ZMP
inppl1a
Ensembl ID:
ZFIN ID:
Description:
Phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase 2A [Source:UniProtKB/Swiss-Prot;Acc:Q2I6J1]
Human Orthologue:
INPPL1
Human Description:
inositol polyphosphate phosphatase-like 1 [Source:HGNC Symbol;Acc:6080]
Mouse Orthologue:
Inppl1
Mouse Description:
inositol polyphosphate phosphatase-like 1 Gene [Source:MGI Symbol;Acc:MGI:1333787]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2819 | Essential Splice Site | F2 line generated | Not yet available |
sa32068 | Nonsense | Available for shipment | Available now |
sa7296 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa7295 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2819
Status:
F2 line generated
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041897 | Essential Splice Site | 101 | 851 | 6 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 46455128)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 47002411 |
GRCz11 | 15 | 47466690 |
KASP Assay ID:
554-3263.1 (used for ordering genotyping assays)
KASP Sequence:
TTAAAGTATTTCTGGATTTAATGATCTGCTTTTATTKATTTGTRTTTCTC[C/T]GTGATTGTTGGTTTTCTAGGAAACAAAGGTGCAGTGGGCGTGTCCTTCAT
Long Flanking Sequence:
TTGTTCTCAGTAAAGTGTTTAATCTGCGCTGTGCTGTGTGCGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNGCTCTCAACCACACAGCTGTAAAAGTTGCTGAGGATCTTAGATGACAGACTGAAATGTCCTGATTTAAGAGTTTTACATCAGTATTATTAAATCTAACTCAATGTCAAACCATTGTTACTTTAAATAAACAATAAATAAGAATGTAAACGTTCAGAAATATTGCTTGTTTCGTGTAGTTTAACTTGATGTACTGAAGTAAAAATAAAATAACAACATAGGACAAAGTTACCAAAACTTAAACATTATTATGAAAATGGGAAGCATTAAAATAACATTAAAGTATTTCTGGATTTAATGATCTGCTTTTATTTATTTGTATTTCTC[C/T]GTGATTGTTGGTTTTCTAGGAAACAAAGGTGCAGTGGGCGTGTCCTTCATGTTTAATGGCACATCGTTTGGATTCGTTAATTGTCACCTGACGTCCGGCAATGAGAAAATCCACAGGTATGTGCTTTAAAATACAGAATACAATAGTATTAATAACAATTCATAAAGATAAGAAAAATACCTTGTTTATTTGTGTTTATACTCACAAATACAACAAAAATTGCTTTTATAGAACAGAAAACGCACCTCAGTCATCTCAGTCTGCCTAACAGTGTCACCAACTGAATGATTGAATTTCAGAACAAAGTCTACATAGGTTACAAGTCCTGCCGATTTCCTACACTCGCTGGCCACTTTATTAGGTACACCTCACTAGTACCGGGTCGGACCCTTTTGCCTTCAGATCTGCTTAATCCTTGGTGTCAGAGATTCAACAAGCTACTGGAAATATTCCTCAGAGATTTTGCTCCATACTCTCATGATAGCATCACACAGTTGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32068
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 |
---|---|---|---|---|---|
ENSDART00000041897 | Nonsense | 311 | 851 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 46450777)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 46997936 |
GRCz11 | 15 | 47462215 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCCAGTGTTTATTCCAGCTGTTTCTCTCTGCAGGTCTGCCAAAGTCTT[C/A]AGAGCAGGCCTACATTGAGTTCGAGAACATCGAGGCCATCGTGAAGACCG
Long Flanking Sequence:
ACGTTCCTTCATGGTGCGACAGAATCCTGTGGAAATCATATCCAGAGACACACATCGTCTGCAACTCATACGGTGCACACTCACATGATGAACACACACACACATGCAAACACATGCACACACGTACTGTATGCATACACATATGCATATGCATGTTTATTTGTGTGTGTGTGTGTGTTTTTGTGTTTGTCCTTGTCTGTGTGTGTATATATTTGTGTATCTTGTGCTTGTTTGTGTTTGTTTTTGTGTATGTATTTATTTATTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGTGTGCGTGTGCGTGTGTGTTCAGGCTGTACGGATGATATCGTGACGAGTGATCACTCTCCAGTGTTCGGCACATTTGAGGTCGGCGTCACCTCTCAGTTTGTCTCTAAGAAAGGTAAGTGTGTGTGTGTGTGTGTGTGTGTGTCCAGTGTTTATTCCAGCTGTTTCTCTCTGCAGGTCTGCCAAAGTCTT[C/A]AGAGCAGGCCTACATTGAGTTCGAGAACATCGAGGCCATCGTGAAGACCGCCAGCAGAACCAAATTCTTCATCGAGTTTTACTCGACGTGTCTGGAGGGTGAGAGAGCCATTGAGCAGACAACACACCACAATCACTAGACAGTAACTCAGTCCCAGACGACACTCATGGTCACTTTTCACATTCATTCGTTCATTTTCCTTCAGCTTAGTTCCTTATTTATCAGAGGTCGCCACAGCGGAATGAACCGACAACAATTCCAGGATATGTTTTTCACAACGGATGCCCTTCCAGCAGCAACCCAGTACTGGGAAACACCCATACACACTTATTCACACACTCATACACTACGGCTGATTTAGTTCATCAAACCCTGCATGTTCTCCCCGTGTTGGTGTGGGTTTCCTCCGGGTGCTCTGGTTTCCCCCACAGTCTAAACACATGCGCTATAGGGGAATTGGGTAGGCTAAATTGGCCCTAGTGTATGAGTGTGTGCGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7296
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041897 | Essential Splice Site | 455 | 851 | 15 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 46446776)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 46993936 |
GRCz11 | 15 | 47458215 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGGCGGAGCTTAACAGTTAAACYCCGCCCCTACTCAATATYCATCTTC[A/T]GTTGGAAAYACATCATCAAACTTRATTTCYTTAAGCTGATAATAAWCTTT
Long Flanking Sequence:
GGGTTTCTATGGGAAATGGAGGTGAATTAGAATTTTTAATGCTTAAATGTGTGCTTGAAACTGCTTCAAAATGTAATTGTGTCACTTTTGTGATAATTTATTTTAGTAAATAGGTAATAATGATTATTTAAATAAAATAGATCTCTGATTTTTCATCAAAGTTTATGTGGGTTTCTGTCTCTCTCTCTCTGTGTTTGGGTTTGTGTGTGTGTGTGCAGGCGAGTGTGTTCTGGCTCTGAAGTCTATGATCGGCAGCACAGCGCAGCAGTTTCACACGTATCTCTCTCACCGCGGCGAGGAAACCGGAAACATCCGCGGCTCCATGAGGGTCCGCGTGCCATCAGAGCGCATGGGCACCAGAGAACGGCTCTACGGTGAGAAACACACACACACACACACTCAATCACACATTAATTACACCGACTGTGTGTGTGCTGAGAGCCACAGATAAAAGGCGGAGCTTAACAGTTAAACTCCGCCCCTACTCAATATTCATCTTC[A/T]GTTGGAAATACATCATCAAACTTAATTTCCTTAAGCTGATAATAATCTTTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATTGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGTGTGTGTGTGTGTGTGTGTGTGAGTAGTTGAACACTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGCACGCGTCTCTCTCTGTCTCTCTCTTCAGGCCACTAAAGAGGTGATCGAGCGAGAAGCTCCAGGGATGTCTCTGGCGATGCTGATGGGCTCTCTGAACGTCACTCCTCTCGGGATGCTCTCCAGGTCTGCCTTCAGACATGTGATTGGCTGATTAGAAATTTTCGTTTACGAGCAATTAGACTGGTGTACCTTATAAAGTGTCCAGTGAGTGTGTATATATAATAGTATTTAGCAGTATAGTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7295
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041897 | Essential Splice Site | 482 | 851 | 18 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 46446134)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
NNNNNNNNNNNNNNNNNNNNNCACACACAAACACACACACACACAYACACNNNN[C/A]CACACACACACANNGTAGCAGTGTTTCCATCCAAAGATGCCTATTAGCAGTG
Long Flanking Sequence:
TGTGTGTGTGTGTGTGTGTGTGTGGTGTGTGTGTGTGTGTGTGTGTGAGTAGTTGAACACTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGCACGCGTCTCTCTCTGTCTCTCTCTTCAGGCCACTAAAGAGGTGATCGAGCGAGAAGCTCCAGGGATGTCTCTGGCGATGCTGATGGGCTCTCTGAACGTCACTCCTCTCGGGATGCTCTCCAGGTCTGCCTTCAGACATGTGATTGGCTGATTAGAAATTTTCGTTTACGAGCAATTAGACTGGTGTACCTTATAAAGTGTCCAGTGAGTGTGTATATATAATAGTATTTAGCAGTATAGTAAATTAATGAGTTGCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCACACACAAACACACACACACACACACAC[C/A]CACACACACACAGTAGCAGTGTTTCCATCCAAAGATGCCTATTAGCAGTGTTAATGTGAAGCAGTTAAACGCAGTGACGCTTCTGTTCCTGCAGACCGACCAGCAGCAGCAGCAGCATCAGGAAACACGGATCAGCAGAACTCAGCAGAGTCTCAGAGGAGGGAGAGAAGAGCAGCACCAGCAGACACACACACACTAAAGAGGAGAACACGCACAACAGGTCTACACACACACACACACCCATACTGAGTTGAGTTTAAAAGTAAAGTTAGTTTACGGTGCATTCACACGGGGTGTCAGCGTCATGTTCGACAGTGGGCGTGTCTGAAGTTGGGGCTGACGCGATCATCATAGCAGCATCAGCCAATGAAATTAGTCCGCAATCAACTACTGTCTGAGCTGGTGTATTTGCATACAGCGATCTGATTGGCTGACGCTTCAGTCGGCGCTTGAAAAGTTGAGAAAGTTCCAACTTCTGCAGCGAGCAACGCCACTGAAAC
Associated Phenotype:
Not determined