ZMP
ahr2
Ensembl ID:
ZFIN ID:
Description:
aryl hydrocarbon receptor 2 [Source:RefSeq peptide;Acc:NP_571339]
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 |
---|---|---|---|
sa13202 | Nonsense | Available for shipment | Available now |
sa37461 | Nonsense | Mutation detected in F1 DNA | Not yet available |
hu3335 | Nonsense | Available for shipment | Available now |
sa45759 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18313 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13202
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 |
---|---|---|---|---|---|
ENSDART00000105762 | Nonsense | 69 | 1027 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 13282759)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 13118689 |
GRCz11 | 22 | 13143466 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACCCKTCTCAGAAGACGTCCGTGCACGACTGGACAAACTGTCAGTGCTT[C/T]GACTCAGTGTMGGATACCTGAAGGTCAAGAGCTTCTTCAATGGTGAGATT
Long Flanking Sequence:
ACTGGTGAAGTTTCATTCATTGCTACTGGCTTGCTTAGTTTGGGACTTGTGGAGCTGCGCTTCGATGGATTTATTCTGCAGTGTTTGGACTTTCTGCAGTTAAAATTATTCCACACTGAGATGAACTAAACTGAACATTAACTCTGAAAACTGGACGAACACAGTTTCAATATACAAGAACGTCTATGCAATCTACATTGTAAAAATGCTATGGAAATAAACGTGAATTGAATTGAACCTTCGTTCATTTATATTTGTAAAACAACGAAACACCACTAGACTTGTTACTGTCAAACATGCCACTTATGGTCCATAACAAGCAGACTAACCCAAAATTTCTCTCCTTTCCCTCCAGACCCAAACCACCACCCCCTGATGGTGTGAAATCCAACCCCTCCAAACGGCACAGAGACCGGCTGAACAGCGAATTAGACAAACTGACCAACCTTCTACCCTTCTCAGAAGACGTCCGTGCACGACTGGACAAACTGTCAGTGCTT[C/T]GACTCAGTGTCGGATACCTGAAGGTCAAGAGCTTCTTCAATGGTGAGATTATTACTTTATTTTATCTTGCGTTCTGATTGCTTTTCTTTTTTTTTGGCGCCGTTGTCCTGTGGCTGCCGACGCATCATCCAAGTGTATACTTCACTCTGGTCATGATGTGGAGAGACCCCCCTTATGATTGGGTGTATGGCCATACACGATAGATGTGCTATATAAATACACCCATCACATTACATTTAAATTTTATCATTCCAAAAGTTACATAAAATTACAATTACAGCTGTTGTTTTGTCTTTAAAGGCAGTTTTGTTACAAGCGAAACATGATGTAAAATCTTGAGAAAAAACAAGTTCTGTACCACTGACACAAAATACAGTGAAGTGAGGACAGGAAATGATGTAGAGAATGAGGAACAGAATCAGGAGATGTCAAAAGCATGATTGAAACTCGTGTTACCACATAATCTTTCTGAGAAATTTTAGCAAAACTGATACATTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37461
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 |
---|---|---|---|---|---|
ENSDART00000105762 | Nonsense | 228 | 1027 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 13192810)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 13028740 |
GRCz11 | 22 | 13053517 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACACATCCCTCCAGAAAACTCTTCTTTCCTGGAACGAAGTTTCTGTTGC[C/T]GATTCAGATGCCTCCTTGACAACTCGTCAGGCTTCCTGGTAAACATCCTA
Long Flanking Sequence:
CTGTCTTTACAGTCGGATGTGGTCCACCAGAGTGTATTTGAGCTCATCCATACAGATGATCGGGCAATGTTTCGAAGGCAACTACACTTCGCTCTCAATCCCTCAAGTGACAGTGCTGATGGATCTGAGGGTTAGTAGCAACTCTATCCCTAACACTAATGTGCAAATAGGGTCAGTGAGTTCCTGGTAATGTGTTGTCAACTTGTACTGCAATGCCCAGCCCTGAATGTTTTGTGAATGAGCAGACTTCTGTGGAGAATAAGACAGCTGTGGGAGGATCAGTTCAGATTTATTAAATGGAGCCTTGTATAAACCAGGGATGATGAATATGGGTTGTGATTCATAGCCGATGACATCACTGTTTTTCTCTTTTGCTTGGCACAACCGATTGGTCTCCAGCAATGCAGAGCAGCAGTGATATCACCAGGGACATGGTCAACTACAACCCTCAACACATCCCTCCAGAAAACTCTTCTTTCCTGGAACGAAGTTTCTGTTGC[C/T]GATTCAGATGCCTCCTTGACAACTCGTCAGGCTTCCTGGTAAACATCCTAATCGATATTGTAGAGTTAATTTTGGGACAAATCCTTTGCACTAGACTCAGTATTTGTTTCTCTGCATAAAACATATTGCAGCAACAGCTGTATAAATAAATCTGTTGTTGATTGTTTACTCTCAGTGTCAGACCCTCATGGGTCTAAATATGAATTTCATGTCCTTTCTTTTGTCCCTAAGGCCCTGAACTTCCAGGGGAGGCTGAAATATCTCCATGGGCAAAACAAGTTGGCAGAAGATGGGACTTTGGCTCACCCTCAGCTGGCTCTTTTTATCATTGCTACACCCCTCCAGCCACCCTCGATCTTGGAGATCAGGAGTAAAACTCTCCTCTTCCAAACAAAACACAAGCTGGACTTCACACCCATGGGTATCGACACAAGGTAGCTTTCCTTTTAAAGACAGAATCAGATTGTGCCAAACATTTATTTTAACACACAATGTTAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu3335
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 |
---|---|---|---|---|---|
ENSDART00000105762 | Nonsense | 534 | 1027 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 13191368)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 13027298 |
GRCz11 | 22 | 13052075 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGATTATCGAGGTCGGCAATAATTGCAACAGCCTTGAAGATTTTAATT[T/A]GGACAGGATGGAGCTGAAGGAGTGGGAGAACACTCTGTGCAGGATGAACT
Long Flanking Sequence:
AACCTGATTCTAATGATGTCATTGTTAATCTAATCTTTTGGTATGTCTAATTAATGTAATGCCTGTATTTTATAGTAATGAGGAGGGTGAGGAACATCTCCGTCAAAGGAAGTTGCAGCTACCATTTAACTGCGCCACTGGTGAGGGTGTCTTGTATGAGGTTGGTCCCACACTGGATGTTGCTGAGATTCAAAATCAGAGCAAAGGCCAGAAAATGCTCAATCCTCCATCTCTGGACCCAGATTCTCTTCTCGGCTCCATGCTGAAACAGGACCATTCTCTTTACAGCCAGAATAATGACCCCAATTCCCAGTTTACCATTGACAAAGCGTTTGGGGATAGCCACGCCCTGCTCAATGTCCCTGGGAACACCTGGCAGCCGTCAACCCCAAACACTGTGCCTGGGATAAAGGAGGAAGCTGTAGTAAAAGACATGTTAGAAACCTTGCAGCAGATTATCGAGGTCGGCAATAATTGCAACAGCCTTGAAGATTTTAATT[T/A]GGACAGGATGGAGCTGAAGGAGTGGGAGAACACTCTGTGCAGGATGAACTACAACAACGATATGGAAATTAACGAAATCATCACAGAAGACATCTTCTCTTATGTGGAGGATGTTCTTTTCAAAGAAAATGGCATTCAACCACTGAAGGACCTTGGTCCATTTTCAGAAATGTCTGAGGGTCTATCAGAGTTGGAGTTGCAGAATAACTTGGCTGCTAACCAGGAATTCAGCTGCCAGGCAGGGGTGCATGGTGGATCTCCAGGTCAGGGTGGATTCATCGGAATGAACATCCAAGAGGGAATGGATACTAGTAGTCCTGGAAGAGGGACGGTGAAGCTCTCCCATATGGGGCCGCAGATGCTACCTGGGAACAATTTCATCCAATCATTTGGACTAGATCAGACAACCCAAAAGATGGCCGGCAACAGTAACATTTTGTTTAGGCCTTCTCTTGCCATGCAGCAGAGTCAGCAGCCAAACCAAATCAATCTTGGCCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45759
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105762 | Nonsense | 543 | 1027 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 13191342)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 13027272 |
GRCz11 | 22 | 13052049 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAACAGCCTTGAAGATTTTAATTTGGACAGGATGGAGCTGAAGGAGTGG[G/T]AGAACACTCTGTGCAGGATGAACTACAACAACGATATGGAAATTAACGAA
Long Flanking Sequence:
AATCTAATCTTTTGGTATGTCTAATTAATGTAATGCCTGTATTTTATAGTAATGAGGAGGGTGAGGAACATCTCCGTCAAAGGAAGTTGCAGCTACCATTTAACTGCGCCACTGGTGAGGGTGTCTTGTATGAGGTTGGTCCCACACTGGATGTTGCTGAGATTCAAAATCAGAGCAAAGGCCAGAAAATGCTCAATCCTCCATCTCTGGACCCAGATTCTCTTCTCGGCTCCATGCTGAAACAGGACCATTCTCTTTACAGCCAGAATAATGACCCCAATTCCCAGTTTACCATTGACAAAGCGTTTGGGGATAGCCACGCCCTGCTCAATGTCCCTGGGAACACCTGGCAGCCGTCAACCCCAAACACTGTGCCTGGGATAAAGGAGGAAGCTGTAGTAAAAGACATGTTAGAAACCTTGCAGCAGATTATCGAGGTCGGCAATAATTGCAACAGCCTTGAAGATTTTAATTTGGACAGGATGGAGCTGAAGGAGTGG[G/T]AGAACACTCTGTGCAGGATGAACTACAACAACGATATGGAAATTAACGAAATCATCACAGAAGACATCTTCTCTTATGTGGAGGATGTTCTTTTCAAAGAAAATGGCATTCAACCACTGAAGGACCTTGGTCCATTTTCAGAAATGTCTGAGGGTCTATCAGAGTTGGAGTTGCAGAATAACTTGGCTGCTAACCAGGAATTCAGCTGCCAGGCAGGGGTGCATGGTGGATCTCCAGGTCAGGGTGGATTCATCGGAATGAACATCCAAGAGGGAATGGATACTAGTAGTCCTGGAAGAGGGACGGTGAAGCTCTCCCATATGGGGCCGCAGATGCTACCTGGGAACAATTTCATCCAATCATTTGGACTAGATCAGACAACCCAAAAGATGGCCGGCAACAGTAACATTTTGTTTAGGCCTTCTCTTGCCATGCAGCAGAGTCAGCAGCCAAACCAAATCAATCTTGGCCTGCAAGGTGTTGTGCAAGAGAATGGTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18313
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 |
---|---|---|---|---|---|
ENSDART00000105762 | Nonsense | 984 | 1027 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 13190017)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 13025947 |
GRCz11 | 22 | 13050724 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCAACTACCACTTGGATTACCTCCAGATAACATAATTTCTCAGCAGTA[T/A]CTCTCCTGCAATASCCAGACACAGGTAAACTGTACTAATATGATCCATGG
Long Flanking Sequence:
GGCTGGCAGCAATCCCAAACTACCCCTCAGGGAGTCCCCACATCATTTTCCGGCGGGCATCAGCCGGGTTTCATCAGCCAAGTTACAGACTTCCAAAGAGGCACACTTAATCAAATGATGCCGCACACAAACGGACAAGGAATCGGATCTGGCTTCTTGCCCCAGACATCTGCAAGTGCCATTTATCCTCAGCAAGGTGATTTCATCAACAACAGCCCTCAAAAGACTTCTACCAGTTGCATGTTCATGAACAACGCTCAACCCTCTGTGAACGGAATGCAGTATGGTTCTGCCAATCTGGTATCTGGGATGTCATCCTGCCAAGGGACTAAAGGTCTGCTTACCCAGAGCCCTACACAAGCATCCTGCTACTTCCAGAGAGGTCCCAGTGAGACCATTGTGGGCACAGCGGTCATCCCACAAGAGGACAACAACATTAGCCCCATGGCTTGTCAACTACCACTTGGATTACCTCCAGATAACATAATTTCTCAGCAGTA[T/A]CTCTCCTGCAATAGCCAGACACAGGTAAACTGTACTAATATGATCCATGGTGTAATTATAACTTCAGATCATTATTTGCTAGCTCGATGATCAAAGCACCAGGTGTGTGCTCACTCCCTATTTTTAGATTAGGTCTTTAAGTTTGTTGAGAGTAGCAGAACTGCCCTGTTCCTACCCCAGGCTCAATGTGTCATGCCACAATCAAGGCTTTTGAAAGATTGAGTTATCTCAACTTTACCTTTCACAGTGTGTTATTTACGTGAAAGACAAGCTCTCGAATTTTGTATCTTATAATTTTGTAAATTATACAGACTCAGAGCCGGTTTTCAAATTGTTTGGTTATTATTCAGTTCGTCTTCAATGAGATCAGTTCTTTTAAAAGTGAATTCCTACAGTTCTCACAGAAAGTACTAAACCCTGAATTGTAAATTAAGCCGTCAAAACAGTTTGTCAGTAACCAAAGGCTGGACACAAAGACTTGGAGAGAAAGTTCTGCTTTA
Associated Phenotype:
Not determined