Busch Lab

ZMP

si:ch211-157c18.2

Ensembl ID:
ENSDARG00000025108
ZFIN ID:
ZDB-GENE-060503-115
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]
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

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa21277 Essential Splice Site Available for shipment Available now
sa34384 Nonsense Available for shipment Available now

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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
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