATTGAAAATCGAATGGGTTTAAACAGTCACAAAATACAAGCTACTATTCTACTGAACACATGATCACTATGAAAAAGTGCATTTAAACAATAAATTCATATTTCATAGTATTGTACTTGCCATTTAAATTCACCTTTTCATTCATTTTCTTTCACACACACTCTAAAGCAAGTAGTATTTATGCATCACACTAAGCTCTTCTGCTAAAATGATGTAGAGGGAAACAAAATAACAGTGAAGGGTCTTGATTCAATCTAAACATAAGTGGTCACAAGAGTCACATTTGAATTCATGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45401
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 |
---|---|---|---|---|---|
ENSDART00000127848 | Nonsense | 557 | 648 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 20444277)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 20453058 |
GRCz11 | 10 | 20410439 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTGGACTAGGTATTTCGAAGCGGTACCATTGTGCTAACTTTGGTGAA[C/T]AGGGCATCACTGTTGGCTGCTGGGACACTTACAGACATGACATTGATTGT
Long Flanking Sequence:
CTCTTCCAAAGGCTTTAACTGACACAGTAAAACTGACACCATTGTTACTGTCCATTTGTCTGATTTTACTGATGACCAATCAGAGCAGAGGAGAGGTTTAAAGAGACTTTAATTTTAGACACTGAGAGAAAAGAGCTTTAATATTTGCTATTTATGAGTAAATAAAGTGCTTTTTGACCTTGAACTGACCTTTAAAATAGCACAACTGGGGCACTTAATTATGATACACAATAAAACTCTCACATTGTATTGTTGTGTGTCTGCACAGGCATTATCACAGCATGGAGGTCTTTACTCATTATGACCTGCTGAGCTTAAACGGCACCAAGGTAGCAGAGGGTCACAAAGCCAGTTTCTGTCTAGAGGACACTCATTGTGATGAAGGTGAGAATGCGAGGGCTGATCCCCTGAACTTTATTCAGTTCAAGCTGAATTCCTAACTGGTTGTTTTCTTTGGACTAGGTATTTCGAAGCGGTACCATTGTGCTAACTTTGGTGAA[C/T]AGGGCATCACTGTTGGCTGCTGGGACACTTACAGACATGACATTGATTGTCAGTGGATTGATGTGACGGATGTCAAACCAGGAGACTACATTTTCCAGGTACAGTTTCAAATCACTGTTGGTGTGAATTTTAGACAATGAGTTTTTGAGGGAATTCTCTTATGTTCACCGTAGGTGGATTTATTAAGTTAAGACATTCAATTCAATCAGTTGTAATTTACAAGTTGGATTAAGTGTATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATTTATTTCTTCCTGTCATGCAAAGCTTTTCCTGCATCTAGTCCTCACATGATCATCGAGAAATCATTTATGCTAATTGTGTTCTCAAGAAACATATTATTATTATTTATTTTTTTTAAAATAAATTTTAGAAACTGCTTTTTTATATATTTTGTAAACTGATACATGCCATTTTAAACTG
Associated Phenotype:
Not determined