ZMP
si:ch1073-93e12.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
EPM2A
Human Description:
epilepsy, progressive myoclonus type 2A, Lafora disease (laforin) [Source:HGNC Symbol;Acc:3413]
Mouse Orthologue:
Epm2a
Mouse Description:
epilepsy, progressive myoclonic epilepsy, type 2 gene alpha Gene [Source:MGI Symbol;Acc:MGI:1341085]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17655 | Essential Splice Site | Available for shipment | Available now |
sa24236 | Nonsense | Available for shipment | Available now |
sa13005 | Nonsense | Available for shipment | Available now |
sa24235 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17655
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082045 | Essential Splice Site | 142 | 322 | 3 | 5 |
ENSDART00000136436 | Essential Splice Site | 141 | 310 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 1571705)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAACTTCTACTTCAGYATAGCMGGACAGCAGGCCATGCACTTCTCTCAG[T/G]AYGTGCGAATAAACTTCCTATCCTYTAGGTCAGGRCTATCAGTCCTTTNAG
Long Flanking Sequence:
CTGTTGTGGCGACCCGAGATTAATAAAGGGAATAAGCCGACAAGAAAATGAATGAATGAATGAATGAGATAAGAAAACAACAGAAACAGAATGTCAAAAAAGCTCTTTTATTTGCATAATCCACACAAAAAAAGCATTTGACATATACGAAATATTAATGAAAAATGCTTTTGCACATCACACATGCAGTCACATGAGATTTCTAAGACATTATATCAATGATTTTGTTGAAATGGCGAGAATTCTAGGCAGTTAATACAGTAGGTTTCTTCTCATCCTCTCATTTATCCCAGTTTGAAGTGTTGTGTTGATGTCTGTCTGTAGGCAGTGGGCCACATCACAACCGGTGCTGTGTGTATGATGACAGAAACATGGTGGATGGGATTCACTGTCATCCGATTGGTCACTGGATCCAGGAGACGGGCCACACAGATGAGATGAAACACACCACCAACTTCTACTTCAGCATAGCAGGACAGCAGGCCATGCACTTCTCTCAG[T/G]ACGTGCGAATAAACTTCCTATCCTCTAGGTCAGGACTATCAGTCCTTTAGGGTGGAGCTATTAGTCCTTTAAGGAGGGGCTATCAGGATTTTTAGGGTGGATCTCTCAGTCATTTAGGGCTGGGCTATTAGTTCTTTTGAAGGGAGCTGTAAGTCCTTTAGGGCAGGGCTATCAGTCATTTAGGGTGGTGCTATGACTGCATTAGGGCGGAGCTATCAGTTATTGTGGGTGGAGCTTTCATTATGTTAGTGCAGGGCTATCAAGTCATTTTGGATGGGGCTGTAAGTTCTTTAGGGCAGGGCGATCAGTCATTGAAGGCAGAATTATAAGTGTCTTAGGCCGGGGCTATCATTAATTTTGGATGGGGCTGTAAGTCCTTTAGGGGGGCGGAGCGATCAGTGTTTTAGGGGCCGATTCTCAAATCCACAAATAGTAGCATCTAATTACCCAGAAGCATTTGTATTTTATTTCCCTGCTCTCTCTTTAATCGTGTGTGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24236
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 |
---|---|---|---|---|---|
ENSDART00000082045 | Nonsense | 185 | 322 | 4 | 5 |
ENSDART00000136436 | Nonsense | 184 | 310 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 1551276)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 1519651 |
GRCz11 | 23 | 1528758 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCACGGCGGTGATGAACTTTCAGACCGAGTGGGACGTGATAAACAACT[C/A]GCACGGCTGCCGGCGAGACCTCAGTCAACCCATGACCCCCGAGACCATGA
Long Flanking Sequence:
TCTGCGTCTTGCTACTGAATCTCATAATAATACTATGAAGCGCTGGGGTGATTGTGTTATTGAGGTGGTGCATCATGAGGATGTGTGTTTTGTAAGAACGTTGACCTGCGTACAACATCTATCCAGCCAATCTAATAGATTTCATGACCTCTTTCACCTCAGATCTTCAAAATAAAATAACAAACGTAGAGAAATGACAATAAAGCTCAACTTGAACTTGAACACATTCTGAGGACAACGATTATTTACACAATATGTCTACTTTAACTGATTTCTGGGGGCTTAGCCTTTCTTGTCTCCTCTGAAGAGCTGTGTTGTTTACACACGATAGTTTAAGCTCTGTCTTCATTCGTGCGTCTGTTTTCTCTTTAGGGTGCTGCCGCGTGTCTGGTTAGGCAGCTGTCCTCGACGGGTTGAACATGTAACCCTGAAGCTAAAACAAGAGCTGGGTGTCACGGCGGTGATGAACTTTCAGACCGAGTGGGACGTGATAAACAACT[C/A]GCACGGCTGCCGGCGAGACCTCAGTCAACCCATGACCCCCGAGACCATGATGCATCTGTACAGAGACTCTGGCCTTTCTTACATCTGGATGCCCACGCAGGACATGAGCACAGAGGGTTAGTGTGTGTGTACTTGTTTTTATATCCTGCTGGGGACTTAAACCTGAATACGCATAGAATCATGGAGACGTGTGTCACTGTGGGGACCAAACTTGAGGTCCTGATGGGTAAACATGCTTGTAAATCAGACAGAAGGAAGTATTTTGAAGATGTAAAAGTGCAGATTGTTTGCTGTGAAGGTTGGTTTAGTGGTAGGGTTGGAAGAGGGGAAAGAATATACAGTTTGTTTAGTAGAAACATCATCACTTTACTTACTTCAGCCGCATGTCAGTAGAGTTTTAAAGAAGACGCTTCAATCCCGGTTTGTTGACGTTAAATCAGGTTCATTTTGTGCACTAACATAACGGATATCCATACAGCTGTGGATATTAACCTGTATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13005
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 |
---|---|---|---|---|---|
ENSDART00000082045 | Nonsense | 267 | 322 | 5 | 5 |
ENSDART00000136436 | Nonsense | 266 | 310 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 1549358)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 1517733 |
GRCz11 | 23 | 1526840 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATGCAGGAGTGGGTCGCWCCACTGCTGCCGTCTGTGGACTTCTCATGTA[C/A]GTGTTCGGGTGGAAACTCAGGAAAGTGCAGTACTTCCYCACCGCCAGAAG
Long Flanking Sequence:
TCTCTGGGAAACATCCATACACACTCATTCACACTCATACACTATGGCTAATTTAGTTCATCAATTGCCCTATAGCGAATGTGTTTGGACTGTGGGGGAAACCCACGCCAACACGGGGAGAACATGCAAACTCCACACAGAAACGGCAACTGACCCAGCTGAGGCTCGAACCAGTGACCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCACCACTGCGTCTTCCCTATAAATAAATCATTTTAAATCAAATTATGGCTCTGATAGAAACTAATAACCTTAAGTTTTCTGAATGTCATTGTGATGCAATGTAATGCTGCTTTGCAATAATAATTATAAAAAGCATTGAATACTTCTCTATCTCTGCAGGGCGTATACAGATGCTGCCCCAGGCAGTGTTTCTGCTGTTTGGGCTGCTGGAAAACGGTCACAGCGTCTACGTCCACTGTAATGCAGGAGTGGGTCGCTCCACTGCTGCCGTCTGTGGACTTCTCATGTA[C/A]GTGTTCGGGTGGAAACTCAGGAAAGTGCAGTACTTCCTCACCGCCAGAAGGGCGGCAGTCTATATCGATGAGGAGGCCCTGCTGAGGGCCCGAGATGACTTTCATATGAAGTTTGGACAGCTCTGTCCATCTGTCCGCAACACAGAGACGCAAGACAGCACCCTCTAGTGCAATGAACGACTGCAGTTCAGTCATATCAAGGTTTAAAGGATTATGCAATAATCACTATTATAAGGGGTTTACACACAGTTGTGTGTCAGCAGTGTGTGAATATAAGCAGCATCTAATGGTCAAAATTAATTGTTTTTACTAATCAGACTTGATAAAATCAGTCTGCAGAAACTCTTTGATTGACATTCTCACTTTGTACGTGTCATCAGAGGGGGAAAGCCCCGCCCACTAGTAACCATCTCTCTCTTATTAGCATAGGACGTTAGTCTTGTTTTTGAATCTGCCACTATGCTGTCACACAGGCGTTTGTAGCTCCGCCCTCTTCTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24235
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082045 | Nonsense | 271 | 322 | 5 | 5 |
ENSDART00000136436 | Nonsense | 270 | 310 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 1549346)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 1517721 |
GRCz11 | 23 | 1526828 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCGCTCCACTGCTGCCGTCTGTGGACTTCTCATGTACGTGTTCGGGTG[G/A]AAACTCAGGAAAGTGCAGTACTTCCTCACCGCCAGAAGGGCGGCAGTCTA
Long Flanking Sequence:
ATCCATACACACTCATTCACACTCATACACTATGGCTAATTTAGTTCATCAATTGCCCTATAGCGAATGTGTTTGGACTGTGGGGGAAACCCACGCCAACACGGGGAGAACATGCAAACTCCACACAGAAACGGCAACTGACCCAGCTGAGGCTCGAACCAGTGACCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCACCACTGCGTCTTCCCTATAAATAAATCATTTTAAATCAAATTATGGCTCTGATAGAAACTAATAACCTTAAGTTTTCTGAATGTCATTGTGATGCAATGTAATGCTGCTTTGCAATAATAATTATAAAAAGCATTGAATACTTCTCTATCTCTGCAGGGCGTATACAGATGCTGCCCCAGGCAGTGTTTCTGCTGTTTGGGCTGCTGGAAAACGGTCACAGCGTCTACGTCCACTGTAATGCAGGAGTGGGTCGCTCCACTGCTGCCGTCTGTGGACTTCTCATGTACGTGTTCGGGTG[G/A]AAACTCAGGAAAGTGCAGTACTTCCTCACCGCCAGAAGGGCGGCAGTCTATATCGATGAGGAGGCCCTGCTGAGGGCCCGAGATGACTTTCATATGAAGTTTGGACAGCTCTGTCCATCTGTCCGCAACACAGAGACGCAAGACAGCACCCTCTAGTGCAATGAACGACTGCAGTTCAGTCATATCAAGGTTTAAAGGATTATGCAATAATCACTATTATAAGGGGTTTACACACAGTTGTGTGTCAGCAGTGTGTGAATATAAGCAGCATCTAATGGTCAAAATTAATTGTTTTTACTAATCAGACTTGATAAAATCAGTCTGCAGAAACTCTTTGATTGACATTCTCACTTTGTACGTGTCATCAGAGGGGGAAAGCCCCGCCCACTAGTAACCATCTCTCTCTTATTAGCATAGGACGTTAGTCTTGTTTTTGAATCTGCCACTATGCTGTCACACAGGCGTTTGTAGCTCCGCCCTCTTCTGAAAAGTGCACAATC
Associated Phenotype:
Not determined