ZMP
als2a
Ensembl ID:
ZFIN ID:
Description:
Als2a protein [Source:UniProtKB/TrEMBL;Acc:A8KB94]
Mouse Orthologue:
Als2
Mouse Description:
amyotrophic lateral sclerosis 2 (juvenile) homolog (human) Gene [Source:MGI Symbol;Acc:MGI:1921268]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10766 | Essential Splice Site | Available for shipment | Available now |
hu3525 | Nonsense | Available for shipment | Available now |
sa17354 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10766
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 |
---|---|---|---|---|---|
ENSDART00000108652 | Essential Splice Site | 723 | 949 | 8 | 13 |
ENSDART00000108844 | None | None | 704 | None | 21 |
ENSDART00000128630 | None | None | 401 | None | 4 |
ENSDART00000135877 | Essential Splice Site | 58 | 992 | 1 | 25 |
ENSDART00000143432 | None | None | 126 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 13918073)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 13670638 |
GRCz11 | 9 | 13641841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCCTYAGTAAACTGAAGAWCCAGATCCTGAGCCCTCTGTTAGCCCGTGG[T/A]ACGTAACACACTTCTTCACTCATCAGTGATCACACATTTTTGTTTGCATT
Long Flanking Sequence:
AAGTTTAAACGCTGGTTTTGTGGTGAGGACGTAGAAGAGGTTTCTGTATATATATATATATACATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACACACACTATAGAAAGTCAGAATTATTAGCCCCCTGAATTATGAACTCATTTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAAATTTTATTTGACTAGATATTTTTCAATCAATGGGGGGCTAATAATTCTGACTTCAACTGTACATATATATAGCAACTATTTACTTTATTTGTTAATGTCTTTTAAGATTGGCTACGTGAACCAGGTTTTTGGGGGAGGACTGAATTGTTTGGCTTTGGCCGATCAGAATGCAATGGGTTTTATATCAACAATCCATGAGCTTGCATCGGCAGAGAGGAAATTCTACTGCAGCCTCAGTAAACTGAAGAACCAGATCCTGAGCCCTCTGTTAGCCCGTGG[T/A]ACGTAACACACTTCTTCACTCATCAGTGATCACACATTTTTGTTTGCATTTGAATATTAATTGAATCTGCTTTGTCATAATGCAGCAAGTTTGGCCTTGTCTCTGGGTGAGTCGTCCATGTTGCTCTTTCAAGAAATGGCTGGTAGTTTCAGCAAGCTTTGCCATCTGACAGGGCAACACTCAGTGTCCCTCACCAACTTCCTGCAGCAGGGCAAAGTGATCGAAACGCTGGTCTTGATCAAACACACAGCCATTTTTATGGATACCTATAAAGAGTAAGGATACCATTCATACTTAAAAAGCTGTTTTTAATCTTTTTGTTAAAGGCCAAATGGTGGATTTTGAGTGTGTTATGTATCTGTCTTTATATGATCTGCAAAGTCACAAAGCTTGAAGTTGCCCACAAAAGCATTTTTTTTTTATCTAGAGTAGAAGAGCTACCAAAAATGCCTGACAAAGTTTCTCTGTCATATCTACATCACTATTTAGAAGTGTTTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu3525
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 |
---|---|---|---|---|---|
ENSDART00000108652 | Nonsense | 838 | 949 | 11 | 13 |
ENSDART00000108844 | None | None | 704 | None | 21 |
ENSDART00000128630 | None | None | 401 | None | 4 |
ENSDART00000135877 | Nonsense | 173 | 992 | 4 | 25 |
ENSDART00000143432 | None | None | 126 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 13922932)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 13675497 |
GRCz11 | 9 | 13646700 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTAGAATCCAAGGAGAAGAACCCGTCGCTCTATGATCTGTTAGTAAACT[T/A]GTTTTACATGCCCTTGCAACACTTGAATGGGTATAACAGGTTACTTCTGA
Long Flanking Sequence:
TGCTGAAACCCTCACAGTGAGTCTGTGTACTCAAAAAATACAGTACAATTCAATATAACCATAAGATCATCCTTTTCATCATTGGTTTTAACCCTTGTGTGCTGTTGGTTGTATTTTCATCCACTCTGGGGTGATTTTGTGTCTTAATTTGGCCACAACTTTATCTGTTTCTCAGCAAATGGAATGATTTTGGTGAAAAATCTTATTTTGACACATATTTTGGGAAAAGGCTTACTACACTCTGCGCAAAGTTACTACCCCTTTGTTACATTATCTTCCTAACAGGAAAAACCACTAACAATTAAAAATACATGATTATTTGGTGTCGAGGCTTTGCAATCAAGGCTAGTCAATTTAAACAATACACAAGGGTTAATACAATCTTTGGTCATGCCTGATTTTCTTCACCAGAGAATGCTTTGGGAAGAAACTGGAGTTGATACAGGCTCTACTAGAATCCAAGGAGAAGAACCCGTCGCTCTATGATCTGTTAGTAAACT[T/A]GTTTTACATGCCCTTGCAACACTTGAATGGGTATAACAGGTTACTTCTGAAACTAGCCAACTGTTTTGAAGTGGTAAGGAAATGATCCAATTTTCATTATTTAGTTTATTAAAGCACCAAAATAATGCATGGCATAATGTTTTATTTTTTAGAACACTGATGAATACCAGAGGATTCAAAATGGCTGCTCCAAATATGAGGCTTTAGCTCGCCTTGTCAGCAAGCAGAGAAAAGATGCTGAGGCCACTTTCCATTTCTGGAAGAACTTCAAAGGAAAGAATTTGGTAGGAAACAGATGCCAACTTTTATAGAAATTACTGCGTAGTTACAAAGCAGATAGTTTACTGATTTCTTTCGCACAATAATACCTATCCAACATGCCACTCCATTCTTGTAAACGCTTTTAGCATTTTTGCTTTATTTCAGCATTCTTTTTTACATATGTATTAGTATTGTCACAATACTGGAGTTCTGTACCAATCGGTGCTGAAATTTTAAAA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa17354
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 |
---|---|---|---|---|---|
ENSDART00000108652 | None | None | 949 | None | 13 |
ENSDART00000108844 | Nonsense | 598 | 704 | 18 | 21 |
ENSDART00000128630 | None | None | 401 | None | 4 |
ENSDART00000135877 | Nonsense | 886 | 992 | 22 | 25 |
ENSDART00000143432 | None | None | 126 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 13945499)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 13698064 |
GRCz11 | 9 | 13669267 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGATCATTTKGGTTTAATGGACAGGTTCTGCCTAGTACTAAAGACGCCTG[C/A]TTTTCCACTGCTGTTGAAACCCTGCAACAGATCAGGTAAAGAYAGCTTGG
Long Flanking Sequence:
TTTTATCAACCAAAATTTTTATTTCGTTGTATCACTACGCCATTTACGAATACCTGTATAATGCATCATAAATGTAGGATTCACAGAAAGTGTTATCATTAAATTTTAAAAAACAAACAAATTTGATATATTTAAAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTAATGCAATAAGGCTGGCTTAAGTATCCAAATAATTTTTATGGATCCTGTATTTTAAGACCAGAAAGTTACAATGGCTTTTGTTATAGTTGAATGTTATCATCTTGTTTTTCAGAAAATTCTGGCCGGTTTCTATCTCTGTATTGGGGGAAATAAAGAAGGTGACGTTTTCTCTCATTTTAAAGACAAAATGTTGGAAAAGTTAACAGTATATAATATCTCATGTTCGATCATTTGGGTTTAATGGACAGGTTCTGCCTAGTACTAAAGACGCCTG[C/A]TTTTCCACTGCTGTTGAAACCCTGCAACAGATCAGGTAAAGACAGCTTGGTGCAACAAAATTAGAAAAACCACAGCAACACTTTATTTTTAACACTATCTTTTGAATTACTCCTTTTTTTTTTGTACAGCACAGCATTCACTCCTTCAGACAAGTTGCAGGTGATACAGCTGACTTTTGAGGAGGTCACCCAGGACGTGCAGGCTATTCTTTGCCAGGACTTTTTGTGGTGCATGGACGACCTCTTTCCAATTTTCCTCTATGTGGTGCTGCGTGCACGGTACTAACTTTGATTGCATTTTGACCTTAAAGGGATAGTCCACCCAAATATGAACATTTCTGGTTAATTTACTCACCCTCAGGTTATCCAAGACGTATGTGAATTTTTCCTTCTGTATAGCATTTAAGAAGATTTTTTAAGCTGTATCCTTGGTTATTCCTAAAATGGCAGTGAATGGTGATAAGTTTTTTTTTTGTTTAAAAATAATCCTATGCAAACAG
Associated Phenotype:
Not determined