ZMP
tlr4bb
Ensembl ID:
ZFIN ID:
Description:
toll-like receptor 4b, duplicate b [Source:RefSeq peptide;Acc:NP_997978]
Human Orthologue:
TLR4
Human Description:
toll-like receptor 4 [Source:HGNC Symbol;Acc:11850]
Mouse Orthologue:
Tlr4
Mouse Description:
toll-like receptor 4 Gene [Source:MGI Symbol;Acc:MGI:96824]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35456 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa35457 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa9527 | Nonsense | Available for shipment | Available now |
| sa12965 | Nonsense | Available for shipment | Available now |
| sa31917 | Nonsense | Available for shipment | Available now |
| sa31918 | Nonsense | Available for shipment | Available now |
| sa15774 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35456
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 |
|---|---|---|---|---|---|
| ENSDART00000034852 | Essential Splice Site | 30 | 819 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 18575292)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 18395327 |
| GRCz11 | 13 | 18526319 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTATATGCAAATATAAAATATGTAAAACATGTCTTGGTCCTTTAATA[G/A]CTGATAAAGAATAAGGAATATTCATGTTCTGGAAGGAATCTGACTTGTAT
Long Flanking Sequence:
ATCTAAATGTCTTCCAATCTTTCTTTAAGGAACATTGGTTTTAAAGGTTTCAATAATTTTCTCACATATTTGTTGGCAAACTGACAATCCTCAGCCCATCTTAGCTCCTAAAGTACTAGACCTTTCTTGGATGCTGCTTTTGTAACAAATCATAATTTCAATGACCTGTTAACATGACCTGTTTCAAATCGCTTAAACAATTGACCTGATTGCTAGCCCTAAATTGCACTTGTCCCAACTTTTTTGTTATATGTTGCAGGTCTGAATGACAGGAAAGGATGTATATTTACAAGTGAAATAAAGTTGACCAGAACAAACATTAAGTATTTTGTGTTCATATTGTCTGCAATGAAAAACAGGTTAAAGTAAATTTAAAAAATCGCTACTTTCTTTTTTTATTTGCGTTTTCAATACTGTCTCAACTTTTTCTGATTTAGGGTTGTATACTATAATGTATATGCAAATATAAAATATGTAAAACATGTCTTGGTCCTTTAATA[G/A]CTGATAAAGAATAAGGAATATTCATGTTCTGGAAGGAATCTGACTTGTATTCCTGGTAGTCTTCCCTTCTCTGTGGCATCTCTGGATTTCAGTTTCAATTTCTTGACCTCATTACATAAGCGTGTATTTCCTGTGATGTTGAATTTACAACTCCTGGATCTCACAAGGTAAATCAGTACTATTCTTCAGTGTGTTACAATTTAAACATGATTGTGTTCTATGTTTTTATTTTTATGTTGTGTCCTTTCAGATGCTACATCAGACAGATTGAAAAAGATGCTTTCTACAATGTGAAAAATTTGATGACATTGATTCTTACTGGAAACCCTATAACATATTTAGCACCTGAATGCTTGAATTCTTTATACAAGCTGCAAAGACTAGTTCTTGTGGATGTTCGTCTTGAATCCTTACAACTTCAAATTAATAACCTTACCAAGCTACAGGACCTTAAAGTCGGAACAAATTGCATCCAGTCCATGACTCTTCCTTCATTCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35457
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 |
|---|---|---|---|---|---|
| ENSDART00000034852 | Nonsense | 488 | 819 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 18576750)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 18396785 |
| GRCz11 | 13 | 18527777 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAAATGGCAGGAAACAGTTTTAGTGGAGATAAATTGAGTTACTTCTTA[C/T]AAAACCTAACAAGCTTGGAGGTTCTTGACATTTCACAGTGTGGCATTGAG
Long Flanking Sequence:
TTCCATTCCACCGTCTTAAGGAACTGTATTTAAGTGACACTGGATTATCTGTTGTACCATTTATTTCACACATTCCAAGCTTGGAAAAACTGGTGATGAAGAGTCCCTTTCCTATTACCTTCACTGGAGTCAGTGACCTTCCCCTGCTTCAATATGTAGACTTGAGTGGAAACATGTTGATTTTGCATGAATGCTGTTCCATTCTTTTTCCAAGGACACCAAATATTCAATACTTGAATCTTAGTCAAAACTCAGAAATAACATTTGTTAATGAGCCATTTTCTGCACTTGACTTGCTTGAAGTGTTGGACTTCCACCATACAAAACTAGTCATAGTTTTTTACTTTGGATTCTTCAAACATCTGAGAAATTTAAAGTATTTGGATATTTCTTATACACGTGTTCATTTCAATACCTTGACTTTTCAGGACCTGCATAATTTGACTGTTCTTAAAATGGCAGGAAACAGTTTTAGTGGAGATAAATTGAGTTACTTCTTA[C/T]AAAACCTAACAAGCTTGGAGGTTCTTGACATTTCACAGTGTGGCATTGAGAAAGTCTCCATGAGATCTTTTACTGGCACGCAGAAACTACGACATTTATATTTAAGTCGAAACAAATTGATGGTTTTGGACTTTTTAACTCAACCAGAGCTGACACATCTTACATCAGTGTATATTGATAAAAACAGTATAACCACCATCCCACTTGATGTTCTACAAAAGTTGCCCATGAACCTTTCTGAGTTTGATTTGTCCTCTAACTCCATCGATTGCTCCTGCTCTCAGACTGATTTTATTTTGTGGATTATTCAAAAACAAAACATTTTAAAACAACTGGAAAACATTCGGTGTAAAACTTTTTCTGCAAATACAGATTTCAAAGCAATAGACTTTGACATTGACTACTGTGTGCACAAGAAAAGACTCACAATTGTTTTATCAGTAATTTGTGTTACGTTTGTAGTTGTGTTAGCAATTTTGCTTTATAAATTCTGGTTCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9527
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 |
|---|---|---|---|---|---|
| ENSDART00000034852 | Nonsense | 518 | 819 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 18576840)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 18396875 |
| GRCz11 | 13 | 18527867 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGCATTGMGAAAGTCTCMATGAGATCTTTTACTGGCAYGCAGAAACTA[C/T]GACATTTATATTTMAGTCGAAACAAATTGATGGTTTTRRACTTTTTAACT
Long Flanking Sequence:
TGGTGATGAAGAGTCCCTTTCCTATTACCTTCACTGGAGTCAGTGACCTTCCCCTGCTTCAATATGTAGACTTGAGTGGAAACATGTTGATTTTGCATGAATGCTGTTCCATTCTTTTTCCAAGGACACCAAATATTCAATACTTGAATCTTAGTCAAAACTCAGAAATAACATTTGTTAATGAGCCATTTTCTGCACTTGACTTGCTTGAAGTGTTGGACTTCCACCATACAAAACTAGTCATAGTTTTTTACTTTGGATTCTTCAAACATCTGAGAAATTTAAAGTATTTGGATATTTCTTATACACGTGTTCATTTCAATACCTTGACTTTTCAGGACCTGCATAATTTGACTGTTCTTAAAATGGCAGGAAACAGTTTTAGTGGAGATAAATTGAGTTACTTCTTACAAAACCTAACAAGCTTGGAGGTTCTTGACATTTCACAGTGTGGCATTGAGAAAGTCTCCATGAGATCTTTTACTGGCACGCAGAAACTA[C/T]GACATTTATATTTAAGTCGAAACAAATTGATGGTTTTGGACTTTTTAACTCAACCAGAGCTGACACATCTTACATCAGTGTATATTGATAAAAACAGTATAACCACCATCCCACTTGATGTTCTACAAAAGTTGCCCATGAACCTTTCTGAGTTTGATTTGTCCTCTAACTCCATCGATTGCTCCTGCTCTCAGACTGATTTTATTTTGTGGATTATTCAAAAACAAAACATTTTAAAACAACTGGAAAACATTCGGTGTAAAACTTTTTCTGCAAATACAGATTTCAAAGCAATAGACTTTGACATTGACTACTGTGTGCACAAGAAAAGACTCACAATTGTTTTATCAGTAATTTGTGTTACGTTTGTAGTTGTGTTAGCAATTTTGCTTTATAAATTCTGGTTCTATGTTCAGTATTGTTTTATTTTATTCAGTGGCTACAGATCACCTGGACAGCAAGAATGTTCTTATGACGCATTTGTGATTTTCTCCAGCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12965
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 |
|---|---|---|---|---|---|
| ENSDART00000034852 | Nonsense | 562 | 819 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 18576973)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 18397008 |
| GRCz11 | 13 | 18528000 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTGATAAAAACAGTATAACCACCATCCCACTTGATGTTCTACAAAAGY[T/A]GCCCATGAAYCTTTCTGAGTTTGATTTGTCCTCTAACTCCATCGATTGCT
Long Flanking Sequence:
TATTCAATACTTGAATCTTAGTCAAAACTCAGAAATAACATTTGTTAATGAGCCATTTTCTGCACTTGACTTGCTTGAAGTGTTGGACTTCCACCATACAAAACTAGTCATAGTTTTTTACTTTGGATTCTTCAAACATCTGAGAAATTTAAAGTATTTGGATATTTCTTATACACGTGTTCATTTCAATACCTTGACTTTTCAGGACCTGCATAATTTGACTGTTCTTAAAATGGCAGGAAACAGTTTTAGTGGAGATAAATTGAGTTACTTCTTACAAAACCTAACAAGCTTGGAGGTTCTTGACATTTCACAGTGTGGCATTGAGAAAGTCTCCATGAGATCTTTTACTGGCACGCAGAAACTACGACATTTATATTTAAGTCGAAACAAATTGATGGTTTTGGACTTTTTAACTCAACCAGAGCTGACACATCTTACATCAGTGTATATTGATAAAAACAGTATAACCACCATCCCACTTGATGTTCTACAAAAGT[T/A]GCCCATGAACCTTTCTGAGTTTGATTTGTCCTCTAACTCCATCGATTGCTCCTGCTCTCAGACTGATTTTATTTTGTGGATTATTCAAAAACAAAACATTTTAAAACAACTGGAAAACATTCGGTGTAAAACTTTTTCTGCAAATACAGATTTCAAAGCAATAGACTTTGACATTGACTACTGTGTGCACAAGAAAAGACTCACAATTGTTTTATCAGTAATTTGTGTTACGTTTGTAGTTGTGTTAGCAATTTTGCTTTATAAATTCTGGTTCTATGTTCAGTATTGTTTTATTTTATTCAGTGGCTACAGATCACCTGGACAGCAAGAATGTTCTTATGACGCATTTGTGATTTTCTCCAGCTATGATGAAGCTTGGGTCATGAATGAACTTATGGAGAATCTGGAGAACGGTGTGCCACCTATTCAGCTTTGCCTTCACATGCGGGACTTTCAAGCCGGGAAGTCAATCGCCTCCAACATTATAGATGAAGGAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31917
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000034852 | Nonsense | 588 | 819 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 18577052)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 18397087 |
| GRCz11 | 13 | 18528079 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTCTAACTCCATCGATTGCTCCTGCTCTCAGACTGATTTTATTTTGTG[G/A]ATTATTCAAAAACAAAACATTTTAAAACAACTGGAAAACATTCGGTGTAA
Long Flanking Sequence:
GTGTTGGACTTCCACCATACAAAACTAGTCATAGTTTTTTACTTTGGATTCTTCAAACATCTGAGAAATTTAAAGTATTTGGATATTTCTTATACACGTGTTCATTTCAATACCTTGACTTTTCAGGACCTGCATAATTTGACTGTTCTTAAAATGGCAGGAAACAGTTTTAGTGGAGATAAATTGAGTTACTTCTTACAAAACCTAACAAGCTTGGAGGTTCTTGACATTTCACAGTGTGGCATTGAGAAAGTCTCCATGAGATCTTTTACTGGCACGCAGAAACTACGACATTTATATTTAAGTCGAAACAAATTGATGGTTTTGGACTTTTTAACTCAACCAGAGCTGACACATCTTACATCAGTGTATATTGATAAAAACAGTATAACCACCATCCCACTTGATGTTCTACAAAAGTTGCCCATGAACCTTTCTGAGTTTGATTTGTCCTCTAACTCCATCGATTGCTCCTGCTCTCAGACTGATTTTATTTTGTG[G/A]ATTATTCAAAAACAAAACATTTTAAAACAACTGGAAAACATTCGGTGTAAAACTTTTTCTGCAAATACAGATTTCAAAGCAATAGACTTTGACATTGACTACTGTGTGCACAAGAAAAGACTCACAATTGTTTTATCAGTAATTTGTGTTACGTTTGTAGTTGTGTTAGCAATTTTGCTTTATAAATTCTGGTTCTATGTTCAGTATTGTTTTATTTTATTCAGTGGCTACAGATCACCTGGACAGCAAGAATGTTCTTATGACGCATTTGTGATTTTCTCCAGCTATGATGAAGCTTGGGTCATGAATGAACTTATGGAGAATCTGGAGAACGGTGTGCCACCTATTCAGCTTTGCCTTCACATGCGGGACTTTCAAGCCGGGAAGTCAATCGCCTCCAACATTATAGATGAAGGAATAATGGGCAGCCGTAAGATCATTGTGGTTGTGTCTCAACACTTCATTGATAGTTCCTGGTGTCGCTTTGAGTTTGAATTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31918
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000034852 | Nonsense | 614 | 819 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 18577128)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 18397163 |
| GRCz11 | 13 | 18528155 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAACTGGAAAACATTCGGTGTAAAACTTTTTCTGCAAATACAGATTTC[A/T]AAGCAATAGACTTTGACATTGACTACTGTGTGCACAAGAAAAGACTCACA
Long Flanking Sequence:
ATTTGGATATTTCTTATACACGTGTTCATTTCAATACCTTGACTTTTCAGGACCTGCATAATTTGACTGTTCTTAAAATGGCAGGAAACAGTTTTAGTGGAGATAAATTGAGTTACTTCTTACAAAACCTAACAAGCTTGGAGGTTCTTGACATTTCACAGTGTGGCATTGAGAAAGTCTCCATGAGATCTTTTACTGGCACGCAGAAACTACGACATTTATATTTAAGTCGAAACAAATTGATGGTTTTGGACTTTTTAACTCAACCAGAGCTGACACATCTTACATCAGTGTATATTGATAAAAACAGTATAACCACCATCCCACTTGATGTTCTACAAAAGTTGCCCATGAACCTTTCTGAGTTTGATTTGTCCTCTAACTCCATCGATTGCTCCTGCTCTCAGACTGATTTTATTTTGTGGATTATTCAAAAACAAAACATTTTAAAACAACTGGAAAACATTCGGTGTAAAACTTTTTCTGCAAATACAGATTTC[A/T]AAGCAATAGACTTTGACATTGACTACTGTGTGCACAAGAAAAGACTCACAATTGTTTTATCAGTAATTTGTGTTACGTTTGTAGTTGTGTTAGCAATTTTGCTTTATAAATTCTGGTTCTATGTTCAGTATTGTTTTATTTTATTCAGTGGCTACAGATCACCTGGACAGCAAGAATGTTCTTATGACGCATTTGTGATTTTCTCCAGCTATGATGAAGCTTGGGTCATGAATGAACTTATGGAGAATCTGGAGAACGGTGTGCCACCTATTCAGCTTTGCCTTCACATGCGGGACTTTCAAGCCGGGAAGTCAATCGCCTCCAACATTATAGATGAAGGAATAATGGGCAGCCGTAAGATCATTGTGGTTGTGTCTCAACACTTCATTGATAGTTCCTGGTGTCGCTTTGAGTTTGAATTAGCTCAGTCTCGGTTTTTGATGGAACGCAATGCCAATATCATCATCATTATTCTGGAAGATGTGGCGGAGAGAAAAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15774
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000034852 | Nonsense | 688 | 819 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 18577351)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 18397386 |
| GRCz11 | 13 | 18528378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAATGTTCTTATGACGCATTTGTGATTTTCTCCAGCTATGATGAAGCTT[G/A]GGTCRTGAATGAACTTATGGAGAATCTGGAGAACGGTGTGCCACCTATTC
Long Flanking Sequence:
TTTAAGTCGAAACAAATTGATGGTTTTGGACTTTTTAACTCAACCAGAGCTGACACATCTTACATCAGTGTATATTGATAAAAACAGTATAACCACCATCCCACTTGATGTTCTACAAAAGTTGCCCATGAACCTTTCTGAGTTTGATTTGTCCTCTAACTCCATCGATTGCTCCTGCTCTCAGACTGATTTTATTTTGTGGATTATTCAAAAACAAAACATTTTAAAACAACTGGAAAACATTCGGTGTAAAACTTTTTCTGCAAATACAGATTTCAAAGCAATAGACTTTGACATTGACTACTGTGTGCACAAGAAAAGACTCACAATTGTTTTATCAGTAATTTGTGTTACGTTTGTAGTTGTGTTAGCAATTTTGCTTTATAAATTCTGGTTCTATGTTCAGTATTGTTTTATTTTATTCAGTGGCTACAGATCACCTGGACAGCAAGAATGTTCTTATGACGCATTTGTGATTTTCTCCAGCTATGATGAAGCTT[G/A]GGTCATGAATGAACTTATGGAGAATCTGGAGAACGGTGTGCCACCTATTCAGCTTTGCCTTCACATGCGGGACTTTCAAGCCGGGAAGTCAATCGCCTCCAACATTATAGATGAAGGAATAATGGGCAGCCGTAAGATCATTGTGGTTGTGTCTCAACACTTCATTGATAGTTCCTGGTGTCGCTTTGAGTTTGAATTAGCTCAGTCTCGGTTTTTGATGGAACGCAATGCCAATATCATCATCATTATTCTGGAAGATGTGGCGGAGAGAAAAACCAAGAAAGTGTTTGGTCTACATAAGCATCTGAAGAAGAACACATACCTGAAGTGGAGCAGAGACCCTTTGAGCAACATGAGATTCTGGATACGACTCAGGAAAGCAATTTTACAGAAATAATCAATGCACTAAACATGTTTTTTTTTTTTTTAACTGAATGTAATTTGGTCAAATAAAACAATGCATTGCACATTCTTCACATGACAATCTCTCTAATGGTATT
Associated Phenotype:
Not determined