ZMP
pdpk1a
Ensembl ID:
ZFIN ID:
Description:
3-phosphoinositide-dependent protein kinase 1 [Source:RefSeq peptide;Acc:NP_001070812]
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 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa5221 | Essential Splice Site | F2 line generated | Not yet available |
sa20114 | Essential Splice Site | Available for shipment | Available now |
sa38407 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa5221
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102245 | Essential Splice Site | 90 | 536 | 1 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 45336265)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 47345818 |
GRCz11 | 3 | 45298152 |
KASP Assay ID:
554-3499.1 (used for ordering genotyping assays)
KASP Sequence:
AGGAGGACTTCAGCTTTGGCAAAATTTTAGGAGAGGGCTCCTTTTCAACG[G/A]TGGGTGATTTTGCTGTTTTCAATAGCCCAGGTAGCAGATATTATGAAAYA
Long Flanking Sequence:
GTTGTGCACAAAAAGAAAAAAAAAAAGATGTTTTTGTCACTTCGACAGGGTAAATATTTTGCGCTCTCTGCAGCGTAAACAAAGGCAGGTCTGAGTGAATGAATTTGAGTACTCGTAATCCTGGCTGAACACAAACAGCCCTCCCCTCTGCGGAAGCTCTACTGTACTTTATCAGCTGCTGGTTTTACTGCTTCTAAGGTGGTTTGGTTCCTCATTGCACACGCACCCGCATGTCTGACTCTGTGTCATGTTTGCTTTGTGTGTGTGTGTGTGTTTTGCTCGTTCAGTACGATGCTGCTCTCATCCAGCCTAGCGTGGCGTTGCGTTCCTGTGCTTCTTCATCAATGGTAAGGACTCAGCTGAACTCCAGGCTTCCTCAGCATCTCGGCATGGAGGTCCGTGGGGGGGAGTCCAGCACGCCTGCTCTCAAGCCTCCGCAATCATTCAAGAAGGAGGACTTCAGCTTTGGCAAAATTTTAGGAGAGGGCTCCTTTTCAACG[G/A]TGGGTGATTTTGCTGTTTTCAATAGCCCAGGTAGCAGATATTATGAAACAAAAACATACATGGAGAGATGTATTGTAAACTGACAGCTATTATTAGTAGTTGATTTGCTGTTGTAAGTTTGGTTTCATTTATTTGTTCAGACTCTCAAAAATGTGATTCTTTCCAGAACAAAATAATAATAATTAATGCTGCAAGCAGCAATGAAAGGGACCTCGCATTTAATTGATGTAATTAAATCATCTATGATTAATTATTTATGCTGTAAATATAGTATTTAGACAGATGTATAGTATAGTATAGTATAGTATAGTATAGTATAGTATAGTATAGTATAGTATAGTATAGTATAGTATATAATGAGCCTGTTTGCCACACCCACTTCTGAACCCCATATCAAACGTAAATTTTTGCCACTTCTGGTGTGTGTGCAAACTTTTATGAGTTTCTTTGCATGTTCAGACTCTCAAAATTTGATTTATTTCAGAACAAACAAAAATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20114
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102245 | Essential Splice Site | 312 | 536 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 45329942)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 47339495 |
GRCz11 | 3 | 45291829 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTGAGAAGTTCTTCCCAAAAGCTAAAGATCTGGTCCAGCGTCTGTTGG[T/C]AATCATGTTTGTTTTCATGATACATGCTTTCGGTTTGTTTTGCATGGTGG
Long Flanking Sequence:
GTGAGTTACTGATCACTTGGGTTTTGGTTCAATCAAACATTGTGAAATATGTCACGATGGCATTCTGCACTGTAGCTGAAGAGCTGGTGGTTGATCACTGGTTGTAATTGCAGTTTTTGAAAACATGGTGTGAAATAACAGGAAGTGTTGGCTTTGGTGTTTATGACTTGTTTGTGTAGACAGTACAGAGGGCTTCTGAGGAAACCCCAACCACCGGGTCACATGACCCGCCTGTCGTTTTTAGTTACATTACAACCAATATACTGGCCTGGACGACCGTTGAAAACAAAACACTCCGCCACGTGACTAAATTTCACCCGTTGTTTGTCTCGAGCTGTGTAAAAACAGTGAAAGCTGGTATTGATTCACTACTGTTAGTCATTTACTTTTATCTTTTAATAGGAACGAGTACTTGATTTTCCAGAAGATAATAAAGCTGGAATATGAATTCCCTGAGAAGTTCTTCCCAAAAGCTAAAGATCTGGTCCAGCGTCTGTTGG[T/C]AATCATGTTTGTTTTCATGATACATGCTTTCGGTTTGTTTTGCATGGTGGTGTTGAAGGAGATTCATTGTTTTTTCCTGTGTCTTTCAGTCTTTGGACCCTAGAAAGCGGCTGGGATGTGAGGAAATGGGAGGGTTCGGTCCGCTGAAAGGCCACATGTTCTTTGAGACTGTCTCATGGGAGAACCTGCCGCTTCAGACTCCACCCAAACTGACCCCTTACCTGCCAGCCATGGCTGAGGATGATGAAGACTACTATGGCAATGTTAGTTCAATTTATCAGACCCGTTATTCCCAAACTGTGCTAAAATTTAAATATTTAGCATTATGTATCTGGTTGATTTTTTTTTTTATTATCATTTTGAAATGCTTATTTAATTTATTTTATTGCATTTTATTTTATTTTATTGCATTTTATTTAGCGGTTTGTGTGCATTTTTGCTTTTTCTATTTTGAATGTTTTTATTTTTGGTTGTATGATTTTGTTTATTTGTTTATTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38407
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 |
---|---|---|---|---|---|
ENSDART00000102245 | Essential Splice Site | 456 | 536 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 45326438)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 47335991 |
GRCz11 | 3 | 45288325 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGACTGCAGTTGGTAATAACAGCTTTTTTCTTGTTTGTTGTTGTCAC[A/T]GGGGCTGTTTGCTCGACGCCGTCAGCTTTTACTAACTGAAGGACCGCATC
Long Flanking Sequence:
ATAACCTATATAAATATATGATGGTTTCTATTGTTTGTATGTTTTTCTTCAGCAGGGTCATCTTGTAGTGACAGCACATTTTGTTATTGTACACAGTAATGGGGCGCGTGCATGCGCGTATGTGCTAATAATGATCTCTTTATCTCTCACATTTCCTGTTAGCTTTTTATAGCATGTTGTAAAAGGAACTCTTGATCATTATAGTTCTGTTTTCAATCGGTCAACAACACAAGTGCCACTAACTGCTGGCTTGTTATTCATTAACATGTCTTTTTTTTCTGTCTTCAAGGCACCAGTTTGTCGAAAATAACTTGATATATAAAATGGGACCAGTTGACAAAAGAAAGGTAACGTTTTTTTTTTCTTTGTCTCTCATATCTAGAGTCAAAAACAGGTGCATGACTGCTTGATTTCTTTAAAGAGTCGAGTGAGTAAATAAATAGCGCCCTCTTTTGACTGCAGTTGGTAATAACAGCTTTTTTCTTGTTTGTTGTTGTCAC[A/T]GGGGCTGTTTGCTCGACGCCGTCAGCTTTTACTAACTGAAGGACCGCATCTGTATTATGTGGATCCTGTTAATAAAGTACTAAAGGGGGAAATTCCGTGGTCTCCAGAATTGCGTCCTGAGGCCAAGAATTTCAAGACGTTTTTTGTCCACACGGTAAAATACTGATATACTTATAGTTTCCTCATTGCATATTATTTGTGTAACACTCATCTTCTCTAGCAGTTTAGTCATGGTTTTAAATCAATTTTCATGGTAAATAATATTTGATAAATGCATCAAACTGGATCTGGGTTTCCACAGATTTTGTATGCTTGGAGGAAGTTGGTTTTGTAATAAACAAGGAATATGGCAAGAACAGTAAACAATACTCTTGTAATCAAATTAAGCTATATTTAAAGCTACAATCTTTAACTTTGTTTTAGTTAAGTATGATCTAAAATTCAGTGAGTACATAAACAGCCAATGTTCAAAACTGTCTCCTTTATACCAATTCACAGTG
Associated Phenotype:
Not determined