Busch Lab

ZMP

tlr5b

Ensembl ID:
ENSDARG00000052322
ZFIN ID:
ZDB-GENE-040219-15
Description:
toll-like receptor 5b [Source:RefSeq peptide;Acc:NP_001124067]
Human Orthologue:
TLR5
Human Description:
toll-like receptor 5 [Source:HGNC Symbol;Acc:11851]
Mouse Orthologue:
Tlr5
Mouse Description:
toll-like receptor 5 Gene [Source:MGI Symbol;Acc:MGI:1858171]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa6655 Nonsense Mutation detected in F1 DNA Not yet available
sa16424 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa6655
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000074153 Nonsense 37 875 2 2
Genomic Location (Zv9):
Chromosome 20 (position 51811084)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 51660523
GRCz11 20 51473635
KASP Assay ID:
554-4600.1 (used for ordering genotyping assays)
KASP Sequence:
AAAGCACCTCCGWGTGTTCAGTTATCGGCTATAATGCCATCTGCATAAAC[A/T]GAGGTCTTCATCAGGTGCCAGAGCTGCCCGCGCATGTCAATTATGTGGAT
Long Flanking Sequence:
AACATGAACAAACGGTAAACAATACATTTATTACAGTATTCATCTTTGTTAATGCTAATTAATGTTCTTTAATGTTGCTTAGTTCATGTTAACTGTGCATTAACTGTTACTAAGCATACATTTGGATTTTAATAATGCATTAGTAAATGTTAAACTATGATGATTTATGAACGTTGTACAAATATCGTTAATTATTAGTTAATGCACGAACATTAACTAATGAAACATTACTGTGAGGTAGTTTTTCATGTGGGTTATGTGTGTGTGTTGCAGCTTTTCTTTTAAAGCCACCAAACCTTGAACTTGTTAAGCAAACAAAATAATATCCCTGTTTGACAAATATTTTAACTGTAAAATGCATGTGATTTTTTTTTGTTTCCAGTGCTCACAGAATGGGATATACATTCATACTGATCCTTTTTGGATTGTGCCTGAACACTGAAGTCGTGAAAAGCACCTCCGAGTGTTCAGTTATCGGCTATAATGCCATCTGCATAAAC[A/T]GAGGTCTTCATCAGGTGCCAGAGCTGCCCGCGCATGTCAATTATGTGGATCTGAGTTTAAACAGCATCGCTGAACTCAACGAAACATCTTTTTCTCGTCTTCAAGATTTACAATTCCTCAAAGTGGAGCAACAAACACCAGGACTCGTGATCAGAAACAACACGTTTAGAGGACTCTCCAGTCTAATAATACTTAAATTAGACTACAACCAATTCCTACAATTAGAGACGGGCGCGTTTAATGGATTAGCAAACCTTGAAGTGCTCACTCTCACGCAGTGTAATTTAGATGGTGCTGTTTTGTCTGGTAACTTCTTCAAACCTCTGACATCTCTTGAGATGCTTGTCTTGCGTGATAACAACATTAAAAAAATCCAGCCAGCTTCATTCTTCCTTAATATGAGGCGATTTCATGTGCTGGATCTGACTTTCAACAAAGTGAAGAGCATCTGTGAGGAAGACCTCCTGAACTTTCAGGGTAAACATTTCACACTCCTCAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16424
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000074153 Nonsense 857 875 2 2
Genomic Location (Zv9):
Chromosome 20 (position 51813544)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 51662983
GRCz11 20 51476095
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTTTTATGACCAACTTCTGCACAAGATAAGAAAARATATCAAGATTAAT[C/T]AAACGACCAAAGAAAYAAAGCRTGAGGAAGCCAATTTCAACACCAACACA
Long Flanking Sequence:
AACTTGTGGATGGAAAGCGTGAGGAGCCTGATCCTGATAGATTTTTGTACGATGTGTACCTGTGTTTCAGTTCTAAAGACATGAAGTGGGTAGAAAGAGCGTTGTTGAAGAGGCTGGACTCTCAGTTTTCAGAGCACAACACACTCCGCTGCTGCTTCGAGGAGCGAGACTTCATCCCCGGGGAGGACCATCTTACCAATATGAGAAGTGCCATCCAGAATAGTCGAAAAACCATTTGCGTGGTGTCTGAACACTTCCTGAAGGACGGCTGGTGTCTAGAAACATTCACCCTGGCACAAAAAAGGATGCAAGCAGAGCTTGAGGACATTCTGGTGGTGCTTGTTGTAGGAAACATACCGCAGTACAGGTTACTGAAGTACAAACAAGTGAGATCCTTCATTGAGAACAGAAGTTACCTCGTGTGGCCTGATGACTGTCAAGACTTGGAGTGGTTTTATGACCAACTTCTGCACAAGATAAGAAAAGATATCAAGATTAAT[C/T]AAACGACCAAAGAAATAAAGCGTGAGGAAGCCAATTTCAACACCAACACAGCAGTATAATCATGGTAGACTTATTATACATTTAGTATGTTTTTCATTACAGTTTTAGAATTTACCTACACTGTAAACCATAATGTTGTCTTTACTTAAACAAATCAAGTAAAGTTGACTGAACATTACTAAAAATTTAGCATTTTGATCATGTCACCTAAAAATACAAATTAATTTAACTTATATACCATGAAAATGCATAAACTTAAGATTTCAAGTATACTAAGCTCAAAATCACAAATAATCCTTTGAAAAATAAGGTTGTTTTTAATGTAGTCTTGACTGTAATTCTAATATGTGCAATTTTTTAATGCAAGTTCTTTTTTTAAATTAGAAAACAAGGCTTTATGTATTATTATTCACCATAAAAGGAATAAATGGTTACTTATTTTTCTTTTAAGCATTTTTTTCATAGTGTATAATTACACACACAGAACTGATCAATTTAAG
Associated Phenotype:
Not determined