ZMP
si:ch211-222n4.6
Ensembl ID:
ZFIN ID:
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 |
| 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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa23899
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 > 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