ZMP
pi4kab
Ensembl ID:
ZFIN ID:
Description:
phosphatidylinositol 4-kinase, catalytic, alpha b [Source:RefSeq peptide;Acc:NP_001106813]
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 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27124 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11490 | Essential Splice Site | Available for shipment | Available now |
sa12448 | Nonsense | Available for shipment | Available now |
sa41098 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa27124
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 |
---|---|---|---|---|---|
ENSDART00000091235 | Nonsense | 319 | 1099 | 10 | 30 |
ENSDART00000114476 | Nonsense | 353 | 1986 | 10 | 52 |
ENSDART00000140077 | Nonsense | 353 | 907 | 10 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 1988286)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 1800668 |
GRCz11 | 8 | 1805874 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGAATGCAGGCGTGGATCTGTTCTACAAAGGCTTCAGCGACCCGCTGTA[C/A]GTCAGCATGTTCAAGATGCTCAGAGACACGCTTTATTACATGAAAGGTGA
Long Flanking Sequence:
CTGGAAGGGCATCCGCTGCGTAAAAACTTGCTGGATAAGCTGGCGGTTCATTCCGCTGTGGCAACCCCAGATTGATAAAGGGACTAAGCCGACAAGAAAATGAATAAATGTGTTGGAAAAATCTTTGTTAAAGTGTAATTGGGGGAAAAATACAGGGCTCTAGTAATGCAGGAGGGTTAATAATTCTGACTGTATTTATTAATCTATATTATATAAAACACGACAGAAATAACATGTGGTTTGTCTTGTTGGTGCAGGTGAAGCAGTTTGTGTCAGATTCATTCCTCAAGTCTCTGGATGCTGTAGTGACTGAGGTTACTGAGGTAAACTCACATCTTTCTTCATACCTGCAGGATCTGCATGCATGCATTGCTATTTATTTGTCACAAAGCAGACAGTGAAGCCTGCTGGCGTTTTCTGCTCTTGCTTATTCTTTTATTTACATTTAAGGCGAATGCAGGCGTGGATCTGTTCTACAAAGGCTTCAGCGACCCGCTGTA[C/A]GTCAGCATGTTCAAGATGCTCAGAGACACGCTTTATTACATGAAAGGTGACTAAACTCTGCTGTTTGCACTCATTTGTTAAATACTCATAAGATGATATTATTAGCCCCCCCTGTGTATTATTCCCCAATTTCTTTATAATGGAGAGAAGATTTTTCTTTGTTTATTGTCTCCTCTCAGACGTGCATGCGGGTTTCGTGAAGGAGGTGCATGACTTTGTGCTGGAGCAGTTCAGCAGCAGTCAGTCGGAGCTCCAGCGGGTCCTGCATGAGGAGCGTCTGCCAGGTGAAGCCAGTCCTCTGAAGCTCCGCTGCCATGCAAATGCAGCCTGTGTGGACCTGATGGTGTGGGCCGTCAAAGATGAGCAAGGTCTGTCTGTTACTGACACTCAGCCATTTGCAATCATCAATTGTTTCTAAGGGCTGGGACACAACAAGATGGTCGGCCGTTGGGCTTTGTTGGTGAACATGGGTCCGGCTAGTGTGTTTGGTGTGTTCCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11490
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 |
---|---|---|---|---|---|
ENSDART00000091235 | Essential Splice Site | 939 | 1099 | 25 | 30 |
ENSDART00000114476 | Essential Splice Site | 973 | 1986 | 25 | 52 |
ENSDART00000140077 | None | None | 907 | None | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 1934262)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 1746426 |
GRCz11 | 8 | 1751951 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGGATCCGCAGGGTGGCAGATAAATACCTGTCAGGACTCGCAGAAACG[T/G]AATGCTCTTCTCTGCTTGGTGCACACTAGAGAGATCCCTAAGTAGACAAC
Long Flanking Sequence:
AGGGGTGTGTCAAATAACCTGTATAAAGATTGTGGAAAACACAGAAACTTTAGAAAGAGTAAGAGAAAGAGGAGGAGAATGCTATGAGGTCTGCTCTGCTCTTTCTCGGCTTTATTATAGAGAATAAAGTCTATTTTCTGATATTCAAAACCTCTGGTCTGATCATTTCTAATTGATAAGAAGTCGATTTACAACACTGTGATGGTTAAGTTTAGGGTTGGGGTAGAAGTGGATGTTAATAAAATAAACTTGGTGGGTAATTTAAAAATAATTTCTCGTTAACTTCCGTCCACAGCTGTATCCCTTCTAGCAACAACCCAGAACATTATTGATGGCTCATCATTATTGATGCGTTCTGTTGCTTTCTGTTTCAGCCCAAGACTAAAGAGCATGAGGAGGAGCTTGAACGCCACGCTCAGTTCCTATTGGTCAACTTTAACCACACCCACAAGAGGATCCGCAGGGTGGCAGATAAATACCTGTCAGGACTCGCAGAAACG[T/G]AATGCTCTTCTCTGCTTGGTGCACACTAGAGAGATCCCTAAGTAGACAACACTTTAATCATCATGTGGACTGAGCAGATTCATCCAGTATTTGTGTGTTTCTTTAAAGTATTGGTGCTTTTCTATGGGTATTGGAGTGTAAATAAAAGCTGTGCGACACTGGCGCAGTAGGTAGTGCTGTCACCTCACAGCAAGAAGGTCGCTGGTTCGGGCCTTAGCTGGGTCAGTTGGCGTTTCTGTGTGGAGTTTGAATGTTCTCCCCTTGTTGGTGTGGGTTTCCTCCGGGTGCTCCAGTTTCCTTCACAAGTCCAAACACATGCGCTATAGGGGAATTGAGTGAGCTAAATTGTCTGTAGTGCATGTGTGTGAATGAGTGTGTATGGGTGTTTCCCAGTACTGGGTTGCATCTGGAAGGGCATCCGCTGCGTAAAACATATGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCTGATTAATAAAAGGACTAAGCTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12448
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091235 | Nonsense | 945 | 1099 | 26 | 30 |
ENSDART00000114476 | Nonsense | 979 | 1986 | 26 | 52 |
ENSDART00000140077 | None | None | 907 | None | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 1932919)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 1745083 |
GRCz11 | 8 | 1750608 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAATAAATAAAAGCTGTGTGTTTGTGCTGTAGGTTTCCTCATCTGTTGT[G/A]GAGCGGAAGAGTTTTGAAGACGATGCTGGATATCCTGCAGACTCTTTCTC
Long Flanking Sequence:
AAGTTAGTCAGATCACGTTTATATGTTCTTCTTAATGCCAACTGTGTAAATAATCATCGATGAGATGCTTATGATAAGCCGTTGTTTGTTTACCTTCAAGCTTTGCGTGTGCCTGTGAAACAGCCTGTGAGCGCCTGCACACGCACATATTATGAACATCTCGACATGTGAAAGTGATCCTGCGAAAGTTGTTCACAATATTGATCATCCACAGAGTTTGTAATTTAGTCAAATGTTTACAAACACAAGCGCAGCCGTTTAAAGCTCATTTGTGGTGAATGATGTCAGAATTTACCGGTATTTTGGAATGGATGTGTGAATGCTCTTTTCCGGAAAATTTCCGTAACGTCCTCGCCTGTGTGAACAGCGCTTTTTTGAATATACCGGTAAAGTCGTTCCGGAAATTTTCCGGATATTTACCGGTATCACTGTGTGAAAGGGGCTAATGACTGAATAAATAAAAGCTGTGTGTTTGTGCTGTAGGTTTCCTCATCTGTTGT[G/A]GAGCGGAAGAGTTTTGAAGACGATGCTGGATATCCTGCAGACTCTTTCTCTTTCTCTGAGTGCTGTCAGTACAACAAAACACATAACACGCACAACACATAACAACACAACTAAACACACAACACAAAGCACAGCACAACGTACAAAACAACACACACTCCCACACAAGCAAAATGACAGTGTATTATCTGTCTGCGAACAAAACACACAACACAACAAACACAAGGTACAACAAAAGTCACATGACTGAACACACAACAACACACAATACAAAACAAACAACACAACACAACTAAACACACAACACAACATACAAAACAACACACACACACCCACACAACCAATAATACAGTGTATTATCTGTCTGTGAACAAAACACACGGCACACAACACAACAAAACACAAGGTACAACAACACAAGTCACACGACTGAACACACAACACAAAACAACACACCACAACTAAACATACAAAACAACACACACTCCCACACAACCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41098
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 |
---|---|---|---|---|---|
ENSDART00000091235 | None | None | 1099 | None | 30 |
ENSDART00000114476 | Nonsense | 1168 | 1986 | 31 | 52 |
ENSDART00000140077 | None | None | 907 | None | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 1915517)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 1727681 |
GRCz11 | 8 | 1733206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTCAGATGAGTGACGCTCTGGAGGCCAAAGACCCGGACGCTTTCACA[C/T]AGAACATGTTCAAGATGACGGCGCTGCTCATCAGCACTAAAGGTACAGGA
Long Flanking Sequence:
GTTATGCATTATTTATTCACTCAGTAGAGCATTTGTTTATCCACTAATTTGTTGCACTGCATACTTAGTTCTGCATTTTTAGACATCCATGCACTCATAGTTCTGCACTTGTGCATTATTTATTCACTCATTTGTTTGTCTTGTTATTTGTGCATTTATTCATGCACTTAAACTGTATATTTATCCATCGCATGCTTATTTTTGCATTGTAGACATTCATGCACATATTTGTGGACTTGAATATGCATACTAATGTGTACGTTTATTTTTTGCATGCATTCTTGCTATTATTTAGAGATTTGCATTTAATCAACAGTTAATAGACACTGTTATGGAAAGTGTGTGTTTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTTCAGGTTGCAGGGATGCTGCAGTTTGCTGAAGCGACACACAGCGAGTCAAACCTCAGTAAACTGATGGTTTCTCAGATGAGTGACGCTCTGGAGGCCAAAGACCCGGACGCTTTCACA[C/T]AGAACATGTTCAAGATGACGGCGCTGCTCATCAGCACTAAAGGTACAGGATATACTGTATATGAGCACACAGAACATGACGATGAAACTACACAGAGAAAGAAATAACAGTGAAAGAGATGCAGTATGAACTGTGGCTCATTCGTGTTTCCAGATATTACCAGAAAAGCAGCAAACAGACAAAGACAAAAGCATTATATTGCATTATATTGCCCCTGTTTAATTTCTGTTTAATGGAGGCAAGATTGTTTCAGCACATTTCTAAGCATAATAGTTTTAAAAACTTATTTCTAATAACTGATTTATTTTATCTTTGTCATGATGACAGTAAATAATATTTTACTTGATATTTTTCAAGACATTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGTTAACTAGGCAGGTTAGGGTAATTAGGCAAGTTATTGTATAATGATGGTTTGTTCCATAGTTCTTTTGACTATCGAAAAAAGAATTAGCT
Associated Phenotype:
Not determined