ZMP
si:dkey-24l11.7
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate phosphoinositide-3-kinase, class 2, alpha polypeptide (PIK3C2A)
Human Orthologue:
PIK3C2A
Human Description:
phosphoinositide-3-kinase, class 2, alpha polypeptide [Source:HGNC Symbol;Acc:8971]
Mouse Orthologue:
Pik3c2a
Mouse Description:
phosphatidylinositol 3-kinase, C2 domain containing, alpha polypeptide Gene [Source:MGI Symbol;Acc:M
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6522 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10124 | Nonsense | Available for shipment | Available now |
sa25065 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12328 | Nonsense | Available for shipment | Available now |
sa679 | Nonsense | Available for shipment | Available now |
sa18446 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6522
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 |
---|---|---|---|---|---|
ENSDART00000086131 | Nonsense | 579 | 1725 | 8 | 32 |
ENSDART00000133547 | Nonsense | 579 | 1725 | 9 | 33 |
Genomic Location (Zv9):
Chromosome 18 (position 26982525)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 27055780 |
GRCz11 | 18 | 27038158 |
KASP Assay ID:
554-4679.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGTGTCTCTTTTTAGAACAACCAATATAAAACAGTGGACAATGTGGTT[C/T]AGTCTGTTAAGAATCTGTSCTGTGCTCTGGATGAAGTTGAGACACCAGCC
Long Flanking Sequence:
TGTTGTGAAGGTTTTAATGCACATTTTCTAAAATTTAATTTCTATATAAAACATTTTTTATTCAGTTCAGTTCAGGTAATCTTTATTTCTTTCACACTTTTTACAATGTAGATTGTGTTAAATTAGCTTAACTTGGATAAAGAAAAGATAAAGAGTAAAATAATATTTTTTTAAATTGATTTGTGGAACATTCCAGCAGTTCAGGCAGGCAGGAGAGTAGTGTAGAATGTGAGTGTATTTCTAATAAATTGCTTCTATTCACTTTAATTCTGATCGGTTTAATGCAAAAGTTAATGCTGAAGGAAGATTTACCGAAGAGCAACTCCACAGATGCGATATTCCAAACTTCACATAAAAATAGCTAGATGAAAACATACAGTAGCTACTGTATCAAAATAAGTCAAGAACTCCTTGAAACTATTGTTATATATTTTTAATTGTAAGCATTTTTCTGTGTCTCTTTTTAGAACAACCAATATAAAACAGTGGACAATGTGGTT[C/T]AGTCTGTTAAGAATCTGTGCTGTGCTCTGGATGAAGTTGAGACACCAGCCATCACTGATGCCGTCAAGAGGCTCAAGCGCTCTGTCAACCTTCCTAGAACACGCTCACCAGAGGTCAGAGACCCTTCAGTATAAACCTTCAGCCATGTGCGATATTAATACAATGGTTCTCAAGTCCAGTCCTCTGGCCTCCTTCTCTGCACATTTTATATGTCTTGGTTACAAAAAGACATACAACTGTGCAAGGCAGTGGGCCTGAGGACTGGAATGGGGAACTACTGTATTAATTTGATGACTGTTACTCATAAGTCAGGAAGTATTTTTCATGTTTTGACAGATCAATTGTTAATAAATTGATTTATCTAGCACTGACTAAAACCACTTTAAAATTAATAATAATAACAATAATAATAACAAAATCAGTGCTGACATGTTGTTCCCTGTACCTAGTCTAAAATGTTTTTTTATTGTTATATGTGCGCATGTTTCATAAAGCACTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10124
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 |
---|---|---|---|---|---|
ENSDART00000086131 | Nonsense | 585 | 1725 | 8 | 32 |
ENSDART00000133547 | Nonsense | 585 | 1725 | 9 | 33 |
Genomic Location (Zv9):
Chromosome 18 (position 26982545)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 27055800 |
GRCz11 | 18 | 27038178 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCAATATAAAACAGTGGACAATGTGGTTYAGTCTGTTAAGAATCTGTS[C/A]TGTGCTCTGGATGAAGTTGAGACACCAGCCATCACTGATGCCGTCAAGAG
Long Flanking Sequence:
ACATTTTCTAAAATTTAATTTCTATATAAAACATTTTTTATTCAGTTCAGTTCAGGTAATCTTTATTTCTTTCACACTTTTTACAATGTAGATTGTGTTAAATTAGCTTAACTTGGATAAAGAAAAGATAAAGAGTAAAATAATATTTTTTTAAATTGATTTGTGGAACATTCCAGCAGTTCAGGCAGGCAGGAGAGTAGTGTAGAATGTGAGTGTATTTCTAATAAATTGCTTCTATTCACTTTAATTCTGATCGGTTTAATGCAAAAGTTAATGCTGAAGGAAGATTTACCGAAGAGCAACTCCACAGATGCGATATTCCAAACTTCACATAAAAATAGCTAGATGAAAACATACAGTAGCTACTGTATCAAAATAAGTCAAGAACTCCTTGAAACTATTGTTATATATTTTTAATTGTAAGCATTTTTCTGTGTCTCTTTTTAGAACAACCAATATAAAACAGTGGACAATGTGGTTCAGTCTGTTAAGAATCTGTG[C/A]TGTGCTCTGGATGAAGTTGAGACACCAGCCATCACTGATGCCGTCAAGAGGCTCAAGCGCTCTGTCAACCTTCCTAGAACACGCTCACCAGAGGTCAGAGACCCTTCAGTATAAACCTTCAGCCATGTGCGATATTAATACAATGGTTCTCAAGTCCAGTCCTCTGGCCTCCTTCTCTGCACATTTTATATGTCTTGGTTACAAAAAGACATACAACTGTGCAAGGCAGTGGGCCTGAGGACTGGAATGGGGAACTACTGTATTAATTTGATGACTGTTACTCATAAGTCAGGAAGTATTTTTCATGTTTTGACAGATCAATTGTTAATAAATTGATTTATCTAGCACTGACTAAAACCACTTTAAAATTAATAATAATAACAATAATAATAACAAAATCAGTGCTGACATGTTGTTCCCTGTACCTAGTCTAAAATGTTTTTTTATTGTTATATGTGCGCATGTTTCATAAAGCACTATGCTGAATTGCAGGCTGGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25065
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 |
---|---|---|---|---|---|
ENSDART00000086131 | Essential Splice Site | 985 | 1725 | 16 | 32 |
ENSDART00000133547 | Essential Splice Site | 985 | 1725 | 17 | 33 |
Genomic Location (Zv9):
Chromosome 18 (position 26996706)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 27069961 |
GRCz11 | 18 | 27052339 |
KASP Assay ID:
554-7869.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGACCACTTTATTGGTTTTATAACCTGCTTTATGACTGGTTTGCTGTA[G/A]GTTTGCCGACACAGAGGTGAGGAAAGTGGCTGTGAGCTGGATCCAGAGCA
Long Flanking Sequence:
GTGGATTAAGAGGTTGGAGTGTCTGGAGTGTTGGTTCGAAGCCCACTGGAAGTATTTTATTAATTTTAAGATTAACCAGCAGTTTTTTTTTGTTTGTTTTTTTCCACCAGACTGTCACGGGCGGACAGACAGCTGCTTTGGGACCAGAGGTACTATTGTCGGGAATATGAATACAGTTTGCCGAAAATCCTGGCCAGCGCTCCCAGCTGGGACTGGGGCAGTATGGGGGAAATCCACGCACTTCTGCACCACTGGCCTGCTCTGTCACCCGTTTCAGCTCTTGAGCTCCTTGAATCCAAGTATGTGTCCAACCTGCTCTCTCTAGATTTTATTATCTCCTATTTTTTATTGCTCAAGCTCATTGTATCCGTATGATCTTTTTAATGTGTCACTTTGGTCATATGATCTTTTCAGTTGTTGTAATGTTGCACTTTTAAACTTGTGACCACTTTTGACCACTTTATTGGTTTTATAACCTGCTTTATGACTGGTTTGCTGTA[G/A]GTTTGCCGACACAGAGGTGAGGAAAGTGGCTGTGAGCTGGATCCAGAGCAGCAGTGATGATGAGCTGGCTGATTATCTCCCCCAGCTAGTGCAGGTATACACACACACACACACACACACAAACACAAACACACATGTTGTTTTTTCATTTTATTTTAGGAGACATTCCATAGATTTCCATTATACACCTTTAATACCAATATTCAACTTTAATACCTCTCCTGCACAATGTCCTGCACAACATTGTTCATTCTTATGTAAAAGTATGTGTATGTACTTGTCTTGTGTGTTTAGTTAAGTATCTTAAAGTAAATGTCAGTTGTTTAGGTTTTTTAAACTAGCTTTTGTGTCCAATGTTGTGTTTGTATTAATTAATTTATTCAGCACCTTTGTACTGCGAGACACATGTAGTTGAATGACAATAAAGCTTAACTTGACTTCTTTTATACTGTAAAAACTGTATTTTCTGTCTCCCTACTCAAACTCCATCCCTAATTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12328
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086131 | Nonsense | 1236 | 1725 | 22 | 32 |
ENSDART00000133547 | Nonsense | 1236 | 1725 | 23 | 33 |
Genomic Location (Zv9):
Chromosome 18 (position 27006252)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 27079507 |
GRCz11 | 18 | 27061885 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGAKTTGGTACCATCTTCTGAAACGCTGAGAAAGATTCAGGTGGAGTA[T/A]GGAGTGACGGGTTCCTTCAAGGACAAACCTCTTGCTGAGTGGCTTCGCAA
Long Flanking Sequence:
TGTTTAAGAAACTTTAATAATGAATAATGTTCAAGGATTTCCTTATTTTATCTTATGATTTCTTATTAAATAGAAACAGTATTTGAATAGCATTTACACTCACTTTTTAAAAATTGGTGGCATTTTTCTTTTTAGATGATTAGTCTCTTGCTAATTTTTAAATGTTTGCTTAACTTTGTTTAGGGTTTGTTGTATCATTTTAGTATCTTGTATGCATGTTGTGTTGATTTGTATTGAAAGCGCTTTGAGAAACTAACTTTTATAGGGGCTATATGAAATAAATGTATTATTGTAGGTAAACCTCACTCCCATGACCTCTAAAGGCACTCTAGAGAATGTTGATAACAGGCATGCAAACATAATTATGAGTTTTTGATGAAATATGAACATGATAGGTTAATTTATTTCTCATATTATGGGTTCTTTTTTTTGTTAATTGACGCAGGCATGGTGGAGTTGGTACCATCTTCTGAAACGCTGAGAAAGATTCAGGTGGAGTA[T/A]GGAGTGACGGGTTCCTTCAAGGACAAACCTCTTGCTGAGTGGCTTCGCAAGTATAACCCTGCTGAGGATGAGTATGAGAAGGTACATTTAAACGTTTTAGACTGCATAATAATCCATTGGTATCTTTAGTCAGATCACTTCATTAGGTTCACCTGTTTAATGCAAATCTAGTCAATCACATGGCAGCAGTTCTGTTGCTTTAGCCATGTAGACGTAATCAAGATTATCATCTGAAGCTCAAAGAGAACATGGGAATGAGGAAGAAAGGTGATTTAAGTGATTTTAAATGTGACAGTTGTTGATGCCTGATGGGCTGGTTTGAGTGAGTATTTTACAAACTCTGCTAATCTGCTGGAGTTTTCATGCACAGCCATTTCTGGGGTTTACAGAGAATGGTCAAAAAAAGCTAATTATACAGTGAGCCTCAGTTCTGTTTGCTCTGTTGATGTTAGAGGTCAAAAAAGAATGGCCAGGCTTCTTCAAACTGATAGAAAATCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa679
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086131 | Nonsense | 1480 | 1725 | 27 | 32 |
ENSDART00000133547 | Nonsense | 1480 | 1725 | 28 | 33 |
Genomic Location (Zv9):
Chromosome 18 (position 27010652)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 27083907 |
GRCz11 | 18 | 27066285 |
KASP Assay ID:
554-0587.1 (used for ordering genotyping assays)
KASP Sequence:
AATTAATAAAAATTCACCTGATTTCTTATGTTTYTTTGTTTTTAGACGTA[T/A]GTCATTCGGATTCTAAGGGAAGGTCAGAGCGAGCCACAGTTTGTTTTCCG
Long Flanking Sequence:
AAAGTTCAGAACCACTGGAGCAAGTGGGTGTGAATCTAAATGATATACATTTTACAGTATACTATATGTCAGTCTTTAGATGGGTTTAAAAATATCTGTCTCTCCGTTTTTCATTGTAGGTTGATTGAATCCAGTCTGGGCAGTGTGGCTACAAAGTTTAATTTCTTTATCCACAATCTGGCTCAGTTGCGTTTCTCTGGCCTTCCCTCCAATGATGAACCCATCCTGTCGTTTGCTCCTCGGACATACACTATGAAGCAAGACGGCAAGATTCGGGACGCCTCTGTGTTTTCATTTCAAAAGAGATATAACCCAGACAAGCACTATGTAAGCACATCTAAATTCTAGTATAGTACTAAATAAAACATTCTTAAAAAATATACATTTTGTGATGTGCAATGTATATTTTCTTACAACTCAGTGTGTAATAAACGCTTAACATGTTCAAACAATTAATAAAAATTCACCTGATTTCTTATGTTTTTTTGTTTTTAGACGTA[T/A]GTCATTCGGATTCTAAGGGAAGGTCAGAGCGAGCCACAGTTTGTTTTCCGCACATTTGATGAGTTTCAGGAATTGCACAACAAATTGACCATCCTTTTTCAGTTGTGGAAGCTGCCAGGGTATGTAAATTTACCATTTGTGCCAGATTCATCAAATACTGCTAGATTTGTCAAATACTCTGTCTTCCTAAGAATATTCTTCTTTTATAGGTTTCCCAGTAAGATGGTGCTGGGACGCACACACATCAAGGATGTGGCATCCAAGAGAAAGGTTGAATTGAATAGTTATGTGCACAATCTGATGAGGAGTTCAACAGAGGTCGCCCAGGTGGGTATTTGGTAGGGCCAGACAGAATTTGTGGACATTTTTTGCTATTTCTGCAGAGACTTTTGTAAAAAAAATCTGCAGATTTATGCGGAATGTTTTAGGGAGTATCATAACTAAAAGCGTATAAAAAAAATATTACTACAGAAATGAATATAAAAACTGAATAAATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18446
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086131 | Nonsense | 1546 | 1725 | 28 | 32 |
ENSDART00000133547 | Nonsense | 1546 | 1725 | 29 | 33 |
Genomic Location (Zv9):
Chromosome 18 (position 27010940)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 27084195 |
GRCz11 | 18 | 27066573 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACACATCAAGGATGTGGCATCCAAGAGAAAGGTTGAATTGAATARTTA[T/A]GTRCACAATCTGATGAGGAGTTCAACAGAGGTYGCCCAGGTGGGTATTTG
Long Flanking Sequence:
TTTTCATTTCAAAAGAGATATAACCCAGACAAGCACTATGTAAGCACATCTAAATTCTAGTATAGTACTAAATAAAACATTCTTAAAAAATATACATTTTGTGATGTGCAATGTATATTTTCTTACAACTCAGTGTGTAATAAACGCTTAACATGTTCAAACAATTAATAAAAATTCACCTGATTTCTTATGTTTTTTTGTTTTTAGACGTATGTCATTCGGATTCTAAGGGAAGGTCAGAGCGAGCCACAGTTTGTTTTCCGCACATTTGATGAGTTTCAGGAATTGCACAACAAATTGACCATCCTTTTTCAGTTGTGGAAGCTGCCAGGGTATGTAAATTTACCATTTGTGCCAGATTCATCAAATACTGCTAGATTTGTCAAATACTCTGTCTTCCTAAGAATATTCTTCTTTTATAGGTTTCCCAGTAAGATGGTGCTGGGACGCACACACATCAAGGATGTGGCATCCAAGAGAAAGGTTGAATTGAATAGTTA[T/A]GTGCACAATCTGATGAGGAGTTCAACAGAGGTCGCCCAGGTGGGTATTTGGTAGGGCCAGACAGAATTTGTGGACATTTTTTGCTATTTCTGCAGAGACTTTTGTAAAAAAAATCTGCAGATTTATGCGGAATGTTTTAGGGAGTATCATAACTAAAAGCGTATAAAAAAAATATTACTACAGAAATGAATATAAAAACTGAATAAATATATATTTACACACATTTACAGAAGTAAATTAATAGACTCAATGATTGGCTAAAATCTGCATATTTCTGCATGTGCAGATTCCATATGGGTCTAGTAATCGGATGTTTAATTTAATATTAAGTGAAATAAAACTGTTTACGCTTTGTCAGTGTTACATTTGTACATTTTTGCTTTTTATGAAAACATGTTGCTTTATTACTTTTTATTTAAATGTTTTCATGTATTATCACTGGTCAGCATTTTTTTTCTTCTTTTTTTGGTACAAATATATTACTATTTTTAGGATTAATT
Associated Phenotype:
Not determined