ZMP
aip
Ensembl ID:
ZFIN ID:
Description:
aryl hydrocarbon receptor interacting protein [Source:RefSeq peptide;Acc:NP_999877]
Human Orthologue:
AIP
Human Description:
aryl hydrocarbon receptor interacting protein [Source:HGNC Symbol;Acc:358]
Mouse Orthologue:
Aip
Mouse Description:
aryl-hydrocarbon receptor-interacting protein Gene [Source:MGI Symbol;Acc:MGI:109622]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6597 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39650 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6597
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 |
|---|---|---|---|---|---|
| ENSDART00000016877 | Nonsense | 134 | 342 | 3 | 7 |
| ENSDART00000101617 | Nonsense | 134 | 342 | 3 | 7 |
The following transcripts of ENSDARG00000069699 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 40395054)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 39283751 |
| GRCz11 | 1 | 40001824 |
KASP Assay ID:
554-4644.1 (used for ordering genotyping assays)
KASP Sequence:
AGGACAGAGACACTGCTGCGGGATCGCTCAGGTTCACTCGCATCACTCTT[T/A]AGGTCACCATGATCTGGATAAGTTGCAGTCCAATCCTCAGCCTCTGATAT
Long Flanking Sequence:
GATGTATATTCATAGATTATTTTGACCTGATGATCTGAACACAAAACATAGAACATTTTTAAATGTACACATCTTAAAAACAATGGTTAAAAAAGATGTTTATATTGACAGTCATAAAGCTTTATCAGACTTTATTTACTTTCTAAAAATTCTGTAATGTTTGTAAAGTTCTACATGTCTCTTTCTCAAACAAATGTATTTAAATGTATTATGATGTATACAAAGATATTCTATATGTGTTTTATCTGAAACGTTCTATTCTTTGGTTTTTAATTATATAAATATCACTGTTAATAGGAAACTAGATTATATAAATGTGTATTTCCACAGCATGTGTTTATCGTGTCAGTACTGATTTTTGTTTGTGTTTGTACTGTAACAGCACACAGCTCTCTACCCTCTGGTTTCTCTGTCACTACGAAACATCAGCCAAGGAAAAGACCCGCTGGAAGGACAGAGACACTGCTGCGGGATCGCTCAGGTTCACTCGCATCACTCTT[T/A]AGGTCACCATGATCTGGATAAGTTGCAGTCCAATCCTCAGCCTCTGATATTTACCCTGGAATTGCTACAGGTGAGAAACAATTACGTCATATCTTTTGTATTTTTCATGAGTGAGATGATAAACATACTTACCTCAATTACAAAGTAGCTTTTGGTGATTACTTGAAGCTTTTTATGATGTCTTTCTGTTTCCTTCATCCAGGTCTTGTCTCCTGGCTCCTACCAGCAGGAAATATGGGCAATGACAGATGATGAGAAACTGGGGGCCATACCTCAGATCCATGAGGAAGGAAACGCACTCTTCAAGAGTGGAGATATTTCAGGAGCTGCTGAGAAATACTATAACGCCATCGCCTGTCTGAAGAGCTTACAGATGAAGGTAAGCTGAGAGGGACGTTTCCACATTAAATATTGCATTTTAAAATACTGATTTATTTTAACATCTTCACACACCTGCAGTGTTTCCAAAAAAAGAGTTTCCAAAAAAGAGTTATCAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39650
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000016877 | Essential Splice Site | 216 | 342 | 4 | 7 |
| ENSDART00000101617 | Essential Splice Site | 216 | 342 | 4 | 7 |
The following transcripts of ENSDARG00000069699 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 40395434)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAGAAATACTATAACGCCATCGCCTGTCTGAAGAGCTTACAGATGAAG[G/A]TAAGCTGAGAGGGACGTTTCCACATTAAATATTGCATTTTAAAATACTGA
Long Flanking Sequence:
AGCACACAGCTCTCTACCCTCTGGTTTCTCTGTCACTACGAAACATCAGCCAAGGAAAAGACCCGCTGGAAGGACAGAGACACTGCTGCGGGATCGCTCAGGTTCACTCGCATCACTCTTTAGGTCACCATGATCTGGATAAGTTGCAGTCCAATCCTCAGCCTCTGATATTTACCCTGGAATTGCTACAGGTGAGAAACAATTACGTCATATCTTTTGTATTTTTCATGAGTGAGATGATAAACATACTTACCTCAATTACAAAGTAGCTTTTGGTGATTACTTGAAGCTTTTTATGATGTCTTTCTGTTTCCTTCATCCAGGTCTTGTCTCCTGGCTCCTACCAGCAGGAAATATGGGCAATGACAGATGATGAGAAACTGGGGGCCATACCTCAGATCCATGAGGAAGGAAACGCACTCTTCAAGAGTGGAGATATTTCAGGAGCTGCTGAGAAATACTATAACGCCATCGCCTGTCTGAAGAGCTTACAGATGAAG[G/A]TAAGCTGAGAGGGACGTTTCCACATTAAATATTGCATTTTAAAATACTGATTTATTTTAACATCTTCACACACCTGCAGTGTTTCCAAAAAAAGAGTTTCCAAAAAAGAGTTATCAATATGCAAAAATCAAGAAAATCTTTGGATTTGTTTGATTCATGGATTATGTTGGCTATTTTAAAAATTGATATTATATAAGAACTATTGATAACTGTAATTTTTCAATTGGAAAAAAGGTTGGTTTTGCACTAAATTATCAAAACTATAGTCTGTTTGTTGAGTTTATGATGCAGATTCAGGACAGAGGCTATCAGCATCAGCACTGGTTTGGCAACAACTCGTCTGTATCAAACAATATTCTTTCATCTTGACCACAGCGAACGTGCTTTTCCGTTTCAAAGACGCGAGGTGCACCACACTGCCATTTTTGTTGACAAGAAAAAAAGAAGCACGGTGCTCTTTTTTTTTTGTCATTAGGAAATGACTGAATTAGCTATTGTGC
Associated Phenotype:
Not determined