ZMP
ASCC3 (1 of 2)
Ensembl ID:
Description:
activating signal cointegrator 1 complex subunit 3 [Source:HGNC Symbol;Acc:18697]
Human Orthologue:
ASCC3
Human Description:
activating signal cointegrator 1 complex subunit 3 [Source:HGNC Symbol;Acc:18697]
Mouse Orthologue:
Ascc3
Mouse Description:
activating signal cointegrator 1 complex subunit 3 Gene [Source:MGI Symbol;Acc:MGI:1925237]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39074 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12811 | Nonsense | Available for shipment | Available now |
sa7238 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39074
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 |
---|---|---|---|---|---|
ENSDART00000114325 | Essential Splice Site | 369 | 761 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 2500779)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 1530431 |
GRCz11 | 16 | 1554319 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATGTGCAGAAAGTGGCCATTCTCATCATTGACGAGATCCATCTTCTGG[G/A]TAAAGCGTCTGACAAAACACCACTAAAACTGCCTTCCCACTGCACAAACG
Long Flanking Sequence:
TCTTAATAAGGTTAAGTTCGGGTAATTAGGCAGGCCATTCTATAGCAGTGGTTTGTTCTGGAGACAATCCAAAACAAATATTGCTTAAGGGGGCTAATAATATTGACCTTAAAATGGGTTTTAAAAAAATGCTTTTATTCTGGCCAAAATAAAACAAATAAGACTTTTTGCAGAAGAAAAAATATTATAGGAAATCATGTTGAAAATTCCCTGCTTTGTTTAACATCCTTAGTGAAAAAATCACAGGAAGGATAATACTTTTGTCTTCAACTGTATCAGCGTATGTTACACCCTGACGCTTTATTTGCTGATGATCGTACTGTTTCTGTCTAGGGTGGTTGAGTTAACTGGTGACAATACTCCGGACATGCGAGCCATAGCACAGGCTGACCTGATCGTCACGACACCAGAGAAGTGGGATGGAGTGAGCCGCAGCTGGCAGAACCGCAGCTATGTGCAGAAAGTGGCCATTCTCATCATTGACGAGATCCATCTTCTGG[G/A]TAAAGCGTCTGACAAAACACCACTAAAACTGCCTTCCCACTGCACAAACGACAAGCCACAGACTGGAAGTCGCTAGCTGTTTGTTTTTAAATGTCTGACAGTTTTTAAATGTTATTTCTGTTATTTTTAAGTTTAATATTGGTTTCATTTTACCTTTATTATACAAATTTGACAATTTTTTGATTTGCTGGTAATAAAAAAATAGTATTGATAGTTTTTAAATGTCCTATCTGCCATTTTTAAGTTAAATATTGGTTCCATTTTACCTTTATGATGCAAATTCGATAATTTATTTTAATGTATTGCTAATAAAAAAAATTGTATTGATACAGTTTTTAATGTCATCTACCATTTTCAAGTCATATGTTGGTTACAATTTACCTTATATGTAAATTTGACCGTTTTTTATTGTATTACTAATAAAATAAATAGTGTTGATACAGTTTTTAATGCCATATCTGCTGTTTTTAATTAAATGTTGCTTGCATTTGACCTTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12811
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 |
---|---|---|---|---|---|
ENSDART00000114325 | Nonsense | 408 | 761 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 2501864)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 1529346 |
GRCz11 | 16 | 1553234 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCAAAAACGGTCAGAGTAGTAGGACTGTCCACSGCGCTGGCTAATGCA[C/T]GAGATCTAGCCGACTGGCTGGGCATCGGACAGGTTAGAAAGACCACTGCG
Long Flanking Sequence:
GGTCCCATTTTACCTTTAAAATTTAAAATTTGACTATTTTCGGTGAAATAAATAGTATTGATGGTTTTTAAATGTCATATCTGCCATTTTTAAGTCTAATATTGATTTGATTTTAAATATATTGCTAATAAAAGAAATAATGTTGATGCAGTTTTTAAATGTAATATCTGCCTTTTTTAAATCAAATATTGGGGCAAAATTTTTGCCATTTTTGATGTATTGTCAATAAAATAAATAGCACTGATAGCTTTTAAATGTCATATCTGGCCTTTTTAAGTCTAATATTGATTCCATTTTACCTTTGTGATGCAAATTTGACCATTTTTGATGTATTGCTGTCAAAGAAATGGTATTGCTACAGTATTTACTTTTTGTTTGGCTTCACAGGTGAAGACCGAGGGCCGGTTCTTGAAGTCATTGTGTCCAGAACCAACTTTATTTCATCGCACACCTCAAAAACGGTCAGAGTAGTAGGACTGTCCACCGCGCTGGCTAATGCA[C/T]GAGATCTAGCCGACTGGCTGGGCATCGGACAGGTTAGAAAGACCACTGCGATATACAACCTGCAATATTTTACAATTGAACATGTTTTTGATCAAACAAATGTTTTTCTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCGAGGGCCGGTTCTTGAAGTCATTGTGTCCAGAACCAACTTTATTTCATCGCACACCTCAAAAACGGTCAGAGTAGTAGGACTGTCCACCGCGCTGGCTAATGCACGAGATCTAGCCGACTGGCTGGGCATCGGACAGGTTAGAAAGTCCACTGCGATATACAACCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7238
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114325 | Nonsense | 629 | 761 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 2515647)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 1515563 |
GRCz11 | 16 | 1539451 |
KASP Assay ID:
554-4409.1 (used for ordering genotyping assays)
KASP Sequence:
GTTATCCTTGTGCACGACATCAAGAAGGACTTTTATAAGAAGTTCCTGTA[C/G]GAGCCGTTCCCTGTGGAGTCTAGGTGTGTACAGAGCCATAAATCTCCCGG
Long Flanking Sequence:
TCCGCTGTGTAAAACATATGCAGGAATAGTTGGCGGTTCATTCCGCTGTGGTGACCCCTTATAAATAAAGGGACAAAGCCGAAGGAAAATGAATGAACGAATGAACATGTAACATAATTTCAAATGTTAATAATAATATCACATTCAGGACAAACCAGATTCCTCACAGCAGCTCACTTCACGTCCTCTGTTTGCTCAGTATAGTGTTATTAGCCCTCCTGAATGTTTGATGGAGAGAAGATTTTGTTCAGCACATTCCTGAACATAACAGTTGTAATAACTCATTTCTCAAAGCTGATTTCTTTCCTCTTTGCTACGATGACAGCACATAATATTTGACAAGACATTGTTCACTAGTGTTCAGCTTAAAGTGAGATCTTCTCCATTCCAGATGTTCTCCAGATGATGGGGCGGGCAGGGCGGCCGCAGTTCGATGACCAGGGCAAGGCTGTTATCCTTGTGCACGACATCAAGAAGGACTTTTATAAGAAGTTCCTGTA[C/G]GAGCCGTTCCCTGTGGAGTCTAGGTGTGTACAGAGCCATAAATCTCCCGGTCTGTCCTTTGTGTTAATGGAGCAATTGCATCGTTTTGCATGTGACATTTGCAGTGAAAACTCAAAACATAAATGAACAGAGTACATGTTAACATTATATTAAAACATCAGTTCATATTTTACAACACTACTAAATACAGAGTTCTGGGGTCAGTAAAGTATCAATCTGTAAACATTTGTTTACATATTAAATGAGGAAAATAAGCATGCGTTATGATGTGACTGAAAAAGTGTCTGAAAAGAGCTTTAAAGAATTATTAAGGAAATGGACGTCTGTGTTTTGAGCAGAACCTGCATTTAACCAATCAGAGTCTCGTCTCTCATTCCCTTTAAGAGTCAGTTGCGCCTCACCATGGTGTATTTGCTCTTTACATATCGGAGTGTAAAAACTGAACGCTTCAGTAGCGAGAAAACAGTTAAACAGATCATCTGCAGCACGAGGATAAAGAA
Associated Phenotype:
Not determined