ZMP
pdpk1b
Ensembl ID:
ZFIN ID:
Description:
3-phosphoinositide dependent protein kinase-1b [Source:RefSeq peptide;Acc:NP_991262]
Human Orthologues:
AC141586.1, PDPK1
Human Descriptions:
3-phosphoinositide dependent protein kinase-1 [Source:HGNC Symbol;Acc:8816]
Putative 3-phosphoinositide-dependent protein kinase 2 [Source:UniProtKB/Swiss-Prot;Acc:Q6A1A2]
Putative 3-phosphoinositide-dependent protein kinase 2 [Source:UniProtKB/Swiss-Prot;Acc:Q6A1A2]
Mouse Orthologue:
Pdpk1
Mouse Description:
3-phosphoinositide dependent protein kinase 1 Gene [Source:MGI Symbol;Acc:MGI:1338068]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17656 | Essential Splice Site | Available for shipment | Available now |
sa24545 | Nonsense | Available for shipment | Available now |
sa39462 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17656
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003789 | Essential Splice Site | 87 | 537 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 38834987)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 37434205 |
GRCz11 | 24 | 37321925 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTACAGGTTGTCTTGGCAAAGGAACACACGACGGGGAAGGAATATGCAA[G/A]TAAGTTGTCYTGTCATTTAGGGCTGTGCATTATGATGATGATGATNNNAT
Long Flanking Sequence:
CACACATACATACATATTCTGCTTAAAATATTTTTTATAAAAATGTTATCTTATGTAATGCAATAATTGCTATGTTTCTCCCATTTAGGATTTAGTAGTTATTAGTATGAGTTATATTTAATAGTTCCTACTATACTTGTGTTTTTCTCTCATCAGTATGATGTTGCATCCCTCCACTCCTCTGTTCTCATCTCCTGTCCATCCATGGTAAGAGGCCAGCAGGACACGCCTCGTCTCCACGGCAACAGCATGGAGGGACCGGCACCAAACGCCCAGCCCGCCCAGCCTCGCAAGAAGAGACCCGAGGACTTCCGATTCGGCAAAATCCTGGGAGAAGGCTCTTTCTCTACTGTACGACACACACACTCCGACTGCGCCACACACGCACACACCTGACAGAGCCCAGAGAGTGTGACTCTGTTAATGGACTAACCTTTGCTGTCTTTTATATTTACAGGTTGTCTTGGCAAAGGAACACACGACGGGGAAGGAATATGCAA[G/A]TAAGTTGTCCTGTCATTTAGGGCTGTGCATTATGATGATGATGATGATATACTCTCACCGGCCACTTTATTAGGTACACCTGTCTGTTGACTGGTTGTTAACGCAAATTTCTAATCAGCCAATCAAATGTCAGCAATTCAATGCATTTAGGCATGTAGACATGGTCAAGACGATCTGCTGCAGTTCAAACCGAGCATCAGAATGGGGAACAGAGGGGATTTAAGTGACTTTGAACGTGGCATGGTTGTTGCTGATCTACTGGGATTTTCATGCACAACCATCTCTAGGGTTTCCAGAGAATGGTCTGAAATAGAGAAAATATCCAGTGAGCGGCAGTTCTGTGGGCGCAAATGCCTTGTTGATACCAGGGGCCAGAGGAGAATGGCCAGACTGGTTCCAGCTGATAGAAAGGCAACAGTAACTCAAATAAGCACTCGTTACAACCGAGGTCTGCAGAAAAGCATCTCTGAACACACAACACGTCCAACCTTGAGGCGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24545
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003789 | Nonsense | 109 | 537 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 38832918)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 37432136 |
GRCz11 | 24 | 37319856 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGCGCCACATAATGAAGGAGAATAAAGCGCAGTATGTCAAGAGAGAA[C/T]GAGACATAATGTCACACCTGGATCATCCGTTCTTCGTCAAACTCTACTTC
Long Flanking Sequence:
ATTTCCGAATATATACTTTAAAATAAATTTTTTAAAAAGTCACTTAAATGTGGTGATTATAAATAAACTATTAATTGATTGAATGCAGAAATGGCACTATATTGTGATGTGTGTGTGTGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATACATACATACATACATACATACATAAATACATATATATATATATATAAATACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATACATATATATATATATATCAGGATCTTAAATGACTTATCATGATTTAATACTTGGGCACATCGTGCAGCTCTTTAATAGCCTTTGCACTGACATTTGAGCATGTACTGGAAAGTGTTTGTGTTTCCTCAGTTAAGATCCTGGAGAAGCGCCACATAATGAAGGAGAATAAAGCGCAGTATGTCAAGAGAGAA[C/T]GAGACATAATGTCACACCTGGATCATCCGTTCTTCGTCAAACTCTACTTCACCTTTCAGGACGAGGAGAAGCTGTGTATCCTTCACACAAACTCTGATGCTCAACTAGTATGGGTTGCACAGCGTCAATATTAAGGAGCACAATAAAGATGGCTGTTGTGTTTCTTTCAAATGAGCTAATATGACATGGACATGCTTATTTTTGTGGCATTTTTTACACTAAAAATACATGTTTTTAATTATTTTGAGCACATTTTAGGTAGCTTGACGTTTATCATTAGGTTTGTATGGTATGCCGTTTATTGAACTATCCCTTTAAGATGTTACTCAAGATATATCTATTAATGGCATATTAGGCTTCTCCTAATTTCTTTCAGCACTATACATGTATACATGTCAGCATATGTTAATGAAGGATTTGTCAAAGCCTTGCTTATGTCAACGCTGCATTTTATAGCTTGTTTTCCTGAATGTCGTGTCAGATTTTGGATTAAGCTACGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39462
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 |
---|---|---|---|---|---|
ENSDART00000003789 | Essential Splice Site | 134 | 537 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 38832841)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 37432059 |
GRCz11 | 24 | 37319779 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTTCTTCGTCAAACTCTACTTCACCTTTCAGGACGAGGAGAAGCTGTG[T/A]ATCCTTCACACAAACTCTGATGCTCAACTAGTATGGGTTGCACAGCGTCA
Long Flanking Sequence:
ATTGAATGCAGAAATGGCACTATATTGTGATGTGTGTGTGTGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATACATACATACATACATACATACATAAATACATATATATATATATATAAATACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATACATATATATATATATATCAGGATCTTAAATGACTTATCATGATTTAATACTTGGGCACATCGTGCAGCTCTTTAATAGCCTTTGCACTGACATTTGAGCATGTACTGGAAAGTGTTTGTGTTTCCTCAGTTAAGATCCTGGAGAAGCGCCACATAATGAAGGAGAATAAAGCGCAGTATGTCAAGAGAGAACGAGACATAATGTCACACCTGGATCATCCGTTCTTCGTCAAACTCTACTTCACCTTTCAGGACGAGGAGAAGCTGTG[T/A]ATCCTTCACACAAACTCTGATGCTCAACTAGTATGGGTTGCACAGCGTCAATATTAAGGAGCACAATAAAGATGGCTGTTGTGTTTCTTTCAAATGAGCTAATATGACATGGACATGCTTATTTTTGTGGCATTTTTTACACTAAAAATACATGTTTTTAATTATTTTGAGCACATTTTAGGTAGCTTGACGTTTATCATTAGGTTTGTATGGTATGCCGTTTATTGAACTATCCCTTTAAGATGTTACTCAAGATATATCTATTAATGGCATATTAGGCTTCTCCTAATTTCTTTCAGCACTATACATGTATACATGTCAGCATATGTTAATGAAGGATTTGTCAAAGCCTTGCTTATGTCAACGCTGCATTTTATAGCTTGTTTTCCTGAATGTCGTGTCAGATTTTGGATTAAGCTACGCTAAAAATGGCGAATTGCTGAAATACATTCGAAAAATCGGCTCATTTGATGAGACCTGCACACGCTTTTACTCTGCTG
Associated Phenotype:
Not determined