ZMP
asb2a
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate ankyrin repeat and SOCS box-containing 2 [Source:UniProtKB/TrEMB
Human Orthologue:
ASB2
Human Description:
ankyrin repeat and SOCS box-containing 2 [Source:HGNC Symbol;Acc:16012]
Mouse Orthologue:
Asb2
Mouse Description:
ankyrin repeat and SOCS box-containing 2 Gene [Source:MGI Symbol;Acc:MGI:1929743]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37047 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa5953 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39284 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa23721 | Nonsense | Available for shipment | Available now |
| sa8807 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37047
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000026088 | None | None | 672 | None | 9 |
| ENSDART00000130533 | Essential Splice Site | 121 | 661 | 3 | 9 |
| ENSDART00000148361 | None | 1 | 1077 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 20 (position 27351616)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 27422919 |
| GRCz11 | 20 | 27322009 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATATAAGTGCTATTCTTAAGATTGGTTTGCATATTTGTTCTTCTTTTC[A/T]GTGATTTGGACCCCTTTCTCTCAGCTATTTGGAAGGGAGATGCAAAGACT
Long Flanking Sequence:
AGACTTATCTGACTCCAAATGGCTTGAATAAAAAACAAATCACTCATAACTCATCTTTCATTCATTCATTTTCTTTTCGGCTAAGTCCCTTTATTGATCTGGGATCGCCACAGCGGAATGAATCACAAACTTATCCAGCATATGTTTTACGCAGCAGATGCCCTTCCAGCTGCAACCCATCTCTGGGAGAACCATACACACTCATTCGCACACATACATACATATGGACAATTTAGCCTACCCAATTCACCTGTACCACATGTCTTTGGACTGTTGGAGAAACCGGAGCACCCGGAAGAAACCAACGCGATTGCAGAGAGAACATGCAAACTCTACACAGAAACGCCAACTGACCCAGCCGAGGCTCGAACCAGCGACCTTCTTGCTGTGAGGCAACAACTACTGCATATTTTGAGTTAAAATCAAATAAAATGCTTAATCAAAATCCTCTGATATAAGTGCTATTCTTAAGATTGGTTTGCATATTTGTTCTTCTTTTC[A/T]GTGATTTGGACCCCTTTCTCTCAGCTATTTGGAAGGGAGATGCAAAGACTTTACAAGACCTCGTTCATAGCAAATCTAAATATCTCGAAGAGCCCAATAAAGATGGCTGGTTACCGCTTCATGAATGTGCCTGCAACGGCCATGTGGAGTGCCTTAAGGTTTTGCTCAAAGGTAAGAAATTAATCATTTGTGTCCAGCTCAGAGTCAAACACTCAAACCATCTCGTCTTTCCTCACAGCCAAACCAGATACAATCAACAAAAGAACACACAGAAATCAGACCCCGCTCATTCTGGCTGTGGGTCGCAAGCATGTTGCTTGTGTCGAGCACCTTTTGGAGCAAGGAGCTGATCCAAACATTGCGAATAACCAGTGGGAGACCCCATTGTACAAAGGTACAATAGTGACTATGTTTACAAGGACATCAGTAATCAAATTATTTGCTATAATCTGAGTAAGACAATAATATAATTAAGGTGTTAACGCTTGTTGTTTTTTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5953
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 |
|---|---|---|---|---|---|
| ENSDART00000026088 | None | None | 672 | None | 9 |
| ENSDART00000130533 | Nonsense | 175 | 661 | 3 | 9 |
| ENSDART00000148361 | Nonsense | 55 | 1077 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 20 (position 27351453)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 27422756 |
| GRCz11 | 20 | 27321846 |
KASP Assay ID:
554-3780.1 (used for ordering genotyping assays)
KASP Sequence:
ACCGCTTCATGAATGTGCCTGCAACGGCCATGTGGASTGCCTTAAGGTTT[T/A]GCTCAAAGGTAAGAAATTAATCATTTGTGTCCAGCTCAGAGTCAAACACT
Long Flanking Sequence:
TTCCAGCTGCAACCCATCTCTGGGAGAACCATACACACTCATTCGCACACATACATACATATGGACAATTTAGCCTACCCAATTCACCTGTACCACATGTCTTTGGACTGTTGGAGAAACCGGAGCACCCGGAAGAAACCAACGCGATTGCAGAGAGAACATGCAAACTCTACACAGAAACGCCAACTGACCCAGCCGAGGCTCGAACCAGCGACCTTCTTGCTGTGAGGCAACAACTACTGCATATTTTGAGTTAAAATCAAATAAAATGCTTAATCAAAATCCTCTGATATAAGTGCTATTCTTAAGATTGGTTTGCATATTTGTTCTTCTTTTCAGTGATTTGGACCCCTTTCTCTCAGCTATTTGGAAGGGAGATGCAAAGACTTTACAAGACCTCGTTCATAGCAAATCTAAATATCTCGAAGAGCCCAATAAAGATGGCTGGTTACCGCTTCATGAATGTGCCTGCAACGGCCATGTGGAGTGCCTTAAGGTTT[T/A]GCTCAAAGGTAAGAAATTAATCATTTGTGTCCAGCTCAGAGTCAAACACTCAAACCATCTCGTCTTTCCTCACAGCCAAACCAGATACAATCAACAAAAGAACACACAGAAATCAGACCCCGCTCATTCTGGCTGTGGGTCGCAAGCATGTTGCTTGTGTCGAGCACCTTTTGGAGCAAGGAGCTGATCCAAACATTGCGAATAACCAGTGGGAGACCCCATTGTACAAAGGTACAATAGTGACTATGTTTACAAGGACATCAGTAATCAAATTATTTGCTATAATCTGAGTAAGACAATAATATAATTAAGGTGTTAACGCTTGTTGTTTTTTGAATGTTCCCATCATGATCCAGTTTTACATGTTACTGTATAGCTCATAATTAAAGTCATTACGTCACCAGGCTATCCACATATCCTCCGGAATTTCATGTAATTTTGCGTGTTTCGTTTTTAATTTGTCGACTTTAGCTGCAGTTTGGCACTTTCACTTTCATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39284
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000026088 | None | None | 672 | None | 9 |
| ENSDART00000130533 | Nonsense | 540 | 661 | 7 | 9 |
| ENSDART00000148361 | Nonsense | 420 | 1077 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 20 (position 27348475)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 27419778 |
| GRCz11 | 20 | 27318868 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTAAATGTCAGTATGGAAGTAATCCTCATCCCCCTTTAAAACCAAGAT[C/A]AACTGGAAGAGAAACAATGTACTTATTAAATGAAGATCCATCAGACTACT
Long Flanking Sequence:
GTTAATTCCTAAAACCAGCACAACCAAAGTGAGACGCTCCGGCATCAGTCCCCTTCATTTCGCAGCTGAGCGTAACAGAGATGACGTTCTAGAAATACTGATTGAGGCTGGATATGATGTCAATGCCATGCTCTCAGACGACTGGTCAAAACTGCATGAGGATCGCCGCAGCACAGCTTTATACTCGGCTGTGGTGAACAGAAACATTGAGGCCGCCATTATGCTTTTAGAAGCTGGTGCTGACCCAAACCTGGACATATTCAACCCTCTGCTTGTGGCTGTGAGGAAAGGAAATATAGAAATGGTGACCCTGTTGGTGAAGTACGGTGCCAATGTTAATGCCATGCTGCCCACTCATCCCACCAGCTTCCCAGCAGCTCTGGTTTTCTGCATGAGGTACATTATGATGATGAAGTATCTTCTGGACAATGGCTGTGATGCACTGGCATGTTTTAAATGTCAGTATGGAAGTAATCCTCATCCCCCTTTAAAACCAAGAT[C/A]AACTGGAAGAGAAACAATGTACTTATTAAATGAAGATCCATCAGACTACTGTGTACAGGTATATTTTTAAATAAAATGATAACACTGTGTTTAAAACTACACCATAACTATTTACACATACAGTGTGCTAATGTTCAGTAACGTACACTTAACTCAGATTTCATCATTCATCTTGATTTTTGTAACCATCTGTACAAAGTACTGTACTGAACAGATCAGACATACACTTTATATTGTTTTTGGACTGGTTACAATGTTGCTTGCTTGCAAAGAACAGCTTACTGAGAAAGAAAGGTGATAGAAACAGACAACAAGAAAAACACACTACTGAAGACACTTTCAAGTTGTTACAAAGTCGCATGAGTCTTTTCTCTGCTTAGATATTTTGAAAAACGAGAGAGTGAAAAACAGCCCGTCAATTCCACAGTAAAAAAATAGTAGTATGGAAATCTTTGGCTAACTATTTGGTTACCAATATTTTTCAAAGTAGCTGCTGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23721
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 |
|---|---|---|---|---|---|
| ENSDART00000026088 | None | None | 672 | None | 9 |
| ENSDART00000130533 | Nonsense | 609 | 661 | 8 | 9 |
| ENSDART00000148361 | Nonsense | 489 | 1077 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 20 (position 27347114)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 27418417 |
| GRCz11 | 20 | 27317507 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTAACCGAACACCTAGACAACAACAAAGACTGGGCTCATGTAAAAGAA[A/T]AAGCAGGTGAGAACATTCTTTGTAATTCTTCTTCTATTCTTTTCATTTTC
Long Flanking Sequence:
ACCTTTTATCTGCTCATTGTAATTGGAATAATGAGAGAATAACACACCTTGCCATGGAACAGCTGAGAAGCCGATTGTCCAATTACTTTTGAACCCTTAACAAGTGGGAGGCACATATGCAAACTGTTGTAATTCCTACAGCGTTCACCTTATTTGGATGTAAATAGCCTCAAATCAAAGCAGTTAAAGCACATCTTCATTTAATTTCAAATCCATTTGTGTTTTATACAGAGCCAAAAAAATTTTTAGAACTGTGTCAATGTCCAAATATTTATGGACCTAACTGTACAACTGTTATTTTGTACATTTCTTTTACAACAAAATGAAGTACTTTTTTTCTTTTTTTTTCACAGTTTTGTGAGATAATCTCTGCTCCCTCAGTCAGTGGTTTGGTTGGACCCATTATTGACACTTTACTTAACTACGTGGGTCACGTTAAACTCTGCTCTAGATTAACCGAACACCTAGACAACAACAAAGACTGGGCTCATGTAAAAGAA[A/T]AAGCAGGTGAGAACATTCTTTGTAATTCTTCTTCTATTCTTTTCATTTTCACACTGTAAAAAGTGTAATAATAAATAACAAGTTAGTCCGGTTTCAACTACACCATTTTTAGTATCTTAATATTTATGTAATATGGAAGTTGAGATGACTAGAAAAGTTCATTTGACTCAACTAAATAAATTAAGGCAGCGATAATGTTTTTGCAGAATTTGTCATATTACTGACAATATTGTCTAAATATTTTTTTTTTAATTAACGGAATTAAAAATAAAAACTGACGCTTCTCTGTTTCAGTTCTTCCATGCACATTGATGAATCTGTGCAGAATAAAGGTTCGCCAACAACTCGGAGTCCACAGACTGCAGCAAATCCACACTCTTCCTCTACCAGCAAGACTAAACAAGTTCTTGATTTATGAACGAGAATCATTTGAGGGAATCCTGTCATAAAATTCTGTGCCATTTTTCAATATTTACAAAACATGTTGTCTTGAATTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8807
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 |
|---|---|---|---|---|---|
| ENSDART00000026088 | Essential Splice Site | 194 | 672 | 3 | 9 |
| ENSDART00000130533 | None | None | 661 | None | 9 |
| ENSDART00000148361 | None | None | 1077 | None | 14 |
Genomic Location (Zv9):
Chromosome 20 (position 27336087)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 27407390 |
| GRCz11 | 20 | 27306480 |
KASP Assay ID:
2261-4416.1 (used for ordering genotyping assays)
KASP Sequence:
TGAGGCGGCATATTATGGACAAGATCAATGCGTTAAAATTCTCCTGAGAG[G/A]TAGAGTGCACTYATTTRTAAATTCCTCAAATCCWAWTTTCCAAGCTGTRA
Long Flanking Sequence:
AAGTCCACAGGTTTGTCCTTGCAACTGGGATGTTTGGTTTCTAAATGTCGTTTCAATTTAGAAGGTTTCATGCTCTCTTGTGAGAGCAACACACTACATATAAGCCTCCTTTTGTTGTCAATATATTTATTCGGGGTACTACTTGCGCTTCAACATATTTGTTGCTATAATTAAATGAAATTTCACATGTCAAATGGTACGGTTGTCATGCGCGCATTTCAAAACAAAAATTCATATTAAATAAAGCACTCATGGAAGATTCATTTCATTATGGCATGACATTTTAGAAGTTTAAAGCAAAGCATTGCATAAACAAATTGTCTATTGTAGGGAACTTGAGCCCATTGCTAAGGCCATTTCGGAGGGGGATGTAGGGACAGTGAGACTAATGGTCAAGCAACCAGGCTGCAACCTTCTTAAACCTAATAAAGAAGGGTGGATTCCTTTGCATGAGGCGGCATATTATGGACAAGATCAATGCGTTAAAATTCTCCTGAGAG[G/A]TAGAGTGCACTCATTTGTAAATTCCTCAAATCCTATTTTCCAAGCTGTAAAAGAATGTTGTGATTCTTATCATGAATGTAGCTCAACCTGGGATGATTAACCAGCGCACTTTGAGAGATCAGACTCCTTTAATGTTAGCTGTGTCCAGAGAGAATCTGGCATGTGTGGAGATTCTTCTGGAGAAAGGAGCTGATCCTGAGATTCCCAACAAGGAAAAGGAGACTCCACTTTACAAAGGTATTGTACCGCTTTAATATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTTCATGTCCACCCAACTGTTATCTATTCATCCATCAGTCTGTCTGTCATCTCTCTATGCATTCATCTAACTGTCAACCATCCATCTGTCCAT
Associated Phenotype:
Not determined