ZMP
ENSDARG00000026663
Ensembl ID:
Mouse Orthologues:
Tlr11, Tlr12
Mouse Descriptions:
toll-like receptor 11 Gene [Source:MGI Symbol;Acc:MGI:3045226]
toll-like receptor 12 Gene [Source:MGI Symbol;Acc:MGI:3045221]
toll-like receptor 12 Gene [Source:MGI Symbol;Acc:MGI:3045221]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22826 | Nonsense | Available for shipment | Available now |
sa42711 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa28651 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39098 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22826
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 |
---|---|---|---|---|---|
ENSDART00000036422 | None | None | 103 | None | 2 |
ENSDART00000132944 | Nonsense | 157 | 851 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 24908945)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 22813261 |
GRCz11 | 16 | 22728651 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTGGGGTTCAAAATCTGTATTTAATTGGGAACAATATTAAATATATT[C/T]AAGCAAACTCCTTAATTATATTCCAGAACCTCTCAAGCCTTTTTCTGGAG
Long Flanking Sequence:
TTGGAGATATTACGAGCATTCCTGCTAAAGCCTTTTCACACTTACCTTCTCTGGAGGTACTTCACATAGATGGAATACGTCTGGAGAGAGTTCAGGCTGGTGCCTTTGAAGGACTCCCCAATCTTAAGTATCTGTCAATGCTTTTCAGTGATGAACTCTACAGATTGGTCAGAATAGATAATCGGTCATTTGCTGGTCTGAATAATTTGGAGGAGTTGTCACTGACAGGTCTGATGCTGCTCAATGGATCCAGTGGTATATTTGACCCATTGGTTAGTTTAATCAGATTAGACATTGTCAGAACTTGCGCACAAGACCTTGGTGAAATTTTCTGTTGTATTTCGAATGGAATGACCCGGCTAAGACACCTAAATGTAGAAGACAGTGAGATTTCAACAATTGAGAACAAAGGATGTCCAGGGGGCTCAATGACCTGGCCGCTTACTGCCCTTTCTGGGGTTCAAAATCTGTATTTAATTGGGAACAATATTAAATATATT[C/T]AAGCAAACTCCTTAATTATATTCCAGAACCTCTCAAGCCTTTTTCTGGAGTTCGAGGGCAAGTCCCTGGGCAGTATTTGGGAGTCTGGAGTTGGAAAAGTCAATGATTTGACTTTGAAAGGGAAAGTATTAAAAAAATACTCAACAAACTTCAAAGATTTGTGTCATCTTGTATCGAGTCTTTATTCGCAATCACTCAGCCTTGTTTATACATCAATAGACAGACTAACTGCTGAGGACTTGAAGGACTGTGGGACTAAGTTGACAAAGTTATTAATCCAGAATTCCAAAATAGACAACCTAGACTTTAGGTTTTGGACCAGTAAACTGGAAATGCAGGCCCTTCAAATGGCCTACATGAAGTTGACAGATGCTCCCTTTTGTTTTGTTGCGAACAGCACAATGTGGTCTTTAACCTCACTGGACCTCACTGGAAACTCTATCACCAATATTGAAGGAGATCAGTTTGCATGTATGCCTTTTCTTGAGCAGCTCTATCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42711
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 |
---|---|---|---|---|---|
ENSDART00000036422 | None | None | 103 | None | 2 |
ENSDART00000132944 | Nonsense | 419 | 851 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 24908159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 22812475 |
GRCz11 | 16 | 22727865 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGTTGCATCTAGAGAACATTTTTTTTGAATTTCCACCAAAGTTACAG[C/T]GACTCAGCATCGATGCACATTATGGAACTAATATTTACATTGGAAACGCA
Long Flanking Sequence:
CCAAAATAGACAACCTAGACTTTAGGTTTTGGACCAGTAAACTGGAAATGCAGGCCCTTCAAATGGCCTACATGAAGTTGACAGATGCTCCCTTTTGTTTTGTTGCGAACAGCACAATGTGGTCTTTAACCTCACTGGACCTCACTGGAAACTCTATCACCAATATTGAAGGAGATCAGTTTGCATGTATGCCTTTTCTTGAGCAGCTCTATCTGAGCCAGAATGCCATTAAAACCCTACAGCTGCATGCATTTCGAGGTTTGCCTCGACTTAAAATCCTGCAACTTGACTCAAACAAGATCTGGCAGCTTTCAGCCAATGATTTCAAAAACCTTCGGGCTTTAGAGGTTCTGCTGATTAACGATAACATCATTGAGACCATAGAGACAGGAACATTTTGGGACCAGCGGGAGCTTTGTGAACTGTCATTTGGTAGACTGGAATATGTTTATGAGTTGCATCTAGAGAACATTTTTTTTGAATTTCCACCAAAGTTACAG[C/T]GACTCAGCATCGATGCACATTATGGAACTAATATTTACATTGGAAACGCATCACCACCCAATGGAACATTTGCTTTGGAACTAAATGGAGAGAGACTGGGTTTTGTGGGCTGTGATAGTGATGTTTTAATGGCAGTCCGTGAGTTGAAAGTCAATTGCACCTACTTCCTTTGCAAGGACAGTTTTATGGCTCCCTATTTCCTAAACCTGGAATCTCTCGAGATCTCAGGCGGAGCTGAAAGGGCACCTCTCAATTACGCTACAATCAATAATCTTCACCATCTCAAGCATCTCAAACTCGCAAGGTTGAACTTCCCCAATTACACAGAATCTAGGAGTGCCTTCTGGAACCTGACTCAACTCCAGACCCTCGTGGTGGTAAACTGTCATCTTAGTTTCCTCACCAAGAGCATGTTCAGAGATCTGACCTCTCTGCAGCTGTTGCGTCTCTACAGTGACAGTCCTCTGATCTTGACTGATGGTGTGTTTGGGGTTTTACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28651
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 |
---|---|---|---|---|---|
ENSDART00000036422 | Nonsense | 77 | 103 | 2 | 2 |
ENSDART00000132944 | Nonsense | 781 | 851 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 24905138)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 22809454 |
GRCz11 | 16 | 22724844 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAGCATCCACAACAGTCAGTGCACTGTTTGTCTGATCAGCCGGCGGTA[T/A]CTGCGCAGTGACTGGTGTGGTCTGGAGATGCGAGTGGCCACACACCGGCA
Long Flanking Sequence:
CCAAGTAGCATAATATAATAAGAAAATATTAAATTGCAACATCAAGCAGCGTAACGAGCAGTTGTTAACGTCAAAAAATGAATGGAAGTGAATGTGACCGGAAGTCGCGAGACAAAAAGATTCAAATGGCAGCGCCCACTCGACAGCTGAGAATAGTGTGAATATAATATAATTTAAATAGGTCTTTAGGTTCGATCATCAGACTTGCTGTTGGTCCTCAGTCTGGCAACCTGCGTTTGCATTTGTTTTGATACAGGAATGTAATATCTAGTTCAACCACTGGGTGTCAAACTTACATACTGCACCTTTAAATATGTTTGGTGACCTTGAAGTTTTGGCAGTTGTTGGTTTTCTCTCATTTTGATCTCCATTGTATTAAAACAAAAAATCTGCAACCTCACCTATTATTGTTAACAACAGGTGGGTAAAGATATCATGGACAACATCACAGACAGCATCCACAACAGTCAGTGCACTGTTTGTCTGATCAGCCGGCGGTA[T/A]CTGCGCAGTGACTGGTGTGGTCTGGAGATGCGAGTGGCCACACACCGGCAGCTGGAAGAGCAGAAACACCGTCTCATCCTCATCTTCCTCCAACACATCTCTCCCTTTGAGCTCTCAGCCTTTCATCGGTAAGTGGCGGTGCATTTACATAAAACGGCAACATTTAGTGTAACAAAGGTCACCAAAAGGGGTCGGGTTGGTTAAAGAGGGGGGAGGGGGGACATTAACTTTATTATCATGATGGACTCATTCAGAAGAAGCCAACTTGCTTTTATGTGACAAACTTTTCGTTGAAAAAAAGCTCCTTATGTCCACCTTTCTTTCTCATCCTCACTTGCGTGTCACACACCTCACATACCTTCACACAAATTCACCTGCGCAGTTTTGGCGCTCGCTGAATGTATTTGAACGCAGCTACAGCTTCTCACATGACAGCAGGGGAAGGCGCAAACAAGCAATGTTCATATGTGTTTAGGGGGCGGTGCGACTCGAAGAGAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39098
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000036422 | None | None | 103 | None | 2 |
ENSDART00000132944 | Nonsense | 848 | 851 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 24902654)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 22806970 |
GRCz11 | 16 | 22722360 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTACATATCTGGACTGGCCAGAGGAAGAAGGAGACCGAGAGCACTTCTG[G/A]GATCGACTAAGGAGGAACATTGCAGAAGATTCTGTAAGTACAAAAACATC
Long Flanking Sequence:
CCGTTGCGTAAAAACTTGCTGGATAAGTTAGCAGTTCATTACATTGTGGCGACCCTGGATTAATAAAGGGACTAAGCCGACAAGGAAATGAATGAACTATTGACTGCTGTGAAAGTCAATGTTTTCAGCTTTCGTCACAATAAAATGTTGTGTTCAACAGAAGAAAGAAACTCATTAAGATTTGGAACAACTATAGTGTTAATGATGAGAATATTTTAGGGTAAACTAAAACTTTAAGATAAAAACAAATTGATTTATGAGAACATGTTAATTCGATTAACATGTTAAATCGATGTTTCGAGGAGAAAATTAATTATATCTTTTGTAAAGAGGACAATTGCTGTATGCAAGTTTTAATGGACCACTTTAAGACATTCCTTTTCTCATTTTACACAGCGTAATACAGTATATTTATTGTTTTTCTATAGTTTGGCAAAACTGGTGAGATCCCGTACATATCTGGACTGGCCAGAGGAAGAAGGAGACCGAGAGCACTTCTG[G/A]GATCGACTAAGGAGGAACATTGCAGAAGATTCTGTAAGTACAAAAACATCTGAACTGAAGCTTCAAGAAAGAGTCGTGTTTATTGAAATAAAATCTCACTTGTGTTACAGGAAGCTTCTTAAACTACTAGCAGGTTCCTGCTCCATGAATGAATACAAGGAACGTTTATATATATATATATATATATATATTTTTTTTTTTTTTTTTTTTTTAAAGAAAAGTTATTCATTCAATTATCTTCCTTTGGCTTAGTCTCTTATATATCAGGGGTCATCATAGTGGAATGAGCCGGCAATGATTCCGGCAAATGTTTTACACAACAAACGCCCTGCCTGCCACAAACCAGCACTGGAATTTTATTTTATTTTATTTTTTTATGTTTGTTTTATATACTGTAATGCTTATCAGTGTTAACCACTTATATTTATGCATTAAAAATGTCTCTATGAATTTAATCCTAACCAATATTAAACTGAAACTATAATTAAACTGCTCTTGTA
Associated Phenotype:
Not determined