ZMP
pi4kaa
Ensembl ID:
ZFIN ID:
Description:
phosphatidylinositol 4-kinase alpha [Source:RefSeq peptide;Acc:NP_001030144]
Human Orthologue:
PI4KA
Human Description:
phosphatidylinositol 4-kinase, catalytic, alpha [Source:HGNC Symbol;Acc:8983]
Mouse Orthologue:
Pi4ka
Mouse Description:
phosphatidylinositol 4-kinase, catalytic, alpha polypeptide Gene [Source:MGI Symbol;Acc:MGI:2448506]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8479 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8903 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41573 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44718 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2547 | Nonsense | F2 line generated | Not yet available |
sa2563 | Essential Splice Site | F2 line generated | Not yet available |
sa34812 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8479
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113162 | Nonsense | 40 | 2097 | 2 | 55 |
Genomic Location (Zv9):
Chromosome 10 (position 3265570)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 3257764 |
GRCz11 | 10 | 3258068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTWAWATGCACATTTGTTAAATATAGGTCCAGAAGCTACAATGCATGTG[T/A]CCTGTGGACATCCGTGGTGTTTTCCAGCTGGACGAGCGGAGGAGAGATGC
Long Flanking Sequence:
TTGTGGAACCCAGCTTTTTTTTTACAGTGAAGCGTGATGTATTTTTATCTTTAGTTTTTAATTGTATTTAGTTTTTTTAATATTTAATTTAAATATTACTGTTTAATATGCATTTTTATGTGACATGCTGTGAATATTTGCTGTCTTTATGGCCATTTTTGGCCACATTATATTGTTTTACTGAAGACGTAATGATTCTCTTTTAAATAAATATGTTAATTTGTTTTGATTGAGTAATTTCAGTGCTTTCTATTTGAAGTATAGCTTCCAAAGAAACATTTCCAATTGTCCAAAAGCATTTTAATGATTTTAGCTAATAAATAAATGATTGTAGTGGTGTGATCTTTTTTTTTTGGTTCACAAAATATATGATGAAATATTTTTACAGATTATAATACTGACACAAAAAGAAATCTCCCTGCTTCGGCAATAAAAAGTATTTCACAATTTTTTAAAATGCACATTTGTTAAATATAGGTCCAGAAGCTACAATGCATGTG[T/A]CCTGTGGACATCCGTGGTGTTTTCCAGCTGGACGAGCGGAGGAGAGATGCTGTGATCGCACTTGGGATCTTCCTAGTGGAGTCTGAGTTGCAGGTATTGGTTTAACATAGTCAAACTATATGTTTCATTGATTAAAATCAGGACTAATGAGGCACATTTAAAGCACTTTAAAAACACTTTTTTCCCCAAAATATAATAAAGGGATAGTTAACTCAAAAAAGTTCCTCACTCTTTACTAACCAGGGTGTCCGCGGGGCTTTAAAAAGTATTAAAAGTTGATAAATCAAAAAGCTATAACCCGGAAATGGTATAAAGAAGAGCCACCAACTAAAGATAAATGGTTTAAAGTTATAGCAGAAGTTGAGGAAATGTAAAAAATGACACATGCACTTTGATTACAGGGCTCGAAATTAACTTTTTTACTTGGTAGCACCGGTGCTCCCAACTTCAAATATTTAGGAGCAACAAAAAAATTTTAGGAGCACCAGAAAAAATTTAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8903
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113162 | Nonsense | 405 | 2097 | 11 | 55 |
Genomic Location (Zv9):
Chromosome 10 (position 3254886)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 3247080 |
GRCz11 | 10 | 3247384 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAGCAGCAGTCAGTCTGAGCTGCARAGGATCCTGCACGATGTGGAGTA[T/A]CTGCACAGTGAACTGAACCCGCTTAAGCTGCGCTGTCAGGCCAACGCCGC
Long Flanking Sequence:
TTCAGCCTTCTCAATTATATTAACGCATATTTTTTTGTCAGTAATGGAGAGGGCGTTGTAACAGGGAAACAGTAATTCGTTAATAAAGATGAAGGAAAGACTAGTGGTTGCTGTTTGGAGTTTTCCAGCGCTGTATAACTTCACAAATCTTGAATATCACAATTTTATTATAATGTTAAAAAGCAGCAGGCCTGGAAGTAAGTCAGTCTTTTTCTTGTCAACAAAAAGGCAGTGTGCTGTGCCTTGCATTCATAGAATGGAAAAGGGTGCACAGTGTGATCGGCCACTAAGAAAGTGTTGTATTTAAATAAAAGTGTTTTATTTACATTAACCAAATCAGTCACGCTTTTTCTACAGATGTTTTATCACATTTTTTGCGCATTTTTTTTTGTGTGTGCAGATCTGCAGGTGTCGTTTGTGAAGGAGGTCCATGACTTTGTTCTGGAGCAGTTCAGCAGCAGTCAGTCTGAGCTGCAGAGGATCCTGCACGATGTGGAGTA[T/A]CTGCACAGTGAACTGAACCCGCTTAAGCTGCGCTGTCAGGCCAACGCCGCCTGTGTGGACCTCATGGTGTGGGCCGTCACGGAAGAACAGGGTAAGACTTGACAGAGAAATACACCACAACACTTATGTCTTGTGAACAGCGGTGTAAAGTAACATTACAAATACTCAAATTTCTGTAATTGAGAAGTTTTTCACCAGTTTTTAAGTGGTTTTAAAAATGTGTACTTTTGCTTTCCCTTCAGTACAGTTTTAGTGCAGTATCGGCACTTTTACTCCACTGTTTTTTATTAATCTGCAGCCACTTTTTTATTGTCGAAAAATCGAAAGATCACTCCTGCGATTCCAGTCCAATCAAATAATAATAATTTTCAACCGTAATGAACAATTTCGAGGCATGTTTGGAAGGTGTCCTATAGAGTTTAGTTTCTCTGTCTGAGCCCAAGCCCACATGGGCAGGGCCGTGATCGAGCATTTGTGGGTCATTACTTAGGCCGTACGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41573
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113162 | Nonsense | 620 | 2097 | 16 | 55 |
Genomic Location (Zv9):
Chromosome 10 (position 3247174)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 3239368 |
GRCz11 | 10 | 3239672 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATCGCTGTGGCTCTGAGAGACACTCCACGAGTGATGGAGCCCATCTTA[C/T]AGATCCTGCAGCAGAAGTTCTGCCAGCCGCCGTCTCAGCTCGACGTGCTC
Long Flanking Sequence:
GTTAAAAATATCCTGGATTTGAAAATATTGTGTTCCTAGCCTTCACCGATCTCAAGTAATAGATTAATGTATAAAAATTGTGAATAAACTTAACTGTTGATGTCTTAAATAATAATGTCATGTAATAATGTAAATGGATATATCTCGTTTTGCAACGAAACTCTTCATTCATTTTATGAAATATATCAGGATCTAATATTTTTTTGTTAATCTAGGTGTTTAAAAGCAGGATTGACCATGGATTCAGTCATCGTTGAAGCTTTCCTCGCCAGTCTTTCCAACCGTCTGTACATTTCGCAGGAAAATGACAAGTATGTTGCATTTGACAGATGATAGCTTGAATAATTTTACAGCCCTTAAAAGAGATTTGTAAGAATGAACATCATTTGTGCTGTTTTCCTCTCAGGGATGCCCATCTAATCCCGGACCACACCATACGGGCGTTAGGACACATCGCTGTGGCTCTGAGAGACACTCCACGAGTGATGGAGCCCATCTTA[C/T]AGATCCTGCAGCAGAAGTTCTGCCAGCCGCCGTCTCAGCTCGACGTGCTCATCATAGATCAGCTGGGCTGTATGGTCATCACTGGAAACGTATGCCAGCTCCTCTGTGTTCTGAAAATCAGGGTTGTATGTTTGGATCCGTGCTAACATCTCCGCGTTTCTGTCCCACAGCAATATATTTATCAGGAAGTGTGGAACCTGTTCCAGCAGATCAGCGTGAAGGCCAGCTCCATGGTTTACTCCACCAAAGACTACAAGGATCATGGATACAGGTGATTTATTTTTACATGTATTTATTATTTAGTGAAATGTTTTGACCTACAGGTTTTTGCGTCATGCTGATGGATAAATAATAGGGGTGTCACGATTTCGATTTTTAATCGAAATCGATCGAAATTTATGCTCAATTTCGATTATCGAATCAAAAAATAGAATCGTCGATGCTGCCACGCCCCCATGTCACGTCAGCTTGGCTTGCCAAGCAGGAAAAAACAGGCTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44718
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113162 | Nonsense | 759 | 2097 | 20 | 55 |
Genomic Location (Zv9):
Chromosome 10 (position 3240141)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 3232335 |
GRCz11 | 10 | 3232639 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGGGATATGTTGTTCATAATCTGTCTGTTTTTTACCCTATAGCTAACC[A/T]AACGTTTGCCGGCCATAAAAGAAGCCAAACCGAGGCTGCAGAAGCTGTTC
Long Flanking Sequence:
AATAAAACGAAACATTCATTAATTTTGTAAAAATGTTTATTGCTCATTGTGAGTTAATACATTAGCTAACGTTTCATTTCATTTACAAATAGCAGGGTATTTGCAGCTACTGTCTATTTCTGTCCATTTGTATCGCTCCCTTTGTGCCCCCTGGTGGCATTGTCGCAAACTGCTGTTAGTCCTAAACACATTTCTGTAATGGTCATCCTGAACTGTCACTCATTGTGTGTGTAAAAAGGCATCTGACCTATTTTATTTTTAACTAATATTTACTTTAATGAACATATAAATCGATATACAGTAAATGACGCTTAGAAAAGGGTATACATTTAGCTTTTACTCATTTAAAAAAATAAATTCTTTTTCGAGTCTGTTTTTGCTGCTAAAATGAACATTATTTTACCTCAGTTGCCGACAGTTTACACAATTAATGTTTTTGGTTGAGAGCCGATTGGGATATGTTGTTCATAATCTGTCTGTTTTTTACCCTATAGCTAACC[A/T]AACGTTTGCCGGCCATAAAAGAAGCCAAACCGAGGCTGCAGAAGCTGTTCAGAGATTTCTGGCTGTATTCGGTTGTGATGGGCTTCGCTGTTGAGGGCTCAGGTTAGACATCCATATTAATAAATGTTCACATGTACATCATTTAGTTTAAGATTTTGTAGCATTTTTGTCTGTTTATTTGTTGAATGTTGGACAAAACACAGTACTTTGCAAAAGTTTTAGGCCAACATTAAATCTTTTACTGACGATATAATGGATAAATGTGACTCTTTTTCACCCATAAAAGTCATAAGTGTATATTTTTAGTCAATTTATTTTAAATTGAGATATCTTCAGGGTGAATAAATGATCTTTCAGTTGATGTACGGTTTGTTAGGATAGGAGTTAGGTTAGAGTTTGAATTACTTTGGTTTATATGTTTAAGACATGTGAAAGACAGTGTTGGAGAGAGGCTGTTTGTCCTAGTTTGAGCTGCATTTCTAGCAGTGTTGTTGTTAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2547
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113162 | Nonsense | 1156 | 2097 | 31 | 55 |
Genomic Location (Zv9):
Chromosome 10 (position 3228369)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 3220563 |
GRCz11 | 10 | 3220867 |
KASP Assay ID:
554-2640.1 (used for ordering genotyping assays)
KASP Sequence:
TCTCYGAGGCCACGCGGAGCACATCAGACCTGAATAAACTGATGATCCGA[C/T]AGATGAATGAAGCTCTGGATGGAGGACAGCCCGAAGCCTTCACCGAAGCC
Long Flanking Sequence:
CGCCATTTTAAAAACTTAAACCACTAGTGTAAACGGGGCCTAAATAGACACTATTTAATCAACATTTTCCCTGTACCCATAATGCCCATTGGTTAATCCGGCCCTGACTGTGGAACTTTGTAGTGTAAATTCATCGCAGTTTGGTTTGGAACAAGTGAATATTCAAAAAATTGAGAATCGATCGGTGCATTTCTACTGAATTGATTTATTGACTAGTCCTTCAGGTTGCAAACAGTCATTAAAAGTTTGTTCCCCATCATTTCAGACCACTCAGCTGACCGAGAGACCCGCATGCGTGAAGAAAGACTACTCCAACTTCATGGCCTCCCTCAACCTGAGAAACCGCTACGCTGGAGAGGTGCTGCTAAATAATGAAGCAGGGCTTTTTGTGTTTGTTTCACCGAGTCTTACCCCCTGTGTCTCGTATGCAGGTCGCAGGGATGATCCATTTCTCCGAGGCCACGCGGAGCACATCAGACCTGAATAAACTGATGATCCGA[C/T]AGATGAATGAAGCTCTGGATGGAGGACAGCCCGAAGCCTTCACCGAAGCCCTGTTCAAGATGGCAGCGCTGTTGATCAGCTCCAGAGGCACGTTTTATTGTGTTTTATAAGCTGTACACTAGCAGATGGTCAAATGTTTTAAAGGGACAGTTCAATCCAAAACTGAATTCAACTTTTAAACTTTATCTTCTGTCCAACACACATAAAGATATTTACACTCACCGGCCACTTTTTTAGGTACACCTGTCTAACTGCTCGTTCACGCAAATTTCTAATCAGCCAATCACACGGCAGCAACTCAATGCATTTAGCCATGTAGACATTGTCAAGACGATCTGCTGCAGTTCAAACTGAGCATCAGAATGGGGAAGAAAGGGGATTTAAGTGACTTTGAACGTGGCATTTTTACTCACAACCATTTCTAGGGTTTACAGAGAATGGTCCGAAATAGAGATAATATCCAGTGAGGAGCAGTTCTGTGGGCGCAAATGCCTTGTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2563
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113162 | Essential Splice Site | 1367 | 2097 | 36 | 55 |
Genomic Location (Zv9):
Chromosome 10 (position 3217790)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 3209984 |
GRCz11 | 10 | 3210288 |
KASP Assay ID:
554-3190.1 (used for ordering genotyping assays)
KASP Sequence:
GTAATTTTKGCATAATAGCTTTAATTCTAATATATTTTGTTGTTCTCTTT[A/G]GTGTGGCATCAAAGTTCCCCACTYAGGGAGACAAGCGTCTGCGGGAGGAC
Long Flanking Sequence:
TCGGCTGATTATGTCCATTCTTTCAAGATGTACAATAACCTCCCTAGTGTGTGTATATGAAGTTTCAACTCAAAATATCCCACAAAGAATGTTTTATAACTCTTTGAAACTGCCCCTTTTATGCTTTGATCCTAATGGTGCCGTTTTGGTGACTGTCACTTTAAATTCAAATTAGATTGTGCTCTTTTCAAAAGTGGGCGGAGCTACAAATGTCCGTGTCAGTATAATGGAAGATTCAAAATCAAAACTAACCTCCCATGCTAATTAGGGAGAGATGGTCACAAGTGGGCGGGGCTTTCCCTCTCTGATGACACATACAAAGGGAAAATGTCAATCAAAGTGTTTTTATCAAATGTGATTATAAAAATAGAATTAATTTGTTTTTACTATTAGAGGTTGGTTATATTTACAGACTGCTGACCCACACCTGTGATTAAACTCCTTCTAAAAGTAATTTTTGCATAATAGCTTTAATTCTAATATATTTTGTTGTTCTCTTT[A/G]GTGTGGCATCAAAGTTCCCCACTCAGGGAGACAAGCGTCTGCGGGAGGACATCAGCATCATGATCCGCTTCTACGCCAGCATCCTCTCCGACAAGAAGTACCTAGGTGCTAGCCTGCTCGTGCCACCTGGTGAGCTCGGTGCCAATCCCCCTCAAAGCTCCCTATCTGCCGGGATTTTCGGATCGCTTATCGTTTCCAGCACTTCTCCGATATCGATCTTAAGTAAGCCTCTACTTGCTCCGACTGTGCGACTACAGTGCGGCAGGAGCATGTTAATGCGGTTTCAAATTAGCATGACCGCCAATTTGAAACCCATACTACAAAACTGCACGGCAATCATCCGGACGGCCGAATTGATCAATTTGACGCCAAGCGCAAATTGAGAAATGCAACCGTCCCATCTTACCCCACCCCCCTCCCGACCCGTACCGCCACCACCCTTTATTGTAGAAGAACATGATCTCATCGCTTCTCATGTAAAATGCATGATCATTTCAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34812
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113162 | Nonsense | 1819 | 2097 | 48 | 55 |
Genomic Location (Zv9):
Chromosome 10 (position 3203481)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 3195675 |
GRCz11 | 10 | 3195979 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTATGTGTTCTCCTAAGTGGTCTCTCTGTGTGTGTGCAGGTCTGCGCTG[T/A]CCGTCCGACTCTCAGGATGAAGGAGATGAGAGCTCACTGACGGCTCAAAG
Long Flanking Sequence:
CACGTAGATACAGTAGGCGGGAAAGACTTGAATTAAAGGCGCAGTACGACAAAACCACCCCCTGCTGGAAATGAGTATAAAATATGATCTTGTAAAAGGTATAATGAAAAATCTGGTGGGTGTTTTGAGCTGAAACTTTATATACACATTCTAGAGACGCAAAAGACTTATATTAAATCTGAAAAAAGGGGTAACCTAGGTGCCCTTTAAGCAATATATGTTTTCAGATGTCTACAGAACAAACCATCGTTATAGAATGACTTGCCTATCTACCCTATTGAGTTATTAAAACTATTATGTTTAGAAATGTGTTGAAAAAAATCCTCTCTCCTTTAAACAGAAATTGGGAGAACAATTATACAGGAGGGAGAATAATTCTGATTTGAACAGTATCTAGTATATCAATGACATCCAGGGAATGTGAGAATTGAGGGACTGATGTATTTCAGTTGTATGTGTTCTCCTAAGTGGTCTCTCTGTGTGTGTGCAGGTCTGCGCTG[T/A]CCGTCCGACTCTCAGGATGAAGGAGATGAGAGCTCACTGACGGCTCAAAGGGTCTGCTGGCAGGCGGCCATCTTTAAAGTGGGCGATGATTGCAGACAGGTCAGTCTCATAGGAAACATCCGGTTACCTTTATTCCAAATTCATTCAGTAAATAAAAACTATTATTTAATGTAAATAGGAAAACCATATGAAATCCTCACAATTTTTGTTTTTTATTCCAAGAACCAATTACTGTTTTCTTTTCACAACACATTTTTTGCTATGAAATAGAATAAAATGTCATAATTCTAATGCCAAAAATTATAATAAATATAATGTGCAAAGTGTGCATCGGATGCAAGTTGACATTTACACTCACCGGCCACTTTATTAGGTACACCCATCCAACTGCTTGTTAACACAAATGTCTAATCAGCCAATCACATGGCAGCAACTCAATGCATTTAGGCATGCAGACATGATCAAGATGATCTGCTGCAGTTCAAACTGAGCATCAGAAT
Associated Phenotype:
Not determined