Busch Lab

ZMP

si:ch211-222n4.6

Ensembl ID:
ENSDARG00000009386
ZFIN ID:
ZDB-GENE-091118-7
Human Orthologue:
MPP4
Human Description:
membrane protein, palmitoylated 4 (MAGUK p55 subfamily member 4) [Source:HGNC Symbol;Acc:13680]
Mouse Orthologue:
Mpp4
Mouse Description:
membrane protein, palmitoylated 4 (MAGUK p55 subfamily member 4) Gene [Source:MGI Symbol;Acc:MGI:238

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa16012 Essential Splice Site Available for shipment Available now
sa15310 Nonsense Available for shipment Available now
sa29558 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa23899 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa16012
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
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000012574 Essential Splice Site 92 641 3 25
ENSDART00000144086 Essential Splice Site 89 331 3 11
ENSDART00000147246 None None 263 None 6
Genomic Location (Zv9):
Chromosome 21 (position 17807697)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 18955949
GRCz11 21 18992585
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGGTCCAGCCAGGYCATATGTCTCATATTCAWCTGGACTTTCTCTRCAG[G/A]TTAGCTTTAAAGTTTATTGGCATANTTTTTTAACCAGTTTGTTCCACTCA
Long Flanking Sequence:
GACTGATCCTGGATCAGCTCCACTGGAGGTGGGAGACAAAGGTAGGAAGCTAAACATTGCTCCTTAAATCTGATGGCAGCCAACTTATCTATTCAGTTTGCCTAGCTGATTAGAAACATGTTAATATTAATACTATTAAGGCTGTTTAAGAAGCCAAACAGCATGACACATAACTGAAACGTACTGAGTGTCCAGTCCTAGATGTTTTTGCTTTGTATGTTTCAGGTCTGGCACAGATCTTGGCACATGTGATTGCTGAGGTGAGAGGCTCTATTAATAAAGATATAAATGGAGCTGAACTATTGTATGGTCTTCTCAACGCCCCCTGGTTGCAGTCACTACTAAAGGTAGAGTCCATCCAACATATATTATTTGTAATTAGTACAAATTGAGAGCTCATTGTCTGCTTTTTTTCTCTGCAGGTGTATGAATGTCTACAGAGGCATCTAAGGGGTCCAGCCAGGCCATATGTCTCATATTCATCTGGACTTTCTCTACAG[G/A]TTAGCTTTAAAGTTTATTGGCATAATTTTTTAACCAGTTTGTTCCACTCATAACGTTTGCATCTACTCTGTCAAAGCCAATAGCGTATAGAGCTGTTTCCTCTGCTAGCTGTTACTGTCCATTTTCACATCTTGCCAGTCTATACCAGGGATCACCAAACTTGTTCTTGGAGGTCCGGTGTCCGGCAGGTTTTAGCTCCAATGCTAATCAAACACACCTGAACAAGCTAATCAAGGTCTTAGTAGGTATACTTGAAACACCCTGGCAGGTGTGTTGAGGCAAGTTGGAGTTAAACCCTGCAGGGCACCGGACCTCCAGGAACGAGATTGGTGACCCCTGGTCTATACTGCCCTTTCTCAAAAAAATGTCAAAAACCTCCCAGTGTCTTAAATGTCTTAAAGTAAGTGAGGACTTTTTAAATAGTACCATTTAGAGTTGTAATCTTGAAGTGTGTGTAAAGTGAGTATTGTCAAATATGGTTACCTGTACTTGGAATTCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15310
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
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000012574 Nonsense 388 641 20 25
ENSDART00000144086 None None 331 None 11
ENSDART00000147246 Nonsense 10 263 1 6
Genomic Location (Zv9):
Chromosome 21 (position 17797421)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 18945673
GRCz11 21 18982309
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CRATGTTTCCTTGTCATATTAGCTGGATTTCGTAGWAGTTTGCGTCTCTG[T/A]CGCCGGCGAAGGGSTCAGGCTTTCGGAAYGTCTCARTTCTGCTCCSTTYG
Long Flanking Sequence:
TTTTCCTGGAGAGCAACCCATATCAAACACACCTGCCTGTAATTATCACATGTGTTCAGCTCCTAATTAATTGGTTCAGGTGTGTTTGATTTGGGTATCAACTGAAATTTGCTGGAAGGTGGCTCTCCAGGAACAGGGTTGGCCATCCCTGCACTAGAGGGTGAGTAAATACATTCATTTTTGGGTGAACTATCATTTTACGTACTGATATGTACCTTTAATGTTGCTTTAACGCACAATATGGGCACTTTGGGTACGAATATGTACTTTTAAGTACAAAAGTGTTTCTTTTGAAAGGGTACTGCTCTGGTGACAGCATTTGTACATTTATTTCTGAGAGTATATTACATGCATTCATTATACTAGATTAATTACAAAATACAATGCATTCCACTTACTGCTGTATCTCTTCCTGATTCATTAGCCTGTTTGCATGTTTGACTGTGTGTTCAATGTTTCCTTGTCATATTAGCTGGATTTCGTAGAAGTTTGCGTCTCTG[T/A]CGCCGGCGAAGGGGTCAGGCTTTCGGAACGTCTCAATTCTGCTCCCTTCGCTGCCCCGCTAGCTGCTACAGTTCACTATCAAACCCTTATGAGGACGTGGTGCGATACCAACACCATCCAGAACACACACACCGCCTCATAGCACTGATAGGTGAGTGTGTCTGAAGAGCTCTTCATAGTTCTATTAGTGGGTATCTAAAGGGTTAGTTCACTTAAAAAATAATGTCATCATTCTAAGTATAACAATTCTGTCATATCCTTCACTTGTCACAAACCTGTTTTAAAAACATTAACCATTGACTCCATAGTATTTGTTTGGAAGTCAATGGCTAGTTTTGGGGGAACTGTTCCTGAGGACATCTAACCGTAAAATTCTCCATTTAAACAGTAATATTGTAGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTAGTCAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29558
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000012574 Essential Splice Site 439 641 None 25
ENSDART00000144086 None None 331 None 11
ENSDART00000147246 Essential Splice Site 61 263 None 6
Genomic Location (Zv9):
Chromosome 21 (position 17797268)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 18945520
GRCz11 21 18982156
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGATACCAACACCATCCAGAACACACACACCGCCTCATAGCACTGATAGG[T/C]GAGTGTGTCTGAAGAGCTCTTCATAGTTCTATTAGTGGGTATCTAAAGGG
Long Flanking Sequence:
CTAGAGGGTGAGTAAATACATTCATTTTTGGGTGAACTATCATTTTACGTACTGATATGTACCTTTAATGTTGCTTTAACGCACAATATGGGCACTTTGGGTACGAATATGTACTTTTAAGTACAAAAGTGTTTCTTTTGAAAGGGTACTGCTCTGGTGACAGCATTTGTACATTTATTTCTGAGAGTATATTACATGCATTCATTATACTAGATTAATTACAAAATACAATGCATTCCACTTACTGCTGTATCTCTTCCTGATTCATTAGCCTGTTTGCATGTTTGACTGTGTGTTCAATGTTTCCTTGTCATATTAGCTGGATTTCGTAGAAGTTTGCGTCTCTGTCGCCGGCGAAGGGGTCAGGCTTTCGGAACGTCTCAATTCTGCTCCCTTCGCTGCCCCGCTAGCTGCTACAGTTCACTATCAAACCCTTATGAGGACGTGGTGCGATACCAACACCATCCAGAACACACACACCGCCTCATAGCACTGATAGG[T/C]GAGTGTGTCTGAAGAGCTCTTCATAGTTCTATTAGTGGGTATCTAAAGGGTTAGTTCACTTAAAAAATAATGTCATCATTCTAAGTATAACAATTCTGTCATATCCTTCACTTGTCACAAACCTGTTTTAAAAACATTAACCATTGACTCCATAGTATTTGTTTGGAAGTCAATGGCTAGTTTTGGGGGAACTGTTCCTGAGGACATCTAACCGTAAAATTCTCCATTTAAACAGTAATATTGTAGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTAGTCAAGCCTGAAATTATTTATACCCCTGGAAAATTCTCACTTAAAGTTTTTGTTCAAATGTAAATAAAAACAGCGATGCGTCTTGTACATCGTCTTAATCGTTTGATGCCACAAGCTTGGCATATCTGTCTTTTGGGAATTTTTACCCATTCCTCTTTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23899
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000012574 Nonsense 572 641 24 25
ENSDART00000144086 None None 331 None 11
ENSDART00000147246 Nonsense 194 263 5 6
Genomic Location (Zv9):
Chromosome 21 (position 17793365)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 18941617
GRCz11 21 18978253
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCAGATGAAGCGCACTCGGATGAACTCCAATATCATCACAAATTACTA[T/G]ACAAGCCGACCTTTTAGGGTAACTGTTCATCTTTACCTTTGCCTACTGAT
Long Flanking Sequence:
GATACACAGGCATTTTTTAGCTTCGCCCTCTTTTGAAAAGAGCACAATCTCATTTGATTTGATCTCTCCCCCCAAAGTTGTGAATATTTTTTTCATCTTCTCACAGAAGCTCTCATCAACATTAAATATTTTATGTTTTTTACTAATTTTAGCAGTTTACTGTTCTTGTTTGTACTTTTTCTGTAACAGTGATGAAAGTTATGAAGTCTTTTCGGCAAATTAATTAATGCAAAAACCTTTTATTTGAAGTGCATGTGCAGGATGCATCATTCACAATGTAATATGGAAGGATATGGAGGCAGCAAGTCTTTAAATGAAAAGTCTGAAATTTGACTTTGTCAACCAGCACAATTGCCACTGAACTTACTCTTTTACTGTTTTCAGGCACTGGAGTCAGTGAGGACCCCCGAGCTGAGGGCCTACGTCATCTTTATAAAGCCTCCTACTGTTGAGCAGATGAAGCGCACTCGGATGAACTCCAATATCATCACAAATTACTA[T/G]ACAAGCCGACCTTTTAGGGTAACTGTTCATCTTTACCTTTGCCTACTGATTAGCTGATGTTTATTAGATATGTACTAGTAACTTTTTTTTAAATACCAGTACTTGTGACATACTATTTTAATTTGATCTGATTTTGATTTCTTGCTTATTACATATAAATACTTATTTAATAGACACTAATAGTTGTTCATGATTTCCACTTAACGGTATGGTTCTGTACAGTTCAGGTCAGCATGGTTTACTACTGAGCACAATCATTGTAGTACAGTGTCATGTTTTTACCTGTGTATGTTCTTTAGATTAAATATTAAGACTGTCTTACCATACCACACCATACCATATTTCGGTGCCCGCAGGGTCTAAAAATGTCCTAAATTTCAAAAACTAAATTTTAGACCTTAAAAAGTCTAGAATTTGTGCATTGTAGGTCTTAAATCGTTTTAAACAGGTCTTTTAATGCCCTATTGTAATGTGAATAGGACGCTGACAACAGAATTGCA
Associated Phenotype:
Not determined