ZMP
magi2
Ensembl ID:
ZFIN ID:
Description:
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 [Source:RefSeq peptide
Human Orthologue:
MAGI2
Human Description:
membrane associated guanylate kinase, WW and PDZ domain containing 2 [Source:HGNC Symbol;Acc:18957]
Mouse Orthologue:
Magi2
Mouse Description:
membrane associated guanylate kinase, WW and PDZ domain containing 2 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17077 | Nonsense | Available for shipment | Available now |
sa9085 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18564 | Nonsense | Available for shipment | Available now |
sa30610 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20277 | Nonsense | Available for shipment | Available now |
sa30850 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40297 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17077
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 |
---|---|---|---|---|---|
ENSDART00000009768 | Nonsense | 15 | 1140 | 1 | 20 |
ENSDART00000133644 | Nonsense | 149 | 1274 | 3 | 22 |
Genomic Location (Zv9):
Chromosome 4 (position 21814320)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 23157655 |
GRCz11 | 4 | 22878630 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGGTACAACCAGGCAGCCCAGAGAAGGAGAAGTTCCTGGAGTAGACTA[T/A]AATTTTGTGACCGTTGAGCGTTTTGTGGAGTTAGAGAGAAGTGGAGCTTT
Long Flanking Sequence:
AAACACACAATAAACCTGGAACTCTAAAAGAACAGATTCAGGGGTTTGGAAGATTTTTGGCCATTTTAGTAAAGTGGATGTGGAATATGTATGGATCAAAATGTAATATGTAATTTGGTAGTCTTCAATCAAAATATGACCATTTGCTTTTTTATTTGAAGTGGTGGTCCTTCTCTGTAAAGATGCACAAAAAGAAAGCTCCGCCCCCCTACACAATATTCAGTTTTAATTGGGAGTACATCAACAAACTAAATTAAAAGTCTCAGTAACTTCCGGTTCACCCAGTCTTTAATGCACTGACCTCACAAAGTTTTAGCCATATCAACACGGCATTCATAAATTGTACCCGCTGGCAGTTTTTAAGTATACAAAGACCCCTGGCGGTTTCATTGTTAAGCCCATGGCTCAAAGCTAAAGCTCACTGACCTGAAATATCTCTCTCTTTTCTCTGCAGGTACAACCAGGCAGCCCAGAGAAGGAGAAGTTCCTGGAGTAGACTA[T/A]AATTTTGTGACCGTTGAGCGTTTTGTGGAGTTAGAGAGAAGTGGAGCTTTGCTGGAAAGTGGAACTTATGAAGGTACGTCAACTGAGTTTCACAATCAGATTTCAAGTTATAGTTTTTGTCCCAATATCTCATTGCTGTGATTAGAGATTTGAGCAATCCCTAAACTAATTAACCACACCACCCAAGTATTAAACTTTGGTTTGGGACTACAGACGTTCCCCACAATGTAAGCTTAACCCTTTATAGGGTAGTCATTGAAAGACTCAATAGACCAAGTCTGGAGGGTTACTTTGGGTTGTTTCAAAACTTTTAAACCTTTATAACAAAACAAAACAAAAACCTGTCAGTAAATGTACCATATATGCTGCCCAACAAAAGCAAAGTACGGTATCTACGTAAACAATGGAACACATTTTGTAGTTACTGCTATTTTGACACTCTTTTTTTTTCTCTGATACAAGACAAAATTTAACCAGGAGACTTTGTCACAAGACAGAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9085
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 |
---|---|---|---|---|---|
ENSDART00000009768 | Nonsense | 72 | 1140 | 2 | 20 |
ENSDART00000133644 | Nonsense | 206 | 1274 | 4 | 22 |
Genomic Location (Zv9):
Chromosome 4 (position 21809061)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 23152396 |
GRCz11 | 4 | 22873371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCTGCTGAATGTAGCAGAGCAGCTGCTGCCCGGAGCAACACCCACATCA[C/T]AGGGCAAAYGCAGRCGCAACAAGTCCGTCAGCAACATGGAGAAGGCTGGC
Long Flanking Sequence:
ATTATTATGATTATTATTGTTGTTATTATTATTATTAATTAATTTATTTATTTATTTTAATTATTTTATTTAAATACAGACACAATATTATTTATATAAATTTTATATTTTAAATTTTATATATATTATAAATAAATAAACAAGCAAGCACGATTTACTTGATGAACATATCCAAGTCATGGTGCAGGAAGTCCTTAAATGGTGATAGAAGCAGATGTTGCTCAGTTCTGGAAACAATGTTGTCCCCAAAGTATTGTTAAGTAAAAAAACACCTAATGGAAAACTGTTGCCTCACTTATTGCCTGAGAAGCTGCTGAACAACACACAAGCCACAACATCTTCATTGTAAAAGTTGCCATCGTCACGATGGCACATCTTACATTCTTAACTCTGGATTGTTGACAGATAACTATTACGGCACACCAAAGCCCCCGGCGGAGCCCAGTCCACTGCTGCTGAATGTAGCAGAGCAGCTGCTGCCCGGAGCAACACCCACATCA[C/T]AGGGCAAACGCAGGCGCAACAAGTCCGTCAGCAACATGGAGAAGGCTGGCATTGAGCCTCCCGAGGAGGAGGAGGAGGAGAGACCCGTCATTAACGGCAATGGAGTCGCCATCACACCAGGTGAGGAGATAAACACTGCTCTATCATACCTGTACATGCACTATTTTGGGCTTTTTGATTGGTCATAGAAGCGAATACACTTCATTCTACAATGCATTTTGTGGAGTCCATGTAAAATCAAAATTTGCTGGCAAGCATTGTTATTCTTTAGTCAGTGCAAGTTAATCATCTTGAAAAAAAAAGTTTGCTTTGGTAATTTTCAATCAAAATTTACCATTTGCGTCCATGTTTGGAGTACCGGTCCTTCTCTGATGATGTCAGTTTAATGGCTTCAGCTACAATATTCCTAATCACACCCCTCTTACTGTTTGTTTGCTACGAGGGGATGATGCACAAAAAGAAAGCCCCGCCCCCACTCAATATTCTGTTTCAGTTGGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18564
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 |
---|---|---|---|---|---|
ENSDART00000009768 | Nonsense | 309 | 1140 | 7 | 20 |
ENSDART00000133644 | Nonsense | 443 | 1274 | 9 | 22 |
Genomic Location (Zv9):
Chromosome 4 (position 21767465)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 23110800 |
GRCz11 | 4 | 22831775 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGGATTTGGCTTCACTATCATTGGCGGTGATGAACCWGATGAGTTTCTA[C/T]AGGTCAAAAGTGTCATACYGGACGGGCCTGCAGCACAGGATGGCAAAATG
Long Flanking Sequence:
AATCACTCTGCCTGTGCTGGTTCTTCTCCTGGCTTTTTTTTTTTTTTTGCTTAAGTCTTGTCTGTCCTAAGAGACGGCCCTGGACGAGGCTCAACACTGTTGAGTGTAACATTAGGATACGTTTAAAGAGCCAAAAGTGAGGTTTGAGCAAAAAAAAAAAAAAAAAAAAAAAACAAGCCATCATGTTCCTCTCTGCTCTTGTATGTTTGGCTGTAAGCAAAGCGCTTGGCCTTCTACCCACAATTCCCCAGTGTGATGTGATCTGCTGCTTTTGATGGGTTTGGAGTGGCTTTTACAAAGTAACCCGTTAATTTCTGGATGTCTTCTCCTGGGTTGCAATCTCATGTTTGTATCTGCATTTCTTCACCTTGGCAGAGAAGCCTCTGTTCACGAGGGACCCCACGCAACTGAAAGGCAGCTTTCTGTCTACACCTCTGCAGAAAAGCAACATGGGATTTGGCTTCACTATCATTGGCGGTGATGAACCAGATGAGTTTCTA[C/T]AGGTCAAAAGTGTCATACCGGACGGGCCTGCAGCACAGGATGGCAAAATGGCTACAGGTAAATACAGTACACCCAGACTCAATGTTTGAACGGTGCTAATGTGCTATTCTCACTCAAACAGAGCTCCCAGCTGCTCAGTCTCTCTCAATCTGTGGTTGTGCCCACACTACTGCAGAGGTCGCAGTGTGAATCTGACATTTTATTGGTTGATAGCGCGTTAGGGACATCCAGGGGTTAAGTGCATTTACGGACAGTGTATTTATTGGCTTTGTGTGTCATCCACAGCAGGGCATGTGTCCATTAATCACAGTGGGGCTTTATGAACTCTGTAGCATCAGTCCAGCCTAGTGGGAGTGTGACTGCGGCAGCTTTACACACACACACACACACACACACACACACACACACACACACACACACACATACATCAGCATTGAAATATCTCATATGTTCAGAGGGACCCACAGTGCAGAGTTCAGAATATAGTCAATACATCTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30610
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 |
---|---|---|---|---|---|
ENSDART00000009768 | Nonsense | 358 | 1140 | 8 | 20 |
ENSDART00000133644 | Nonsense | 492 | 1274 | 10 | 22 |
Genomic Location (Zv9):
Chromosome 4 (position 21758478)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 23101813 |
GRCz11 | 4 | 22822788 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACCACCCATGCTGATGTTGTAAAGCTATTCCAATCAGTGCCAATTGGA[C/T]AAAGCGTAACCCTTGTCCTTTGCAGGGGTTACCCTCTTCCTTATGACCCA
Long Flanking Sequence:
GGCACAGGTACATTATAAATAGCTGTTTTCATGTCGATCGCAACAGACGCAGACAGCGTGTGAACCTAGCATGAGTTTTATCCTATTTAGCTAAACTACAGCGATAATAATAATTCTAATTTGATATATTTATAAAAAAACATCCCTTAATCATGTTCCCATCTCTTTTTTTATAAGTCAATGAAAATGTCAGTATATTTATTATAGTTGTAGTCATCATCACTTTCGTCTAGTTTTTGTTGTTAGAAACTTGTTTGTCACGAAAATTTTGCATCAACAAAATTAACACTGTTTGTAAACAGAACTCACTTGTATTTAACTTTTTTAAACTGAATCAAACACAGACACACACACAAATATACTCTACCCACCAGAGCTTATGTACCTTTCTTTGTGTGTAATTGTTTCTAGGAGATGTGATCGTCTATATCAACGACGTCTGCGTCCTGGGCACCACCCATGCTGATGTTGTAAAGCTATTCCAATCAGTGCCAATTGGA[C/T]AAAGCGTAACCCTTGTCCTTTGCAGGGGTTACCCTCTTCCTTATGACCCAGAGGATGCAGCAAACACCTTACTATCCCCCCTCGGCCTCATTGATCGCCCTCTGCTGGTCAACGGACGGAATAGCTACGACAGCTACATGGAGTACATCTCCCGCACCGCCCGTTTCGTCGACCCCCTTCAAACAACGATGGTGCAGCCTCACCCTGGAGACACCCACCTGGACGCCGGGCCACTGGAGGACAGCGTCTCGATGGCGTCGTCTGGAGCGGCTGGAGGAGAGCTGCTAACGATTAACATGGTGAAGGGGGCAGATGGGTTTGGATTCACCATAGCAGACAGTAATGGAGGGCAAAGAGTGAAGCAGATTCTGGAGGCTCAAGGATGCCCGGGGCTGTGTGAGGGAGATCTGATTGTGGAAATTAACCAGCAACCTGCGCTAACACTGTCACACACGCAAGTGGTGGAGCTGCTAAAAGAGTGTCCGATTGGGACGGAGGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20277
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 |
---|---|---|---|---|---|
ENSDART00000009768 | Nonsense | 535 | 1140 | 9 | 20 |
ENSDART00000133644 | Nonsense | 669 | 1274 | 11 | 22 |
Genomic Location (Zv9):
Chromosome 4 (position 21738228)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 23081563 |
GRCz11 | 4 | 22802538 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGTTGTTTCCCTCTTTAAATTTAAAGATCCAGCAGGTTTCAAGTTTTG[T/A]TCTTTTACATTGCAGGTCACTTTTCCCCTTGGAAGACCACTAAACAGGTA
Long Flanking Sequence:
AGCAGTGCTCTACCATTGGATTTGGGAGTTGTTTCATTGATTGCAACGGAAGGTTTTTAAAATATATATTTTTTGTCATCAAAAACGAATGCAGTTCTTGAGGACAAACTCCCTTATTCGCTCAACAGATACATAAAATATTCAAACAATCACCACTTGTCCTTAAAGAAGCAAAGCAATTCTGAAAGGACAAAATTCTTTCGATTGAATGAATTAATTGTTTCTTTTTGTTACAGATTTTTGAAGCACTTTAAATATAATTTAATTCACTTAGAACTATTCCGAGGTTTAACAGCAAAACAATTTAACATAATTTGGCAGACATTAATAGAATGATTGAATACGCTTCACTGTTATGATTCACTTCAAAGGAAATAATAGGTTAGCTAAAGAATAAACATCTCAGCACGAACCACAACAGTCTGATAAAAGCTTATCACTAAGGGTTTTTGAGTTGTTTCCCTCTTTAAATTTAAAGATCCAGCAGGTTTCAAGTTTTG[T/A]TCTTTTACATTGCAGGTCACTTTTCCCCTTGGAAGACCACTAAACAGGTAAAACGTATCGTATTCAAGCCCTCTAATTGTAATTAATAAACTAACAGCAACTGTCCTCTAACAGTTATGTCAGATTATACATTATACAGAAATAACCATTGAGCTTTATTACTAAGATAAATGCATAGTAGATGCTTTATTATATTACTATAACACATTACTACTAACACATTATTATAACTGCATTCTACTAAGCCAACAAAAAGCACTAATTTTCCTCATATATACACCAATACAACATATACCACAACTTATTTAGAATTTTGTGGGATTCAAAACATACACACATTATAAATAGAGTATAGAGAGCTTGTTTGGCATGCTTTCCCGGGAGAGAGCCACATAAGATCTTCGAGCCCGGGGCTCCCTCCCCGTTTGCAAGGCGAGAGGGGAGTTTGAGCCAAGGTAGATCTCGAACTCCCCAGCTGTAGTAACTAATGAACAGATAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30850
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 |
---|---|---|---|---|---|
ENSDART00000009768 | Nonsense | 873 | 1140 | 15 | 20 |
ENSDART00000133644 | Nonsense | 1007 | 1274 | 17 | 22 |
ENSDART00000009768 | Nonsense | 873 | 1140 | 15 | 20 |
ENSDART00000133644 | Nonsense | 1007 | 1274 | 17 | 22 |
Genomic Location (Zv9):
Chromosome 4 (position 21709310)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 23052645 |
GRCz11 | 4 | 22773620 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAACACTGTGAACCAGACCGGTGCAGCCCCTCTAGCAAACTCCAATGCT[C/T]AACAAAACTCTGCTCCTCAACCCAGTCCCATAAAGCAACCCATTTCAGAA
Long Flanking Sequence:
TAATATTTAGTTTTTTATTTGTACATGCCACATTTGACCACTTTAGATAAATCAATGTGTCTATGATCTTGGAACAAATACTGTAAACTGGACTTAATATTGATTTTGCCTTATTAAAAAGATTAATTTTTCACACTTACATGAACTACCACTGCAGGATGGAAAACTGACATGCAAATTTATTCAATTATTGTAATAAATTTGCTTCTAAAAGACCACAGAAAGTACATGCAAAAAGCTATCAAAAGCCATGGTTATTTTTTGCACTCATGTAACCTTTAATCTGCTACCTTAACAGATGTTAAATATAGACACCTGTATAACAAAGATAAGATTTAGAAATTACTTATATTTTGTCTTTTCTCCACTTTTCAGAGACTAACAGCACTCCTTCTGCAGGCAGCTCAGAGAAGCAAAGTCCTATGGCCCAGCCAAGTCCAGTGTGTCAACCTAACACTGTGAACCAGACCGGTGCAGCCCCTCTAGCAAACTCCAATGCT[C/T]AACAAAACTCTGCTCCTCAACCCAGTCCCATAAAGCAACCCATTTCAGAAGCACAGCCGAGCCTTGTCACTCAAAACAGCCCAGCCAATCATCCCAGCTCAGTGACCCAACAGAACCCGCAAACTCAGCCAGTACAAACTTACAGCCACGACAGCAGGCAAGAAACTAACTTAAATTACTTTATTGCTTAAATATGGTTTTCAGGATTAATGGTTTACTACTACAACAACACTATTTTTAGGTTGACACTTTGTTTTCTGAAGAAAATGTGTATAGTGTTTGACCCTGATGGTTGCTCAGTTCCTTGGACATTTGTTGAGGACATTAAATAATATTTTAATGTGCTAGTCATTTTTACCATTGCTTATTAAAATTGAGCAAAACCTATTAATATATTATGCATTTACACTCTTCTTCAGTTAAAGCAAGTAGGAATCTGAATTGCAAAAAAATTAATATGTGTGAGGTGAAATGTTGTGTTTGCACGTAAAACACAGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40297
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 |
---|---|---|---|---|---|
ENSDART00000009768 | Nonsense | 873 | 1140 | 15 | 20 |
ENSDART00000133644 | Nonsense | 1007 | 1274 | 17 | 22 |
ENSDART00000009768 | Nonsense | 873 | 1140 | 15 | 20 |
ENSDART00000133644 | Nonsense | 1007 | 1274 | 17 | 22 |
Genomic Location (Zv9):
Chromosome 4 (position 21709310)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 23052645 |
GRCz11 | 4 | 22773620 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAACACTGTGAACCAGACCGGTGCAGCCCCTCTAGCAAACTCCAATGCT[C/T]AACAAAACTCTGCTCCTCAACCCAGTCCCATAAAGCAACCCATTTCAGAA
Long Flanking Sequence:
TAATATTTAGTTTTTTATTTGTACATGCCACATTTGACCACTTTAGATAAATCAATGTGTCTATGATCTTGGAACAAATACTGTAAACTGGACTTAATATTGATTTTGCCTTATTAAAAAGATTAATTTTTCACACTTACATGAACTACCACTGCAGGATGGAAAACTGACATGCAAATTTATTCAATTATTGTAATAAATTTGCTTCTAAAAGACCACAGAAAGTACATGCAAAAAGCTATCAAAAGCCATGGTTATTTTTTGCACTCATGTAACCTTTAATCTGCTACCTTAACAGATGTTAAATATAGACACCTGTATAACAAAGATAAGATTTAGAAATTACTTATATTTTGTCTTTTCTCCACTTTTCAGAGACTAACAGCACTCCTTCTGCAGGCAGCTCAGAGAAGCAAAGTCCTATGGCCCAGCCAAGTCCAGTGTGTCAACCTAACACTGTGAACCAGACCGGTGCAGCCCCTCTAGCAAACTCCAATGCT[C/T]AACAAAACTCTGCTCCTCAACCCAGTCCCATAAAGCAACCCATTTCAGAAGCACAGCCGAGCCTTGTCACTCAAAACAGCCCAGCCAATCATCCCAGCTCAGTGACCCAACAGAACCCGCAAACTCAGCCAGTACAAACTTACAGCCACGACAGCAGGCAAGAAACTAACTTAAATTACTTTATTGCTTAAATATGGTTTTCAGGATTAATGGTTTACTACTACAACAACACTATTTTTAGGTTGACACTTTGTTTTCTGAAGAAAATGTGTATAGTGTTTGACCCTGATGGTTGCTCAGTTCCTTGGACATTTGTTGAGGACATTAAATAATATTTTAATGTGCTAGTCATTTTTACCATTGCTTATTAAAATTGAGCAAAACCTATTAATATATTATGCATTTACACTCTTCTTCAGTTAAAGCAAGTAGGAATCTGAATTGCAAAAAAATTAATATGTGTGAGGTGAAATGTTGTGTTTGCACGTAAAACACAGATT
Associated Phenotype:
Not determined