ZMP
si:dkey-226b20.7
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate inositide-3-kinase adaptor protein 1 (PIK3AP1) [Source:UniProtKB
Human Orthologue:
PIK3AP1
Human Description:
phosphoinositide-3-kinase adaptor protein 1 [Source:HGNC Symbol;Acc:30034]
Mouse Orthologue:
Pik3ap1
Mouse Description:
phosphoinositide-3-kinase adaptor protein 1 Gene [Source:MGI Symbol;Acc:MGI:1933177]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38935 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16590 | Nonsense | Available for shipment | Available now |
sa42191 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42192 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10642 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38935
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110266 | Nonsense | 264 | 837 | 4 | 16 |
ENSDART00000144020 | None | None | 237 | None | 6 |
ENSDART00000148034 | Nonsense | 263 | 464 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 23253942)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22983280 |
GRCz11 | 13 | 23113730 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGATGATTTGTTTTTCTCTTTTAGATATGCCAGCTGGGGAAGTATCAT[T/A]GACGGTTTATAAAAATCAGTCTGTGTTATGCTCATCAACTGTAACATATT
Long Flanking Sequence:
AATGTCTGAAGTTGGGGCTGATGCGATCATCACAGCAGCGTTAGCCAATGAAATTAATCCGCAATCGGCTAGTGTCTGAGCTTGTGTGTTTGCATGAAGCAATCTTATTGGCTGACGTGCGTGTTGGCATTTGAGAAGTTGAGAAATTTCCAACTTCTTCAGCGAGCAACGCCGTAGTGGTGCCAATGGATCCACAATGCAGTTCAGCAACGCCTGACATCACCCATTCAAAGTGAATGAGAAGCGTTGATGCTGGCGCCCTGTGTAAATGGGGTGTAAGAGATTAAGCACAACCCTGTTAGACCATGCATCAAGGTGCAAATGTGGATTCGGACATGCCTTTAATGCTTTTTCTTTATGTACTTTAAACTTTGCGCCTAGATAAAATAAAATAGTCCAATGATTTAAATAATTTTATGTACAATATATGCCTGCAATTCTTAATTCAGCTGTGATGATTTGTTTTTCTCTTTTAGATATGCCAGCTGGGGAAGTATCAT[T/A]GACGGTTTATAAAAATCAGTCTGTGTTATGCTCATCAACTGTAACATATTATACAGAAATGGAGGAAATTTGCAGATATCTAAAGAAAGCAACTGATCCAGTGCAGTTCATGTGTCAGGTAATAGCATGAAACAAACAAACAGTTGATAGAAGCAATAAACAAAAATCTTTTGCAAAAAGGACACATAAACTGAAATGACTTTTGAATATGACCTTTTTATTTGTATTGTATTATGCATCTTGCTTCGAACATCACATAAATGTTACATGTTGAAATTTAAACTTGTTTTATAGTACTAAAAATAAAAGAAAAAAACGTCAATTTTAGAAGTTAAAATTTGTTATTATTTTTACATAAAGTAAAAATTTTGTGAGAGCCAAGAAAAGATCAGAAGAAGACAGTAAAATGTAAAAAAGTAAAAGGAAATGCTGATGTATTCAAACTGTCTAATAATTTTCAGGTTTTATTATTGTCTTTTAAAAAAAGTAGTTTCAGAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16590
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 |
---|---|---|---|---|---|
ENSDART00000110266 | Nonsense | 299 | 837 | 4 | 16 |
ENSDART00000144020 | None | None | 237 | None | 6 |
ENSDART00000148034 | Nonsense | 298 | 464 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 23254046)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22983384 |
GRCz11 | 13 | 23113834 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAAATGGAGGAAAKTTGCAGATATCTAAAGAAAGCAACTGATCCAGTG[C/T]AGWTCAWGTGTCAGGTAAWAGCATGAAACAAAYAAAYAGTTGATAGAAGC
Long Flanking Sequence:
TTATTGGCTGACGTGCGTGTTGGCATTTGAGAAGTTGAGAAATTTCCAACTTCTTCAGCGAGCAACGCCGTAGTGGTGCCAATGGATCCACAATGCAGTTCAGCAACGCCTGACATCACCCATTCAAAGTGAATGAGAAGCGTTGATGCTGGCGCCCTGTGTAAATGGGGTGTAAGAGATTAAGCACAACCCTGTTAGACCATGCATCAAGGTGCAAATGTGGATTCGGACATGCCTTTAATGCTTTTTCTTTATGTACTTTAAACTTTGCGCCTAGATAAAATAAAATAGTCCAATGATTTAAATAATTTTATGTACAATATATGCCTGCAATTCTTAATTCAGCTGTGATGATTTGTTTTTCTCTTTTAGATATGCCAGCTGGGGAAGTATCATTGACGGTTTATAAAAATCAGTCTGTGTTATGCTCATCAACTGTAACATATTATACAGAAATGGAGGAAATTTGCAGATATCTAAAGAAAGCAACTGATCCAGTG[C/T]AGTTCATGTGTCAGGTAATAGCATGAAACAAACAAACAGTTGATAGAAGCAATAAACAAAAATCTTTTGCAAAAAGGACACATAAACTGAAATGACTTTTGAATATGACCTTTTTATTTGTATTGTATTATGCATCTTGCTTCGAACATCACATAAATGTTACATGTTGAAATTTAAACTTGTTTTATAGTACTAAAAATAAAAGAAAAAAACGTCAATTTTAGAAGTTAAAATTTGTTATTATTTTTACATAAAGTAAAAATTTTGTGAGAGCCAAGAAAAGATCAGAAGAAGACAGTAAAATGTAAAAAAGTAAAAGGAAATGCTGATGTATTCAAACTGTCTAATAATTTTCAGGTTTTATTATTGTCTTTTAAAAAAAGTAGTTTCAGAAAGAAATTTGGATTTAAAGACTAATATTAAGCTGATTTTGTATTTAACATGATTATATTTTCAGGCATTTGATATCACATCAAAGCTCCAAGAGTCGTTAGATAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42191
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110266 | Nonsense | 315 | 837 | 5 | 16 |
ENSDART00000144020 | None | None | 237 | None | 6 |
ENSDART00000148034 | Nonsense | 314 | 464 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 23254538)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22983876 |
GRCz11 | 13 | 23114326 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGATTATATTTTCAGGCATTTGATATCACATCAAAGCTCCAAGAGTCGT[T/A]AGATAATTTGCTTGCTACCTCTCTTGAAGAACGGATGCCTGTAAATGGAT
Long Flanking Sequence:
ATCCAGTGCAGTTCATGTGTCAGGTAATAGCATGAAACAAACAAACAGTTGATAGAAGCAATAAACAAAAATCTTTTGCAAAAAGGACACATAAACTGAAATGACTTTTGAATATGACCTTTTTATTTGTATTGTATTATGCATCTTGCTTCGAACATCACATAAATGTTACATGTTGAAATTTAAACTTGTTTTATAGTACTAAAAATAAAAGAAAAAAACGTCAATTTTAGAAGTTAAAATTTGTTATTATTTTTACATAAAGTAAAAATTTTGTGAGAGCCAAGAAAAGATCAGAAGAAGACAGTAAAATGTAAAAAAGTAAAAGGAAATGCTGATGTATTCAAACTGTCTAATAATTTTCAGGTTTTATTATTGTCTTTTAAAAAAAGTAGTTTCAGAAAGAAATTTGGATTTAAAGACTAATATTAAGCTGATTTTGTATTTAACATGATTATATTTTCAGGCATTTGATATCACATCAAAGCTCCAAGAGTCGT[T/A]AGATAATTTGCTTGCTACCTCTCTTGAAGAACGGATGCCTGTAAATGGATTACAAGTATTCGGAATTAGTCAAATTGAAGAAAACACAGCAGCAAGTGAGTCAATTCATTCATAAACACATTCATGTGATTACGCTCTTAAAAATAAAGTTTCTTTATTGGCATTAATGTGAAGAGAATACAGTATTTACATCAACATATGTAAACCATCAACTTTCAAGAAGAACCTTTAACATAGACTGGAATATTTCCAGTCTACAAATGGTTCATTAAATGGTTTCTTTAGATGTTCTCACTTTAAATCATGTGGCCTCAACTAATATGAACTTACAGTCAAATGAGTAATTCATTACAGTGTACTTATTGTGTAAATAAATGTTTTAAAATTGCACTTAATTAACTAATTAATTTCTGTAAGTACATTTATAATTACATGTTGACCATCTCTTACACTTTAACCCACCTTTAAACCTATCCTTTATTATCCTTATGCATTTCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42192
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110266 | Nonsense | 435 | 837 | 7 | 16 |
ENSDART00000144020 | None | None | 237 | None | 6 |
ENSDART00000148034 | Nonsense | 434 | 464 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 23255816)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22985154 |
GRCz11 | 13 | 23115604 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGACGCACATTGAGGAATCTCAGAACGCCCCCGAAAGTGAGGACATCTA[T/A]GAGGATATGCTGAGAGCTTCCCAGAACTTCATCTCTGAGTTCGATAATGA
Long Flanking Sequence:
ATCATGTAGAAGGAACTGGTGTTGATGGCTAATTGTTATTAAAGACAGGAAACAGTAAGTAGAAATGACTTTGTTTTCAGATCACCGTGATGTGGAACTCCCAACGCTGCTTCACTTTTCTGCCAAATATGGCTTAAAAAAGTTAACATCTTTGTTAATGCGGTGCCCCGGAGCCATGCAGGCTTACAGTGTGATGAACAAGGATGGGGATTACCCCAATAAGCTGGCCGAGAAGAGCGGTTTCTCTGATTTAAGACAGTTCATGGATGAATATGTTGTGAGTTCACTGCTGAATGTTGCATTGTAAAAGAAATATAAGAATATAATGCAATTGTTAGTTAACAAGTATGGGATACATTTATATAACAATATTTCCTTTATTATATAGTGTTGGTGATGCCAATTACTTGTTTCTTTTATTAATCCAAACAGGAGACAGTGGATTTAGTGAAGACGCACATTGAGGAATCTCAGAACGCCCCCGAAAGTGAGGACATCTA[T/A]GAGGATATGCTGAGAGCTTCCCAGAACTTCATCTCTGAGTTCGATAATGAGAACATTTATGAGTCTATGGTGAAGCTCAATCCTGAGATGGGTGTGTGTGTTGTAATATTTTATATTTTCATTAATAATTAATGAAGTTTTTATTTTAAGAAACAATATTGTTTTGTTACTACTGCTAAATGGATCAATGGCTAAAGTTTTTTTTTTTAACAATAGTTACAGCTTATTATATGTTTTTACTATAGTTTACACAATAGACCCTCATTTTAACTATAATTTATATACCAAAAAAACACTGTCAGGTGTAATAAATATTTTCAGGCTATAGTCTACCAAAATAATTGTCAAGCATATGGATATTATTAAATATTGTCAGACTGTAGAATCTATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATGTTTTTACATAAATATATAAGTTTTGCTGAATGGTGATGGAACATTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10642
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110266 | Nonsense | 825 | 837 | 16 | 16 |
ENSDART00000144020 | Nonsense | 225 | 237 | 6 | 6 |
ENSDART00000148034 | None | None | 464 | None | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 23268189)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22997527 |
GRCz11 | 13 | 23127977 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCGTTAYGTATCCAATCCATCCCGCCCTGTTCCTCAGAATCCTGCACAA[A/T]GAYCTATACCACCTCCGCCGGTACCCAGACGGACATGGTGARGGTCTGGC
Long Flanking Sequence:
ACCTAATAAATTGGCCGATGAGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTATGTATATATATGTATATATATATATATATATATATATATATATATATATGTATATGTATGTATGTATGTGCGTATATATAAATCAAATGTATATATATATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTGCGTATATATAAATCAAATGTATTTACAAAATTTTAAGCAATAAGTAACCAATGTTTCTTAAGCAACAGATCAGCATACTCGAATGGTTAATTTATTGTTGAAATTTCAAGGATAATAGTTCATGAAGTTGATTCTAATGATCATTTCTGATTTGTCTCTGAAAATAACTGAACTTGAACCCACTGTCTCTTAGGAGCCCAGAGATACTGAACGAGCGTTATGTATCCAATCCATCCCGCCCTGTTCCTCAGAATCCTGCACAA[A/T]GACCTATACCACCTCCGCCGGTACCCAGACGGACATGGTGAAGGTCTGGCTTTCCTTCTGTGTGAATCTGCACTTTTTCTTGACGAGTCTCTTCAAGATGGAGCTAAAGATGCTGACTTTGATTCCACTGCGCTGTCAGTCAGGGATCTTACAGAGGTTTTGTATGAAGGCGTCTCTGAAGAGCACTGCTTTAGATTCTTTTAACCAACTGCAGAATGTGCAGGGGATTGTGGGATATCATAGACAGAAAAACCCATCTATGATACTGCCAGATAGCAAACAGGATATTATGCAAACATCTTGATGCTGTCTTTTCAAATCTGCCTGTGAATGCAGCATGTTTTAAGTTTTGGTCTCAACAAATCGAAGACTTCTTTGAAGACTTCTTTGAGCGTTTGAACCGATCTAGACACAATGAACTTAATTTATATATATTTTAAGTGATATATCGGTTTTTGCTCTTTGAGTGTTGTGTTAGTGACAGCAAATGGCAAGCTTAA
Associated Phenotype:
Not determined