ZMP
zgc:92316
Ensembl ID:
ZFIN ID:
Description:
phosphatidylinositol-4-phosphate 5-kinase type-1 beta [Source:RefSeq peptide;Acc:NP_001004579]
Human Orthologue:
PIP5K1B
Human Description:
phosphatidylinositol-4-phosphate 5-kinase, type I, beta [Source:HGNC Symbol;Acc:8995]
Mouse Orthologue:
Pip5k1b
Mouse Description:
phosphatidylinositol-4-phosphate 5-kinase, type 1 beta Gene [Source:MGI Symbol;Acc:MGI:107930]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7122 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41132 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13090 | Nonsense | Available for shipment | Available now |
sa21206 | Nonsense | Available for shipment | Available now |
sa34316 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa7122
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 |
---|---|---|---|---|---|
ENSDART00000008215 | Essential Splice Site | None | 527 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 11417647)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 11251477 |
GRCz11 | 8 | 11289182 |
KASP Assay ID:
554-4906.1 (used for ordering genotyping assays)
KASP Sequence:
GCAGCAGCGCTGAACCAAACACCAACACCTGTGCTCTTGGTTAAATCAAG[G/A]TAAACCATAATTGCATMATWTATTATTAACAGAACCRCACATTTGCTGCA
Long Flanking Sequence:
AATAATTACTAATATTATTAATTCATATACAATTTCTGTTTTGCCTTTTAATATATTTTAAAAACTTTTAGTTTATTTCTGCACATCAATATTAACCAATAAATGTAATAAAAGCCACATAAAATATCAGATCAATTTCAAAATCTTATTTATTGCTCCTCATCAGTATTAGCCAACTAATAAAATGCATATAAAAAGTATTAATCTATATAAAAATAAAACATTTTATAACATAAAATGTGAGACCTTATAAATAAAATCCAATCCTTTTCTTCAGATTGTGAGTTGAATTATGACCTCGACATGTTCTTGACCTCATGCTCACGTCGTTGTCGGTCATTAAAACCCAACCGCTGCCTCATTAACTCTGCTTTAACCTTCTGGTTTTACAGGAGGAACATCATCATTGTGAGCTCCACTTGTGCTTTCTGGTCCACATGACTGCGCAATGCAGCAGCGCTGAACCAAACACCAACACCTGTGCTCTTGGTTAAATCAAG[G/A]TAAACCATAATTGCATCATTTATTATTAACAGAACCACACATTTGCTGCATTTACAAGGCACTCGAGTTCTCCATCAGGACGTCCTGCTGTGCGTGTCGGGCTCTTTTGCAAATCAGATGGTTTCTGGTTTGTGGATGGAGCCTGAGGAGATTATTTACATGCCCTGCTGATGGTTTTGTGTGACGTTTAACTCTTTGTTGTCTCGTGCAGATGTCATCAGCCAATGCCAATGGAGTCGGGAGCTCTGGAAATAACCGTAGAGAAAAAACATACAAAAAGGTGCATCAACTGTTTTTCAGTCTTGTGTTTGTTGCTGAAATATGGAGAATGCTATGTTTTTTTGTGTGTTTGTGCATACATACAGTTGAAGGCAAAATGATTAGCCGTCCTGTAAAATTTATTCATTTCCCTTCAGCTTAGTCCCTTATTTATCAGTGATCGCCACAGCGGAATGAACCGCCACCTATTTCAGAATGTTTTAAGCAGTGGATGCCCTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41132
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008215 | Essential Splice Site | 106 | 527 | 5 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 11428258)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 11240866 |
GRCz11 | 8 | 11278571 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCCGCTACTTCCGGGAGCTGTTCGGGATCAAGCCGGATGATTATTTGG[T/G]AAACTTTTTTAAATTTGTTGTTGTTATTAGTATATTTATTCTTTGTTTTT
Long Flanking Sequence:
GTCAATATTAGTAGCCCCCTTAAGCAATATTTTTTATTATTTGTCTACTGAACAAACCATCATTATACAATGACTTTCCTATTTACCCTAACCTAGTTAAGCCTTTAAATGTCACTTTAAATGTCACTTTAAGCTAATACTAGTATCTTGAAAAATATATTTAATACTAGTATCTAGAAAAATATCTAGTAAGATATTATTTAATGTCATCTTCAGCAACGATAAAATAAATCAGTTATTAGAAATGAGTTGTTATAACTATTATGTTTAGAAATGTGTTGGAATAAAAATCTTCTTTCTGTTAAAAATAAAGAGAGAGGCTAATAATTCTGACTTTAACTGTATGCTTCATTTTTTAAGCAAGTACTTTTACTTTTTCAGTGAAGGAAGCAACCTGACACCAGCACACCATTATCCAGACTTCCGGTTCAAGACTTATGCGCCACTGGCTTTCCGCTACTTCCGGGAGCTGTTCGGGATCAAGCCGGATGATTATTTGG[T/G]AAACTTTTTTAAATTTGTTGTTGTTATTAGTATATTTATTCTTTGTTTTTGGTGTGAAATGCGCTTTATAAATACACTTAATTTTTAAAATGTTACAAAGGTTTTTTAAAGTCTGTGTGAAATCCATATTTACTATGTGTTTTTCACATAACACACATTGTTAAGCCGCCTTTCCACTGCACACGACAAATGACAAGTGACAGACCGTCTAGTTTGCTACAAAATAATGATGTGCAAAAAGAAAGCCCCGCCCACTACTCAGTTTTTGGTTTTAGTTGGAAGTACATCAACACACCGAAATAAGTCTCAGCAGCTTTTGCTTTACATTTACTTTTAAAAAAAGCAATACAGTTTCTATACTTTTATTCAAGTCAAGTTTTTTTATGTCTTCTATATTGTCCCAACTTTTCCTGATTTGGGGTTGTATTACAATTTAAAACAATACTTTTACTCATCAAGCGTGCATTATATTGATGATAAGTGACAGTAAATACACTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13090
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008215 | Nonsense | 225 | 527 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 11439383)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 11229741 |
GRCz11 | 8 | 11267446 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACAAGAGACGKGCGTCAYGAAAAGAGCGGGAAAAGCCCTGTCCCACATA[T/G]AAGGACCTAGACTTWGTGGACATGCATGATGGYTTGYACTTTGACCCAGA
Long Flanking Sequence:
TTAGCTTTTTGTGTTTGTTTGCTCTAAAAACTATAAATCAAAGTTGACAGGGCTCAGATGTTTTGTTTGCTGGAGTAAATGAGGCACAATCTGTAAAGGAACTGCCCCCTTTAGAAAGGTGGGGCGGGGAGTAGCAGCTCATTTGCATTTATAGAGATATATGCGAAACTGCCTAAAATAGGGTATATAAAGTGTGATATATTAAGTGATATGTGAGGTATTTTGACCTGGAACTTTAAACACATTAAAAAAAATAATGCATAATAGGCTTTAAATAAATCTATTTCTCCTTCTCAGAACCTCAACCAGAACCCCAGGACGCTCCTACCCAAGTTTTACGGCCTGTACTGTGTTCAGTCTGGAGGAATCAACATCCGTCTCGTGGTTATGAACAACGTCCTGCCGCGATCAGTGAAGATGCACTACAAATATGACCTCAAGGGCTCCACATACAAGAGACGGGCGTCACGAAAAGAGCGGGAAAAGCCCTGTCCCACATA[T/G]AAGGACCTAGACTTTGTGGACATGCATGATGGCTTGTACTTTGACCCAGAGACATATAATGCCCTGATGAAGACACTACAACGGGACTGTCGGGTGAGTTATACAGTATTTTGTCCTTTTACAAAGAAGCTGTGAGTGGTGAGCAAAGTTGCGCACAATTCTAGTTTGTTTTTAATGGTACTCTATGTAAAGCAACTTGAAAACTAAGTGGCTTAGGGAATCACGAGGTGGACACTTGGGGTTTAGAGATTTATTTGCTTAATTTAATCATACAATAGGGTATTATGACCGTGACAGAGGGCTCTGTCACGATCACGACAGTAGGTGATTTCATTTACACACAGTGTAATATCCATCAGTGATTCTGCCGTTCCCAACCCTTTGGTGCACATAAAGGTTGGGACAATGTTACCATTGCATATATAACGCACACACATACATTCACTCATCACCACAATTCCCAAAAAACACACACACAGACACCAAATACATTTATTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21206
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 |
---|---|---|---|---|---|
ENSDART00000008215 | Nonsense | 266 | 527 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 11456011)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 11213113 |
GRCz11 | 8 | 11250818 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGTTAAAATGTGCTGTAGGTGCTGGAGAGTTTTAAGATCATGGACTA[C/A]AGTCTCCTGCTGGGGGTTCATGTTCTGGATCAGAGTCACAGAGATGGAGA
Long Flanking Sequence:
TAATATAATATAATATAATATGAGTATAATTTAATTAAAAATAATATAATATAATTTAAAATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATTCCCAGAGATGGGTTGTGGCTGGAAGGGCATCCGCTGCATAAAAACTGGCTGGATAAGTTGGTGGTTCATTCCGCTGTGCCGACCCCAGATTAATAAATGGACTAAGCCCACAAGAAAATGAATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATTAATATAATATAATATAATATAATATAATATAATATAATATAATATTTAAATTTCTAATATTGTTTTGCATGTTACCATGGCACCATTTTTTATCTCGGTGTGTTAAAATGTGCTGTAGGTGCTGGAGAGTTTTAAGATCATGGACTA[C/A]AGTCTCCTGCTGGGGGTTCATGTTCTGGATCAGAGTCACAGAGATGGAGACGGCAGTGCTGTGGACGGGAAGAGAACTGTGGGACAGAAGGTGCTTTACTCCACCGCCATGGAGTCCATTCAGGGAGACGGAAAAGCAGCAGAGGCTTTGACCACAGACGACACGTAAGTTCAGGCTCTTTATGTCTGCATATATATATATATATATATATATATATATATATATATATATATATATCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTCATTTAAATTGAAATGTTGGTTTAAAGAATTGTAAACTTTGTTGACTTTTGTGAAATAATACTTAGAAAATAAATCATTACATACACTATAAACCAGGGGTGCCCAAACTTTTTCTTATAAAGGGCCAAAAACCAAACTTGATTGAGGCTAGTGGACCGAAGATAAATATAGTTGACATGAGTAATTTCCTTATTTGTTTAATAATGTTTATAAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34316
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008215 | Essential Splice Site | 394 | 527 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 11457849)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 11211275 |
GRCz11 | 8 | 11248980 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAGATTTCTCAAGTTCATGAGCAGCCGAGTGTTCAGAAAGAATCAGCG[T/G]AAGTCTACAATATGAAGATGCATTTTTGATGCAGATGCAACATTACATGC
Long Flanking Sequence:
GTAGTGAAATCTTAATGTACTTGTCCTGATCTTTTTTTTTTTTTTACACAGAATGGGAGGCATTCCTGCAAAAACACACAGGGATGAGAAAGTACTTATTTTCCTAGGCATTATCGACATCTTGCAGTCTTATAGGTAAGTCTGTTCTTGGTTTACAGCAAACCCAAGAGATCCAAATGTCAAATTACACACCATCAAATGACTGATTCCAGCTTCTTTGAACAAACTCCATTATCCCTCATCTCGCTCCTGTTTTTGCACCCAGATTCATCAAGAAGCTGGAGCACTCCTGGAAGGCGCTGGTCTATGATGGCGTAAGTCTATATGTCTTCTCTTATGAATAGACTATTCATAGCGCATGAGGGAATTAAAGACTCTTCCTGGTTTGATTGTGTTGTATTCTGTTTCTCCTAGGATACTGTGTCTGTGCACAGGCCGAGTTTCTATGCAAACAGATTTCTCAAGTTCATGAGCAGCCGAGTGTTCAGAAAGAATCAGCG[T/G]AAGTCTACAATATGAAGATGCATTTTTGATGCAGATGCAACATTACATGCGGTGCAAGTTGCAAAGGCAAAATGTGTGTTTTTGTTCTGAAAACTGGGTAACAATTTGCATTCGGTAATCCTTGTGTATTGTTCAAATTGACTACCCTTTCATTAGGTTCGTGGCTGTTTTTGCATTGGCTTCCATTATAATGACATTTTTTGATTGCAAAGCTTTGATACCAAATAATCATGCACTCCTTATTGTTGATGGTTTTACCAGTAAAGTTTGTAGGGCTCTATTTTAATGATCTAAGCGCAAAGTCTAAAGCGCATGACACAAAAGCATTAAGAGCATGTCCGTATCCTCTTTTGCTATTTTAAGCATGGACAAATATGGTCTGCACCCTGGCATATGGTCTAACAGGGTTGTGCTTATTCTATGAGTTATGGGTGTGTTTTGAGCATAACTTGCATTAAACCAGTCATAGTTTCATCTCCCATTCCCTTTAACGCCCGATT
Associated Phenotype:
Not determined