ZMP
arnt2
Ensembl ID:
ZFIN ID:
Description:
Aryl hydrocarbon receptor nuclear translocator 2 [Source:UniProtKB/Swiss-Prot;Acc:Q9DG12]
Human Orthologue:
ARNT2
Human Description:
aryl-hydrocarbon receptor nuclear translocator 2 [Source:HGNC Symbol;Acc:16876]
Mouse Orthologue:
Arnt2
Mouse Description:
aryl hydrocarbon receptor nuclear translocator 2 Gene [Source:MGI Symbol;Acc:MGI:107188]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20863 | Nonsense | Available for shipment | Available now |
sa15572 | Nonsense | Available for shipment | Available now |
sa20864 | Essential Splice Site | Available for shipment | Available now |
sa11162 | Nonsense | Available for shipment | Available now |
sa20865 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20863
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 |
---|---|---|---|---|---|
ENSDART00000129575 | Nonsense | 270 | 738 | 8 | 20 |
ENSDART00000130997 | Nonsense | 119 | 586 | 3 | 15 |
The following transcripts of ENSDARG00000058449 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 11591830)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 10532182 |
GRCz11 | 7 | 10773822 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTGTTTCAGGTGTGGCAGTGCACCTTTGGATCACATCTCATTGAAT[C/T]GATTGTCCAGCATGAGAAAGAGATACAGGTATGTTTGAAAGATTCACTGA
Long Flanking Sequence:
TTCGGTTTCCCCCAAAGTCCAAAGACATGCAGTATGGGTGAATTGGGCAAACTAAATTGGCCATAATATACGAGTGTGAATGTGAGTGTGTATGGGTGTTTCCCACTACTGGTTTGTGGCTGGTAGGGCATCCGCTGTGTAAAATATATATTGGAATAGTTGGTGGTCCATTCTGCTGTGGTGGCCCCTAACAAAATAAAGGGACTAAGCTGAAGGAAAGTGAATGAATGAATGAAATTCTTAATAAAAATGTGTTAAATGCATCTGTTTTTCATTGTTTAATCTAAATCTCCTTCTTGCTGAATACGTACACAATTTTTTATTATATGTATTAACATCAGAGCCGGTCACAATTAAGTTTGGTTTTTCCATATTTTAGCTTGTAACATGAATGTATGTTTATTTTAATTTGTATTTCTTAGAGATGAGAAACTAACAATGTTTTATGTGTGTTTTGTTTCAGGTGTGGCAGTGCACCTTTGGATCACATCTCATTGAAT[C/T]GATTGTCCAGCATGAGAAAGAGATACAGGTATGTTTGAAAGATTCACTGAATCACTCAAGTCACGTATGAACTTTGGCATTAAAAAAAATGATTCACTGTACTATACGCATCACTGCATGTAATTTAGATTCTTTCAAAAAAGATTCACTGAATCTTTTTCATTACATTGTGTGATTTTGATGTGCTCAAAAATGATTCACAGAGTCATTTGCATCACATCGTCATATTATTTTGATTCTATCAAAAAAGTTCACTAAAGCACTCACGTTACTGTATAACCTTTGGTACTTAAAAAAGAAAGAAAAAAAGATTCACTGTATTATTCACATCACTGCATGTATCTTAAATTCTTTCAAAAAAGATTCACTGAATCTTTTTTATCACTTAGTGAATCAGTTTTGAGCACATTAAAACCACACGTCATTTGAATCACACCTTCTTGCTTTGTGGTTTCTAAAAAAGATTCACTGTATTATTCACATCACTGCATATTATTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15572
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 |
---|---|---|---|---|---|
ENSDART00000129575 | Nonsense | 368 | 738 | 11 | 20 |
ENSDART00000130997 | Nonsense | 217 | 586 | 6 | 15 |
The following transcripts of ENSDARG00000058449 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 11614265)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 10554617 |
GRCz11 | 7 | 10796257 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATTCCTTTCRCGCCACAATTCGGATGGCATCWTCACAKTYGTGGACCCT[C/T]GATGCATCAACGTGATTGGCTACCAACCTCAGGTCATTATCACMTTGAAA
Long Flanking Sequence:
TTATGGGTGACACCATTACATTTAATGCAATTTCAGTTAAATGCCTCTTCATGTAAAATTGCTAAACTCCTCATTTGTAAGTCGTTTAGACAAAAGAATCAGCTAAATAATTAAATGAAATGACTAAATGTCTACCCTGCCCATTCCTCAATCACACACACTCAGGGGATGGAGAATTACCCTGTTTACTTCACAGTGAAGCCACATCTTTGCATTTGAATCAAACATTACATCCATTCAGTTTAATAAATACTCTCCCACATCTTAAACCATACAGACAACTGTAACTAATGTTTTGACGATCCCATGACAGTGTTGCGCAATAAAGCATGCATCTGCTGGTTTGAGAACCAGACCATCTGTTTGTATGTAAAACTCTTCATCATCTCGTCCCTCAGGTGACCAGCTCTCCTGTTTCAATGGATATGAACGGACTTTCAGTTCCGACTGAATTCCTTTCACGCCACAATTCGGATGGCATCATCACATTCGTGGACCCT[C/T]GATGCATCAACGTGATTGGCTACCAACCTCAGGTCATTATCACCTTGAAACTTCATATTAAATGAACACCACACGTTTTTATTGAAAATATAGGCTCCTTTTACAGCTCTCCTAGAGTTAAACAGATGAGTTTTACCATTTTTTAATCCATTGAGCTGATGTTTGGGTCTGACAGGAGCACTTTTAGCTTAGCTTAGCACAATTAATTGAATCGGGTTAGACCAGGGGTGTCAAACTCAATTCCTGGAGGGCTGAAGCCCTGCACAGTTTAGTTCCAACCCTGCTCCAACACACTTACCTTTAGGTTTCAAACAAGCCTGAAGGACTAGTTTAGATCAAAATTAGTTTGATCAGGTGTGTTTAATTAGGGTTGGAACTAAACTGTGCAGAGCTGCGGCCCTTTTGGAACCGAGTTTGACACCTGTGGGTTAGACCATTAGCATCTCGTTCATAAAATGACCAAAGTGTTTAAGAAAAAAAATTTCTTAAAGCTTGACTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20864
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129575 | Essential Splice Site | 404 | 738 | 13 | 20 |
ENSDART00000130997 | Essential Splice Site | 253 | 586 | 8 | 15 |
The following transcripts of ENSDARG00000058449 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 11638530)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 10578882 |
GRCz11 | 7 | 10820522 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAATGGGGACAATAAAGTGTAAACAAACAAACAAATGTTTCTTGTGAAT[A/G]GGTGGTGAAGCTGAAAGGCCAGGTTCTCTCAGTGATGTACCGCTTCCGGA
Long Flanking Sequence:
GAATGACAAACTCTTTAGCCATATTGACTTTATTTACATCGGTGTATAATTATTCAGAGACACGGAACGGAACGAAACATACAGCATAATCATAATCGAGCGAACACGAACCAACACACAAGAGCACTCTGTAAAACAAGGCGTGCCGGTCGAATTTAAAGTCCACAGAACGAAGTCCGATTGGTCCACGAGGAAATGCCCTAATGAGGAGTGACAGGCTCAGGATCCAATCAGAAGGTATCTGGTAGAGAGAAAATAGTGGAACAAAAGGTGATAGTGCGAGACACAGAGCGAATGACAGACAAGGAGAGGGACAGCGAGAGGAGAAAAGCAAAAACAGAAAGGGTGAAAGCACAGAAATACAAACTCCCACAGACCGTAATGATGTTATTGATGTTTGTTTCAGCTCAGTGTATGCAAATGTGGGCTCACAGTCCAAGACAGATTTTCCCAATGGGGACAATAAAGTGTAAACAAACAAACAAATGTTTCTTGTGAAT[A/G]GGTGGTGAAGCTGAAAGGCCAGGTTCTCTCAGTGATGTACCGCTTCCGGATGAAGAACCGAGAGTGGATGCTCATCCGAACCAGCAGTTTCACCTTCCAGAATCCTTATTCAGACGAGATTGAGTACATCATCTGCACCAACACCAACGTCAAGTAAGTCCAACCTTCTCACTAAATGATAACATTCAAAGCAATACACAAACAGGCTCTTCTGATTGGATAGTTTGTGGATTTTGCAGGGGTCAAACATAACCTCGTGACCAATCTTGAGACATCTGGGCCTCCAGAGAAATCGATACCATTTATTTTTGTGTTTAACCATTCTGGTATAGGTGTCTGTTCGTCTGGTGTTGGAAGGATATGTTTGATTTATGCCAACATCTGTACTCTGAACTTGATGATGTACATTTAAAGCAGGTTGTATTTGCTTTGCTTTCAGAGGATCTTTAGGGATTGGCTTTTATTTATTTATTTTTTATGGTTGGTGTGTCTAAGAAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11162
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129575 | Nonsense | 524 | 738 | 16 | 20 |
ENSDART00000130997 | Nonsense | 373 | 586 | 11 | 15 |
The following transcripts of ENSDARG00000058449 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 11665279)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 10605631 |
GRCz11 | 7 | 10847271 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCTCNNNGATGATGTWTTGTGTGTKTTTATGTGTGTTCAGCTGAAAAG[A/T]ARATGATGGTTCCCTCATCCACCTCTGGCGGGCAGCAGTTGTATTCTCAG
Long Flanking Sequence:
TAAATATTGGGACATCAACAAAATTCTAACATTTTAGGCTCTATACAACAACACAATAGATTTGAAATGAAAAGACTGAAAATGAAATGAAATGAAAGACTGCAGTCTGTCAGCTTTAATTTGAGGGGATTTAAATCCAAATCAGGTGAACAATGTAGGAATTACAACAGTTTGCATATGTGCCTCTTACTTGTTAAGGGGCCAAAAGTAACGGGACAGTTGGCTTCTAAGCTGTTCGATGGTCAGGTGTGTGTTATTCCCTCATTATGCCAGTATTTTCCCAATATTTATGGACCTAACTGTATATACGTCCTCTATTTTTGTCTTTATTCTTGTCAAATCATGTAGATTGTAGTATTTGTAAAATTAGTTTATTTTACAAATTTATTGTCTCCTCTGTGTGATCCCAAAGATAAAGCTGTAATGTGATGTTTCTCTGTCATATTTGAGCTTCTCGATGATGATGTTTTGTGTGTTTTTATGTGTGTTCAGCTGAAAAG[A/T]AGATGATGGTTCCCTCATCCACCTCTGGCGGGCAGCAGTTGTATTCTCAGGGCAGCCCGTTTCAGCCAGGACACTCCGGAAAGAGCTTCAGGTACACATTCAAAATCTGTGCGGGACTGAATTTTTAGTCCCGATCCCATCAGGTTTTATTCCACACCCGACTGCTCCCGCTGTATATTCATCCTTTGTTCACCCGCTGCCCGACCCTCCCCGTTTTCTACACAACCCGACAGTTTCTGCCTAAATTTAGATCTGGTTTCCAAAATCTCACATTTAAATTAGGCACTACCAAAAGAGAGAGAGATAACAGATAAATGCGTAGGTTGTGCAAGGATTGCAGGCTAAATGTCAGTTTTGTTTGCCTCTTTGTGATGAGACATGAGTGCTGCCTTAAGCAGTGACGTTTGGTGAGGTTTGTGGTTGGTGAGGCACTACCTCTTTCAAAGTCAGATTTACAAACATATCCACTCAATATGTTTGCCAACTACAGATTGTGTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20865
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129575 | Essential Splice Site | 658 | 738 | None | 20 |
ENSDART00000130997 | Essential Splice Site | 506 | 586 | None | 15 |
The following transcripts of ENSDARG00000058449 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 11672899)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 10613251 |
GRCz11 | 7 | 10854891 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTCCGGAAACGCCTACTCCAACCTCGCCAATCGCAACACTGCTTTCGG[T/A]AAGAAAATCTGCTCATTCATTATAATACATGACTACATTGCTCATTGATA
Long Flanking Sequence:
GCGGTTTTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTATATATATATATATATATATATATATAAATATATATATATATATATATATATAACTATATATATATATATAACTATATATATATATATATATAAAACTATATATATATATATATATATATATATATATATATAACTATATATATATATTTATACATATATATATATATATATATACATACACATATAGACTGAAGCTGTGGATCTGGAGTTTAGCCTAATAGGTCTAATATGGTCTCTGTTAGATCTATGTGTTATATCTCTTCATGTCTCTTGTCGTTCCTTCAGCAGCAGATTCCCGCTCAGTCTAATAAGGCTCAATCGTCTCCATTTGGCATCGGCTCCAGTCACAGCTATCAGGCAGACCCGTCATCCTACAGCCCTCTGTCTAGCCCCGCCACCTCCTCGCCCTCCGGAAACGCCTACTCCAACCTCGCCAATCGCAACACTGCTTTCGG[T/A]AAGAAAATCTGCTCATTCATTATAATACATGACTACATTGCTCATTGATAACCATGCATTATCCAAGAAGTTACTTCCAGGAACATTAGACTCATTGAAATCCTAATTTTATTATTGTTTTTGAGAGAAATAGAAATCTAAATGCGAAATGAAATCTAATTTTCCTTTTTAATGATGGTTCTTAAATGTTTTTGTAGCATTTTAGTTTTTAATACTTACTATTTATTTAGTTTTTAATAATTTTAATACTTACTATTTCTGATTTCAAGAGATATTGGGATCTCAATGTTCAAGTTGTAAACATTTTGTTGTTTAAAATGCAAATAATCACTGTACATGAAGCTAGTACTTTTTATAAAAAAAAAATGAATGTCTGGAAGATTAATAATATTGAAACTTGTCACGTTTACTTTCATCAAAACAGCTGCAAGAAACATACTCCAATTAATGTAAAAAAAAATTACATTTTCAATGTTTGCAGAGCCTTAACTCTGGAAATG
Associated Phenotype:
Not determined