ZMP
ascc2
Ensembl ID:
ZFIN ID:
Description:
activating signal cointegrator 1 complex subunit 2 [Source:RefSeq peptide;Acc:NP_956736]
Human Orthologue:
ASCC2
Human Description:
activating signal cointegrator 1 complex subunit 2 [Source:HGNC Symbol;Acc:24103]
Mouse Orthologue:
Ascc2
Mouse Description:
activating signal cointegrator 1 complex subunit 2 Gene [Source:MGI Symbol;Acc:MGI:1922702]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa33558 | Nonsense | Available for shipment | Available now |
| sa31421 | Essential Splice Site | Available for shipment | Available now |
| sa10074 | Nonsense | Available for shipment | Available now |
| sa26429 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33558
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 |
|---|---|---|---|---|---|
| ENSDART00000048859 | Nonsense | 177 | 768 | 5 | 19 |
| ENSDART00000139431 | Nonsense | 177 | 243 | 5 | 7 |
| ENSDART00000142562 | Nonsense | 177 | 192 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 5 (position 19688319)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 17515946 |
| GRCz11 | 5 | 18019942 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATTCCCAAAATTCTGGATCTGTGTGTTCTGTACGGAAAAGGAAATTCC[C/T]AACTGCTACATAAAATGATCGGTACACAAAATCTGTTAATATCACAGTAC
Long Flanking Sequence:
ATGAGGAAGAGATTGTCACTGATGGATAGGACTTTCCCACCTCTGATGACATGTGCAAGGGGCGAATGTCAATTAAAAGTGTTTTAACAGACTGTTTTTTATGAAGTGTGATTATAAAAGAATAAAAAATCAAAATTTTTACCATTAGAAGCTGGTTATATTCACAGACTGTTGCCACACAACTGTGTTTTAACCTCTTTTAAAAGTGATTTTTAATAAGAGGTCCCCTTAAATGTATTCTTGTTAAATAAAGTTATTAATTCTTTATAAAATAATCTTACTTAGTCAAAAATTGGAAAGGTAGTGTAAATGTGTGCTGGTAGTTTTATATTAAGTTACAATAAATGTATATTGATCCTGATTTTAAAACACTGCTCTGTTGTCTTCCTTAGGAGCACTTCATTACCCCTGCAGTGTTTGCAGAGATTATTTACAACAACTATCTGTTTGACATTCCCAAAATTCTGGATCTGTGTGTTCTGTACGGAAAAGGAAATTCC[C/T]AACTGCTACATAAAATGATCGGTACACAAAATCTGTTAATATCACAGTACATTTTTAAAAAAACAACAGAGAAATACATAAATACCTTATTATTCTTTTTAAATAACTCATATTTATTACAGTGTTTACATATTTGAAACTTATCATTTCAATTTTTGCCCCAGACAACATTTTTACGCAACAGCCCAGTTATTATGGAGACCTAAATGAGACTATACCCTCCATCATCCAGGTACTTTATGAGATCATGTTACGTAATCAACTATTTTCATTGACTTAATTGTTTACAAGTCGTCTGAACTTCCGGAAATCTCTGCATGTGCTTTCTAGGTGTTTGATATAATATTACAGAAGTGTGGTATTCAGTCAGAGGACACAGGAGCCGGTCAGCCCCTAAAACTCAATGCTAACAGATGCCTAACTGCCATGACCATGCCAGAGGAGGTAAAATATAATAATAATAAAAAGTAATTATACACACATTAACTGACTCTGCCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31421
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000048859 | Essential Splice Site | 244 | 768 | 7 | 19 |
| ENSDART00000139431 | None | None | 243 | None | 7 |
| ENSDART00000142562 | None | None | 192 | None | 5 |
Genomic Location (Zv9):
Chromosome 5 (position 19687873)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 17516392 |
| GRCz11 | 5 | 18020388 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACTCAATGCTAACAGATGCCTAACTGCCATGACCATGCCAGAGGAGG[T/A]AAAATATAATAATAATAAAAAGTAATTATACACACATTAACTGACTCTGC
Long Flanking Sequence:
TTTGACATTCCCAAAATTCTGGATCTGTGTGTTCTGTACGGAAAAGGAAATTCCCAACTGCTACATAAAATGATCGGTACACAAAATCTGTTAATATCACAGTACATTTTTAAAAAAACAACAGAGAAATACATAAATACCTTATTATTCTTTTTAAATAACTCATATTTATTACAGTGTTTACATATTTGAAACTTATCATTTCAATTTTTGCCCCAGACAACATTTTTACGCAACAGCCCAGTTATTATGGAGACCTAAATGAGACTATACCCTCCATCATCCAGGTACTTTATGAGATCATGTTACGTAATCAACTATTTTCATTGACTTAATTGTTTACAAGTCGTCTGAACTTCCGGAAATCTCTGCATGTGCTTTCTAGGTGTTTGATATAATATTACAGAAGTGTGGTATTCAGTCAGAGGACACAGGAGCCGGTCAGCCCCTAAAACTCAATGCTAACAGATGCCTAACTGCCATGACCATGCCAGAGGAGG[T/A]AAAATATAATAATAATAAAAAGTAATTATACACACATTAACTGACTCTGCCATCAGTGTCTTTTCTGGCAGATTAATATGCTTATAATTAAATATGCATCACTTTTATGTCTCTTAGGAGCTTGCAGACTTGGTTTCTTACATGTGTGATACCTGCACTACTATCCATTCTTTCCTGGACATCTTCCCTGAGGCTTGTTCTACTTTCAAACAGCACAACTTTCTTAACAGGTGACAAATACACATCCACATCCTGGTATTAAGATGCCTATTGTCCATTAAATGATAAATGGGCGATGCTGAATATAGATGTGAACATGATTGAAAATGAAATGAAATTTTGTATTTTTATTATATTTAGTTTATTATTATTATTATTAATTTATTTTTTTAATCTGTCCCATTTTGAACACTTGCAAAAGTAGACAATAACCTAACTGATTCAATTGCTTTCATAGTAAAAAAAAACAACATTTAGAATAAGTGGGTCTTGAGCTTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10074
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000048859 | Nonsense | 317 | 768 | 10 | 19 |
| ENSDART00000139431 | None | None | 243 | None | 7 |
| ENSDART00000142562 | None | None | 192 | None | 5 |
Genomic Location (Zv9):
Chromosome 5 (position 19683871)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 17520394 |
| GRCz11 | 5 | 18024390 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTGCACTCTGTCTCAGTTTACAGGAGGACATGTGGAGACGAGTATCTTA[T/A]TCTAGAAAGAAAATGGTGGAGATTGCTCACCTGCTGCTCCARCACGCGTG
Long Flanking Sequence:
GTGTATATCTTTTGTATAATGAATGCTTATTAATATGTCGATATGCTTGAATGTTTTACATTGTAAATATCAAGTATAGGTTTTTCCATGAATATAGCCAATGCTGCTGATATGAAATTAAAACATAAACAAAATAAATAAGTAAATAAACAGTAAAAAGAAATAGTTTTTTTTACATGTGGTCAATATATATAAACTATTAATTTATTTAATTTACAAAAAAATTGTGATACATATTATTATAAATCATCCTTATCTTATTTATCTTACCTTATCTTAATGTTACAAAATATTGACCGGAGCCTCTCTGAATGTAGATTACCATCATTTTATGAGATGGCAGTTCCAGACCTGGAGAAAGCAGTGAAGAAGAGGAATTTCGATAAAAGGTTAGAATAGCAAACTTGACTTCTCTTTTTGATGAATTTGTACAGATTAAACCTTAAACTTGTTGCACTCTGTCTCAGTTTACAGGAGGACATGTGGAGACGAGTATCTTA[T/A]TCTAGAAAGAAAATGGTGGAGATTGCTCACCTGCTGCTCCAGCACGCGTGTTTACAGCCCATACTGGAGGGGTACATGATTTTAGAGCTGATTAGACAGGCAAAGATTGGAATGGATACCAGATATTCTTGTCTTAACACAAAGCGCTGATTATTTTCACAGCTCTGAAAATGTGGCATCCTTTGTAGAAGATCTTCTACAGAACTTCACAACTTTCCTTCAAGAGAAAAGGTAAATGATGTTTATGTGTTTTAATGGTTGTGTATCAATATGTTAAAGGTGTGCAATGTTGCCAGACGTTGCTGACTTTTTCCAGGCCAAAAGCTGTCCAAAACCCGCCAAAACATACAAAAAACATACAAAAATGTATACTTTATTTACTTTTAGTTTATTTAAATCGAAATTAACCTAGATACTTTAACTGTTATAATTTTTAACAATTCAGCAACCAACACCAGCCGTTACAGAATCACAACATAAGTGGATCACATCATAACACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26429
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000048859 | Essential Splice Site | 533 | 768 | 14 | 19 |
| ENSDART00000139431 | None | None | 243 | None | 7 |
| ENSDART00000142562 | None | None | 192 | None | 5 |
Genomic Location (Zv9):
Chromosome 5 (position 19680454)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 17523811 |
| GRCz11 | 5 | 18027807 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGATAAACTAGCTCCTTCTCTTGACAAACTAGACCGGGCAATGGCCAGG[T/A]AAAGTATAAGATACAACGATTTATAACACTTTAGAATGGGATCACATTGG
Long Flanking Sequence:
TCATCATATTCATTTTATGTCAATCTTAGCACTTGATGTAACTACAGAAGAGTCAAGCCTTTTCTATTTTTGAATTATTTGAGCGACATGCTAATAGTCTAATCTGATTCAACGATTTATGCTAAGCCAACCTAAAATTGCTTCTGCAGACAAGGAGATTGGTTGAATAAATTAATAAAAATGATAAAACGCAACTGTTTAACTCAAAGGGACTTGTAAAACTAGTCTATTTCCAAAAAAAAATGAAGTGTTCCTTTAAAAATTGCATTCCTCCTTTTGTTTTGTTTTTGTCTGGTGTTTAGGGTGCAGTGTGCACCGTGAGTGCTGGAGAATTAGAATCTCTGCTGTCCCATATCCGAGACCTGCTTCCAGACTTGGGAGAGGGATTCATACTGGCATGTTTGGAAGAATATGGCTACAACTCCGAACTTGTCATTAACAACATCCTAGAAGATAAACTAGCTCCTTCTCTTGACAAACTAGACCGGGCAATGGCCAGG[T/A]AAAGTATAAGATACAACGATTTATAACACTTTAGAATGGGATCACATTGGTTAGTGTTAGTCAATGCCTTAACTAAAATGTAACTAACAGTGAGCAGTTTGTTATTTATTAGTTTGTCTTACTGTTAATTCATTTTAATTGAATTAACATCATTTAAAAAAGTATTAAAGTTAATAAATCAATTATGAGAAAATGAAGGCTCTTAAAAGGTATTAAAAAGTCTTAATCACAGTTTTATGAGGTCTTAAATTTTGTTTAAGCGTTGTCCAAAGTGTTTGACTCCAAAAAAGCATATGATATATTTATTTTTCTCCTAATAATAACAACGCCGTGCTCAATCCACTTGATTGGTTCGGGCCAGGACACTTCCAGCCTAGCTCCTTTGTCTATGTGATGTCACGTAATTTGTGACCATTGCGGTAAAGTGATGTGACACTCTCCATATGTAGCGAAACAGACGGTAAAATGGGAAAACGTATGTTTGCGTACTCCTGGTTGGA
Associated Phenotype:
Not determined