ZMP
ahr1b
Ensembl ID:
ZFIN ID:
Description:
aryl hydrocarbon receptor [Source:RefSeq peptide;Acc:NP_001019987]
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 |
---|---|---|---|
sa32390 | Essential Splice Site | Available for shipment | Available now |
sa37460 | Essential Splice Site | Available for shipment | Available now |
sa37459 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa188 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa32390
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028787 | Essential Splice Site | 232 | 940 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 13126176)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 12962106 |
GRCz11 | 22 | 12986883 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTTGTGTGTCGTTTCCGATGCCTCCTAGACAATTCCTCAGGATTCCTG[G/T]TCAGTGTCAACAAGCTATGCTAAGCTAAAGTATCCATTTTGCTATTAACT
Long Flanking Sequence:
TAGGTAGTGAGAGCATAAGAGAAGAAGTATGTGTTTTGTGGTTTGACCTTTAGTGGAAACTCCTGGAGTTGCAAAATAATTGTTATGGTCACTAAAATGTCTATTTTAATTAAGCATAACAGCAAACAGAAATGATGGTCAGTGGATAATTCATCTTCGTCTTCTGAAGGGCAAGTTATTTGTTATAGAAGTCCCACTGTGACTTTTCCAACCACAGCAAATTCCATTTTTCTTTTTGATATTTGTCCCCTCTTGATATTTGTTCACATCTTTGAATGGAAACACAGCTAATGAGCCATTGTTGAAAAAAAATCAAGACATGCTACCAATGTCTGCTTTCTCTCTTCTTCTGTTTTCTTTTCCTAGATGGAGATCCTGCCCCAAATATGTCTCTTGTGTTGTGCAACCCAGACCAGCTGCCTCCCGAAAACTCTTCTTTCCTGGAAAGAAACTTTGTGTGTCGTTTCCGATGCCTCCTAGACAATTCCTCAGGATTCCTG[G/T]TCAGTGTCAACAAGCTATGCTAAGCTAAAGTATCCATTTTGCTATTAACTGCCAACAAAGTTGCCTACTTAGGAATGTCATACATTTGACTGATTTGATATTACAATGGGTTGAAATATATCTGGCTATTCAGAGTCCCTAAGCCCTAACGTTCCAGATTACAGAACGAGTTAGCATCTGGGTTAGTGCAGGTTAGCGGATTGTAGCCATAGATTTGAGAATTGTTGGAACACCTCTGTAATCCCTCTTAAAGGAGCAATAAGGTCATGGGGAAAAGGTTTTAATTTGTGCTTGAAGAAACACATGAAAATGGTGAGAAGAATGAGACGTTAAGCTATCATTTCAAATTAGCCAGGTTAGCCTAAAATCAAAGCTAATTGGAGGAAAGTCAGGCTTCAGCTATAGAAACAACAGTGAATACTGATGTTTCCAGCAGGCTTTGTTCCTAAAGTATTCCTTTTCCCCACAAGTCTCTTTCTGTGCTAATCTTGGCATTGCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37460
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028787 | Essential Splice Site | 233 | 940 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 13124787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 12960717 |
GRCz11 | 22 | 12985494 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTTTTGTATATTGATATTCCAGTAATTGTTTGTACTTGTATTCTTGA[A/T]GGCTTTGAATTTTCAAGGACGTCTGAAATTCCTGCATGGGCAAAACAGGC
Long Flanking Sequence:
ATGAAATCTAATGCTAATTTGTGTGTTTGTGTACAAGTATGTGTGTCAGTGGTTTAATATGCCGTGAAGTCATTGACAAACTGAGACATTTGTTGTGTGGCCTTACATAAGTAGAACTATTTTAAACAGGCCTTGCACAAGGCGCCATGTAATTCCACATATGACACACTCTGACTAGCTTGCACTGCGTTTGTTAATAGATGACCTGACATGAGCTCTGTGGCCCACATTGAGTCAGAGACAAATGATGTGGTTTGCCAAAAGCACAGAAACAAAATCATCAGCTCCAGCTGTATATGTATTTATTCTACGTGTATCAGTTGTGTACGTCTTTCATGCAAATGTATTGACATGTATTTTATTTGCTCCTTTTGTTAGAGTTGCCAAGATTTACGTTTATTTAAATTTACAGTCCAAATAAACTCTGGTTTGGAATTGCTTTCAATGCTTTCCTTTTTGTATATTGATATTCCAGTAATTGTTTGTACTTGTATTCTTGA[A/T]GGCTTTGAATTTTCAAGGACGTCTGAAATTCCTGCATGGGCAAAACAGGCGATTGGATGATGGAGGCCAAATGCCACCCCAGCTTGCCCTGTTTGCCATTGCGACGCCCCTACAGCCTCCTTCCATAATGGAGATTCGAACCAAGAACATGATATTCAGAACCAAACACAAGTTGGATTTCACCCCAATGGCCTGCGATGCAAAGTAATCATGGACGACTGTGTTGATTAAAACAATAAGACGTTATATATGTTCATCTGTACAATATAATATGGTACAAACATCAGCGATGTTGTTCTGCCTGTTTTTTAGGGGTAAAATAGTTCTTGGCTACACAGAGGCGGAACTGCGAGTTCGAGGTTCAGGGTACCAGTTCATCCATGCAGCTGATATGCTCTACTGTGCTGAGAACCATGTCAGGAGTAAGATTTTCAGATTTCTTATTAAAGGTGTTAAATGTTTTAAAGTTGCCCACTTTAGACTACTTCCATAAATCGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37459
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028787 | Essential Splice Site | 300 | 940 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 13124476)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 12960406 |
GRCz11 | 22 | 12985183 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAATATAATATGGTACAAACATCAGCGATGTTGTTCTGCCTGTTTTTT[A/C]GGGGTAAAATAGTTCTTGGCTACACAGAGGCGGAACTGCGAGTTCGAGGT
Long Flanking Sequence:
GTGTATCAGTTGTGTACGTCTTTCATGCAAATGTATTGACATGTATTTTATTTGCTCCTTTTGTTAGAGTTGCCAAGATTTACGTTTATTTAAATTTACAGTCCAAATAAACTCTGGTTTGGAATTGCTTTCAATGCTTTCCTTTTTGTATATTGATATTCCAGTAATTGTTTGTACTTGTATTCTTGAAGGCTTTGAATTTTCAAGGACGTCTGAAATTCCTGCATGGGCAAAACAGGCGATTGGATGATGGAGGCCAAATGCCACCCCAGCTTGCCCTGTTTGCCATTGCGACGCCCCTACAGCCTCCTTCCATAATGGAGATTCGAACCAAGAACATGATATTCAGAACCAAACACAAGTTGGATTTCACCCCAATGGCCTGCGATGCAAAGTAATCATGGACGACTGTGTTGATTAAAACAATAAGACGTTATATATGTTCATCTGTACAATATAATATGGTACAAACATCAGCGATGTTGTTCTGCCTGTTTTTT[A/C]GGGGTAAAATAGTTCTTGGCTACACAGAGGCGGAACTGCGAGTTCGAGGTTCAGGGTACCAGTTCATCCATGCAGCTGATATGCTCTACTGTGCTGAGAACCATGTCAGGAGTAAGATTTTCAGATTTCTTATTAAAGGTGTTAAATGTTTTAAAGTTGCCCACTTTAGACTACTTCCATAAATCGTCAAAATCCCATTTGACGCTATTACATTTGTAGTGTAGAAGCTATTATTGTTCAAATAGCCACAAAAGGCCACCCACTATCAACATACTGACCTAAAACATTAAGAAAGTGTACCAGTACTAGGTTTTCGTACTTTGCTGTGTTGTTCCAAAATTCCTGGATTACGATCAAAACCATAGCTGCCATCCATAGTCTTTTGTTTGTTAGCTTTCCTGCTTGCCTGTAAGTTGCGTAACATGGAGACATTCATTCAGTAGCACTTACGCACAGTGAATGTTTCCGAGAAAATTATGTGAAACAGGGTGAGAGAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa188
Status:
F2 line generated
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028787 | Nonsense | 368 | 940 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 13123409)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 12959339 |
GRCz11 | 22 | 12984116 |
KASP Assay ID:
554-1011.1 (used for ordering genotyping assays)
KASP Sequence:
ACAAAGGACAACCGTTGGAAATGGGTACAAGCTAATGCTAGACTTGTCTA[C/A]AAAAATGGCAAGCCTGACTACATCATTGCCACCCAGAGGCCACTTGTGTA
Long Flanking Sequence:
ACATTGGACTTTTTTGGCAAAAAAAAAACATTAGCCCTGTTCATTTTGGCAAATAATGTCAGTTTTCTCATTCAGTGTGGTTAGCAGGAGGCAATCCATAGATGTTATAGGAAAAAAGTACATTGCTTATAATGTCAGAAAGGAGACAGACAGATGAGCTAAACACAGGAGAAGGAATTCTTTCCTGTAATCCTATAGATTATGGATGAGATTGGATAAATCCTTGATGTTATGACTAGAGAAGACATGTGAACTAGAGCAGTAAATCCATATCAGTAATTTAATATGGAACCAAAAGCCCGTAGCAGAAAAAAAGGTACAATGCAAAAAAAAATAAAAATAAAAAACTGTTCTATATATTTAAGTCAATAAATGTGATTACAAATTGTTGCATTGTCCATTGCAGTGATCAAGACTGGAGAGAGTGGTCTGACTGTTTTTAGACTGCTTACAAAGGACAACCGTTGGAAATGGGTACAAGCTAATGCTAGACTTGTCTA[C/A]AAAAATGGCAAGCCTGACTACATCATTGCCACCCAGAGGCCACTTGTGTAAGTATATCATCCTACTGTCTTACATTCTTTACGTAGCTTTGCAATTTAGCTTGATTTTGATGAAAGACATTTCTTTTATTTGTTCATACAGAGAAGAAGAGGGTGGAGAGCACTTGAGGAAACGATCTATGCATCTTCCATTCACCTTTGCTACTGGAGAAGCTCTGCTGTACCAAATCAACTACCCCATGTTGGGCTTCCCCGACACCCTTCAGGACAAAGGCAAGAACAACAAAACCAAAAAGAGCAAGGTGAACAAAAGCTCAAAGGACGATCTGGATCCAAGTTCCTTACTGGGAGCCATGATGAGACAGGACGAGTCTGTTTATGTTTGCCAGCCAGCTATGGAGCCTAGAATGTCATTCCACAGTAGCCTCTTTGGTGAGCAAGGAGAGACTAGCACTTTCTCTTCTTCTGCTGAGAATGAAAGTTGGAATCCAGTGCAGAATG
Associated Phenotype:
Not determined