ZMP
ahi1
Ensembl ID:
ZFIN IDs:
Description:
jouberin [Source:RefSeq peptide;Acc:NP_001071029]
Human Orthologue:
AHI1
Human Description:
Abelson helper integration site 1 [Source:HGNC Symbol;Acc:21575]
Mouse Orthologue:
Ahi1
Mouse Description:
Abelson helper integration site 1 Gene [Source:MGI Symbol;Acc:MGI:87971]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15936 | Nonsense | Available for shipment | Available now |
sa36321 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36320 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32121 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15936
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 |
---|---|---|---|---|---|
ENSDART00000064668 | None | 17 | 936 | 1 | 21 |
ENSDART00000130253 | Nonsense | 172 | 1190 | 3 | 26 |
Genomic Location (Zv9):
Chromosome 17 (position 8101681)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8104455 |
GRCz11 | 17 | 8261633 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGACTCGAGTCAACAGAAAGAGCAGACGGAGACAGAAGATGATTATTTA[C/T]GAGCGTACCAACATCAGATCTCACAGGAAGAAGAGACGGCGGGAAAGAAA
Long Flanking Sequence:
TTCATGCAAATATCACATCCACAATGCTGGAATTGCTCATGTAATCTTTATTTGAACCAGAAAAATGTTGCTCATTGAAAAATAATCACTGTAAATATTAACTTAATCGCGTTTTCTTTCAGCTTCAGACCTTAAAGAAGAACCTAGATTTGAGTAAAGACACTGAAGATGATGAAGCCATCCTACATAACACATACGATCCGGCTCAGGGCAGCCCTAGATACACCAAAAACAGGCGCAGGGAGAGGGAAGTATCAGAAAAGACTAACTTAAACAATGCTGTGAGTGAGGAGGAGTCCACATTGACCAGCGGGAAGAGGAAAAGCAAGAGGAAGCTCCCACAACCACCACCCAGTGTTCAAGACGCAGATGACAATGACAGAAGGACTGATGCAGAAACTGATGGAAAACCTATTAGGAGGATAAAAAAAGGGAAAAACAAAGCTGCTAATGACTCGAGTCAACAGAAAGAGCAGACGGAGACAGAAGATGATTATTTA[C/T]GAGCGTACCAACATCAGATCTCACAGGAAGAAGAGACGGCGGGAAAGAAATCGACACGAAAGAAAGCCGCAGAGAAGCTTGAGGAGAAGCAGCTGCTAAACAATGAGCTGGAGAAGAAAAAGAAGAAGGCGAAATCAAGCAAACATGATGCTGAAAGAAGGTAATACAATTATTTTAAAAAAAAGTAATATGTTGTTCTTATTATTTAAGATTGAACATTTGCAGGGCTGAAGTAAATAATGTTGTTTACATTACGTGATTATCCCTATGTAATAAAGGTAACACTTTAATTTAAGTACCAATTCCAGTTAATTATTCATTTTCCTTCGGCATAGCCCTTTATTTATCAGGGGTCGCCACAGCGGAATGAACCAGCAACTATTCCAGCATATGTTTTACGCAGTGGATGCTCTTCCAACCCCGTACTGGGAAACACCCATACACTCAGGCCAATTTAGTTTATTCAATTCACGGTTAGAAAATGCAAACTACACACAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36321
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 |
---|---|---|---|---|---|
ENSDART00000064668 | Essential Splice Site | 693 | 936 | 14 | 21 |
ENSDART00000130253 | Essential Splice Site | 922 | 1190 | 17 | 26 |
Genomic Location (Zv9):
Chromosome 17 (position 8081127)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8083901 |
GRCz11 | 17 | 8241079 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATGTCCCTGAAGATGCAGCGGGTCAAACAGAAACTAGACTCTGTGCTG[G/A]TAAAAATGGTGATTTATAGAAAATGAAGCAAAATATAATTCAGTCAATAA
Long Flanking Sequence:
ACAGCATATAACATTTAAAAGGCTCAAATGCGAATATGCAATTTCAGAAGGGTTGTAAAAACAAGTAAAGTTGCAGCGTGTCTAATGTGAGGTGGAAGTTTATTCCAGCATTTTGGAGCGATAACAGCGAAAGTCAGATCCTTTTTCCACTAACCTAACCTAACTGTCCTTGGTACAGACAGATAAGACTGATCTGATGATCGTGTCTGCATTCTCGAGTAATAAGTAACATAATTAAACTTTTTGGGTGAACTAACAATTTAAGCGGTGTTTAAAAAACAAAGGTTATATGATTTCTACCATACTCAGTGGCTCAGATGGAGGTGGAGAGTTTGCGAGGCTGGAGTCGCTCAGAGAATCTGGACAGTAAGACGGGCAGGATTTCATCAGAGTTCATGAGCATCCAGAACCCCACGGCCACCAGCATGGACCGATTTGCCAACACTGCACGCATGTCCCTGAAGATGCAGCGGGTCAAACAGAAACTAGACTCTGTGCTG[G/A]TAAAAATGGTGATTTATAGAAAATGAAGCAAAATATAATTCAGTCAATAATAGATCAGTAACACAGCCATTTTCTTACAGGAGCCTCATCGCAGTTCCTCTAATGTGGACATGTATGAGCAAGGCAAGTAATGTATATGATGTATATTTGAAATTAAAGGGATACTTCGCCTAAAAACACTGATTTGGTATAAACCTTTTTAAATTTCTTTCTTCTTTTGAACAAATATTCTGAAGAATGTTGGGGATAAAGGACACAAAAATATATATTTTCTTTTATAAATCAATGGGTGTTTTTTTTTAATCCAACATTCTTCTTTCTTTTTGTTCAACAGAAAAAGGAAACTCAAAGAGGTTTGGAACAAGTGGAGAATGAGTAAATGACAGAAATTATTATTATTTTTGGGTAATCTGTCCCTTTAAGAAAATAAGATGTGTTGGTAACACTTTATAATAACTACACACTATAAATCATTTATTAAGCATTAGGAAATAGTGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36320
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064668 | Essential Splice Site | 694 | 936 | 15 | 21 |
ENSDART00000130253 | Essential Splice Site | 948 | 1190 | 20 | 26 |
Genomic Location (Zv9):
Chromosome 17 (position 8078501)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8081275 |
GRCz11 | 17 | 8238453 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTCTGCTCTGTAATACTAAACTGAGCTCTTGTTATTGTTTTTTTTTTC[A/G]GGGCCTGAACTCATATCTTCCTCCTCCATCTCTACTGTCTCCTCACTCTA
Long Flanking Sequence:
CCCTGCCGTTATCAGTGCGCAATTAATCTTAGGAGGTTTGAGCTTGTGTCCTTCATTACCTGGAAAATACAGGGCACATTTTGAGGCTAACTTGAAGGAGCCTTTAATTTTTTTTTTTTAAATAAGAGAGCCTTCGTCGCGCCATGATGACGCAGCCCCCTTCGGAGGATGCAGCCTCTGAAATGAGACACAGCTTGTGAATCTTTTATTTGTTATTTTCTTTAAAGGTGGAATGTCTTCCTTGGGAAGGAGTATAGAGGTGAATATTACATCATTTCTACTTGGTTCACTAAATATTATATTGCAGTTAGCATGTTGAATTTAAAGACAAATAGTTGTAATTTTAATAAACAGTTTTAGTTGTAATAAAATTATTAAAGGAGCTTCTATTTATACCGATTAGTGATGATTAAAAACGTTTGCCGTTACATTGAAATGAACTACAGCAGTAGTTCTGCTCTGTAATACTAAACTGAGCTCTTGTTATTGTTTTTTTTTTC[A/G]GGGCCTGAACTCATATCTTCCTCCTCCATCTCTACTGTCTCCTCACTCTAAACTGCAGATGTCTTCTTCACTGAGCGCTCAGCTTATTCCTCAGGCCACACTGACCTCACACACCAGTATGAGCGTTACCTTTAATCATTTTAACCTCACCTGTATATGAATTTAATGGACATGGACATGTACGTACATGAAGAAACGGTTAGCGATCTGATGTTAGAATTTAACATTGCTTTTTCTGGGTTAATTTACTTGACCCAGCTGCAAAGACGTACATCACTAGGTACCGTAAATATCAATATTGTGTGACATAGATAAAATGTATGTAACCCACTAGCGCGAGTCATTTTTACATGGGAACTGATATAGCGCAATAATGAACTTCTGAAAATAAACAGGACATCTCAATAGTGGAATAAAAAAAAAAAAATTTAACAGTAATTTGTTGTCATTATACAAAATAATAAATTTTTTTCTATAAAAGTCTTCAAAGCAAATTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32121
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 |
---|---|---|---|---|---|
ENSDART00000064668 | Nonsense | 910 | 936 | 21 | 21 |
ENSDART00000130253 | Nonsense | 1164 | 1190 | 26 | 26 |
Genomic Location (Zv9):
Chromosome 17 (position 8070267)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8073041 |
GRCz11 | 17 | 8230219 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGGATTGAAGTTCCCTCTGAAGATCTGCCTCCATCTTCAGGATCTTCC[A/T]GAAGAAGGAGACCTCTTCCCAAACTCGGCCAAGCCAACGGTGCGTTTGAA
Long Flanking Sequence:
TATAAATATGACGCTTTTACACCTAATGGTGTAAAATTGGTGCTTTTTGTTTAGTCACAAAGCGTTAAACCTCACCATCACCTGGAGTGAACAGCCCTTTAGTCAGCAAAAATGTATGACACCATTCTAATGGTTTTTAGATATTTAAATAAAAAAGGTTGTGCTTTTAATCTTTCAGTGTTTTTGGGTTCTGTCGACTTCTTTAAAATCACTGATTATGATAATGTGTTTTATTTTGACCCTGATGTTTCAGATGTCCGCAGCCATCAGTGCCTCTGGAGAGCTGAAGATCATCTCAGAGCTGGACACGGATGCTGAAGCCTCCTCCACCACGTATGAATCCAAACGTCATGTCTTCCTGTCATTTATGCATCAATTGTACACGTATTATTCATATAAGTTTCTTCACTTGTTTTCTTCACAGAAGAAAAAAGAAGAAGAAAAAGGTGAAGCGGATTGAAGTTCCCTCTGAAGATCTGCCTCCATCTTCAGGATCTTCC[A/T]GAAGAAGGAGACCTCTTCCCAAACTCGGCCAAGCCAACGGTGCGTTTGAAGGTGAAGGATTGAACTTACGGGATCTGGTCTGATGCTTATGACGGAATTACAGACATAGAAACTTAAATACGTCTTTCTGATAATTTATTTTTATAGTTGGCCTTATTTTTAAAAAGTCTATTTTGTAATTGGATACGTTTGTAATGTATAGTTTTAGATTAGTTTTGTACAGTTTTTTTTGTTTTGTTTTGTACATATTTTATGTTTATACGTTTCATTTAAAGTAAGTTAAGATTACAAATGTAACGGCAACAACTCCAGCGGTGGAGTTATCTAATAATACTAAATAATTTTTCCACATGGGAATGAACCTTTTTATTTATTTAGCACAAGGGTTAATGACAACTGACAATATATATATTTATACAAAACAGTTCTGTTTGTATTCTTTCACAACATTTACAGCATGGGTCTCAAACTCAATTCCTTGAGGGCCGCATCTCTGCACA
Associated Phenotype:
Not determined