ZMP
ap1s2
Ensembl ID:
ZFIN ID:
Description:
AP-1 complex subunit sigma-2 [Source:RefSeq peptide;Acc:NP_991121]
Human Orthologue:
AP1S2
Human Description:
adaptor-related protein complex 1, sigma 2 subunit [Source:HGNC Symbol;Acc:560]
Mouse Orthologue:
Ap1s2
Mouse Description:
adaptor-related protein complex 1, sigma 2 subunit Gene [Source:MGI Symbol;Acc:MGI:1889383]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6197 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa2610 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa6197
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 |
|---|---|---|---|---|---|
| ENSDART00000054837 | None | None | 157 | 1 | 5 |
| ENSDART00000122812 | None | None | 157 | None | 5 |
| ENSDART00000131115 | Nonsense | 1 | 162 | 1 | 6 |
| ENSDART00000135761 | None | None | 157 | None | 5 |
| ENSDART00000144954 | None | None | 168 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 11 (position 12777987)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 12662396 |
| GRCz11 | 11 | 12720055 |
KASP Assay ID:
554-4710.1 (used for ordering genotyping assays)
KASP Sequence:
CATCAGCCACAAAGCTCATGCTGCTCACGGGAACGAGTGTAAAAWAAACT[T/A]GAAGGTAAAAGCAACATTTTATCTCTTGCATTGATGGACGATTACAGATG
Long Flanking Sequence:
CCCAACGACCTTCCATAGGATCTGGTTGGATAAAATTTGATAAGAAAAAGACATAAGTCTGGGTAATAGATGATTGGAGTGTCCAATAGTTTTTTTCAATAATTTTGGGTAAATGTATGCCAAAAATTGCATTTAATAAGTTTCTGTAATTTTTAAACAGAAATAAAAATACTATTTTAAAATTAAGATCATATAAATGTGTCCAATTATTTACTGTGTGTGCGTGTGCGTGTGTGTGTTTCTTTTTTCTCCCCACAGATTCATTTTCATGATCAATATCACTGAATAAAAACCCTCCGTCTCAAAGCTTCACCCATCCTGTTCGGGTGTGGACCAATACAGAGTGTCATCGGTGAGTCTGTGAGCCAATGAGAAGACGCGATCCAGCTATCTAGCAAAAGGGCGATGATGCGTCCATGTAACGGGACTCCTCACATCTGCGTTTACTGCCATCAGCCACAAAGCTCATGCTGCTCACGGGAACGAGTGTAAAATAAACT[T/A]GAAGGTAAAAGCAACATTTTATCTCTTGCATTGATGGACGATTACAGATGTTTCGGACTTGCTTGAGCAAACACACATGGCTTTTTAATGTGTGTGTGTGTAGTTGAAATTAGTAACATTTACAGCGGCCGCAGCCTTCATGCTAACGCGATTCTTCCTTCTTTGTTACGACAAACAGAAGTAATTCACGCAACACGACAGTGCGTCGCTTGGTTCATGTCAAATGTGAAATTACTTTTTGAAATAGGTGACATGATAAATGTTTCCTGTATGAATGGGTGGGAAATGCTAAGTACTATTTGGACTTGACTGGGCATTTACGGTGATACAGCGTACAAACACGGTTTAAGACTCTCTTTTTGTTTGTTTTCTTGTTTTCAGATGCAGTTCATGCTGCTTTTTAGCAGGCAGGGAAAGCTGCGGCTTCAGAAATGGTACGTGCCGTTGTCTGACACACAGAAGAAGAAAATCTCCCGTGAGGTCATTCAGATGGTGCTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2610
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054837 | None | None | 157 | None | 5 |
| ENSDART00000122812 | None | None | 157 | None | 5 |
| ENSDART00000131115 | Essential Splice Site | 147 | 162 | 5 | 6 |
| ENSDART00000135761 | None | None | 157 | None | 5 |
| ENSDART00000144954 | None | None | 168 | None | 5 |
Genomic Location (Zv9):
Chromosome 11 (position 12785094)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 12669503 |
| GRCz11 | 11 | 12727162 |
KASP Assay ID:
554-3261.1 (used for ordering genotyping assays)
KASP Sequence:
TGAGAAACACARACACTGCTTGTTCTGAATCTTGGATTTATTTAGTGAAG[G/A]TATAAACTAAAATCTGATTCTCATCTTTAACAGGAAGCCGAGACACCACG
Long Flanking Sequence:
TTGATAACAAGCAGGAAATGTTCATGAGCCAATGACATGACCACATTGAAGTCTATACACTCTCATTCACACACATTCATTCACCATGGCCACTTAATTAGGTTTTACCCAATTCATCTATGCCACGTCTTTGGACTGTGGAGGAAACTGGAGCACCCAGAGAGAAACCACTGGAACATGGGGAGAACTCACAATCCAGTAGTAAACCCAATACTACTTTAAATTCTAGACATAGTAGCTAATGACCAATAGATCCTTTGAAAAAACTCTTGCAAGTGCTCATTGTGATGCTTTGTGTGTTTGAACACTAGGTGTGTGAGCTGGACATTATCTTCAACTTTGAGAAAGCCTATTACATTCTGGATGAGTTTATACTGGGCGGTGAAGCCCAAGAGACATCGAAGAAGAACGTTCTAAAGGCCATAGAGCAAGCGGACATGCTGCAGGAGGTGAGAAACACAAACACTGCTTGTTCTGAATCTTGGATTTATTTAGTGAAG[G/A]TATAAACTAAAATCTGATTCTCATCTTTAACAGGAAGCCGAGACACCACGTAGTGTTCTGGAAGAGATTGGACTGACATAAATGTCGAGAGCACATCCTACTCCAAACGCATCTTACTGTCTTTTTTTCTGTGGGCATTTTCTCCAAGTCTGTATTTTAGGTTAGCTTGCAGGCTAAAGTAGTGTTTAACATAATCAACACTTCCAGCATTACCCATATAGACTCTTGTATTTCTACTGCCAAACATCTGAGGGAATCGAGCACATGGAAATATTAATCTCAGCAGTTATGCAAATTCCCCATAGCGTTCGACTGTTTGGATTAGAATGCGTGTAGCAAAGATTAGCGTTAGCATTAGCATCCCCACAACTTTCCATCTTCTCTGATTTCAAACATTACCTCTCACCTTCAGCTGCCTTAAAACACTCATCTCCAGCTCACACTGTAACTTATGCAACTCTCTGTAGTTCCAAGTCAGCAGTTCTATACTGAGATTTGCT
Associated Phenotype:
Not determined