ZMP
si:ch211-157c18.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein containing a WW domain and PDZ domains (Also known as DHR or GLGF) [Source:UniProtKB/T
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2451 | Essential Splice Site | F2 line generated | Not yet available |
sa41190 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21277 | Essential Splice Site | Available for shipment | Available now |
sa34384 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2451
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064394 | Essential Splice Site | 94 | 1076 | 1 | 17 |
ENSDART00000146563 | Essential Splice Site | 94 | 1039 | 1 | 15 |
The following transcripts of ENSDARG00000025108 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 23679658)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 22805476 |
GRCz11 | 8 | 22826715 |
KASP Assay ID:
554-3165.1 (used for ordering genotyping assays)
KASP Sequence:
GTTCTCAACTCATGTCCACATCCCATTCGGATCAAAACCGTCTCTCCAGG[T/G]ACTTTAATCACTGATGAGAGCAAACTGAATATGTGTTTGAAAAAGATACA
Long Flanking Sequence:
GCAGGCAAAAGAAATGTTGGGAACCACTGTTCTAAACTGTTCGACCTGTAATAACACAAGCTCACTACAGTCTCATTTGCTAAAATGGTTAAAATTATGCAATGGATGGAGCATTCTGACCACATGGCAAACCCTTGTCATTTTTTTCAGCATAGAACATTTACTTTTAACAATATTTTCCTGACTGGTGTTTTTTCTCTTTCTTCCAGCGCTGTCAACATGTCTAAGGCCACTGTTAAGAAGCTGCACTGGCGCTCAAAAGTGCAGGAGAGCTTCGTCCCGCTGGGCGGAGGCTCGGGAGAGCTTGGCGTGGCCATTGGAGGTGGTGCAGATTATGGAGAGTTCCCATTCGTTACTGCAGCACCTGGGGGAGGAGCCACTGTTGGAGACATCATCCTTGAGATTGGGGGAACACCTGTCCTGGGACTAACTTTGGGAGACGTAAGAGGGGTTCTCAACTCATGTCCACATCCCATTCGGATCAAAACCGTCTCTCCAGG[T/G]ACTTTAATCACTGATGAGAGCAAACTGAATATGTGTTTGAAAAAGATACAATAGTCAGAAAACACTGTCACCATTTACTCACTCTGATGTTGTTTTCATCCTGTAAATCAGTTTTTTCATGCTTTTTTAATAGGAGAGAAAATTATAATAAAATTATTATTATTTTTAGCTACAAAATGCGATTAGTTGACTTTACTTGAAAATCTAGATTAAACTCATTGCCTTAAAATTATTAACTAAATAAACCTATATTGAATCAGATTTTTAGCCATACTATGTTGGTGTGCACCCAATTTACCTAAAGTGCATGTCTTTGGATTTGTGGAGGAAACCCATGCGAACACTGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGACCCAGCCAGGCCTTGAACTAGAGACCCTCTTGCTGTGAGATAACGGTGCTACCCACTGTGCCACCGTGCCACCCCAACTAAATAAACTATGTGCATAATTATAAAAGTTCAGATAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41190
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064394 | Nonsense | 127 | 1076 | 2 | 17 |
ENSDART00000146563 | Nonsense | 127 | 1039 | 2 | 15 |
The following transcripts of ENSDARG00000025108 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 23672815)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 22798633 |
GRCz11 | 8 | 22819872 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGGATCCATGGACAGCCAACTCCAACAAGTCATACGGGAGAACCTCTA[C/A]CTGCGCGCCGTGCCCTGTGAGTGATGCAAACATGTTTAATCCAGTACTAT
Long Flanking Sequence:
CATGTGTTGAGATTGCGCGCGGAAAGGACCACCGGATTATATTAAGTGCAAAAATCAATAGAGAGAAGGCGAGCGGGGAGGATAGGTCCTCGTTAGGGGCTCCGCAGTGCTTGTTTGTGACAACAGCACACTGACCTTAGAGACTTCTGCAGTTGCAGTGCAGTTTCAGTGTGTGTGTGAGGTCTGAAGAGCTGCTGTGGAAATCTGGTATTACGAAGGGCTACTTTTTGGCTTCTGAACAGCGTTTTTAACAGATTCACTTTGCCAGTTTACCTTTTCCTCATATTTCCATGGTGACAGCAGTGAGCTATTTGTGTTTTGGCAACAGTGTTGGTATTACAAAGTGGTTGCAGATCTTTCCAGCTCATTCATGTTCATGTGTTCTGTCTGTGATCTGCAGGCTCGACTCTCTGTAAGGATCTAAGACTTTACCTGAGCAAGTGCTTTACACCAGGATCCATGGACAGCCAACTCCAACAAGTCATACGGGAGAACCTCTA[C/A]CTGCGCGCCGTGCCCTGTGAGTGATGCAAACATGTTTAATCCAGTACTATGGCGTGTTTAACATGAATGTCAAAAAGCTGGGAGAACAATGTTTTAGATGGGTTATGTGAAGAATTGCGAAATTATAGGTATTAGCTACAGTGGTGGACGTTAAGTGAACTTTGTTTGTGTATTGCTTGTGTTTGTGGAGACTGAACATGATCCTAAGTCATCCAGGGGTGCGTTTCCCAAACAACAACATAACTCGTGGCTGAACTATCATAGTACGATGCATCGTTTGGGAAAAGAACCATGTAGTGACGAGTGTTTTCCAAAACCGTAGTTTCTCTGTCGCAGATCCATTGTTTGAATCACATTAGTTATAATGTAAAAAGTACATAATGATGCTCCAAATGGGGTGGAGTTACAAGTTTTTTAGGAAAAAAAAACATACTTTTTTCTGCAAATTATATTGTTTTACACGCACTCGCATTTAAAAAAAATCAACAATAGTTTAGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21277
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064394 | Essential Splice Site | 173 | 1076 | 3 | 17 |
ENSDART00000146563 | Essential Splice Site | 173 | 1039 | 3 | 15 |
The following transcripts of ENSDARG00000025108 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 23659884)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 22785702 |
GRCz11 | 8 | 22806941 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCTCTGGAAGAGTCTGGAGCCTTGCTGGAAAGTGGGAAGTTCAAAGG[T/C]CAGAATCACTGTCTACTTTAAAACCACTTAATGCGTCTAAACTTGTTTCT
Long Flanking Sequence:
AATGAATGAATGTATCTTCGCCTCTATTTATATTAAGGCCAATCATTTTATGTTTGACAGATGTGGATATGTTTCATCCAAGGTCGATGAATCCAAACATCAGACGCATCAAAGCGACTGACCTTAGTCCTAGTGATGTCATCAGGATGTTTTTTTACCAAAGATGCATTAGATTGAAGATGGAAATCCATAAAAAAATAATGAGCGATCTTTTAAAAAGCCCCATGTGTCTTTTGCGCTACAGGCCTTCCTATTTTTACATTCTCCATTTAAAAGGCTTGTTGTTTACTTCTACCAGATACACAGTTGAACAAAAAGCAAAAACATTTTATTTCTTTTAATGATTACAGTTATGTTTTCTCTTTTTGTGTTTACAAAGGTACAACAAGGCAACCACGGGACGGAGAAATCTCAGGGGTGGATTATAACTTTGTGTCCATTGAAGAATTTTTCTCTCTGGAAGAGTCTGGAGCCTTGCTGGAAAGTGGGAAGTTCAAAGG[T/C]CAGAATCACTGTCTACTTTAAAACCACTTAATGCGTCTAAACTTGTTTCTCAACCAAACATCACTTCACAGCCCAACAGAGTAGAACATGGTATTTTCAGGATACTCAGAACATTTAAAGAAACCGATTGCCTCAATAGATTTAAAATTTTTTCCCTTCTAACTGAGACAACGAATAACCAAACTCATGTAGTTTGATTCTTTTTACAAATCAGATTAACTTAAACTCTTTAACTAGAGGTACAGATCTTCTTTGCTACCTCGTTCAATTGTAAATCGAAACAATCCCCATTGTTCTCCAGAGTGTCCCAGCGCAGAAATTTTCTAGGTATTCTTCACATGCTTTCATATTATTGAAGATTGCACATTTTAACAGTGTAAATCTAGTCTGGTTCCCTTGCAAAACCACAGATGTCTCACTGTCAGTCCACACTGTAAACCCTAATGTTGTCTTTACTTAAACAATCAAGTAAAGTTGACCGAACATTACTTAAAATTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34384
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 |
---|---|---|---|---|---|
ENSDART00000064394 | Nonsense | 419 | 1076 | 8 | 17 |
ENSDART00000146563 | Nonsense | 419 | 1039 | 8 | 15 |
The following transcripts of ENSDARG00000025108 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 23642001)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 22767819 |
GRCz11 | 8 | 22789058 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGTTGTTCTTCGTCGAGGTTACCCCATGCTCTACAACCCTGATGGCTG[C/A]CCCAAAACCAGTCTCGCCTCCCCTTCTGACACACCCAACACCAACCCTGC
Long Flanking Sequence:
ATGTGTTTGGAATAATCAATCGGAATGGTCTCTTAACCTTTGCATGACCCAAAACATTTTTAAAGCAATTTTAAAATCTGGAAGTCTTGAATTAGGACAGAACGTTTAAAAATAGTGTTTTCATAACTTCATGGCTATGCTAGCATGTTACACATAACATTAGTTTTGTTAACTGGGAGTCGGTTTGCATTGTAGACTGAACTATTTAAATGTTATGCTTTAGATCTAAATCTTTACATCTCTACACTTTAATTCCTCTTGTACTCTTTGCACTCAAAAAAAAATCGGATTGTTTACAATTTGATTTCCCTTATGCATAAAAATAAATGACAGAAATCTCTCTCTCTTTCAGCGGATATCCTGGTGTACATCAACGACTCATGTGTGCTGGGTTTGTCTCATAAAGAAGTAGTAGAAATGCTGAAATCCGTCCCCATGGGTCACAGTGTGGATGTTGTTCTTCGTCGAGGTTACCCCATGCTCTACAACCCTGATGGCTG[C/A]CCCAAAACCAGTCTCGCCTCCCCTTCTGACACACCCAACACCAACCCTGCAGCCCCTGGTTCTGCTCAATCCCAGGTCCAGCATCCTGATGGACAGCAACCTGCCTTTGTGAACCTCAACCGCTCCATGTCACTCCACAACAACTTCTACCCCCGCATGCAGAAAGAGGCCTTGGATGCCAATGGGAACACTGCACCCCAGCCTTCCTACTCAATGGCCAATGGAAATGGAGTTGGAGGGATTATAGGGCTGGGGGCGGTGCCTTTATCAAACGGCCCCGCCCCTTCAGAGCGAATGAGCTCCAGTCATAGCGATACAGAGGTCAGCTCTGTTGTCACACGCAGGTAACAAAAATTTGACAGTCAGTTCATCTGAAATATCAAACCAGTTTACTTATTTTTTTCTTATTATTATTGATGCCACCCTGTGTACACATGCATTTATTTCCATCCTCTACACAGAGCTTCCCTTATCAGAAGCTACAACAACAACTCTCTTCC
Associated Phenotype:
Not determined