ZMP
ENSDARG00000088608
Ensembl ID:
Human Orthologue:
L1TD1
Human Description:
LINE-1 type transposase domain containing 1 [Source:HGNC Symbol;Acc:25595]
Mouse Orthologue:
L1td1
Mouse Description:
LINE-1 type transposase domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:3578435]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22802 | Nonsense | Available for shipment | Available now |
sa7297 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42697 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14021 | Nonsense | Available for shipment | Available now |
sa13772 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22802
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 |
---|---|---|---|---|---|
ENSDART00000122529 | Nonsense | 3 | 286 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 16 (position 20028205)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 18058438 |
GRCz11 | 16 | 17965142 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCATTTATCTCTCAACAGACTTATCAACCCCGTGCGATCTTCACAGGT[C/T]AGTCAAATAATCATAATAACAAACTTTTCGACATGAAACCGAGTTCGAGC
Long Flanking Sequence:
GATTTATTTTTTGCACTACAGAATTTCATACAAATCCTGCTTCTTTTACAGTAAAATACTGTTTCCTTTCATTACAGCTAAACACTGGCTATTTTACAGTTATTTACTGCATAATCTACAGTAAGGGTTATTAGTGTAGTTGATTTGTTTATAAATAATTATTCATTTTTGGATATTAAATGTAACAATAAGGTCTTGAGATCACTACTGACAAAAGAATATTTTCCTCTTCCTGTTAAAAGAAAAGTTTTATCTGAGAGATTTTCTAAAGCGGACTATTGAAATTAGAAAAAGATACCTTTCATTTCCCTTGTTACCTAAAATGAAAGAAATACATTTCAAAACAATTAATGACATCTATCCATGTAACAAATTTCTTAGAATAAGATTTAGACTTCCGCTTCCGCCCGCATGGAGTGAGCCAGACAGACGGGAGCTCCTCAAATAAATAATCATTTATCTCTCAACAGACTTATCAACCCCGTGCGATCTTCACAGGT[C/T]AGTCAAATAATCATAATAACAAACTTTTCGACATGAAACCGAGTTCGAGCAAGAAAGTTACCTCGTCAATTCAACATAATACAAAAGCAGAAGGCAGTGATAACAAATTTGATGACAAAGACGGCGGCTCTCCCATCTCGCTAACAACACTCCGATCAGAGCTACAAACTCATCGGGAAGCGGTGATTAAGGACATTAAATCACAAATCGAAAACCTCCACCTGGAGATGCAAAAAAAACAGCATGCGCTACGAGAAGAAATTTTCCCGGAACTGGCAACCTTGAACAAAGCGCAATCCGATTCGGCGAAGGAGTGCACAGAGATTAGAAAAACTTTGAGTGACACCATGGATAGAGTGGCAGTACTTGAACAGTCTTACGAACGCATGAGTAAAGAACACAAAAAAATACAAGAGAAGTGTATGGATTTAGAGAATCGTAGCCGGAGACAAAATTTAAGATTCGTTGGAGTCCCTGAAGGGGTTGAAGTGGGAAATCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7297
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 |
---|---|---|---|---|---|
ENSDART00000122529 | Nonsense | 166 | 286 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 16 (position 20027701)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 18057934 |
GRCz11 | 16 | 17964638 |
KASP Assay ID:
554-4489.1 (used for ordering genotyping assays)
KASP Sequence:
ATTTAAGATTCRTTGGAGTCCCTGAAGGGGTTGAAGYGGGAAATCCGGTT[C/T]GATTCATCAAAGACCTGCTACTGGAGCTGTTTGGAGCTGACGAACTTGGG
Long Flanking Sequence:
CAAATAATCATAATAACAAACTTTTCGACATGAAACCGAGTTCGAGCAAGAAAGTTACCTCGTCAATTCAACATAATACAAAAGCAGAAGGCAGTGATAACAAATTTGATGACAAAGACGGCGGCTCTCCCATCTCGCTAACAACACTCCGATCAGAGCTACAAACTCATCGGGAAGCGGTGATTAAGGACATTAAATCACAAATCGAAAACCTCCACCTGGAGATGCAAAAAAAACAGCATGCGCTACGAGAAGAAATTTTCCCGGAACTGGCAACCTTGAACAAAGCGCAATCCGATTCGGCGAAGGAGTGCACAGAGATTAGAAAAACTTTGAGTGACACCATGGATAGAGTGGCAGTACTTGAACAGTCTTACGAACGCATGAGTAAAGAACACAAAAAAATACAAGAGAAGTGTATGGATTTAGAGAATCGTAGCCGGAGACAAAATTTAAGATTCGTTGGAGTCCCTGAAGGGGTTGAAGTGGGAAATCCGGTT[C/T]GATTCATCAAAGACCTGCTACTGGAGCTGTTTGGAGCTGACGAACTTGGGGATTCTAATATGATGGTGGATCGAGCGCACAGGACCCTTGCTCCGAGACCTACAACGGGAGAGAGACCCCGGGCATTAATCGTCCACTTCCACTATTATGCGGACAAAGAGAAACTTCTTAAGTTATCCAGAAATAAAGGCCGTCTTTACTATAAGGGATCCCCAGTACACATCTTCCCTGACATGAGTCCAGAAGTTGGCAAACTTCGCGCTGCGTTCAATCCAGTCAAGGCCAAGCTGCGAGCCGCCGGAATAACCTACAGTCTATTTTACCCTGCCAGATTAACAATTACTGTGGACGGAATCAGGTACACTTTTGAGCACCCTCGAGAAGCTGATACATTTCTGGAAAAGAAGTCTCAAACCTAGATGGCTGAACTGTGAGGCTTGATCATCTGACTGAAAATAAATGTGGTGTCTGTTCTTATTTTTATCAGGCTTGGATACTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42697
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 |
---|---|---|---|---|---|
ENSDART00000122529 | Nonsense | 215 | 286 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 16 (position 20027552)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 18057785 |
GRCz11 | 16 | 17964489 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTACAACGGGAGAGAGACCCCGGGCATTAATCGTCCACTTCCACTATTA[T/A]GCGGACAAAGAGAAACTTCTTAAGTTATCCAGAAATAAAGGCCGTCTTTA
Long Flanking Sequence:
CGATCAGAGCTACAAACTCATCGGGAAGCGGTGATTAAGGACATTAAATCACAAATCGAAAACCTCCACCTGGAGATGCAAAAAAAACAGCATGCGCTACGAGAAGAAATTTTCCCGGAACTGGCAACCTTGAACAAAGCGCAATCCGATTCGGCGAAGGAGTGCACAGAGATTAGAAAAACTTTGAGTGACACCATGGATAGAGTGGCAGTACTTGAACAGTCTTACGAACGCATGAGTAAAGAACACAAAAAAATACAAGAGAAGTGTATGGATTTAGAGAATCGTAGCCGGAGACAAAATTTAAGATTCGTTGGAGTCCCTGAAGGGGTTGAAGTGGGAAATCCGGTTCGATTCATCAAAGACCTGCTACTGGAGCTGTTTGGAGCTGACGAACTTGGGGATTCTAATATGATGGTGGATCGAGCGCACAGGACCCTTGCTCCGAGACCTACAACGGGAGAGAGACCCCGGGCATTAATCGTCCACTTCCACTATTA[T/A]GCGGACAAAGAGAAACTTCTTAAGTTATCCAGAAATAAAGGCCGTCTTTACTATAAGGGATCCCCAGTACACATCTTCCCTGACATGAGTCCAGAAGTTGGCAAACTTCGCGCTGCGTTCAATCCAGTCAAGGCCAAGCTGCGAGCCGCCGGAATAACCTACAGTCTATTTTACCCTGCCAGATTAACAATTACTGTGGACGGAATCAGGTACACTTTTGAGCACCCTCGAGAAGCTGATACATTTCTGGAAAAGAAGTCTCAAACCTAGATGGCTGAACTGTGAGGCTTGATCATCTGACTGAAAATAAATGTGGTGTCTGTTCTTATTTTTATCAGGCTTGGATACTTAAGAAAAAATAGCATTAATATATTGCTGGACATATACATAACTTTATTAAAAAAAAAAAAAAAAAGAACCGCAATGATTATAGTAAAGTGAAAATAGTACATGTAAATTGGTCTAATGAGTAACTTATTTGTTTTTGTAAAGGAGCTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14021
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 |
---|---|---|---|---|---|
ENSDART00000122529 | Nonsense | 286 | 286 | 2 | 2 |
ENSDART00000122529 | Nonsense | 286 | 286 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 16 (position 20027339)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 18057572 |
GRCz11 | 16 | 17964276 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WGTCTRTTTTACCCTGCCAGATTAACAATTACTGTGGACGGAATCAGGTA[C/A]ACTTTTGAGCACCCTCGAGAAGCTGATAMATTTCTGGAAAAGAAGTCTCA
Long Flanking Sequence:
CTTGAACAGTCTTACGAACGCATGAGTAAAGAACACAAAAAAATACAAGAGAAGTGTATGGATTTAGAGAATCGTAGCCGGAGACAAAATTTAAGATTCGTTGGAGTCCCTGAAGGGGTTGAAGTGGGAAATCCGGTTCGATTCATCAAAGACCTGCTACTGGAGCTGTTTGGAGCTGACGAACTTGGGGATTCTAATATGATGGTGGATCGAGCGCACAGGACCCTTGCTCCGAGACCTACAACGGGAGAGAGACCCCGGGCATTAATCGTCCACTTCCACTATTATGCGGACAAAGAGAAACTTCTTAAGTTATCCAGAAATAAAGGCCGTCTTTACTATAAGGGATCCCCAGTACACATCTTCCCTGACATGAGTCCAGAAGTTGGCAAACTTCGCGCTGCGTTCAATCCAGTCAAGGCCAAGCTGCGAGCCGCCGGAATAACCTACAGTCTATTTTACCCTGCCAGATTAACAATTACTGTGGACGGAATCAGGTA[C/A]ACTTTTGAGCACCCTCGAGAAGCTGATACATTTCTGGAAAAGAAGTCTCAAACCTAGATGGCTGAACTGTGAGGCTTGATCATCTGACTGAAAATAAATGTGGTGTCTGTTCTTATTTTTATCAGGCTTGGATACTTAAGAAAAAATAGCATTAATATATTGCTGGACATATACATAACTTTATTAAAAAAAAAAAAAAAAAGAACCGCAATGATTATAGTAAAGTGAAAATAGTACATGTAAATTGGTCTAATGAGTAACTTATTTGTTTTTGTAAAGGAGCTAAGTGGTTTACTACCCTTTGGTTGAAGTAATGGGTAACGTTAACAACAGAAGTCTTCTAAACTTACTCTGCTGTTTTTTGTGTGATGTTCATACACACAGTGGACTGAGAGTTATGTTCAACCCCCAACTCTTTTGTTTATTTTATATTATTTATTTATTTATTTTTATTTTATTTATTATTATTATTTATTTTTTCCCTGTACACTCTAAAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13772
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 |
---|---|---|---|---|---|
ENSDART00000122529 | Nonsense | 286 | 286 | 2 | 2 |
ENSDART00000122529 | Nonsense | 286 | 286 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 16 (position 20027339)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 18057572 |
GRCz11 | 16 | 17964276 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WGTCTRTTTTACCCTGCCAGATTAACAATTACTGTGGACGGAATCAGGTA[C/A]ACTTTTGAGCACCCTCGAGAAGCTGATAMATTTCTGGAAAAGAAGTCTCA
Long Flanking Sequence:
CTTGAACAGTCTTACGAACGCATGAGTAAAGAACACAAAAAAATACAAGAGAAGTGTATGGATTTAGAGAATCGTAGCCGGAGACAAAATTTAAGATTCGTTGGAGTCCCTGAAGGGGTTGAAGTGGGAAATCCGGTTCGATTCATCAAAGACCTGCTACTGGAGCTGTTTGGAGCTGACGAACTTGGGGATTCTAATATGATGGTGGATCGAGCGCACAGGACCCTTGCTCCGAGACCTACAACGGGAGAGAGACCCCGGGCATTAATCGTCCACTTCCACTATTATGCGGACAAAGAGAAACTTCTTAAGTTATCCAGAAATAAAGGCCGTCTTTACTATAAGGGATCCCCAGTACACATCTTCCCTGACATGAGTCCAGAAGTTGGCAAACTTCGCGCTGCGTTCAATCCAGTCAAGGCCAAGCTGCGAGCCGCCGGAATAACCTACAGTCTATTTTACCCTGCCAGATTAACAATTACTGTGGACGGAATCAGGTA[C/A]ACTTTTGAGCACCCTCGAGAAGCTGATACATTTCTGGAAAAGAAGTCTCAAACCTAGATGGCTGAACTGTGAGGCTTGATCATCTGACTGAAAATAAATGTGGTGTCTGTTCTTATTTTTATCAGGCTTGGATACTTAAGAAAAAATAGCATTAATATATTGCTGGACATATACATAACTTTATTAAAAAAAAAAAAAAAAAGAACCGCAATGATTATAGTAAAGTGAAAATAGTACATGTAAATTGGTCTAATGAGTAACTTATTTGTTTTTGTAAAGGAGCTAAGTGGTTTACTACCCTTTGGTTGAAGTAATGGGTAACGTTAACAACAGAAGTCTTCTAAACTTACTCTGCTGTTTTTTGTGTGATGTTCATACACACAGTGGACTGAGAGTTATGTTCAACCCCCAACTCTTTTGTTTATTTTATATTATTTATTTATTTATTTTTATTTTATTTATTATTATTATTTATTTTTTCCCTGTACACTCTAAAAACT
Associated Phenotype:
Not determined