ZMP
auts2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human autism-related protein 1 (AUTS2) [Source:UniProtKB/TrEMBL;Acc:Q7ZZ40]
Human Orthologue:
AUTS2
Human Description:
autism susceptibility candidate 2 [Source:HGNC Symbol;Acc:14262]
Mouse Orthologue:
Auts2
Mouse Description:
autism susceptibility candidate 2 Gene [Source:MGI Symbol;Acc:MGI:1919847]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21753 | Nonsense | Available for shipment | Available now |
| sa45409 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21753
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000078920 | Nonsense | 77 | 1019 | 1 | 15 |
| ENSDART00000137928 | None | None | 995 | None | 14 |
Genomic Location (Zv9):
Chromosome 10 (position 27832306)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 27235100 |
| GRCz11 | 10 | 27196813 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTCTTCATCTTCAGCCACCCCCTTCCAGCAGGGGGTTACCTTTGCCCT[C/A]GAGGCCAGCTCAAATCCAGAACCCTTGCCCAGAGCGCACACTAAGGCCAC
Long Flanking Sequence:
TGTTGTTACTGTATGATGTTGCTCTCATGATTTCAGTTTAAGTGTTTTAGAGCTGGTAGTGCACTATTACAAATTTATTCAATCAAGTAATAAAATAAAAAAACACAATGCAATCATTTTTTAAATGTGAAATATTATACTGTGGCACACTACTTTTTCTTGCACATCATCATCTTGCACATTAATCATGTTCCATTCTGTATTAAATCAAATGTTGATCTGCACATGAGCTTTCTAAAAAGTGCTTTGTTGTTCTTTTGTCTCTACAGTTCCAGATTTTAGTGTTGACACACTCTCCACCAATGCCAGCCAGGAGCTGCGAGGCCTGGGCATTCCCAAGGTGTCAGGCCTAGAGCGCAGTCAAGAGAAGAGCCAGGAGACTTCCCGGGAAATCTCCTCGGCCACCCCCCCACTGGTGCCCACTTCCCATTCCAAACCTCCCCTCCCCGCCCCTCTTCATCTTCAGCCACCCCCTTCCAGCAGGGGGTTACCTTTGCCCT[C/A]GAGGCCAGCTCAAATCCAGAACCCTTGCCCAGAGCGCACACTAAGGCCACTGTCACCCCCTATTGCTCTGCCTCAATCCCAGGGTCAGGAGCTCTCTCAGGCACCCCCGCATCCGTCTCAGCACCCACCTGAATCACCATCTCACCCAAAGCCACCTCGAACCCCAAGTATCTACCACCACCCCCCATCGCCAGCGCTACCAGCCCAGCAGAACCCTACGCAACCCGTGCAGCACAGGCCACCCTCACGCTGTCACCAGCGTCCAATTTCAGCCTACAGTGGCAGCCTTACGCTCAACGGCCTGAGGTGAGTGTGCACCAAATGAGTGTATTGTAAAAGCACAGCAAGAAGTTTCTGTAACAATCCAGATGTGTTGTTTGCTGATTGAGTAGAGCCTCAGCTATTAAATCCTATAATACAACAGCAACGTTTCTGTTTTAGAATGTAAAATATATCAGTCCGCCAGTAAAGATGAGGCACAAATCCCTACATGTTTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45409
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000078920 | Essential Splice Site | 594 | 1019 | None | 15 |
| ENSDART00000137928 | None | 570 | 995 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 10 (position 27821435)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 27224229 |
| GRCz11 | 10 | 27185942 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCAGTCAGCTCACATGAGAGAGAACGAGAGCGGGACAGAGAGAGAGAG[C/A]GGGACCTGGACAAGAGGGACTCATCAGTCAACAAGGATGATAAAGAACGG
Long Flanking Sequence:
ATGGTTTGTCCTTCTTGGTGGTATGCTAACATTACCCTGGATACCATGGCTCTTGACACATCACAAAGACTTGTCTTTGGTCACAGTAGAGCTGAAACCTCCAATGCTAAATTGGCTAGTGTTTCATTCAAATTGGCCAGTTTCATTGTCCATCCCCTGTACACATGTCAGCTATTCTAATAATGTTTAAGAGAGGGAAATTTATGTGATTGTCTGATAAAAGAGTGTCTGATATTTTGCTCCGCATGAAGCAAAATAAAATAAAAAAATCTAATTAATTTCATTGTTTCATTCTCCTAGCATCCAACTCTGTGTTTGGCCACAAAGATTCACCCAGCGCACAACAGCACTTCAGCGGCCCTCACGAGCCATGGAACAGACTCCATCGCACACCGCCATCCTTCCCCACTCCACCGCCCTGGCTCAAACCTGGAGAATCAGAGCGCAGCGCTTCAGTCAGCTCACATGAGAGAGAACGAGAGCGGGACAGAGAGAGAGAG[C/A]GGGACCTGGACAAGAGGGACTCATCAGTCAACAAGGATGATAAAGAACGGTGTGTGGATTATAACAACACACTAATCAACACATCATTTGTCAAGAGTTAGATATGCTTTAGCTAGTGAATTGTTTAATGTGTAAGGCTGATTTGTTTACGGATTATTCACATTTGTACTGCAGCTAGATTTAATCATTACAATGTGATTAATGCTGCGGCCACATCAGAGTTAGTGCGTGCAAAATTCTGTCGTACGGTGCTGTGAAAAGGGGCGGGATTAAACAAGATGATTGGACTTTAAAAACAAACAAGCGATTGGTCCATGTTTTAAACTTCTGTCTAGAGAGGTCATGTTTTAATCTTCAATTTTTATTTAGATCTTCTGGTCTACCTAGAAAATATGTTTAGAATTTAGCCTCCCTTATGTTGAATAAAATAAGTTTCTCCAAATCTTTTAATTACACAGTGTGGAACATATTACCTGTCTGGTTTTACACTTTTTTACTGA
Associated Phenotype:
Not determined