ZMP
si:ch211-139k15.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
MAGI3
Human Description:
membrane associated guanylate kinase, WW and PDZ domain containing 3 [Source:HGNC Symbol;Acc:29647]
Mouse Orthologue:
Magi3
Mouse Description:
membrane associated guanylate kinase, WW and PDZ domain containing 3 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32444 | Essential Splice Site | Available for shipment | Available now |
sa37725 | Essential Splice Site | Available for shipment | Available now |
sa10154 | Essential Splice Site | Available for shipment | Available now |
sa24348 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32444
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113660 | Essential Splice Site | 102 | 1347 | 1 | 21 |
ENSDART00000141091 | Essential Splice Site | 102 | 1027 | 1 | 18 |
ENSDART00000144918 | None | None | 195 | None | 4 |
Genomic Location (Zv9):
Chromosome 23 (position 26728952)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 26561774 |
GRCz11 | 23 | 26488315 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTCATCCGCCACTTTCGCGAACCCCTCCGTCTGAAGACTGTCAAGCCAG[G/A]TTAGTTTGTCTGTTTGCTAATTAAAGCCTGAGTTATCTGTTTGTGACGCT
Long Flanking Sequence:
ATTTCGTGCGTTTTGACTGAACCATACTGGGAGTACAACCGAGCGATGTCAATTGTGAAGTTTTAGGACCTTTTTTTTACCTTTACATCAAGACATGGGAATGAAGCCGCTGTGCTTTTTAGCACTCTAAACGCGCTTGCATAAGGAAATAACCAGTTTGTTTTGAGAGACTCGTGTACGAAAGGGATTAATCATGTCCAAGACGCTGAAGAAGAAGAAACACTGGTCCAGCAAAGTGCAGGAATGTGCTGTTTCGTGGGGTAATGCAGAGGAGCTCTGCGCCGTGTTGGAGATACGCGGAGGAGCCGAGCACGGAGAGTTCCCGCACCTGGGACAGGTGTTGTCGGACGCGCTAGTGTGCCATGTCGGCAGGCTGCCTGGTCCAGGAGATGTGCTTCTGGAGGTGAACGGCACGCCTGTCAGCGGACTGACAAACCGAGACACCCTCGCCGTCATCCGCCACTTTCGCGAACCCCTCCGTCTGAAGACTGTCAAGCCAG[G/A]TTAGTTTGTCTGTTTGCTAATTAAAGCCTGAGTTATCTGTTTGTGACGCTACAATTACACACAAGTTTCTTTTTAAAACTCAAATAAATGCTAGTTTATGCATTTTAAAACTAGCATTTATAAGCAAATAATCTACCACTTTACGTTTCATTTTTGTATGTTTGAAAGTGGGTTAGCATCGCTTTTAGCAGAGCTTGTGCTCAATGTTACAATGTGTTGTTTAGCAACAGACAACCAATCACGAACTGACCCAGTGCCTGCCTTGTGAAAGCTTAAATTGCATTAAACAAAATAAAGATCCTATAAAAGATTTATATCATTTAACATCCATAGAGCCTATATATTCAACAGAATGTTCTTAAAATTCTTTGAAAAGAACATTTTTAATTATTTAGAGTAGCCTAAACAAAATGTATCACAAAAGTACTATACCTTTATATACAGGCCTATACATTCTGCTATACTATATTAGAAAACATATGTGCAGTTTTATTGTATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37725
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113660 | Essential Splice Site | 307 | 1347 | 6 | 21 |
ENSDART00000141091 | Essential Splice Site | 307 | 1027 | 6 | 18 |
ENSDART00000144918 | None | None | 195 | None | 4 |
Genomic Location (Zv9):
Chromosome 23 (position 26535605)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 26368427 |
GRCz11 | 23 | 26294968 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGGTGTTTACTTGCTAACTTTCCCTCCCTTTCTTTCCCTCTCCATCTA[G/A]TCACAACTCCAAGACCACGACCTGGCTCGACCCACGACTGGCAAAGAAAG
Long Flanking Sequence:
AGATCTAATAAAAAATACAGTATAGTTTTTAAAAAATGCACACTATTGTCGTACACCTTTAGTAGTTGAAGAAAAAAATGTTGTTTAATTTTAATGAAAGTTTAATGTATTATAATACATTAAATTCTAAGTAAATTAGATTAGAATATATAATATTTTTTATAGCTGAATATAAGCAGAAGTTTTACCAAATACTAAAACATAAATTTAATCCTGATTTTATGCAAATGTATCATCTAAAAAAAATGCAAATTCATAATTTTTCAATGTCCCTCCAGGTGTACAAAATCACTGCTTGGAAAACATAAAAAAAGATCTCACCATCTGTTGTTAGCTATCACTAAGCAGCATTTACTGATTGTTTGTGTCGTTTTTACATTATTCCAGTGAGTTATAGCAATATTGTGGTCATTTTTCCACTGTAATTACAACTTATGACCTGGAGGGCCTTCAGGTGTTTACTTGCTAACTTTCCCTCCCTTTCTTTCCCTCTCCATCTA[G/A]TCACAACTCCAAGACCACGACCTGGCTCGACCCACGACTGGCAAAGAAAGCAAAGCCTCCTGAAAAATGTGAAGATGGAGGTAAGACTGAATCACACACACAACATAAACAGACCCTTAGCTGAAAACCAGAGACATTAGCCTCTCTCTTTTTCTCTGTCTGTCTCTCTCCGACCCACCTGACTAATGGTTCACAGGAGACGTGCTGAGAGCACATCAATGTGTCATTTTAAACCAGCTTTCTGCAATGGCCACGTACAGTGCCCAGCATAAATAGGACACCCCTTACAAATCTCTCTTTTAAATTATTATTTTTCTATGCCGTATAATAAAGTTTGTGTATTATATACAGGGTGTCCATGAGGTCTTAAAAAGTCTTACATTTGAAAAACAAAAGTTTTGGCTTTAAATTCACTTAAATATTTGTTGTAGGCCTTAAATCATGCTAAACAGGTCTTAATTTTCCTATGTCTAAGTAAAGCTACCCAACATATATTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10154
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113660 | Essential Splice Site | 1019 | 1347 | 18 | 21 |
ENSDART00000141091 | None | 1027 | 1027 | 18 | 18 |
ENSDART00000144918 | None | 195 | 195 | 4 | 4 |
ENSDART00000113660 | Essential Splice Site | 1019 | 1347 | 18 | 21 |
ENSDART00000141091 | None | 1027 | 1027 | 18 | 18 |
ENSDART00000144918 | None | 195 | 195 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 23 (position 26485801)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 26318623 |
GRCz11 | 23 | 26245164 |
KASP Assay ID:
554-6192.1 (used for ordering genotyping assays)
KASP Sequence:
CTCTTCCTCAGGGGGAAATGGGGACTGTCATCACCTCAGGAATAAAGCAG[G/A]TGAGACGTGATACGCTTGCSGTAATAGAGCACACAGATTATTATTATTAT
Long Flanking Sequence:
GTAATCCTGCAAGCATGATATCTATGACCACTTCAATATCCTTTCATTTTCAATCGCATCCTTCCAGTCGTCTTATATGACAAGCACTCTAACAATCTCTTTATTCAGTTCCAGCCTGAGTTAAGGCCCAGGTCATCCTTTTTTAGCCATAAAACTAAGTGGATTTGTAGTTAACTCGCTCTGCTCAGAGCCTTTGCCCACACTTAACATTAACAAAAAGGTGTAATGAGGTCTGGAAGAGACTCATCCTCTCCAGTATTTAACTCCACATTGTCATGAACAAAAGCAGTCTAAACCGTGTCTTCTAACAGGACAGCAGATGAAGGGAGACGCTCTGGTTTTTGTGTGCAGCAGGTCATTTATTGGCCTAAAGCTTTAATTGTGTGTCATTCAGGAATGGTGTGGAGACGGAGGAGAGGAAAGACAGTCTGGGCCGAGTGGAGTATAAAGCTCTTCCTCAGGGGGAAATGGGGACTGTCATCACCTCAGGAATAAAGCAG[G/A]TGAGACGTGATACGCTTGCGGTAATAGAGCACACAGATTATTATTATTATGCAGCGGACTTGTGCACTTCGATTTTATGCAGCCCACGTTTTAGGAAGATTACATTTCTTTTAAAACTTTGAGATTGCTTTTTTAAGTTGGTGTATTTGGTTACCAAGGTGATGAGAATGTCAGTGAAGAGCATGCTTGAGATGAAATATGTAATGTGGAAAATGACATTAATATTTATATTCTGCTCCATCTACTCTTACTATAATTGCACAGGAAAGTAAATGTGCCTATAAAATTGTAATTAGCAAGATATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATGTCTGTCTGTCTGTCTGTCTGTCTGTCTTTTCGTCCGTCCGTCAGTCCTTCAGTGTTTCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCCATCCATCCATCCATCCATCCATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24348
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113660 | Essential Splice Site | 1020 | 1347 | 19 | 21 |
ENSDART00000141091 | None | None | 1027 | None | 18 |
ENSDART00000144918 | None | None | 195 | None | 4 |
Genomic Location (Zv9):
Chromosome 23 (position 26481605)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 26314798 |
GRCz11 | 23 | 26241339 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTAAACAAACTTCTCTGTCTGTCTGTGTGCATGTGTGTCTGTGGTTTTT[A/G]GGGCTGTTATCCAGTGGAGTTGGAAAGAGGACAGAGAGGCTTTGGCTTCA
Long Flanking Sequence:
ACCTAAACATCATGTTTTATTATTAATGTACATTGCTAAAAACTTTATCTGAACAACTTTAAAGGTGCTTTTCTCAATGTTTAGATTTTTTTTTTGCCCCCTCGGATTTCAGATATTGAAATAGTTGTATCTCTTCCAAATAATGTAATATTAATATCAAACAAATCTTACATAAATAGAAAGCTTATTTATTCATCTTTTTGTTGGTGTATAAAGCTCAGAAAACTGATTGTTATAAGAGTATAAGTTTTGTAATCCTGAGTCACATAGTATGTATTGTTAATGAAATTTACAGACACAAACTAATAATAGGAAGCACTTACGCGTGTATTTTGGAGGATTTCTTTGCATTAGACAAAACTTTCCCAAAACAAATATCAAAATTGACAAGTGTATGAAAATGCATCTTGCCTTAACTAAACATTTTAAGTTTTTAAACTTAAAAACTGTTGTAAACAAACTTCTCTGTCTGTCTGTGTGCATGTGTGTCTGTGGTTTTT[A/G]GGGCTGTTATCCAGTGGAGTTGGAAAGAGGACAGAGAGGCTTTGGCTTCAGTCTGCGAGGAGGAAAGGAGTATAACATGGGGCTCTTCATCCTCAGACTCGCTGAAGACGGTCCTGCACTGAAAGACGGAAGAATACATGTGAGTTTACACCACAATCACACACATTAGCAGGACAGATTCTCTCACATTTATTCATGACAAAAGTCCTGCAATAAAAAACTGCATCATGATTTACATATTCAATATCATTCAATTGTCAGTTATCATCATAATGTCAGTTTTTGTATTGTTTACTAACACAAATTATGATATTATTTTGTTAGACAAAAGAAATGAAGTTTTTGATGATGACTAGAAATGTGTGTTTGTGTAATGTCTCAGGTGGGAGATCAGATCGTGGAGATCAACGGTGAACCCACACAGGGCATCACACACACACGGGCCATCGAGCTCATCCAGGCCGGAGGAAATAAAGTCCTGCTGCTTCTAAGGCCTGGAT
Associated Phenotype:
Not determined