ZMP
si:dkey-3n7.3
Ensembl ID:
ZFIN ID:
Description:
ankyrin repeat and SOCS box-containing [Source:RefSeq peptide;Acc:NP_001034979]
Human Orthologue:
ASB15
Human Description:
ankyrin repeat and SOCS box-containing 15 [Source:HGNC Symbol;Acc:19767]
Mouse Orthologue:
Asb15
Mouse Description:
ankyrin repeat and SOCS box-containing 15 Gene [Source:MGI Symbol;Acc:MGI:1926160]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20189 | Nonsense | Available for shipment | Available now |
| sa33365 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa20188 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20189
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 |
|---|---|---|---|---|---|
| ENSDART00000067407 | Nonsense | 75 | 586 | 3 | 10 |
| ENSDART00000146889 | Nonsense | 75 | 584 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 3999672)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 4118285 |
| GRCz11 | 4 | 4127198 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTAAGGAAAATGCACAAATGCAGTGAAGCCTATAAGGAAAGAGACAGC[A/T]GAGGTTTGCTGCCGATGCACAGAGCGTGTGTTCAGCCTGATTCCTGTGTG
Long Flanking Sequence:
ACAAAAGACTCGCTCAGACTGACTCTTTTGAATCAGCAAATTTTTCCGTGAAAACTCACTGCCTGCGTTTGAAACCACATATTTCATAGTACACTAAAATCAGTATGCAAGCCGAGTAGTATGTCCGAATTCATCAGTATGCGAGAAGTACCCGGATGACTTACTACTTCTGGCGAGATTCTGAAGTGGATAGATTAATAAAACTGGTTAACATTGAATATCTGCAGCTATACCTAAAAAATTTAAGTCATTACTTTGCTCCACTGTTCACATATACCACTTTCCCTTCATGCAGTGCTTTGGAAACAGCCAGTGATGAAAACCTGAAGATTTTATCTGCTATAGATCAAGGTATACTTCAAATACATGTGTGCATGATTAAATATCACATGTCAGATATTTGATACCGATGACTGCATATTGTGTGATATCTTCCAGGAGACACGTTTGCTTTAAGGAAAATGCACAAATGCAGTGAAGCCTATAAGGAAAGAGACAGC[A/T]GAGGTTTGCTGCCGATGCACAGAGCGTGTGTTCAGCCTGATTCCTGTGTGCTGGATATTGTGCTACTGGGTGAGCAGACAACATATATTTCATATGCATTCGACAGTATACAGTTGAAGTCAGTATTATTAGCTCTCCTGAATTATTAGCACACCCCCCCCCCCTGATAATCACCCCCCCCCCCCATTTCTGTTTAACAAATAAAATATTTCTCCAATACATTTCTGAACAAAATAGTTTTAATAACTCACTGATTTATTTTATCTTTGCCATGATAACAGCACATATTATTTGACTAGATATTTTACATACTAGTATTCAACTTAAAGTGACATTTAAAGGCTTAACTGGGTTAGTTAGGCAAGTTAGGGTAATTAGGTTTGTTTTGAAGACAATAAAAAAAATAGCTTAAAGGGGCTTATAAAATTGACAAAAAATGGCTTTTAAAAAATTAAAAACTGGTTTTATTCTAGCAGAAATAAAACAAATAAGACTTTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33365
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 |
|---|---|---|---|---|---|
| ENSDART00000067407 | Essential Splice Site | 292 | 586 | 7 | 10 |
| ENSDART00000146889 | Essential Splice Site | 290 | 584 | 7 | 9 |
| ENSDART00000067407 | Essential Splice Site | 292 | 586 | 7 | 10 |
| ENSDART00000146889 | Essential Splice Site | 290 | 584 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 3995416)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 4114029 |
| GRCz11 | 4 | 4122942 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACACTTCCCAACCATATTACAAATCTTTGTGTCTCTTTTTAAACCTCC[A/G]GAGCTCTGAAGACATTAATTCCCATCACCACAAAAAGGGCCATCCGGCTT
Long Flanking Sequence:
CAACCCTTATCAAACACACCTGAACAAGCTAATCAAGGTCTTACTAGGTATACTTGAAACACCCAGGCAGGTGTGTTGAGGAAAGTTGAAGCTGAACCCTGCAGGGCACCGGACCTCCAGGAATGAGATTGGTGACCCCTGGTTTAGGGCATTCCATTTAAACCCATTTACATGTTCCACCCATAGTGAACACTTGTGGGATGTACTCAATGATGTACATCAATGATGTGATGGTGTATTTGGGATAAACCAAATCTCTAAACTATAAACACTGAGCTCATGATGGTTTTGGAAAACACACCATTCTATAGTACAGCAGATCTCAGTTCTGGTCCTCACGACCCCCAGCTCTGCACCTTTTGTATGTTTCTCTTACCGATTCAGAGGTTTGATTCATTTGACCATAATTGCATTAAAAATTGGACTGGAATGGAGCTATGATCAACCTTAACACACTTCCCAACCATATTACAAATCTTTGTGTCTCTTTTTAAACCTCC[A/G]GAGCTCTGAAGACATTAATTCCCATCACCACAAAAAGGGCCATCCGGCTTTCCGGGATGAGTCCGGTTCATTCTGCGGCAGACGGAGGTCAAGCACAGTGCCTCGAACTTCTCATTGAAAAAGGTTTTGATGTCAATCCAATACTGGGCTGTCATATTTCCGAAAACTATGGAGACATGAGGAAAACCCCGCTCTACTTTGCCGTCTGCAATGGAGACGTGACCTGCACAGAGATGCTTCTGAAAGCGGGAGCGAAGCCGGATTTGGACCCGCTGCGCTGCCTCCTGGTGGCGGTCAGAGCTGAGAAGTATGAGTTGGTGCGGCTGCTTCTTGCGCACGGTGCAGACGTCAACTGCATCTTTTCCGTCGTCAGTGACACTTTATTTCCTACAGCGCTGCAATACTGCTTCAAAGATGAGATGATGCTGCGCCTGCTCCTCAACAACGGATACCATGCAGAAAGCTGTTTCGAGTGTTACCATGACAACAGTGTAAAGACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20188
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 |
|---|---|---|---|---|---|
| ENSDART00000067407 | Essential Splice Site | 292 | 586 | 7 | 10 |
| ENSDART00000146889 | Essential Splice Site | 290 | 584 | 7 | 9 |
| ENSDART00000067407 | Essential Splice Site | 292 | 586 | 7 | 10 |
| ENSDART00000146889 | Essential Splice Site | 290 | 584 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 3995416)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 4114029 |
| GRCz11 | 4 | 4122942 |
KASP Assay ID:
2259-4391.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACACTTCCCAACCATATTACAAATCTTTGTGTCTCTTTTTAAACCTCC[A/G]GAGCTCTGAAGACATTAATTCCCATCACCACAAAAAGGGCCATCCGGCTT
Long Flanking Sequence:
CAACCCTTATCAAACACACCTGAACAAGCTAATCAAGGTCTTACTAGGTATACTTGAAACACCCAGGCAGGTGTGTTGAGGAAAGTTGAAGCTGAACCCTGCAGGGCACCGGACCTCCAGGAATGAGATTGGTGACCCCTGGTTTAGGGCATTCCATTTAAACCCATTTACATGTTCCACCCATAGTGAACACTTGTGGGATGTACTCAATGATGTACATCAATGATGTGATGGTGTATTTGGGATAAACCAAATCTCTAAACTATAAACACTGAGCTCATGATGGTTTTGGAAAACACACCATTCTATAGTACAGCAGATCTCAGTTCTGGTCCTCACGACCCCCAGCTCTGCACCTTTTGTATGTTTCTCTTACCGATTCAGAGGTTTGATTCATTTGACCATAATTGCATTAAAAATTGGACTGGAATGGAGCTATGATCAACCTTAACACACTTCCCAACCATATTACAAATCTTTGTGTCTCTTTTTAAACCTCC[A/G]GAGCTCTGAAGACATTAATTCCCATCACCACAAAAAGGGCCATCCGGCTTTCCGGGATGAGTCCGGTTCATTCTGCGGCAGACGGAGGTCAAGCACAGTGCCTCGAACTTCTCATTGAAAAAGGTTTTGATGTCAATCCAATACTGGGCTGTCATATTTCCGAAAACTATGGAGACATGAGGAAAACCCCGCTCTACTTTGCCGTCTGCAATGGAGACGTGACCTGCACAGAGATGCTTCTGAAAGCGGGAGCGAAGCCGGATTTGGACCCGCTGCGCTGCCTCCTGGTGGCGGTCAGAGCTGAGAAGTATGAGTTGGTGCGGCTGCTTCTTGCGCACGGTGCAGACGTCAACTGCATCTTTTCCGTCGTCAGTGACACTTTATTTCCTACAGCGCTGCAATACTGCTTCAAAGATGAGATGATGCTGCGCCTGCTCCTCAACAACGGATACCATGCAGAAAGCTGTTTCGAGTGTTACCATGACAACAGTGTAAAGACG
Associated Phenotype:
Not determined