ZMP
si:ch211-66g24.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate membrane associated guanylate kinase, WW and PDZ domain containi
Human Orthologues:
MAGI2, MAGI3
Human Descriptions:
membrane associated guanylate kinase, WW and PDZ domain containing 2 [Source:HGNC Symbol;Acc:18957]
membrane associated guanylate kinase, WW and PDZ domain containing 3 [Source:HGNC Symbol;Acc:29647]
membrane associated guanylate kinase, WW and PDZ domain containing 3 [Source:HGNC Symbol;Acc:29647]
Mouse Orthologues:
Magi2, Magi3
Mouse Descriptions:
membrane associated guanylate kinase, WW and PDZ domain containing 2 Gene [Source:MGI Symbol;Acc:MGI
membrane associated guanylate kinase, WW and PDZ domain containing 3 Gene [Source:MGI Symbol;Acc:MGI
membrane associated guanylate kinase, WW and PDZ domain containing 3 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34452 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30903 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa772 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa34452
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 |
---|---|---|---|---|---|
ENSDART00000115228 | Nonsense | 26 | 993 | 2 | 16 |
ENSDART00000144255 | Nonsense | 138 | 1074 | 3 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 37823920)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 36679335 |
GRCz11 | 8 | 36711769 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTGTGTTTTCCTGTCTTCCATGTCATGGCAGGTACAACTAGACAGCCA[C/T]GAGACGGTGAGATCTCTGGGGTCGACTATAACTTTGTGTCAGTCGAAGAG
Long Flanking Sequence:
AGCTAAATTATCTGCCAATGGGGGAAAGCAAAATAATCATATTATGCCAAAAAGAAAAACAAGATTATTTTACTTGTTTTAGGGAAAAACACACTTGAATTTGACATTACTTCTCAAAACAAGACAATTTTTGCTTCTCTTGAAAATGCTTCTTGATTTAATAATTTTTAGCTATTTGGAATAGAAACAAGACCATTTTTATTTTTTTGCAGTGAAAAATAAGTTAATTTTTACTTACCCCATTGGCAGATTATTTAGCTATAAAGAAAGCTGTTAGAATAATAATAAGAATAAGCTATACGATAAAAACTCACTGTATTTTTTATATGTAATTTTTACAACTTTTTAAAATTATTTTTAGATACAGTATTTGACTTTTTAGATATTTGGACAAGAAACAAGACAAAAACTTTTTTGCAGTGTCTATGTTATTTGAACTTGCTGTATTTAATGTGTGTTTTCCTGTCTTCCATGTCATGGCAGGTACAACTAGACAGCCA[C/T]GAGACGGTGAGATCTCTGGGGTCGACTATAACTTTGTGTCAGTCGAAGAGTTCTTCTCTCTGGAGGAGTCGGGGGCGCTGTTGGAGAGCGGAAAGTTCAAAGGTCAGACAGTATTCATGACACATCTCCTGAAGAGTTTATAGTGATTATGAAGAAGAAAACTGTAGTGCAGGGGTTCTTAAAGCGATAGTTGACACAAAAATGAAAATCCTGTCATCATTTACTCACCTTTCACTTGTTTCAAACCTGATTGGGTTTTTTCTTCTTCTGAACATAATAGTAGTTAATTTAAAAGAAACATGTAACTCTTGACCTCTATAGTATTTGTTTATAGAAGTCGATGGTTACAGGGTTTCAGTTTTATTTAGAATGACTTATTTGGTTTTCATTAGAAGAAAGAAACTCAAAACAAGGTTTAAAACCACTTGAGCGTGGGTAAATAGTAAGTACATTTTCACGTTTGGGTGAACAAACCCTTTAAAGCCTCAATTTAAAGGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30903
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115228 | Splice Site, Nonsense | 205 | 993 | 6 | 16 |
ENSDART00000144255 | Splice Site, Nonsense | 317 | 1074 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 37852209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 36707624 |
GRCz11 | 8 | 36740058 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATCATGCTGAACTCTGTCACCATCATCTTTCTGGTTTATTATTTGTAG[T/A]AGCAGAGTTTACGGACCAGCCGAGTGAACTGAGAGGTTTCTCCGTCCACA
Long Flanking Sequence:
TTGCTAACAGTTGAGCTACCTGGTTAGAATGTAGGAGTAAATGCCGTTCTTTTTCATCACCTTTCACCATTTATCTTTTCATTTCCCTCCTGAATAAAACTACAGAAATCATCATAGAATTATTACACTTTTAATGCCAATAACGATGGAAATTGTTTTATATTTATTGGAATTTCTAATCGTCTTTTAGGCTTCCAATAGTAACTTCGTTACCCTCAATTGGTGGAATGCTAAAACAATATAGCGAAATATATCCACAAAATACATTATAACCTCTTAAAAAGTAATTACTTTGATGGTTTGTAATGTTTTATGGGTATTTGTAGTGAAACCAATTGATCATCTGTGATGGTTTCTATTGTGTTTTGTTAGTTTGTCTGTTTTTATTTCTCCAGCAGGAATGTCACTTATATTCTGTACTATTAGTGTGTAGATTTTGTCTGTTATTTATGATCATGCTGAACTCTGTCACCATCATCTTTCTGGTTTATTATTTGTAG[T/A]AGCAGAGTTTACGGACCAGCCGAGTGAACTGAGAGGTTTCTCCGTCCACACTCGTCTAGTTAAAGGCGCACGGGGCTTCGGTTTCAATATAGTGGGAGGCAGCAGAAGGAGAGAGTTCCTGCAGATCTACAGCATCACTCCCGGAGGACCTTCAACCCTGAACACAGGTAACCGCACACAGATCTCCTCAGCAGCCCACTGCGGTACAACACTGACTACAAACAAGGAGATTTTCTATAGGTTGCAGTTTGCTCGCTCTCTATTGCTCTCTCGCTTTCTGCATATTGCCATGGATTGTTTGTAAATTGTGTGATACTGTCGAACGACTCTTTCCTTCGCACTATAATCCTAATGACCTGCATGGTGTAATCCAACTATCAATGCTGACACACACAATTGCATGTAAAATGTGACATTATGAACACTTTCTCTATTGCTTTATTGTTGTTTTATTACTAATATACAAAAACATATCATAGTATTTTTGATCTGATTATTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa772
Status:
F2 line generated
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115228 | Nonsense | 285 | 993 | 7 | 16 |
ENSDART00000144255 | Nonsense | 397 | 1074 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 37855298)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 36710713 |
GRCz11 | 8 | 36743147 |
KASP Assay ID:
554-0677.1 (used for ordering genotyping assays)
KASP Sequence:
ATGATACCTGTGTGCTCGGCTACTCTCACAAAGATGTAGTAGAAATGCTA[A/T]AAGCCATCCCTATTGGTCATACTGTGGACATCATGGTCCGAAGAGGTTAC
Long Flanking Sequence:
AAGCTGAATGTCTTGAAAAATATCTAGTAAAATAATAAGTACTGTCATCATGGCTAGAATAAAATAAATCATTTATCATAAATAAGTTATTAAAACAATTATGCTTAGAAATCTGTAAAAAAAAGAAATTCTGTTAAACATAAATTGTTCAAAAAATATAAAGGGGGACTAATAATTCTTCAACTGTAGGCTACTCTGAGAATGTATTCCTTCACACTTTAAGTTTACACAAGTCCTCCACCTGATTAAAAAAGGCGTGCTCAGCCATAAAGAGTGATGCTGTAGTGGAATTGTACCATAGAAAATGTGTCAGAAACATCAAAACAGCATTTTAAAATAATTTCTGTAGGAGGGATCATGTGACACTTAAAGTTTAGTTGGTTCAACTTTCAGAGCCTATAAATCCATTTCTTTTCATTCTTCTTCCAGCTGACATCCTAGTCTACATCAATGATACCTGTGTGCTCGGCTACTCTCACAAAGATGTAGTAGAAATGCTA[A/T]AAGCCATCCCTATTGGTCATACTGTGGACATCATGGTCCGAAGAGGTTACCCCATGCTCTACAACTCAGAAGGTTGTCCTAAGATGTCCAATCCAAGGCTGACTGCATCCCAAAACCAGTCACCACATCTACCTCCACCAACCACCACCCAACCGCAGGCCCAGGCTCCTCTCCCATATGCACAGCTCCACCTCAACCACAACAGCCCCCCGTGGGCTGACTTTGACAGGGGGTCTTCGAGGAATCTCAGAGTGCGAGCTTCAAGGTTTAGTCTGGATGCTAATGGAAATTCACCTCCATTTGCTTCACCTCCAAGACCTCCGTCATCGTACCAGGGCTCCAACGGGTATGGGAGTGGGTTTTTGAGACCGCCACGCACTGCGAGAAGCATACGGAGGTTGCAGAGCGCAGAACTGGCCAGCCAAAGTGACAGTGAGGTGGTGTCTGCAATCGGATCCCACAGGTGAATGGATTTGATGTGTGATGATGTTAGGAGAGTT
Associated Phenotype:
Not determined