Busch Lab

ZMP

mpp5a

Ensembl ID:
ENSDARG00000006272
ZFIN ID:
ZDB-GENE-020712-1
Description:
MAGUK p55 subfamily member 5-A [Source:UniProtKB/Swiss-Prot;Acc:Q8JHF4]
Human Orthologue:
MPP5
Human Description:
membrane protein, palmitoylated 5 (MAGUK p55 subfamily member 5) [Source:HGNC Symbol;Acc:18669]
Mouse Orthologue:
Mpp5
Mouse Description:
membrane protein, palmitoylated 5 (MAGUK p55 subfamily member 5) Gene [Source:MGI Symbol;Acc:MGI:192

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa15209 Essential Splice Site Available for shipment Available now
sa2908 Essential Splice Site F2 line generated Not yet available
sa36468 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa15209
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000014306 Essential Splice Site 437 703 9 15
ENSDART00000084501 Essential Splice Site 437 703 7 13
ENSDART00000136167 Essential Splice Site 437 703 8 14
Genomic Location (Zv9):
Chromosome 17 (position 34398322)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 34283246
GRCz11 17 34231192
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAYAGAGAWGGGGAWGAAGACAACCAGCCTCTTGCTGGCCTCGTCCCTGG[T/C]ACTATGWTTTTACATGCTGTTGTGCTGTTTTTTTTTTTTTTTTCTTTCAT
Long Flanking Sequence:
GTGAAATATCTGCAAAAACACTGTATTTTTATGATTTTAGTCAAAAATGTACATTAATTTAAATATTACTTTAGTATCTGCATGTATTTTTAGGTCACTTATTGTATCCATTCTTACAAAATGAGTGTGTGTGTGTGTGTTCACAGGCGGACATGCATGGTGTACTGTCTTTTGTTCTCATCCCCAGCGCACAGATCAAATCTCCTCCTATTAAAGAGACTGTGGTGAGAACTTCAGTCAGAATTAAATTCATTACTGCTTTAATGAAACAAAGGTCAAATCAATATTTAAAATCATTTCCCTGTGTTCATCCAGGTACATGTGAAGGCACATTTTGACTATGACCCCTCAGATGACCCATATGTGCCATGCCGAGAGCTCGGCCTGTGCTTTCAGAAGGGGGATATACTCCACATAATCAGCCAAGACGACCCCAACTGGTGGCAGGCCTACAGAGATGGGGATGAAGACAACCAGCCTCTTGCTGGCCTCGTCCCTGG[T/C]ACTATGTTTTTACATGCTGTTGTGCTGTTTTTTTTTTTTTTTTCTTTCATACTGTCACACTTAGATGTCTTTTACTTGTGTGATTGTCCAGGCAAAAGTTTTCAGCAGCAGAGGGAGGCAATGAAGCAAACCATAGAAGAGGATAAAGAGCCTGAAAAATCAGGTAAGTGTTGCAGAGCTTGTGCATACTTCTAAACACACACATGCACAGCTCTTTTTTTCTCATTAACACTCATTTTCTGTTTTAGGAAAGCTTTGGTGTGCTAAAAAGACCAAGAAGAAGCGGAAGAAGATGCAATACAATGCTAACAAAAATGATGGTGAGTGTCTTCAGGCAAACATTAGAGTAAACTACACACCTTTAAAACATTTTTACCAAATAATTCAGGGGTAACACACACTTTACCAAGCAGACCCTTAATATTAAAGTATTCATTTTAATGCACACACAGCTAAATGCATTGCATTTCAATAAATACTCCATTTAATGTTTATTAACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2908
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000014306 Essential Splice Site 484 703 11 15
ENSDART00000084501 Essential Splice Site 484 703 9 13
ENSDART00000136167 Essential Splice Site 484 703 10 14
Genomic Location (Zv9):
Chromosome 17 (position 34398643)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 34283567
GRCz11 17 34231513
KASP Assay ID:
554-2827.1 (used for ordering genotyping assays)
KASP Sequence:
GACCAAGAAGAAGCGGAAGAAGATGCAATACAATGCTAACAAAAATGATG[G/A]TGAGTGTCTTCAGGCAAACATTAGAGTAAACTACWCACCTTTAAAACATT
Long Flanking Sequence:
GTGAAGGCACATTTTGACTATGACCCCTCAGATGACCCATATGTGCCATGCCGAGAGCTCGGCCTGTGCTTTCAGAAGGGGGATATACTCCACATAATCAGCCAAGACGACCCCAACTGGTGGCAGGCCTACAGAGATGGGGATGAAGACAACCAGCCTCTTGCTGGCCTCGTCCCTGGTACTATGTTTTTACATGCTGTTGTGCTGTTTTTTTTTTTTTTTTCTTTCATACTGTCACACTTAGATGTCTTTTACTTGTGTGATTGTCCAGGCAAAAGTTTTCAGCAGCAGAGGGAGGCAATGAAGCAAACCATAGAAGAGGATAAAGAGCCTGAAAAATCAGGTAAGTGTTGCAGAGCTTGTGCATACTTCTAAACACACACATGCACAGCTCTTTTTTTCTCATTAACACTCATTTTCTGTTTTAGGAAAGCTTTGGTGTGCTAAAAAGACCAAGAAGAAGCGGAAGAAGATGCAATACAATGCTAACAAAAATGATG[G/A]TGAGTGTCTTCAGGCAAACATTAGAGTAAACTACACACCTTTAAAACATTTTTACCAAATAATTCAGGGGTAACACACACTTTACCAAGCAGACCCTTAATATTAAAGTATTCATTTTAATGCACACACAGCTAAATGCATTGCATTTCAATAAATACTCCATTTAATGTTTATTAACATGCACACAGTTTCGGTCTTGTGCTTAATAGTCACATTTTCACATTGATTTTAGGGGAGGGTGATTTCATAGAGATGTCATATGTTTTTGTTTTGTTTTTGTCATGTACTTTTTGAAAAAAATATTCTCGTAAAATAACAAATGTTTGTTTTGTTGCTTTTACTATTTTGCAAGTCAATTAAAATTGAATTTAAATTAAATAGAATTATTCAAATAAAAAAGATTTCTACTCACTTAAGTTATTTTCAAGATTGTGGGTGACCCAAAAGTTGCTGGTCTCCACTGATTTCTGTAGTAACTGTTTGGCCTGCCACATTCTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36468
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000014306 Nonsense 663 703 15 15
ENSDART00000084501 Nonsense 663 703 13 13
ENSDART00000136167 Nonsense 663 703 14 14
Genomic Location (Zv9):
Chromosome 17 (position 34405922)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 34290846
GRCz11 17 34238792
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAGCTGCGAGACATTATCGAGAAGGCCCGAGAGATGGAGCAGAACTA[C/A]GGCCACCTGTTTGATGCTGCCATTGTGAACACCGACCTGGACAAATCCTA
Long Flanking Sequence:
AAGTAAATAGACAATCTCATACTGTAGATGTTTATATAATTCATGTTTTTAAACGCTGATTGATCAAACAATAAAAGCGTTTATTTATAGATTATTTAAGATGGATTTAAATGCAAAATTTAAATAGCTTTTTAAAATGGCATTTGACAAATGCTTTTCTCTCTCTATTTGCCACTTTCTTGTCTCTCTCTATTTGCTTTTCTTTTTGCTATATGCTTTTCTCAAGTTGAAAATAAATCAAGTTTAAAAATGCCATTGGACAGTCCACACGTGGGAGCAACCAAACAACTTTCACCCTCTCTCACATGTAAATGAAACATGCGTATTTTTGTGGCCAAGTGTGATATATTTTCTTTAGGAAAATAGTTTCTTATAGGATTTAACCTCCTTTTTCAGAAAACATTCACTTTTATTCATGTGGTTTCACACATTGACTGTATTCTCCAGCCCGAGGAGCTGCGAGACATTATCGAGAAGGCCCGAGAGATGGAGCAGAACTA[C/A]GGCCACCTGTTTGATGCTGCCATTGTGAACACCGACCTGGACAAATCCTACCAGGAGCTGCTGCGTCTCATCAATAAACTAGACACTGAACCCCAGTGGGTCCCTTCATCCTGGCTGCGCTGAGATGGGTGAAAATGAAGAGCACGTTGTTTATCAATGCTTTAGAATGCCTCTGTTTTTCTTGTTTTCTTCTCCTCACTCATAGATAAGGACACTATACGCGCCCTCAAGCCCGCACAGAAGTGTCTGTCTGCACTACACTGTCGGCAGGCTGAGGGAATGAGAGTTTTAATGTCATAACTTGTGTTTTCGAGTCCGGTTATCCACATTCCAGTGAGAAAGTTACCAGCACTTGGTGCAGCAGTAGAATTAGGGCTTCTATACTGCTTTTGATAACTATTTATGATTGTAAATATTCTATATGTATTTTTAAAGATGGATTTGGACAAATGCAGAGGTGGGACAAGATAGCTGGAAGTCAGCATTTTTCAAGAGATCTA
Associated Phenotype:
Not determined