ZMP
SACS (2 of 2)
Ensembl ID:
Description:
spastic ataxia of Charlevoix-Saguenay (sacsin) [Source:HGNC Symbol;Acc:10519]
Human Orthologue:
SACS
Human Description:
spastic ataxia of Charlevoix-Saguenay (sacsin) [Source:HGNC Symbol;Acc:10519]
Mouse Orthologue:
Sacs
Mouse Description:
sacsin Gene [Source:MGI Symbol;Acc:MGI:1354724]
Alleles
There are 11 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa42539 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa28446 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa32032 | Nonsense | Available for shipment | Available now |
| sa14729 | Nonsense | Available for shipment | Available now |
| sa35878 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa12071 | Nonsense | Available for shipment | Available now |
| sa18161 | Nonsense | Available for shipment | Available now |
| sa7404 | Missense | Mutation detected in F1 DNA | Not yet available |
| sa10203 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42539
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 |
|---|---|---|---|---|---|
| ENSDART00000090779 | Nonsense | 325 | 4578 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 21874165)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 9413745 |
| GRCz11 | 15 | 9389816 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGCTCTTTCTAAAGAGCGTGCAGAAGGTCTCTCTGCATATACGGGAAT[C/A]AGATGGAACAGAGCGGATGCTTTTCCAGGTCACAGCAAGCGATAGCCAAG
Long Flanking Sequence:
GATCACCTACTGCACCTTTAAATTACTTGATGGAGAGCAGGGATTTTGAATAGCCACATCTACTGTATGTGCATTTGTGTATTTATTTCATTATGGACCAAAATATTCTACTACTATTAATGTACCATCTTTTATAGATGTACCTAGTATATTCAGCGGGGATCAAATTGCGATGCTGGACCCTCATCAGATGTTGTTTGGAGTACATGAGTCTGGCCAGTGCTGGAATCTGAAGTCTGACATTAAAGAAATAACCGAGCTAAGCGATCAGTTTTCCCCTTATTTTGGCTTGCTCGGTAGCTCAGAGAAAACCATTAAAGATGGCAACTTTCCAGGAACACTCTTTCGCTTTCCACTCCGGATGAAACCCTCACAATTAAGTAACAACATTTACAATAAAGAGAAGGTGCTGGAGCTCTTTGAATCCTTCAAAGTCGATGCAGACACAGTATTGCTCTTTCTAAAGAGCGTGCAGAAGGTCTCTCTGCATATACGGGAAT[C/A]AGATGGAACAGAGCGGATGCTTTTCCAGGTCACAGCAAGCGATAGCCAAGAAGATAGGATGGAAAGGCCGAACTCTCTAAAAACCCTGGGACAGGCTATAGATAGCTACAGTAATGGCGTACCGAGCAGTTCGGTCACCTGTGCCACCTACCAGCTCTCCATTGAAGCGCGGGATGAAACTGCCAAGGAGACTCAGAAAACCACCTGGTTAGTGTGTAACAGCGTGGGAGGACGAGGCATGTGCGGTGAACTGGATTCTCTTGCCGATGACCTGAAGTTTATCCCAACCATTGGCATTGCCTTGCCACTCACTCTTATTGATGAGGACAAAGGGGCAACTTCTAGTTTCTCAGGACGCGCTTTTTGTTTTCTCCCTTTGCCACTTGGAGAAGAAAGTATGACAGGATTGCCGGTCCACGTTAGTGGTTTCTTTGGATTGACAGACAATCGTAGGAGCATTAAATGGCGGGAGGTGGACCAATGGAGGGACCCGGCGGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28446
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 |
|---|---|---|---|---|---|
| ENSDART00000090779 | Nonsense | 1306 | 4578 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 21883174)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 9404736 |
| GRCz11 | 15 | 9380807 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCACAGTTTTAAAGCCCATACCAGATTTGGACCTGCAACCTTACTTGTA[C/A]TCGTTACCAAAGACTATTGCAAAATTCAACAAGCTTTTTAAATTCTGTGG
Long Flanking Sequence:
ACAAAGTTAGTGAAGTCCTCTGAGGTACAGACAAATCTGCAAAAATTGAAATGGGTCCCTGTTTGCAAAGACAGACCTTTGAATTACCCAAAGTCACTTGCTTGGAGAGGTGATTCATGCAATATATCGTCTCTTTCTGAAATGTGTGACATTTCTTATGCTGTACTTGTTGGTTCTTCAGTTTCCCTAGTTGAACGTACCTCTGCTGGGATGAAAAAAGCCCTGAAGTTGTCATTAGAGCCTCAAGTTGACCAAGTGCTCCAGCATTTGAAAGCAGTAAATGACTGGCATCAATCTCAAGCATTTACCACTGAAGACTGGTATCAGTTTCAGCAGATCTTGTGTGAGATATATGAATTTATGCAAGCTCACTTGGAAGATGCAAGGGAAGCCTTGAAGTCTCTGTCCTTTGATTGGGTTTGGACAGGGAAAACATTTGCTTCCCCTGGATGCACAGTTTTAAAGCCCATACCAGATTTGGACCTGCAACCTTACTTGTA[C/A]TCGTTACCAAAGACTATTGCAAAATTCAACAAGCTTTTTAAATTCTGTGGCTCCATTGAAGAAGTTGTTCCAAGCCATGTCTTTGAAGTTGTCAAAACGATAAGACAAAGGTGTGAAGAGGAGATGACAAAACAAGAGAGTAAACGCAATGTCCTGCTCCTAATTAATATTTTACGGTGGCTATACAGCAGTCAAATACCAGTCGATGCTGACATGCATGTCCCCATTCTTTACCACAAAGATCCAAGCAAATTGGTTATGAAACCTATCCATGAATGCACTTACTGTGACATCAAAGTAGAAGACCTGAATGACTTACTAGATGATGCTTCCGAGCCCATCATCCTTGTCCATGATGACATTCCAATGAAAACTGCTGAATGGTTGAAAGTCCCATGTTTGAGCACAAGATTGATAAACCCAGAGAACCTAGGGTTTGAACAATCAGGTCAAAGAGAGCCTCTAACTGTGAGAATAAAGAACATTCTAGAGGAATATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32032
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 |
|---|---|---|---|---|---|
| ENSDART00000090779 | Nonsense | 1412 | 4578 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 21883491)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 9404419 |
| GRCz11 | 15 | 9380490 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCCATGAATGCACTTACTGTGACATCAAAGTAGAAGACCTGAATGACT[T/A]ACTAGATGATGCTTCCGAGCCCATCATCCTTGTCCATGATGACATTCCAA
Long Flanking Sequence:
CTGGTATCAGTTTCAGCAGATCTTGTGTGAGATATATGAATTTATGCAAGCTCACTTGGAAGATGCAAGGGAAGCCTTGAAGTCTCTGTCCTTTGATTGGGTTTGGACAGGGAAAACATTTGCTTCCCCTGGATGCACAGTTTTAAAGCCCATACCAGATTTGGACCTGCAACCTTACTTGTACTCGTTACCAAAGACTATTGCAAAATTCAACAAGCTTTTTAAATTCTGTGGCTCCATTGAAGAAGTTGTTCCAAGCCATGTCTTTGAAGTTGTCAAAACGATAAGACAAAGGTGTGAAGAGGAGATGACAAAACAAGAGAGTAAACGCAATGTCCTGCTCCTAATTAATATTTTACGGTGGCTATACAGCAGTCAAATACCAGTCGATGCTGACATGCATGTCCCCATTCTTTACCACAAAGATCCAAGCAAATTGGTTATGAAACCTATCCATGAATGCACTTACTGTGACATCAAAGTAGAAGACCTGAATGACT[T/A]ACTAGATGATGCTTCCGAGCCCATCATCCTTGTCCATGATGACATTCCAATGAAAACTGCTGAATGGTTGAAAGTCCCATGTTTGAGCACAAGATTGATAAACCCAGAGAACCTAGGGTTTGAACAATCAGGTCAAAGAGAGCCTCTAACTGTGAGAATAAAGAACATTCTAGAGGAATATCCATCAGTTGCAGATATCTTCAAAGAGCTCTTGCAGAATGCGGATGATGCCAATGCCACTGAGTGCAGTTTCTTGATTGACATGCGAAAGAATCTTGAAATTCGAGAGAATCTTCTTGACCCTGGCATGATTATTTGCCATGGTCCTGCTTTGTGGTCATTCAACAATTCTGTTTTCTCTGATACAGACTTCCTTAATATAACCAGGTTGGGTGGATCAATGAAAAGATGTGAAGCTGACAAGGTGGGAAAATTTGGCCTCGGGTTCAACTCTGTGTATCATGTGACTGACATACCTATTATTATGAGCAGAGAATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14729
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 |
|---|---|---|---|---|---|
| ENSDART00000090779 | Nonsense | 1897 | 4578 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 21884946)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 9402964 |
| GRCz11 | 15 | 9379035 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCAAAACTGGCTTACCTGTCCACATAAATGGTTGCYTCGCTGTCACAT[C/A]AAATCGCAAAGAAATCTGGAAGACAGACACCAAAGGACAATGGAATTCCA
Long Flanking Sequence:
TATTCTTAAATCTGCTGCCAAAGTCATGAAAAAAGTTGCAGCCACCAGCAAAGTGCCAACTGAGGTACCGAAGTCTGGTTGCATCATCAGGATCATAGTGGAGGAGTACCATAATGTCTTCAGACGCATAGTTGATCTTCAGTCCCCACTTTTCAGAGGTTCTGATGAAGATCCATCATCTTACTTTGAGATGGCAGCTAAAGGTACACAAACTAAGAGACTTACAGATGACATGCCACAAAAGGGAGTTGAAAATACAAACTGGCTAATCTGCTCATGCATGGATGTGACAGAAGCTCTGAAATTCTCCTTAAATGATAGTGGAAAACGCCTTGGTCTGGTACCATGTGGAGGCATTGCTGTGCTGCTTACTGAAGAAGATAATAGAAAATGGACTGTTAAGACAAGTGCGACACCAATTGGGGAGGTTTTCTGCTACCTACCCCTTCGAATCAAAACTGGCTTACCTGTCCACATAAATGGTTGCTTCGCTGTCACAT[C/A]AAATCGCAAAGAAATCTGGAAGACAGACACCAAAGGACAATGGAATTCCATTTTCATGAGGCATGTGATTGTCCAAGCATACTTGGCTGCACTCAACATGCTGAGATCAATGGCAGAAAGTGGGGAGTTATTGGACTACAGCTATTATGCTGCCTGGCCTGACCCTGGAGTTGTCCATGATGATTTCAATCTGATTTGTCAAGGTGTTTATCAAGAAATAGCCAAAGGTGCTGATGATGATCGTGCAAAAGTCTTTTCAGATGGGAAAACCTGGGTGTCAATCAAGAATGTCCGATTTCTGGATGACTCCTTGCTCTGCAGACCAGACATTGGGTCTGCTGCATTTAAGATATTCTTGAAATATCTTAGAAAATGTGGATCCCAAGATCTCTGTGCTGTTGAGCTGCCAGAATGGGTTAAGGAAGGTTTTGATGATGCTGGCTGTAAAGGAAAATTAATGGAGAACACCCTGACTGAGAAGCAGTTTTTCTCAGATGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35878
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 |
|---|---|---|---|---|---|
| ENSDART00000090779 | Nonsense | 1967 | 4578 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 21885157)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 9402753 |
| GRCz11 | 15 | 9378824 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCCTGGAGTTGTCCATGATGATTTCAATCTGATTTGTCAAGGTGTTTA[T/A]CAAGAAATAGCCAAAGGTGCTGATGATGATCGTGCAAAAGTCTTTTCAGA
Long Flanking Sequence:
ACTAAGAGACTTACAGATGACATGCCACAAAAGGGAGTTGAAAATACAAACTGGCTAATCTGCTCATGCATGGATGTGACAGAAGCTCTGAAATTCTCCTTAAATGATAGTGGAAAACGCCTTGGTCTGGTACCATGTGGAGGCATTGCTGTGCTGCTTACTGAAGAAGATAATAGAAAATGGACTGTTAAGACAAGTGCGACACCAATTGGGGAGGTTTTCTGCTACCTACCCCTTCGAATCAAAACTGGCTTACCTGTCCACATAAATGGTTGCTTCGCTGTCACATCAAATCGCAAAGAAATCTGGAAGACAGACACCAAAGGACAATGGAATTCCATTTTCATGAGGCATGTGATTGTCCAAGCATACTTGGCTGCACTCAACATGCTGAGATCAATGGCAGAAAGTGGGGAGTTATTGGACTACAGCTATTATGCTGCCTGGCCTGACCCTGGAGTTGTCCATGATGATTTCAATCTGATTTGTCAAGGTGTTTA[T/A]CAAGAAATAGCCAAAGGTGCTGATGATGATCGTGCAAAAGTCTTTTCAGATGGGAAAACCTGGGTGTCAATCAAGAATGTCCGATTTCTGGATGACTCCTTGCTCTGCAGACCAGACATTGGGTCTGCTGCATTTAAGATATTCTTGAAATATCTTAGAAAATGTGGATCCCAAGATCTCTGTGCTGTTGAGCTGCCAGAATGGGTTAAGGAAGGTTTTGATGATGCTGGCTGTAAAGGAAAATTAATGGAGAACACCCTGACTGAGAAGCAGTTTTTCTCAGATGTTTTCTTCCCCCATATCCAAGACATAGATAAGGACCTACGGGACCCTCTGATGTATTATGTACTCAATGAAAAACTTGAGGATTTTGCATCCATACTGAAGGAAACCCCATGCATTCCATCTTCAGGACCATCAAAGATGCTTGTTTTGCCATCTCGACTCATCCACCCAGAGGGCAGAGTGGCCAAACTTTACAACAGTGAAGACGGAAGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12071
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000090779 | Nonsense | 2081 | 4578 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 21885499)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 9402411 |
| GRCz11 | 15 | 9378482 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCCCCATAWCCAAGACATAGATAAGGACCTACGGGACCCTCTGATGTA[T/G]TATGTACTCAATGAAAAACTTGAGGATTTTGCATCYATACTGAAGGAAAC
Long Flanking Sequence:
TTCATGAGGCATGTGATTGTCCAAGCATACTTGGCTGCACTCAACATGCTGAGATCAATGGCAGAAAGTGGGGAGTTATTGGACTACAGCTATTATGCTGCCTGGCCTGACCCTGGAGTTGTCCATGATGATTTCAATCTGATTTGTCAAGGTGTTTATCAAGAAATAGCCAAAGGTGCTGATGATGATCGTGCAAAAGTCTTTTCAGATGGGAAAACCTGGGTGTCAATCAAGAATGTCCGATTTCTGGATGACTCCTTGCTCTGCAGACCAGACATTGGGTCTGCTGCATTTAAGATATTCTTGAAATATCTTAGAAAATGTGGATCCCAAGATCTCTGTGCTGTTGAGCTGCCAGAATGGGTTAAGGAAGGTTTTGATGATGCTGGCTGTAAAGGAAAATTAATGGAGAACACCCTGACTGAGAAGCAGTTTTTCTCAGATGTTTTCTTCCCCCATATCCAAGACATAGATAAGGACCTACGGGACCCTCTGATGTA[T/G]TATGTACTCAATGAAAAACTTGAGGATTTTGCATCCATACTGAAGGAAACCCCATGCATTCCATCTTCAGGACCATCAAAGATGCTTGTTTTGCCATCTCGACTCATCCACCCAGAGGGCAGAGTGGCCAAACTTTACAACAGTGAAGACGGAAGGTTTCCTGAAGGAAGTCTAAGAGACTATGTCAATCCAGTATGCTTGGTGAAGTTATTGCAGCTGGGAATGGTCAAGGATGACTTATCTTGGGAAGACTTGATTGAAAGGGCTGAGTCTGTACTGGCTCTGAATGAAAATGACCACACAATTGCGTGCCACAGGAGCAGCATAATCCTCAGTCTTATTGACGAAAAGCTAAAAATGAGAGATCCAGCTGCAAATCAGTATCTTGATATATTTCAAAATATCAAGTTCCTACCATTTTTGACAAAGCCAGCTGGATTTTCACTTCCGTGGCATGGCAACAATTTCCCCCAGTTGACCATGTTCTCTGCAAAGGAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18161
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 |
|---|---|---|---|---|---|
| ENSDART00000090779 | Nonsense | 2403 | 4578 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 21886464)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 9401446 |
| GRCz11 | 15 | 9377517 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTTTTGAAAATGTGGGAGTTCACGCAAGCTTCACTGTTGAAACGTTCT[C/A]AGGTGTTTTACAGCYGATAAAGAATGAATGTGGGAGAAAACCTYTMACTG
Long Flanking Sequence:
TTTCCCCCAGTTGACCATGTTCTCTGCAAAGGAGCTTTTTACAACAGAACACCAGGACACTGTGTGTTTGATGAACCCTATTCTGAATGAAAATTCACCCTCCTTTAAAGGATGTGGTCCCATCTCACTGGCTGTGAAGGACTTTCTTGGACTCATAAGAAAGCCGACGGTCTCATTAGTCATCAGCCAGCTAAAAGAGCTCTCAAAGTCCTTTGACGGTGTAACACTGTACCAAGAGAACATAACCAATGCTTGTTACAAATATCTTCATGAGGAGTTGCTTCAGTCCAATGCTGCAAAAGAGGAAATCATGGAAGAGCTAAAAACATTCTCCTCTATTTTAGTTGAGAACACATATGTGGAGCCATTAAAAGTTGCATTTAACTTAAACTTTGATGCTGCACCATACCTTTACCAACTTCCAAACAAGTACAGAAATAGTTGTCGAGAGCTTTTTGAAAATGTGGGAGTTCACGCAAGCTTCACTGTTGAAACGTTCT[C/A]AGGTGTTTTACAGCTGATAAAGAATGAATGTGGGAGAAAACCTCTAACTGAAGAAAACTTTCAACTGTCTCGTAGAATAATTAGTGAGGGAATATGGAGCTTGATCAGAGACAAAAGTCAAGAGTTCTGTCTAAGCAACTACGGGGAGATACTTCTTCCTGACAGCAATTTCACATTACAACCATCAAAATCGCTTTGCTACAATGACTGTCCTTGGATTAAAGTCAGGGACACGACTGTTAAATACTGCCATGGTGATATTCCAAGAGAAGTAGCAGTAAAACTGGGGGCAATTCCGAAACGTCACAAAGCCTTAGAAAGATATGCCTCCAACATTTGCTTCACTACCCTTGGCAGTGAGTTTGGGCAGAAGGAGAAACTCACCAGCAGAATAAAAAGTATCCTCAATGCTTATCCATCTGAAAAAGAGATGTTGAAAGAGCTCCTGCAGAATGCAGATGATGCAAAAGCCACAGAAATATACTTTGTCTTTGATCCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7404
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 > C
Consequence:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000090779 | Missense | 2508 | 4578 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 21886779)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 9401131 |
| GRCz11 | 15 | 9377202 |
KASP Assay ID:
554-4373.1 (used for ordering genotyping assays)
KASP Sequence:
AAGAGAAGTAGCAGTAAAACTGGGGGCAATTCCGAAACGTCACAAAGCCT[T/C]AGAAAGATAYGCCTCCAACATTTGCTTCACTACCCTTGGCAGTGAGTTTG
Long Flanking Sequence:
AGAGCTAAAAACATTCTCCTCTATTTTAGTTGAGAACACATATGTGGAGCCATTAAAAGTTGCATTTAACTTAAACTTTGATGCTGCACCATACCTTTACCAACTTCCAAACAAGTACAGAAATAGTTGTCGAGAGCTTTTTGAAAATGTGGGAGTTCACGCAAGCTTCACTGTTGAAACGTTCTCAGGTGTTTTACAGCTGATAAAGAATGAATGTGGGAGAAAACCTCTAACTGAAGAAAACTTTCAACTGTCTCGTAGAATAATTAGTGAGGGAATATGGAGCTTGATCAGAGACAAAAGTCAAGAGTTCTGTCTAAGCAACTACGGGGAGATACTTCTTCCTGACAGCAATTTCACATTACAACCATCAAAATCGCTTTGCTACAATGACTGTCCTTGGATTAAAGTCAGGGACACGACTGTTAAATACTGCCATGGTGATATTCCAAGAGAAGTAGCAGTAAAACTGGGGGCAATTCCGAAACGTCACAAAGCCT[T/C]AGAAAGATATGCCTCCAACATTTGCTTCACTACCCTTGGCAGTGAGTTTGGGCAGAAGGAGAAACTCACCAGCAGAATAAAAAGTATCCTCAATGCTTATCCATCTGAAAAAGAGATGTTGAAAGAGCTCCTGCAGAATGCAGATGATGCAAAAGCCACAGAAATATACTTTGTCTTTGATCCCAGGACTCACTCAACTGACAGAATTTTTGATGACAAATGGACTCCCTTGCAAGGCCCATCACTCTGTGTATACAATAATCAGCCATTTACAGAGGATGATATCAGGGGGATCCAGAATCTTGGAAGGGGTACCAAGGAAGCAAACCCTGGAAAAACTGGCCAATATGGCATTGGATTTAACTCAGTATATCACATTACTGACTGCCCCTCTTTTATCTCAAATAACGACATTCTTTGCATCTTTGATCCACATGCCCGTTATGCACCTGGAGCAACATCCGTTAGTCCGGGAAGAATGTTTAGAGATTTGGATTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10203
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 |
|---|---|---|---|---|---|
| ENSDART00000090779 | Nonsense | 3377 | 4578 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 21889385)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 9398525 |
| GRCz11 | 15 | 9374596 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCCAGCATACTTCGAGCWCTTGAGTACATGATCCAGATATCCGCTTTC[A/T]AAACAGCAAGTTTGACTGATAAAGATTTCGATGCTTTGCTGTTGTACTTC
Long Flanking Sequence:
CTTTTGACATAAACAGTTTTGGAGACCTTTTGGGATCTGTTCTTCCCCGGGAGTGCAAAGCAAGGAGTTCAGTGAAGTGGAAGGAGAACTTTCCCACTGAATCTTGGCTCAAGAGTTCATGGCATTTTATCAGTGAACAACTTGCAAACAAGGATGACCAAGCAGAAAACAAGCTGAAATTTGAGACCATTCTGGAGATCTTAAAAGATTGGGCCCTCCTTCCAGGAATCAAATTTTTGGTTTCAGGCAACAAATTGGTTGTGCCAGAGCATGACGTTTTGTTACCCCTGAGCCTGATCTTTGCAGCCATCTTCCCGAATGGACAAAATGACAAAGTCTTTCATACCTTGATGAAAGGAGGATGCTTTCAATTGGCTGTGAATAAAATATGTGCCAAAGAGAATCCCATGTTGCCTTTGCTGGCTCAGCATACAGCAAACATAGACAACCCTTCCAGCATACTTCGAGCTCTTGAGTACATGATCCAGATATCCGCTTTC[A/T]AAACAGCAAGTTTGACTGATAAAGATTTCGATGCTTTGCTGTTGTACTTCAACTGCAATTTGTCAAATCTAGCCCAGGATGATATTCAGTGTCTAAAACTGTTGCCATGTTACAAAGCTGTCAGTGGTCGGTACATATGCATTTCAAACTTTGGAGCATGCTATGTTCTAACAAAGAGCATTCCCTCAGCTGACATTGAAAAATGGGCACACAATACATCCTCAGCCTTCCTCGCTGACAATCCACAGCTGAAAGAACTCTACGGCTTCCTTGGGATCACACCAATCGATGATCTTGAGGTATACCTGAATCATGTCCTTCCAAAGTTTGACATTTTATCACATGATGCCAAAATCCAACATGTCATCTACCTGAAGGAGAGGTTATTGGCAATGGAGGAGCAAGTCAGCATCAAGGATAAACTCTTTGAAAAACTAGAAGGTCTGTCCTTCATTTATGACTCCACCAATAGACTGAAACCTGCCAAGGCCTTTTTTGAT
Associated Phenotype:
Not determined