ZMP
LRTM2 (2 of 2)
Ensembl ID:
Description:
leucine-rich repeats and transmembrane domains 2 [Source:HGNC Symbol;Acc:32443]
Human Orthologue:
LRTM2
Human Description:
leucine-rich repeats and transmembrane domains 2 [Source:HGNC Symbol;Acc:32443]
Mouse Orthologue:
Lrtm2
Mouse Description:
leucine-rich repeats and transmembrane domains 2 Gene [Source:MGI Symbol;Acc:MGI:2141485]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12648 | Nonsense | Available for shipment | Available now |
sa44277 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12648
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 |
---|---|---|---|---|---|
ENSDART00000067336 | Nonsense | 22 | 408 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 25 (position 19533760)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 18945737 |
GRCz11 | 25 | 19043688 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATCAGGTCTGATGACCCTAGTGAGTCTGTGTGGWACATCTAAAAGTTG[T/A]CCGTTATTDTGTTCCTGCAACATAAACCAAACAGACTGCAGTCACCTTTA
Long Flanking Sequence:
TCCTTAATCAAAGTCTGTCATGAAGAGGGTTTGGATATTGTTTATTATCGTTACCTCTCAGAACTGTCGTGAGTGGCTGCGCACCCAAATAATCATTGCGTTTCATCTTCAACTTCTGAAGTAGTTTTTATAATATAAGAAAAAAGGTCCACAATGGCTTCTCATACTGCAGCAAATTCTTTTTGATATTTGGCACCAGCTTATCAGGAAGTGATGATTTTGTACTCTCAACTCATTGTATGGATGGTGGATGGATGGAAATGTTGCTTTATTTACAATTGTTTTATGCAATATTCTAGTTATTCATACATATAATTCACATCTTTGGATGGAAACATAGCTATTGATTGACATCCAACGGTTAGTTTGATTTGGTGCATCATGGCTCTAAAGTACCCTTAATCATCTCAAATCTGATGGCTTCCTAAATTCCTTCATTTTCTTGCAGTTTCATCAGGTCTGATGACCCTAGTGAGTCTGTGTGGAACATCTAAAAGTTG[T/A]CCGTTATTGTGTTCCTGCAACATAAACCAAACAGACTGCAGTCACCTTTACCAACTGGCTTCCTTGGACTCCATCCTAGAGCAGCTTCCATTTGACACAACCAATCTCAACCTCTCCAAAAACAACTTCACCACTGTGGAACCTGGGAGCTTTTCCAACCTCAGCGCTTTGCTACAACTAGACTACTCTAGAAACCTTCTCTCTGCCATTAACCCTGGATGTTTTTCCAATCTCAGTGGCCTTTTGCATCTTGACCTCTCCAGAAACCTTCTCTCCAGAGTTTTCCCTTCCAGTTTCTCCCATCTGAATAGCCTGGAGTTCCTGGATCTCTCAGTAAACCTTCTTGTGAGGCTCCCGGTTAACCTGTTCTCTGATCTCAGCAGCCTAAATGAACTGGTTCTACGAGACAACAGGCTAAAGGAACTGAACCCAGCTCAGTTCAAAGGCCTGACTGAGCTCAGGCGTCTGGATCTTTCTTTAAACAGCCTCAGCCATGTGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44277
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 |
---|---|---|---|---|---|
ENSDART00000067336 | Nonsense | 355 | 408 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 25 (position 19535885)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 18947862 |
GRCz11 | 25 | 19045813 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGACGGCCACGTACGGCTGTATCTACGCCACGCTGGTGGCTCATCAA[C/T]AACAGCAGATGCTGCAGAGAAAGCGCCAGCAGCAAGAGCCACTCATGGTG
Long Flanking Sequence:
TAATAAATATACTAAACTATGAAATACAGCAGAAATTAAACATAATTCAACCAATTAAGTTACAGTTCTCAAATACTCTACATGATACAACTATTTCCCACACAGAATGCATTCAAAATTAAACTATTAGATAATTTTTAATGATTTATGATTAACATTTTTTAAAAAACTAAATAATGTCATCCTCTTCCGCAGGTGGCCGTGTGGATTCCCCCAACTGCTCGTTTCCAACTGACCTGCAGGGTAAAGATCTTGCCAGTCTCCCAATGGAGTTGTTCAGACACTGTTACCCCCTGCAGCTCCAAACCAGAAAGCCATCCGCCCCAGAGGCCCACCAGGGGCCGTCAGGAGACTGTATGCGCCAGCGCTACCGGGCCGTGAGCGTGCGTCGAGCCACGGCCACAGTGGTGGTGGCGGGTGTGGTGTGCAGCGTGGTGTGTGTGTTGATGGTGGTGACGGCCACGTACGGCTGTATCTACGCCACGCTGGTGGCTCATCAA[C/T]AACAGCAGATGCTGCAGAGAAAGCGCCAGCAGCAAGAGCCACTCATGGTGGAGAAAGAACCAGCACACGATGAAAAAGAGGATCTGATGCCAACCATCGGAAAGGGAGCCGAAGCTATGGAGTGTGTGGGGTGGATGGCATTTCCTCCGGAAGTGTGTGTTTAAGGGAGACTGTGGTTTATTGTTGAACAACTACATAAATTACATGAGGGCAAATGACTCAGTGTATGTTAAAAGCAATTACTAGTTGGTTGGTTAAGGGATTGTTCATCTGAAAAGCTGTTTATTTGACTCAAGTCATCTAAAATGTACACTGTAAAAATGTAATGACGAATATACAAATATTTTGTATGTTGCTTTAACTTATTTTTCATAATTTAATCAGGTTTCAATGTTTTTTTAAGTTATACAATGTTTAATTTAATATTTTTAGTAAGTTAAGATGACTTGAAAAGCTAATTTGATTCAACAAAAAAATTGAAGCAGCAAGAATTTCTTTTA
Associated Phenotype:
Not determined