Busch Lab

ZMP

tlr7

Ensembl ID:
ENSDARG00000068812
ZFIN ID:
ZDB-GENE-040219-11
Description:
Toll-like receptor 7 [Source:UniProtKB/TrEMBL;Acc:Q6TQH6]
Human Orthologue:
TLR7
Human Description:
toll-like receptor 7 [Source:HGNC Symbol;Acc:15631]
Mouse Orthologue:
Tlr7
Mouse Description:
toll-like receptor 7 Gene [Source:MGI Symbol;Acc:MGI:2176882]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa11566 Nonsense Available for shipment Available now
sa31752 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa11566
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
ENSDART00000130393 Nonsense 952 1051 1 1
Genomic Location (Zv9):
Chromosome 9 (position 56166535)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 54580919
GRCz11 9 54146832
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGATTGGGTTCCTGGATGTCCACTTATTGAGMATCTTTCCCAAAGTATA[C/T]AGTTGAGCCAGCGTACGGTTTTCATCCTGACTGAGAGGTATATAAGGAGC
Long Flanking Sequence:
ACAACAACATGTTTGTGTGTTCCTGCAATGCAACCTGGTTGGTCCGATGGATCAACCGCACCTCTGTAAATATCCCGCGACTTGCATCAGATGTTACCTGTGCTTCCCCCAGTGCTCAAAAGGGCCAAAGTGTAATTTTCCTCAACCTCCAAGCATGCCAACACAACTCCCTATCCATCATACTCTGTATTTTCCAAACCACTCTGATTTTAACCATCCTAACCCTCACCATCTCCAGCCATCTCTTCCTATGGGATGTTTGGTACATCTACCACTTCTGTCTGGCCAAACTCAAGGGATACCGTCGATTATCCTCCAACAGCGCTGTCTACGATGCTTTTGTGATCTACGATACGACAGATCCTGCAGTTCAAGAGTGGGTCATGCAAGAGCTAAGAGTCCACCTAGAGGACAAGGGTGATCCCAGGATGAACCTTTGTTTGGAGGAACGGGATTGGGTTCCTGGATGTCCACTTATTGAGAATCTTTCCCAAAGTATA[C/T]AGTTGAGCCAGCGTACGGTTTTCATCCTGACTGAGAGGTATATAAGGAGCGGGAGTTTCAGGACAGCCTTTTATTTGGCCCACCAGAGACTCATGGATGAGAGGAATGATGTTATCGTACTCATTTTCTTGGAGAGAATGCCTTGTCACTCCAAATATCTCAGACTGAGGAAGAGGTTGTATAAAAAGTCAGTTTTGGAGTGGCCAAGGAACCCACAGGCACAAAGGTACTTTTGGTTCAGTCTCAGAAGCCTAATGGCCACTGAGAGTCAATATAATACACTCTTCCAGGAGACTCTGTGATCAGGACACTTAAACACTTAAAGTGCTGATTTTTATTAAGCCAAAATGTACAAAAGAAGCTGTAAAATGTCCTAAGCATGCCAACACAACTCCCTATCCATCATACTCTGTATTTTCAAATGAGTCTGATTTTAACCATCCTAACCCTCACCATCTCCAGCCATCTCTGCCTATGGGATATTTAGTACATCTACCACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31752
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
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130393 Nonsense 1019 1051 1 1
Genomic Location (Zv9):
Chromosome 9 (position 56166737)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 54581121
GRCz11 9 54147034
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAATATCTCAGACTGAGGAAGAGGTTGTATAAAAAGTCAGTTTTGGAGT[G/A]GCCAAGGAACCCACAGGCACAAAGGTACTTTTGGTTCAGTCTCAGAAGCC
Long Flanking Sequence:
TCTGATTTTAACCATCCTAACCCTCACCATCTCCAGCCATCTCTTCCTATGGGATGTTTGGTACATCTACCACTTCTGTCTGGCCAAACTCAAGGGATACCGTCGATTATCCTCCAACAGCGCTGTCTACGATGCTTTTGTGATCTACGATACGACAGATCCTGCAGTTCAAGAGTGGGTCATGCAAGAGCTAAGAGTCCACCTAGAGGACAAGGGTGATCCCAGGATGAACCTTTGTTTGGAGGAACGGGATTGGGTTCCTGGATGTCCACTTATTGAGAATCTTTCCCAAAGTATACAGTTGAGCCAGCGTACGGTTTTCATCCTGACTGAGAGGTATATAAGGAGCGGGAGTTTCAGGACAGCCTTTTATTTGGCCCACCAGAGACTCATGGATGAGAGGAATGATGTTATCGTACTCATTTTCTTGGAGAGAATGCCTTGTCACTCCAAATATCTCAGACTGAGGAAGAGGTTGTATAAAAAGTCAGTTTTGGAGT[G/A]GCCAAGGAACCCACAGGCACAAAGGTACTTTTGGTTCAGTCTCAGAAGCCTAATGGCCACTGAGAGTCAATATAATACACTCTTCCAGGAGACTCTGTGATCAGGACACTTAAACACTTAAAGTGCTGATTTTTATTAAGCCAAAATGTACAAAAGAAGCTGTAAAATGTCCTAAGCATGCCAACACAACTCCCTATCCATCATACTCTGTATTTTCAAATGAGTCTGATTTTAACCATCCTAACCCTCACCATCTCCAGCCATCTCTGCCTATGGGATATTTAGTACATCTACCACTTTTATCTGGCCAAACTTGAGGGATACCACTGATTATCATTTAGCAGCACCATCTATGATGCTTTTCTAATCTACAATACGACTGATCCTGCAGTTCAAGAGTGGATCATGCAAGAGCAAAAGGTCCACCTGGAGAACAAGGGTGATCCCAGGATGATCCTTTGTTTGGAAGAGCGGGATTGGATTCTTGGATGTCGACTTAT
Associated Phenotype:
Not determined