ZMP
zgc:158309
Ensembl ID:
ZFIN ID:
Description:
phosphatidic acid phosphatase type 2B [Source:RefSeq peptide;Acc:NP_001073447]
Human Orthologue:
PPAP2B
Human Description:
phosphatidic acid phosphatase type 2B [Source:HGNC Symbol;Acc:9229]
Mouse Orthologue:
Ppap2b
Mouse Description:
phosphatidic acid phosphatase type 2B Gene [Source:MGI Symbol;Acc:MGI:1915166]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20132 | Nonsense | Available for shipment | Available now |
sa38409 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12356 | Essential Splice Site | Available for shipment | Available now |
sa40150 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6915 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40151 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40152 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20132
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102202 | Nonsense | 80 | 323 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 48562428)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50563568 |
GRCz11 | 3 | 47374208 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGCCTCCATTCCATTCTTCGCCTGTGAGCTCAAAGCGGTGACACCATA[C/A]ATGAGAGGCTTCTTCTGCGGGGATACCAGCATTACCTACCCTTACATAGA
Long Flanking Sequence:
CAACCATCCAGGTTAGCAATGGATTTGTGTGTTTTCCTAAAAGCGAAAATCCCTTGCACACTCCAAGTGAACCATATCCACTGCAAAATTCGCAAGAAACTTTCCAATCTCTGACCTCAATCCTGTATTCTTCAGGGTCTTTTCTTCTCCACATGCCTCATCTATCCAGGCTGTCATTCTCTTTCAGCCCCCACCCTTTCCTTTACACTTTCTGCCAGAGCTATGCGTGGAATGTCATCTCCTTGGGCTGGATCTCTATTCCCATCAGTAAGATCGAATGACAGTCTCAGTATCTAAGCCACATTCATGATTCTAATTGCACATAATAGAGCATTAAAGATGTATGTGTGTCTGATCGCGTGATGCCAAAGAAACACTGAAAGACAGAGAAGAATGTTCCTCTAGGTAATTCCGAAAGGAACATTAACTCATGTGTATGTCTCTCTCTTGACAGCCTCCATTCCATTCTTCGCCTGTGAGCTCAAAGCGGTGACACCATA[C/A]ATGAGAGGCTTCTTCTGCGGGGATACCAGCATTACCTACCCTTACATAGAAAGTGAAGCCATTCCTGATAGCGTGCTTATAGCCGGGGGCATCATAATCACAGGACTTACGGTGAGAATATGCACACTTACAAAAATATCACTAGCTGAAATCCCTTCAAGGTATTCTGCACCCTACTGTTTTCATCTACTCACCCTCAGGCCAGACATATCTTCTTTCTAGGAACACTAAATTTTTTCAAGAAGTGTATTATTTTCCGTGGAATTGCAAAACATTCCACAAAAACAAAACAAAATAGGGTCCAAAACTAAATTAAATGATTACAGTAATAGTATAAATGACTTGTGCCTTCAGAAGACTTATTTAAAAAGGCCAGGGCAACCAGTTTGATTTAAAAACCAAAAGTAGTGACAACTAAACAAACTTGTTGTCTTGTTGCTGTGACTTGCATCTAGGCCCAGCAAGTTGTTCTTCAGTTTACCACAAGTCTACAGCCTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38409
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102202 | Essential Splice Site | 117 | 323 | 2 | 6 |
ENSDART00000102202 | Essential Splice Site | 117 | 323 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 48562541)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50563681 |
GRCz11 | 3 | 47374321 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGATAGCGTGCTTATAGCCGGGGGCATCATAATCACAGGACTTACGG[T/A]GAGAATATGCACACTTACAAAAATATCACTAGCTGAAATCCCTTCAAGGT
Long Flanking Sequence:
ACCTCAATCCTGTATTCTTCAGGGTCTTTTCTTCTCCACATGCCTCATCTATCCAGGCTGTCATTCTCTTTCAGCCCCCACCCTTTCCTTTACACTTTCTGCCAGAGCTATGCGTGGAATGTCATCTCCTTGGGCTGGATCTCTATTCCCATCAGTAAGATCGAATGACAGTCTCAGTATCTAAGCCACATTCATGATTCTAATTGCACATAATAGAGCATTAAAGATGTATGTGTGTCTGATCGCGTGATGCCAAAGAAACACTGAAAGACAGAGAAGAATGTTCCTCTAGGTAATTCCGAAAGGAACATTAACTCATGTGTATGTCTCTCTCTTGACAGCCTCCATTCCATTCTTCGCCTGTGAGCTCAAAGCGGTGACACCATACATGAGAGGCTTCTTCTGCGGGGATACCAGCATTACCTACCCTTACATAGAAAGTGAAGCCATTCCTGATAGCGTGCTTATAGCCGGGGGCATCATAATCACAGGACTTACGG[T/A]GAGAATATGCACACTTACAAAAATATCACTAGCTGAAATCCCTTCAAGGTATTCTGCACCCTACTGTTTTCATCTACTCACCCTCAGGCCAGACATATCTTCTTTCTAGGAACACTAAATTTTTTCAAGAAGTGTATTATTTTCCGTGGAATTGCAAAACATTCCACAAAAACAAAACAAAATAGGGTCCAAAACTAAATTAAATGATTACAGTAATAGTATAAATGACTTGTGCCTTCAGAAGACTTATTTAAAAAGGCCAGGGCAACCAGTTTGATTTAAAAACCAAAAGTAGTGACAACTAAACAAACTTGTTGTCTTGTTGCTGTGACTTGCATCTAGGCCCAGCAAGTTGTTCTTCAGTTTACCACAAGTCTACAGCCTGTGGCTAACTAGCACAGGTGTTCTTTACCTGTGCTGGAGGAAATAGCTGTCCAAAGCCGCAGGTGGCCATAGTCTGAAACAGGAAAGTCCATGTCTGAAAAAGGAGTTTAAGGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12356
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102202 | Essential Splice Site | 117 | 323 | 2 | 6 |
ENSDART00000102202 | Essential Splice Site | 117 | 323 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 48562541)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50563681 |
GRCz11 | 3 | 47374321 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTGATAGCGTGCTTATAGCCGGGGGCATCATAATCACAGGACTTACGG[T/G]GAGAATATGCACACTTACAAAAATATCACYWGCTGAAATCCCTTYAAGGT
Long Flanking Sequence:
ACCTCAATCCTGTATTCTTCAGGGTCTTTTCTTCTCCACATGCCTCATCTATCCAGGCTGTCATTCTCTTTCAGCCCCCACCCTTTCCTTTACACTTTCTGCCAGAGCTATGCGTGGAATGTCATCTCCTTGGGCTGGATCTCTATTCCCATCAGTAAGATCGAATGACAGTCTCAGTATCTAAGCCACATTCATGATTCTAATTGCACATAATAGAGCATTAAAGATGTATGTGTGTCTGATCGCGTGATGCCAAAGAAACACTGAAAGACAGAGAAGAATGTTCCTCTAGGTAATTCCGAAAGGAACATTAACTCATGTGTATGTCTCTCTCTTGACAGCCTCCATTCCATTCTTCGCCTGTGAGCTCAAAGCGGTGACACCATACATGAGAGGCTTCTTCTGCGGGGATACCAGCATTACCTACCCTTACATAGAAAGTGAAGCCATTCCTGATAGCGTGCTTATAGCCGGGGGCATCATAATCACAGGACTTACGG[T/G]GAGAATATGCACACTTACAAAAATATCACTAGCTGAAATCCCTTCAAGGTATTCTGCACCCTACTGTTTTCATCTACTCACCCTCAGGCCAGACATATCTTCTTTCTAGGAACACTAAATTTTTTCAAGAAGTGTATTATTTTCCGTGGAATTGCAAAACATTCCACAAAAACAAAACAAAATAGGGTCCAAAACTAAATTAAATGATTACAGTAATAGTATAAATGACTTGTGCCTTCAGAAGACTTATTTAAAAAGGCCAGGGCAACCAGTTTGATTTAAAAACCAAAAGTAGTGACAACTAAACAAACTTGTTGTCTTGTTGCTGTGACTTGCATCTAGGCCCAGCAAGTTGTTCTTCAGTTTACCACAAGTCTACAGCCTGTGGCTAACTAGCACAGGTGTTCTTTACCTGTGCTGGAGGAAATAGCTGTCCAAAGCCGCAGGTGGCCATAGTCTGAAACAGGAAAGTCCATGTCTGAAAAAGGAGTTTAAGGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40150
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102202 | Nonsense | 141 | 323 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 48564929)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50566069 |
GRCz11 | 3 | 47376709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGGTACGATTCAGAGATGTGCACTCACGGGCATTTGTACGCAACCTCTA[C/A]GTGTCCTGTCTCTACAAGGAGTTGGGCAGCTTTTTATTTGGCTGCTGCGT
Long Flanking Sequence:
TATTTCCTATTTACCCACACACAACAATTGTAATAGTTTGTGAATTACTTCAGTGCTGTATAATTGTAATGAGTGAAATCTTATAATTTAACATTGTCTTTTTTTGCACTGGAAGAAAGTAAGTCATCAATTATAAACAACATGACAGATGACAGATGCTCATGCATTTTTTTTTTTTTTTTTACGGGGTGAACCATCCTTCGAAGAGCCTTGGTGTTCACAGTAGTATTAGCCCACGGTTCTCCAGTTACTGAGGGCTATTGATTTACTCTTTTCATCTACTTCGCTATTGAACAAGAGTCTCTCTTTGTGCAAGAACGCATGTGTGTGTGTGTGATGCTGTGAATTATTTAAGGCTTCATGGGCCTTGTAGTGTTTAACTCAGTGTTGCATGGCTGTAACCTCAGTGGTGTTCCCTGTTTGTTTCAGATTGCAGTTGGAGAGTGTTACCGGGTACGATTCAGAGATGTGCACTCACGGGCATTTGTACGCAACCTCTA[C/A]GTGTCCTGTCTCTACAAGGAGTTGGGCAGCTTTTTATTTGGCTGCTGCGTGGGGCAATCTTTAACCAACATGGCAAAGCTGAGTGTTGGCCGACTCCGTCCCCACTTCCTGTCGGCGTGCAATGTGACCTATGAATCACTTAACTGCACACCCGGAACCTACATCTCACATGTTGTCTGCAAAAGCTCAAAAAAGATAGTGGAGGAAGCCAGGTAAGTGGTGGAAAAGAGGATTTTTTGAAGCTGTGAAGATGAGATGAGCTCTGTTCCAAAACCTAGGCTGCCTATGAAACTGCATTCTCTCTGAGTAGTTATTTCTTTTGAAAGAGCACTTGATTTGCAACTGTTTAATGTATATTATTTTGACCTTGGTGGCAGCCCCTGTTAATTAAGGGACTATGCTGAAGTAAAATGAATGAATGAGTAAATATTGACCTTGTTCTTCATGTATGAGCAAATCTTTGTTGCTCGGGATTTCCAGTCTCTTTCAGGTCCATTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6915
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102202 | Essential Splice Site | 212 | 323 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 48567108)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50568248 |
GRCz11 | 3 | 47378888 |
KASP Assay ID:
554-4870.1 (used for ordering genotyping assays)
KASP Sequence:
AAGATTATGACATTTGGTTAGTAATATTTCCCTTYTGCTCTTCCTAAACA[G/A]AAAATCCTTCTTCTCGGGCCATGCATCTTTCGCCATGTACACCATGCTTT
Long Flanking Sequence:
AGAAACATCCTTGCAGGTGTGTTGAGGCAAGTTGGAGCTAAAATCTGCAGAACACCGGCTCTCCAAGACCGAGTTTGGACTGCCTTAAAGGGACTTTGCTATAGTATCAATAATGGGGTTTCATTGGTAATGAACACTAAAATATTGGAATTAAGCCATCCCGACATCGCCATCTTGCATTGCGGAATTGGATAAATTTGACAGTTCTTTATAATTCGCCCCAAAATTAAATATCAAAGACTTTAGGAACTGCTCTATTTATGAAGACTTGATAAACCGTCTAGGTTGGGGGCTTACTAGATTTTGGAACAGAGTTTAAATCACATAGTTTGTTTTATGTGAATATAGAGGAATTAATTTAGAAAAACATGTATGCTTGTGATTGCCTAATATAACATCATGCAGACAATGTTACGAGCCATAAAGCAGTGCAGTGGTTTAATGATTTGCAAGATTATGACATTTGGTTAGTAATATTTCCCTTCTGCTCTTCCTAAACA[G/A]AAAATCCTTCTTCTCGGGCCATGCATCTTTCGCCATGTACACCATGCTTTACCTGGCAGTGAGTATCTCTGTGTGTGGGCATGTTTACCACAAGCACACTCATACACTCAAACACAAGTCAGGGTAGCGCTGAACGCCTGTGCTTGCTGCTGGATGCTGCTGCAGAGCTTCACTGCTGTCAGCTTTCACTTCCCATCCCTGCCATGCGGGAGAAATGCCAAAAATTCCAACTGACAAGAAAGTCTCTCAAACTTCAGCTCACACAAGCGCACACAAATACACTCAAACTGAAAGAAGAAGGCTCTGAGAACGCAAAAAAACTCCCAAAAGGCATCTTGCTTCAAGCGGAAAAGAAAGGCTTGAGTGAAAGGGGGAATGTTCTCCAGAGGCCTGATGAATAGATGAGTGGAGAGAGGGAGAGCGAGGGAAAGCTAGCCTAAGACAGAGGAGGCCTTGTTTAGTTGTGGGTTGGGTCGGGAGGGGGGAGCTTTGGCCTGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40151
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102202 | Essential Splice Site | 231 | 323 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 48567168)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50568308 |
GRCz11 | 3 | 47378948 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCTCGGGCCATGCATCTTTCGCCATGTACACCATGCTTTACCTGGCAG[T/A]GAGTATCTCTGTGTGTGGGCATGTTTACCACAAGCACACTCATACACTCA
Long Flanking Sequence:
CTCCAAGACCGAGTTTGGACTGCCTTAAAGGGACTTTGCTATAGTATCAATAATGGGGTTTCATTGGTAATGAACACTAAAATATTGGAATTAAGCCATCCCGACATCGCCATCTTGCATTGCGGAATTGGATAAATTTGACAGTTCTTTATAATTCGCCCCAAAATTAAATATCAAAGACTTTAGGAACTGCTCTATTTATGAAGACTTGATAAACCGTCTAGGTTGGGGGCTTACTAGATTTTGGAACAGAGTTTAAATCACATAGTTTGTTTTATGTGAATATAGAGGAATTAATTTAGAAAAACATGTATGCTTGTGATTGCCTAATATAACATCATGCAGACAATGTTACGAGCCATAAAGCAGTGCAGTGGTTTAATGATTTGCAAGATTATGACATTTGGTTAGTAATATTTCCCTTCTGCTCTTCCTAAACAGAAAATCCTTCTTCTCGGGCCATGCATCTTTCGCCATGTACACCATGCTTTACCTGGCAG[T/A]GAGTATCTCTGTGTGTGGGCATGTTTACCACAAGCACACTCATACACTCAAACACAAGTCAGGGTAGCGCTGAACGCCTGTGCTTGCTGCTGGATGCTGCTGCAGAGCTTCACTGCTGTCAGCTTTCACTTCCCATCCCTGCCATGCGGGAGAAATGCCAAAAATTCCAACTGACAAGAAAGTCTCTCAAACTTCAGCTCACACAAGCGCACACAAATACACTCAAACTGAAAGAAGAAGGCTCTGAGAACGCAAAAAAACTCCCAAAAGGCATCTTGCTTCAAGCGGAAAAGAAAGGCTTGAGTGAAAGGGGGAATGTTCTCCAGAGGCCTGATGAATAGATGAGTGGAGAGAGGGAGAGCGAGGGAAAGCTAGCCTAAGACAGAGGAGGCCTTGTTTAGTTGTGGGTTGGGTCGGGAGGGGGGAGCTTTGGCCTGCTGAGAGATAGACAGGCTTCTTTCAGTTAAACCCCTCTCTCCCGCTCTCTGTTATGGCCTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40152
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102202 | Essential Splice Site | 290 | 323 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 48572904)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50574044 |
GRCz11 | 3 | 47384684 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACGTCCTGACCGGCTTCTTGCAGGGAGGACTGACTGCTTACTGGGTGG[T/A]AAGAATCATGTCACCACAAGCTCTCAGCTCTTACTCTTAGGATCCACTTT
Long Flanking Sequence:
GTATTACAGTGTAGGACATTTTGATTTAGCTTTGAGGATGGTCTATGAAAGATTGCTTTATGGTTTATAAAAAGATAGGTTAGGTTTATTAGCCAACTTCTGGGAGGTTTTTCAGGAAATGTGTCATCAAACATTTAGGAAGGTCAGACACACTCTCTCTCTCTCTCTCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACTGTAACCTTTATTTATCAGTCTGCACACTCTTTTATCAGCTCAAATGTTAATCATTCTTAAAACTTCCTGTGCAGTTCTACCTGCAGGCGCGGTTGTCATGGCAAGGGGCACGGCTTCTACGACCGCTGCTGCAGTTCATGTTGGTGATGTTGGCAGTGTACACAGGACTCAGTCGCATTTCCGACTACCGCCATCACCCCACTGACGTCCTGACCGGCTTCTTGCAGGGAGGACTGACTGCTTACTGGGTGG[T/A]AAGAATCATGTCACCACAAGCTCTCAGCTCTTACTCTTAGGATCCACTTTCCATCAAAGTTTAACTATAATGTTGATCAAACTCACTCTGCTTTAGCCTTATAGACCCTAATTATCTACTTTTATATTATAGTGATTATCTTTTGACTTTGAAGATGTCAAAAGCAACTATCATGTAATGAATCCTATTAGATTGCAGTTTGGGTGACCTTGCAAATCAAGTTAGGACTGCAATCAATTCAAAATGTTTAAGGTATAAAAAGAGGTATAAAGCGAAAAGTGGACTATTACATGCGGAATAGATTTAGTTAAAAAATGTTAAAGATGCAGTGTGTAAGTTTGACACCCAGTGATTGAACATGGTATTGCACCCGTAGTTCAAAACACACGCAAGAGCAGGTTGCCAGATTGATGACGCCAACAAATACTGATTTAAGGTTGATTTAAATTGTGTTCCAAATAAAAGTAACGGCATGCAATAGAAGGAATATTTTCCATATT
Associated Phenotype:
Not determined