ZMP
ENSDARG00000076924
Ensembl ID:
Mouse Orthologue:
Als2
Mouse Description:
amyotrophic lateral sclerosis 2 (juvenile) homolog (human) Gene [Source:MGI Symbol;Acc:MGI:1921268]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15114 | Nonsense | Available for shipment | Available now |
sa33807 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15705 | Essential Splice Site | Available for shipment | Available now |
sa33806 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12310 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15114
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 |
---|---|---|---|---|---|
ENSDART00000108524 | Nonsense | 87 | 1658 | 3 | 37 |
Genomic Location (Zv9):
Chromosome 6 (position 7927698)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 9563367 |
GRCz11 | 6 | 9798906 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAACCAAAYATCATCAGCAGAGCCCATTTTGGAGGCAGTGCTGAGCGAA[C/T]AGCGTGTTGTTTTTGTGGCTGCTGGCTCCGCSCACAGCGGAGTYGTGACG
Long Flanking Sequence:
ATGTATTAGAAGAAAAAGCCTTATTATTATAATTATTATTATTATAATTATAAAAATATGATTTAGTTGTTTAATTTAACAAATTACAATAAAGTACAAATAAAATCATAACTAATCATGTGATTTTGTTAGCTCACATTGTTAGTTTTGTGGCGAACAATTCATCTGTGTCACTGTGTCACAATATAAAAAAAAAAACAGTTGCAGCTTCCGGTTCATGCAGACTTTAACAATTATATTAATATATTTATTTAAAAAGGCTAAAGCATCCTAGGGTTCCCTTAGAAGTTAATTGGGGCCCCCTAGTTTGCACTGGCCCCTGTTTCATAAAAGTTGTTTTTAAAAAATTGATGATTTAGAAAAAAATTATGTTACAATTCAGAAATGTACTAATTTGAATTCTATATTTAGGCGGACAAGTGTACAGTTTTGGTGAGTTGCCTTGGAAGCAGAACCAAACATCATCAGCAGAGCCCATTTTGGAGGCAGTGCTGAGCGAA[C/T]AGCGTGTTGTTTTTGTGGCTGCTGGCTCCGCCCACAGCGGAGTCGTGACGGAGGATGGAGGAGTGCACATGTGGGGAGAAAATGTTCACGGCCAGTGTGGCTTGTTGGGACTGTCTGTTATCCCTAACCCCACCCCTGTGGGTGTGCTTGACTCTGAGGCCACGCCACCTCAGACGGTTAAAATCCTGGAGGTGGCATGTGGCGATCAGCACACCCTGGCTCTTTCAGCCAAGCATGAAGTCTGGGCTTGGGGTAGCGGCTGCCAGCTGGGCCTCAACACTTCAACTTTTCCCGTCTGGAAGCCCCAAAAAGTGGACCACCTATCTGGGAGGCATGTATTACAGGTGGCGTGTGGATCCGCTCACAGCGTGGCTCTCGTACGCTGTCTCCCTCCTCCACAGGAGCCCCGAAAACCCCCTCAAGACAAATGCGGTCAGTGCCATCAGCTGCTCTACACTATGACAGATAAAGAAGACCATGTCATTATCTCTGACGGCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33807
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108524 | Nonsense | 531 | 1658 | 8 | 37 |
Genomic Location (Zv9):
Chromosome 6 (position 7916871)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 9574194 |
GRCz11 | 6 | 9809733 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACTGATGCCCACCTGCCTTCCTTACAGACGGAAGTGTGGAGCTGGGGA[C/T]AAGGCCAGGATGGACAACTTGGACATGGAGACCTCCTTCCCAGGTCAGAG
Long Flanking Sequence:
GTAAAATCTTACCGAAATACGATTAAATATGGTGGGATTCCAATCTGATATGCACAAAAATAGGATTTGGTTTGTTGATTTGGACAATCTTTATAAGATCTACTGTTTGTATATAAATGAGTAAAAAACAATACAAATGCATATTTATTTTTAACCTCACATGATTATATCACAACATATATCAATCAAATGTTTGAGCGGATGTGTGGTTAATTTTAAAGCAGAAAAATCAGATTTGCACTTTGAACAATCTGAACAAGGCTTTCTGTCTTATTAGTACATGTAGAATACATTCAGGCTTTAGATATTAATGTTGCAGGTTTCTTTTAAGGTGTTTTGTGTTGTTGATTCTCTTTCTCCTTCACACTCTCTCAGTATCTCCTCGCCTCCTACGGAGAACAAGTCGCCCCCGTATGCGGGCTGTCCCGCTCGCTTCAGGAGGTATACCTGAGACTGATGCCCACCTGCCTTCCTTACAGACGGAAGTGTGGAGCTGGGGA[C/T]AAGGCCAGGATGGACAACTTGGACATGGAGACCTCCTTCCCAGGTCAGAGTCTTTAAAATCAGCGGGGAGCCATGTGTAGCTCCAATCTTTCCTAACACGTTAGCAACTTAATACAATGTTAGCAACTTGTTAAAAGTGTTACCAATATCCATAAACATGGTCAAATATCCTTGCAACTTATGTTTTTGACTTATTCAAGCATTACACATTCGTTAAAACAAGTTCAGTTGTTAAAATAGTAGCATTTTAGTAGAACATGCTAAAATATGCTAACATTATGTCAAAAAAATGGCAGAAACATTCTACCAAAATCTCAAAACCTACTAATATTTTAAAACGTTAGTGTTACGGAAATGCTAAAAACATGCTATCATAGAACATGCTAACGTTTTGACTAAACAGGAATTGGCTACTGTATACTAGAACATGTTATTAATGTGCCTAGTAAAACAAATTGGCAAACATGCTAAAATTGCTAGCAACTTGTTAAAATGTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15705
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108524 | Essential Splice Site | 604 | 1658 | 11 | 37 |
Genomic Location (Zv9):
Chromosome 6 (position 7908884)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 9582181 |
GRCz11 | 6 | 9817720 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGATTCCTGACTGTTTTGCTTTTTGTWTSTCCTCTTTTGTCTTTGCGC[A/T]GCTGTCAGATGGGATTCRTGTGTGGGATATTGGGGCAGGTCWGCAGCACA
Long Flanking Sequence:
CTAGGTAATTAGGTTAACTAGGCAGGTCAGGGTAATTAGGCAAGTTATTGTATATTGATGGTTTGTTCTGTAGACTATCGAAACAATATAGCTTAAAGGGGCTAATAATTTTGACCTTAAAATGTTTTTAAAAAAATTAAAAACTGCTTTTATTCCTGCCTAAATAAACCAAACAAGACTTTCTCTAGAAGAAAAAATATTATCAGACATACTGTGAAAATTTCCTTGCTCTGTTAAACATAATTTGGGAAATATTTAAAAAAGAAAAACAAACTCAAAGTGGGCTAATAATTCTGACTTCAACTGTATATGTTTGTTTGTGTGTCATCTCTTTATGAAGTATGAAGTTGTTCTTATCATGTAATGTTTTTATGTATATTGATCTTACTATGAAATTGCCATAAGTGGCTGATGTGTCAATAAATGAATGAATGAATGAATGGACAACATCCAGATTCCTGACTGTTTTGCTTTTTGTTTGTCCTCTTTTGTCTTTGCGC[A/T]GCTGTCAGATGGGATTCGTGTGTGGGATATTGGGGCAGGTCTGCAGCACACTCTCTTATTGGCTGACGGAGACTGTATTCAGCCAATCCTGTACTACAGCGGACAGCAGGTGAAGGAAGTGCCGGAGCCAACAGAGGAAGAGGAGCAGACTGCAGAATACACGCAACAACCTGTGCTGCTGCCCTTCTGTATGAACGTGAGCAAGTCTTCTCATCATCAACATCACTTCAAATCATTTTTTTTTTGTAGGGATGGACGATTAATCGATAAAAAAAAAATGCAGTCTAGATTCAGATACTGATGCAGTGTTGAATATAAACGGTCTCAATTTCATCTTTAATATTCCTTCTATAATCAAACTGTACATTTAAATCTGCGTTAGAACCAGAGTCATTTCTACCAGCATTATTATTATTTCTTATACTGATGTTTTAATTATCACAAAAGTACTGGAATAATAGTTATGTCATGAACACTGATGCTTACATGAAGATTTAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33806
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 |
---|---|---|---|---|---|
ENSDART00000108524 | Nonsense | 688 | 1658 | 12 | 37 |
Genomic Location (Zv9):
Chromosome 6 (position 7907154)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 9583911 |
GRCz11 | 6 | 9819450 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAAGCAGTGTGTATGCAGGTGGACGGACGTGTGCAGCGCTGACGGATTG[T/A]AATGTCATGGGTTTTATTGCTAGTCTGCATGAGCTGGCGGCTGCAGAGAG
Long Flanking Sequence:
GCGGTGGCATGACATTAAAAAGGTGGTTTGTGCTCAAAAATCCTTTATTGTGGCTGAATTCCAACAATTCAGAAAAGATGAATGACCAAAATTTGGAGTCAAAATTGTAGCCTTTGGAGAGGCCTAGTCATAGTCCTGACCTGAATCCAATTGAAATGCTGTGGTATGACACTAAAAAGGTGGTTTGTGCTCAAAAATCCTTCATTGTGACTGAACTCCAACAATTTTGAAAAGACGACTCAGCCAAAATTCCTCCACAGTGCTGTAACAGACTCGTTGCAAGTTATTGAAAATGCTTGGTTGCAGTTGATGCTGCTAAGGGGAATCAACCAAAATTGTTCCCTGATTGTTTCAATTATTATTGTATTATGAATTCTTTACCTTGATGTGGTGTTATCACTATTGTTTGAGTTGACTCTACATGATCTTTTTGTGTTGCAGTTGGGCTATGTAAGCAGTGTGTATGCAGGTGGACGGACGTGTGCAGCGCTGACGGATTG[T/A]AATGTCATGGGTTTTATTGCTAGTCTGCATGAGCTGGCGGCTGCAGAGAGAAAATATTACTGCAAACTCAGCAATATCAAGAGTCTTCTGCTCCAGCCATTGCTCAAGCTGGGTATGACTGTGTGTGTCACAATTGCTTGTTTTGTACACTGATTTAGACCTTCATTTGCATCTTCATTATAGCCCTGGAAATCTACACAAGTATCGTCTTATTCAGCGGCACATTTAGTGGAAATAAAACAGCTGAAATCAATGCTTAGTATATGCAAACGCTTTTGTTAACTAAAACTATATATATATATATATATATATATATATATATATATATATATATATATATATATAATTTAATTTATAATGTAAAACGTAATATTAGCATTAAGGGTATTACCCTTAACTAGAACTATTAACATTTTACATATAAAAATATAGCATATAAACCATTTTACTGGAGATATTGAGTTTATGTGCTTACCAATGAACAAATGATATCTGTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12310
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 |
---|---|---|---|---|---|
ENSDART00000108524 | Essential Splice Site | 1467 | 1658 | 31 | 37 |
Genomic Location (Zv9):
Chromosome 6 (position 7879804)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 9611243 |
GRCz11 | 6 | 9846782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGRTCGGCACAGAYGCTGATGGAAAGCTGCTGGAGTCTCCTAAACCTGGG[T/A]ATGGAAAATAGTATTAAAGGACTCTAAGGGTGGTCTATGCAACWGCAGTT
Long Flanking Sequence:
CCGTCGGTACCTGGTGAAGGTAAACATTGTATTTATTAACTGATGCTAAACCACACTTTCCTCCAACACATTAGCTTCCTAGTGTATATTTACCACTTTTGTACCACTGATTATTTTGCTCTGTATATCACAGACGCATGATGTGTGTTTTATTTTAGGCATGTGATACTCCTCTGCATCCTCTGGGTCGGCTGGTGGAGACGCTGGTTTCGGTATACCGGATGACGTATGTTGGTGTTGGAGCAAACCGCAGGTTATTACCGCAGGCCGTCAATGAGATCACGTCCTATCTCAGCCGTATCTTCCAGCTCGTCAGGTAAGATGATCTGTAAAACAGAAAAGGAAGTGTGCTTTTCCATGTCTTTTAAATAACATGCTTGTTTGTGTTTAGATTTCTCTTTCCCGAACTGCCAGAAGAAGGAGGTTCACTAGCCGACCCTCCAAAAGAGAAGGTCGGCACAGATGCTGATGGAAAGCTGCTGGAGTCTCCTAAACCTGGG[T/A]ATGGAAAATAGTATTAAAGGACTCTAAGGGTGGTCTATGCAACTGCAGTTGTTCATATTACAATTAGCTTTTAACTGGAATGTAAAAAAAAAACATTCTTCATTCATTTTCCTTCGGCTTAGTCCCTTTATTTATCAGGGGTCGCCACAGCGGAATGAACCGCCAACTTATCTAGCAAATGTTTTACCCAGTACTGGGAAACATCCACACACACTTGTTCACACACATACACTACGGCCAGTTTAGTTTAAGCAATTCACCTGTATCTCATGTCTTTGGACTGTGAGGAAACTGGAGCACCCGGAGGAAACCCATGCAAACATGGGGAGAACATGCAAATCTCACAAAGAAATGCCAACTGAGCCAGCCGGTACTCGAGCCAACGACCTTCTTGCTGTGAGGAGACAGCGCTAACCAATGAACCACTGTATCGCCTTGGTTAATCATAATTATGGCATTATAATTCCATGAAATTAAGATTATAGGTGGAGGTAACGAAT
Associated Phenotype:
Not determined