ZMP
ppfibp2a
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapien PPFIBP2, PTPRF interacting protein, binding protein 2 (Liprin beta
Human Orthologue:
PPFIBP2
Human Description:
PTPRF interacting protein, binding protein 2 (liprin beta 2) [Source:HGNC Symbol;Acc:9250]
Mouse Orthologue:
Ppfibp2
Mouse Description:
PTPRF interacting protein, binding protein 2 (liprin beta 2) Gene [Source:MGI Symbol;Acc:MGI:894649]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16101 | Essential Splice Site | Available for shipment | Available now |
sa11866 | Essential Splice Site | Available for shipment | Available now |
sa9503 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16101
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 |
---|---|---|---|---|---|
ENSDART00000089031 | Essential Splice Site | 179 | 826 | None | 23 |
ENSDART00000135633 | None | None | 441 | None | 10 |
ENSDART00000143617 | Essential Splice Site | 81 | 209 | None | 7 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 29112526)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 29184783 |
GRCz11 | 18 | 29163037 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTATGGCAGTGAGCCAGCACAAGCTTCTCAGACWGAACCAAAGCCGACGG[T/C]RAGTCTGAGATCTGGACATTTAGACAAATGTAAACAKTCTGGAACTGTGG
Long Flanking Sequence:
AGTTAAAAACTAAAAGAGCACTTTAACCTTTTAGTAGATTTGGAAACATATTCCAAAATTAATCCTATATTAAAGCATAATGATAAAATGTTGATTGCAGTGCATCATTAGTAATAGTATGGGGTAAAAACAGTAATCCAGGAAAGGAAATAATGGGATTTACATCTAGCAAACATAAACCGATACAAATAAGAATAGATATTAAACATAGTAGAGTAGTATATCTGTACAGTAAGTAACCCAGTAGGAAGCCACTGCTTGTCTGTCTCCTATAATCCATCTTTTCCATTACCTTTTTTTATCTGTTCCTCCTCTCCTCCCCATCCATATCCCTCTTTGACAGAGTGTAGTGAATCTGATTAGTGAGCTCCAGGAGCAGATGTGTAGGATTCGTCAGGAGATCTCAAGTAAAAACCCAGAGAAGCCAGCAGAGATGATCCCAGAGGAGGGCTATGGCAGTGAGCCAGCACAAGCTTCTCAGACTGAACCAAAGCCGACGG[T/C]GAGTCTGAGATCTGGACATTTAGACAAATGTAAACATTCTGGAACTGTGGCCATTGTGGAAAAGAAATACTTGGAAGCCCTTTGATCTTAAAGGTTAAAGTCTGTGATTACTGAAAAAAGGTTTCCAACTTTTATATGCATGCATTGTTATTGATTAATGATGTTTGTTTTAGTTCGTGCTCTAATCAAGGACATTAGTGACCACCCACATCTGCTGCTAGGCATTGGTTCTGCAAGTATTTAGCTTTTTTGTCCAAAATATTTTGAATGCTTTTTTAGATGCTGAGGTTTTACAGATGTCTTACTGAATTTCTTAACTGTGACTGAAAAAGTTTTATTTATTTTTATTCTTTTTTTATTGTAATCTGGATTTCTCTCATAATATTATATTATCTCATAAAGTTATTTCACGCATTTCATGTTTTAATGATTATGAATTTTATAAAAAAAAAAAATTCTACAGAACCATGTTGCTTTGCTTGTTTACCATACAACTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11866
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089031 | Essential Splice Site | 584 | 826 | 18 | 23 |
ENSDART00000135633 | Essential Splice Site | 199 | 441 | 5 | 10 |
ENSDART00000143617 | None | None | 209 | None | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 29138527)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 29210784 |
GRCz11 | 18 | 29189038 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ARCAAGACAATGGAGAAATCTTCYGAACTGGATCATATCTGGRTTACACG[T/A]ATGTAATAATCTTWATATTTTAAACYTAATGAAGCTGAACTGTTGCCCTM
Long Flanking Sequence:
TAGCCAAGTAATAAGTATACAGACATCCCAAGTTGGGAAAAGTGACTTCCGGGGGGAAAATACATGATTTGTGGGAGTTGTTTTTGTTGCATGATGTATATGAAGAGTGGTGGGTTGGTGGGGTGGGTTTGTGGTGCTTTTGTATTTGATGAGCTGGGAGTGAAGGGGTTAGGTTGGGCAACATATTTGAAGAGCAAGGGCGTATTTGAGATACTCACGACTTAAGGTAGATTATTATTTCGGGAGTCTCTATGCATATGCGGGAGACTCCTGGAACGTCTGGGAGACTTGGAATGTCTGAGAATATATGGTATATCCACCATGCAATAAAGTCTTTCTGAAACATTAGTAGTACTAATAACGTGTCTTGTGCTCTGTTCTGAATAGGAGATTTGTATTAAACATCCTCTGCACAGAAAGAAATTGCAACTAGCTCTCAGAGCATTCAGTAACAAGACAATGGAGAAATCTTCCGAACTGGATCATATCTGGGTTACACG[T/A]ATGTAATAATCTTAATATTTTAAACTTAATGAAGCTGAACTGTTGCCCTCTGTGGAGTTGCACTACAGCTAAGTCACAACTTGCACCATCAATAACAGCTTGCGATACAGTACATTTTGCTTAAACTGCATGTTCATAAATGAAATTTCATCTGTTTCTGTTTGCCATTTCAAATAAATGCATGTGTTCTGCCAATATTTTCCACATCCTTATTTGCTGTAGGTTGGCTTGATGACATTGGTTTACCACAGTACAAAGATCAGTTTTATGAAAGTAAGGTTGATGGGCGCATGCTACAGTACCTAACAGTGGTAAGATGAAGTTAATTTTACCCCTGTGTAACAACGTTTTCATCTAGGTGAACATGAGTTTGTAAAATGTTAAAATGATGTGCTTTTCTCTCAGAATGACCTCTTGTTTCTGAAAGTCACCAGTCAGCTTCATCATCTGAGCATTAAATGTGCAATCCATGTCCTTCATGTTAACAAGTTTAACCCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9503
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 |
---|---|---|---|---|---|
ENSDART00000089031 | Essential Splice Site | 696 | 826 | 21 | 23 |
ENSDART00000135633 | Essential Splice Site | 311 | 441 | 8 | 10 |
ENSDART00000143617 | None | None | 209 | None | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 29140296)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 29212553 |
GRCz11 | 18 | 29190807 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGAATATGCTCCAAACYTGAGAGGCAGTGGTGTTCATGGAGGCCTAATT[G/A]TGAGTCCCAGGGGCTACATACATATGAGGGGGYACCACACAAACTACTTG
Long Flanking Sequence:
ATTTAAACTGCTAAGTGTGAGTGCTCCAATTCGGGCCCAGGTGTGGTTCAGTTGGCCAACCCTGGCCCAGTTGGAATAGGTGTGCCACAGTGCGGTTCAGTTGGGGTTTGGCGTGGTAGGATTGTAGTGTGAGTGCAAAGCGTGCCTGAGTGCGAAACTGAAGATGCAACTTCACATTTAAGGGACTTCATATGGATTTATTATTCATTCCTTTTTTTTTTTTTTTTAAGATTTATTTTTGCCAAACAAGCTTTATAATCAATCATCAGCTAAGTGTCAACTCTTAAAATGTAAATTTTAGGGTGAAATATCCCCTTAAGTTAACATTTTGTTAGAATTCACTGTTTTAAACTAGATTTAATTCCATTCTGCAGTTCAAGACGTCTCCTTCTGAGGTGGTGCAGTGGTCCAACCACCGTGTGATGGAGTGGTTGAGGTCGGTGGATCTGGCTGAATATGCTCCAAACCTGAGAGGCAGTGGTGTTCATGGAGGCCTAATT[G/A]TGAGTCCCAGGGGCTACATACATATGAGGGGGTACCACACAAACTACTTGTTCTCCCGTAAAACAATTTATGATCCAATTACAGATGTCTAATCAGGTTCTGATACACAATCTGTTTTTTTTATATTTACACACTGTGTAAGTATTGTACTTTCACTTGAACAAAGAGTGTAAAGTGTGGATGAGTTTTCACCTTTTTTTTTAGTTCCAAATCGCAAAAAAATATAAAGCTTAGAAATATTTACTGCAAAAAAGACCAAACACTCATTGTTCTGATTAATGAATACTTAATTTATACTTAAAATTAATAAATAAAGTAATACAAATACAATCTTTAATTTCAATTTCAATTTTTCTTTTTTTTTTTTTTTGCAGAAGAAAGTCCATGTTTTAAATATTTTGTCGTGAAATATCTGTCTATGTTTTGTGTTTATGTATTGCAGATCCTAGAACCTCGTTTTCATTCAGAGACCCTGGCGTTGTTGCTTAACATCCCTCCAC
Associated Phenotype:
Not determined