ZMP
ahr1a
Ensembl ID:
ZFIN ID:
Description:
aryl hydrocarbon receptor 1 [Source:RefSeq peptide;Acc:NP_571103]
Human Orthologue:
AHR
Human Description:
aryl hydrocarbon receptor [Source:HGNC Symbol;Acc:348]
Mouse Orthologue:
Ahr
Mouse Description:
aryl-hydrocarbon receptor Gene [Source:MGI Symbol;Acc:MGI:105043]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1410 | Nonsense | Available for shipment | Available now |
| sa28637 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16655 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1410
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 |
|---|---|---|---|---|---|
| ENSDART00000019024 | Nonsense | 179 | 807 | 5 | 11 |
| ENSDART00000049830 | Nonsense | 180 | 808 | 6 | 12 |
| ENSDART00000136461 | Nonsense | 162 | 790 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 22111742)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 20218185 |
| GRCz11 | 16 | 20024004 |
KASP Assay ID:
554-1331.1 (used for ordering genotyping assays)
KASP Sequence:
AGAGTGTGTATGAACTCATTCATACTGAAGACCGGCATGAGTTTCAGAGA[C/T]AGCTCCRCTGGGCCCTCWACCCTGGCTTTACCCCAGACTCTAGACAGCTT
Long Flanking Sequence:
TGTGCAATTTGATTGTACAGGAATCACAGGACTGACAGGAAATAGTAAATAGTGACAGCAGGTTGAAGGAAAGTAGTGGAGTAAATGTAGACACTGCTCTAACAATGTAAAATTTTTATTTCTTTAAGCATTATGCACCCCATTTGGTAGACTGTTACATTTATGCCCCTTAATTTTGTGAAATTCCAGTGAAATTGTGTGACTTTCTACACAAAAACAATTATAAAAGCACTTTCTCACTTGTGAACAGATGCTAACTTTAACTGAAATGTTTGGGTGACAAACAAAGCAAGCTCTGAAGAATTTACATAAAATAGCCTGATAATCAAGACATTTACCATATTTTTACTTCAACAGTTTCATAATTCAGTTTCCTTAATTTAATCTGGTATAGTTTCTAACTGTATTGAGCAATGGATATGTTTGTTTTGCAGTCGGATGTCATTCATCAGAGTGTGTATGAACTCATTCATACTGAAGACCGGCATGAGTTTCAGAGA[C/T]AGCTCCACTGGGCCCTCAACCCTGGCTTTACCCCAGACTCTAGACAGCTTGTGCAAGGTAGAAAATAACTAAATATCTCTCCAGACAGACCTGATCAGACCTAACCATTGTGTTTTGACAAATGAATGATTCTGTGCCCATTCCATCAACTCAAAGTATAGAAGAAGACAAATTGCAGATATGTTTGCAAGCAAAGTTTGCTTGAGTTCCAAAACATGATTTTAAGTGACCCTTTTATGTTATATTGGTTTTTATATGAGCTTTCTACAATAGTATGCATCTTAATAAACAAAAAAACTTTTATTTTTTAATAATATTTCATATTTCTTAATTTCTCGAAAATAATCCCTGTCTTGAATATATATTTATATACCAACACAATAGATTTGAAATGAAAGGAACAAGATGTGCTTTAACTGCAGACTATCAGCTTTAATCCATCATCATTGCATAATTTACACACTGCTTAAAACCACACGAGGGAGAGTAAGTGATGGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28637
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 |
|---|---|---|---|---|---|
| ENSDART00000019024 | Nonsense | 295 | 807 | 7 | 11 |
| ENSDART00000049830 | Nonsense | 296 | 808 | 8 | 12 |
| ENSDART00000136461 | Nonsense | 278 | 790 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 22107546)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 20213989 |
| GRCz11 | 16 | 20019808 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTCCATACTGGAGATACGCACCAAGAACTTAATGTTCAAAACCAAGTA[T/A]AAGCTGGATTTCACACCTATTGCGTGTGACACAAAGTAAGAAATTAGCTA
Long Flanking Sequence:
TGATGGCATAATTTGTGCCAGAGAAAATCTTCAATCTGAGGGTTCAAGTAAATCAAATTTGAGAAAATTGCCTTTAAAGATGTCTAAATAAAGTGTAATGCACAATACTAATTAAAACAATATGACATTTATAAAATATATTCAAGTAACATGATCTTTCCTTAGTATTATAATGATTTTTTAGCATGAAAGAGAAAACAATTTTAACCCTTACAAGGTATTTTTGACCATTGCTAGAGACAGTATATACATTGTGCAACGTAAGACTGATTTTATGTGGTCGAGGGTCACGTATGTTTAAATGGGTTTAACGAATGGCTTGTATTTTTATAGGCCGTGAACTTCCAGGGCCGTTTGAAGTTCTTGTATGGGCAGAATGAGAGTACAGGAGATGGCAAACGCATCCCGCCTCAGCTGGCCCTGTTTGCCCTGGCCTGCCCTCTACAGCCACCTTCCATACTGGAGATACGCACCAAGAACTTAATGTTCAAAACCAAGTA[T/A]AAGCTGGATTTCACACCTATTGCGTGTGACACAAAGTAAGAAATTAGCTAAGTATCCATCAATGATGTGTCTCAATTGTTTCGTTTTTATTGTACACTCAAAAACTGGTGTTTGCTGTTTGTTCAGTCTACTTATTTAAAGTGAGCTAAAACTCAGGTAATGTTTTCTTGTGGGTGGCAACTCAATTGTTTTGAAATCAGTTGGATTTTTTCTTCAGTGTTTGGACTTCTAACAGAAATTTTAATCACACTGAACTGAACTAAACTGAACTTGATTTTTGACAATTTTAATTTACTAAAACTTCAACGTTAAGCTGCTTTGACAGAATGTACATTGTAAAATCGCTATAGAAATAAACATTAGTTATTAGTTATTTTGTTCAATCCACTTAAATTTGAAAAAAATGTATAAGGTCATTTCATTTCTTTATATTCTTCATATGCAAATCAGTTGTATGGAACCCAGCATTTTTTACAGTGTACTTTCGTTATTTAAATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16655
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000019024 | Essential Splice Site | 391 | 807 | 9 | 11 |
| ENSDART00000049830 | Essential Splice Site | 392 | 808 | 10 | 12 |
| ENSDART00000136461 | Essential Splice Site | 374 | 790 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 22105369)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 20211812 |
| GRCz11 | 16 | 20017631 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACAAAAATGGGCARCCAGATTGCATCATCACCTCKCACAGAGTCATAAC[G/A]TATGCACTTATTTTTGTCTTTGCTATTTATTTGGGKTTTTTTTTTNNTATT
Long Flanking Sequence:
GAGATAAATGGCATCAGCACGTAATAACCTGTTATGATTATTACTGAACCGATATCGAATTGTCCTCATCTGCATCGCGGTGCACTGAAGAAACAATTAATTTTGACACCCCTAGAAAATACACTCACTCATTTATTTTCTCAAATAATGCACAATAATATACATTTTAGTGCTTAAATGTGGTTGCTTGTTTTGCAAGAAACATTGATAAATACAAATACTGTATAGATTTAAAGAGACAGTTCATGCAAAAAATAAAAAATAAATATATACTCACCCTTAAGAGCTCTGTCATTCATAATGATTACAAGACTAGTTAATTTTATTTTAATAATTTCACAATTTCTCTCCCCTGCAGTGATGAGGACCGGTAAAACTGGGTTGACTGTTTTCAGACTGTTGACTAAACAGAACCGCTGGGTTTGGGTTCAGTCCAACGGCAAACTTGTCTACAAAAATGGGCAACCAGATTGCATCATCACCTCTCACAGAGTCATAAC[G/A]TATGCACTTATTTTTGTCTTTGCTATTTATTTGGGGTTTTTTTTTATATTGAACAACCTGCAAACATTTTATTCTGTTTAATTATTAGAAATTTAACAGAATAACAACCTTTGGCAGCCTAGCCAGCGCTTGTGCTTAGTATTGTTGTGCAGGGCGGAAGTGGCTTGGCCTGCAGCAGTGTGGGCTCTAGCCATGAGAGCTACAATATCAAAATCCACATACCTTGGGTGGGGGTCTCGGCATGGAGCCCACCTCAGTGGGGAGCCCACCACCTGGGGAATGGCCTCATATCTGCTGTCGCATGAGCACAAGGATCAGGCAGAGAAAAGCACCCTCCATACCTGCAATAGCTCCTGTACCCCTGGGAAGCAGGGAATGGGGGAGCTGGGAGAATTTACTTTGTTACCCCCACATTGCACTGCTCTAGTTGGTCCCATGGCTGGACCAGCGGTGGTGATACCTCCGGACCCCCCTGTTGAAGCAGCCTTGCAAACAACAGC
Associated Phenotype:
Not determined