Busch Lab

ZMP

pikfyve

Ensembl ID:
ENSDARG00000056112
ZFIN ID:
ZDB-GENE-030131-9636
Description:
1-phosphatidylinositol-3-phosphate 5-kinase [Source:RefSeq peptide;Acc:NP_001120777]
Human Orthologue:
PIKFYVE
Human Description:
phosphoinositide kinase, FYVE finger containing [Source:HGNC Symbol;Acc:23785]
Mouse Orthologue:
Pikfyve
Mouse Description:
phosphoinositide kinase, FYVE finger containing Gene [Source:MGI Symbol;Acc:MGI:1335106]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa21515 Nonsense Available for shipment Available now
sa15086 Essential Splice Site Available for shipment Available now
sa41455 Nonsense Mutation detected in F1 DNA Not yet available
sa12649 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa21515
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078540 Nonsense 366 2084 9 41
ENSDART00000110204 Nonsense 373 2091 9 41
ENSDART00000112453 Nonsense 382 2100 10 42
ENSDART00000123278 Nonsense 242 1922 6 37

The following transcripts of ENSDARG00000056112 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 33118892)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 32274838
GRCz11 9 32085584
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATTGTAATGTATAATAGCTGATTATTTTGCAGGATTCTTTTCAACTT[A/T]AAGATATATGGAAGAAGATTTGCCACAACACTACTGGGATGGAGTTCCAG
Long Flanking Sequence:
TGTGGCTGTTTCATGCTTGAGTGTGAGCATTTTAGCTGGAGCTTTTTGAGGGGAAATGATTAAGCCGTTGCTGAGGATATTTGTTTGTGATCTGCTAGTCATCAGGAATCTCAGAACAGCGGTCTCAATTCCAGACTGACAGTGGTCCAAGAGGATATTGGAAAGTCACCTGCCAGGAAGAGGTGATTATGTTATATTTTCCATTTCTTTTTTTGCTTATTCTTCTATTTATAGCCTATAAATACAATCCATTGCATTTTTTTCTATTAAGGTCAGCTAGTGTGACCAATTTGTCTTTGGACCGTTCCGGCTCATCCATGGTTCCTGCCTATGAGAGTTCGGTTAGTCCACAGAACAGCCGAGCTCTACCCAAGACCGACCACAGCGAAGAAGAGCGAAAGATCCTTCTAGTATGAAATGTTTGCTCTTTTCAAACGCTTCCCTGATTTTTGAATTGTAATGTATAATAGCTGATTATTTTGCAGGATTCTTTTCAACTT[A/T]AAGATATATGGAAGAAGATTTGCCACAACACTACTGGGATGGAGTTCCAGGACCATCGGTACTGGCTGCGCACTTACCCCAACTGCATTGTGGGTAAAGAGTTGGTCAACTGGCTTTTAAGAAATGGCACTATTTCCACTAGGTAGGAACAACCGAAATTGGTTTCAAGAGGCTTTTTTGTTTATTACAACTTCAAGTGGCAGTTTCTCCCCATGTTCGCGTGGGTTTCCTCCGGATGCTCCGATTTTCCCCACAGACTAAAGACATGTGCTATAGGTGAATTGAATACGCTAAATTGACATTAGTGTATGTGTGTGAATGCAGGATTGTATGGGTGTTTCCCAGTGCTGGGTTGCAGCAGGATGGGCATCCGCTGCATAATAACATTTGCTGGATAAATTGGTGGTTCATTCCGCAGTGGCGATCCCAGATTAATAAAGAGACTAGGCCGAAAAGAAAATCAATGAATAAATGAACTTCAAGTGTGGTCAGATATTGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15086
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078540 Essential Splice Site 680 2084 15 41
ENSDART00000110204 Essential Splice Site 687 2091 15 41
ENSDART00000112453 Essential Splice Site 696 2100 16 42
ENSDART00000123278 Essential Splice Site 556 1922 12 37

The following transcripts of ENSDARG00000056112 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 33123890)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 32279836
GRCz11 9 32090582
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGCTGTGACGATGATATGGACATCCGTCAGTTTGTCCACWTCAAGAAG[G/A]TAAAGACAGCAATGGAAGNAAAACTGATGAATYGAGTTTAGTAGAMACAN
Long Flanking Sequence:
GGAAGAGAATGGGGAAAAGAAAGCGATGGAGCGGTTGCTGTAAGACTTTTAATGAATAACTTGCTTTAGCTTGCTTACTTCTATTCATTTACAGTTAGAAGCAACAAAGAAATTGTTGTAGAACAATTCAGGGATGATATCAGTATTTGAATTACATGACTGCCTATAATAAGTTAATTGGTATACTTTTATAAACATGTGAAATACTCTAAATATTATCTAGTGTTAAAGTATGATTATGAAAGCATTACATATAAGGTAGGTGTAAATGATTTCAGGGGATTTCAGTACGACATGATGATTAATGCTTCCTCCTCAGGTCAGCAAATCACAGCCACATGATGGCGCTGCTGCAGCAACTGCTGTACAGTGAATCACTGTCTCTGTCGTGGCGTGACATCATCGTACCTGTGGTGAGGCAGGTGGTGCAGACGGTGCGACCGGATGTGCGCAGCTGTGACGATGATATGGACATCCGTCAGTTTGTCCACATCAAGAAG[G/A]TAAAGACAGCAATGGAAGAAAAACTGATGAATCGAGTTTAGTAGAAACATTTATTATATCTTGGAACGTGTGCTGTTTTGTAGATTCCAGGAGGAAAGAAGTTTGACTCTGCTGTAGTGAATGGTTTTGTTTGCACAAAGAATATCGCACACAAAAAGGTTTGTATTGATTGAACATTATTCCACAAAGGAGGTCATGGTATATTTGTGCTAATTGTGCTGGGACTTTCTCATTAGATGAACTCTTACATCAAAAACCCCAAGATCCTTCTTCTCAAATGCTCCATTGAGTATCTATATAGAGAGGAGACCAAGTTCACCTGCATTGACCCAATTGTTTTACAGGTAACTTCCTAACTAATGTTTACATGTTTGTAATTTTTACAATCTAAGAAATAGTTTCATTTACAATTTGCTGTTTTCAGGAGCGTGAGTTTCTTAAGAACTATGTTCAGAGGATTGTTGATGTCCGACCAAACTTAGTCCTGGTGGAGAAGACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41455
Status:
Mutation detected in F1 DNA
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
ENSDART00000078540 Nonsense 1406 2084 24 41
ENSDART00000110204 Nonsense 1413 2091 24 41
ENSDART00000112453 Nonsense 1422 2100 25 42
ENSDART00000123278 Nonsense 1282 1922 21 37

The following transcripts of ENSDARG00000056112 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 33128951)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 32284897
GRCz11 9 32095643
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCGTCGGGCTAACGCTGAGCCTTGTGGCCACTCTATCCATAAAGATTA[T/A]CACCAGTACTTCTCTTACAACCAGATGGTGGCATCCTTCAGGTCTGCATC
Long Flanking Sequence:
TTGGTATAAGTCAACTCTTGATATTATCTGATACCACAGCAATTAGCTCTTGAGTTGTCATCAGAATTTATGTCATTCAATCAGGTTTTATTTATATTTGTATATGTGGAATTTTAGACCATCTTACCAGTGCCCCAGCATGTACTGTGAGACCCCCATGGTTCACCACATCCGGCGCTTTGTGCACGGTAAAGGCTGCGTCCAGATTGTACTGAAAGAGCTGGACTCGCCTGTTCCTGGATATCAGCACACAATCCTCAACTACTCATGGTGTCGCATCTGCAAACAGGTAAAAACGTTTGGATTGGAAACCGACCAAAAATAAAAAACTGTATGACTTATGTGATACCCGTTTCGTTTTAGGTGACTCCTGTGGTCCCTTTGTCTAATGACTCTTGGTCCATGTCCTTCGCCAAGTACCTTGAGCTTCGTTTCTATGGTCATCAGTACACCCGTCGGGCTAACGCTGAGCCTTGTGGCCACTCTATCCATAAAGATTA[T/A]CACCAGTACTTCTCTTACAACCAGATGGTGGCATCCTTCAGGTCTGCATCTATATAAATATAATTTGTGTGAATATGCAGGATGTACTCTGAATGTATTCCTGATCTTCTGTCATCTGTAGCTACATTCCAGTGAGGCTGTTAGAGATCTGTCTGCCTCCCCCGAAGATCATCATCAGGAACCAAGGTCCATCGAAATCCAGCTTGCAGCAGGATCTCAAAGACTTCTCCCAGAAGTAAAATATCCTGCTGCATATTCTCTCATCTAGTTCCACCAGATGCCAGCTGAATTAATTAATTGTCTATTGTTTTGTAGGGTGGCTCAGGTGTACCTGGCTATAGATGACCGTCTTACCTCCTTAAAAACGGACACATTCAGCAAGACCAGAGAGGAAAAAATGGAGGACATGTTTGCACAGAAAGATGTAATTTTCTTTATATAAATAATAATAATAATAATAAAATAAAAAGAAAATAATAATTTTCTTTTATTTTCTTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12649
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078540 Nonsense 1940 2084 39 41
ENSDART00000110204 Nonsense 1947 2091 39 41
ENSDART00000112453 Nonsense 1956 2100 40 42
ENSDART00000123278 Nonsense 1778 1922 35 37

The following transcripts of ENSDARG00000056112 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 33136559)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 32292505
GRCz11 9 32103251
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTRTATGCYTAYAATKTTATCTGGTGTTTGTGCAGGTGTTTGACCTGAAA[G/T]GATCGCTGAGAAACAGGAACGTGAAGACGGACCAGGGAAAGGAGAGCTGT
Long Flanking Sequence:
ATCCTAGAAACAATCAGGCAGATGTGTTGAAGCAAGTTTGAGCTAAACTATGTAGGACAGCGGCCCTCCAGGACGGAGTTTGGGTACACCTGCCCTAGAGAGTCATACAGTGTAAAAACAACAATGATCTGACATAATTAAAAATGGTAGGGTGAACTCTGCATAAGACAACACAATTGTAATTTCCTAATTTGCTCCATAGTTATATATAGGAATTGCTTTGCTATACCTTTGTATAAGGCAACATGTTCTTGCATCTGTGCAACAGCGACCCACAGCACTTGCTAAGATTCTGGGAGTGTACCGCATCGGCTACAAGAACTCCCAGAACAACACTGAGAAGAAGCTTGACCTGCTTGTGATGGAAAACCTTTTCTATGGACGAAAGATGGCACAGGTACTGGAGCTTAGAACTGGTGTTTCAGAAAAACCCATTGACAAATTGGGTCTTTGTATGCTTACAATGTTATCTGGTGTTTGTGCAGGTGTTTGACCTGAAA[G/T]GATCGCTGAGAAACAGGAACGTGAAGACGGACCAGGGAAAGGAGAGCTGTGAGGTGGTGCTCCTAGATGAGAACCTGCTCAAACTGGTGCATGACAATCCCCTTTATATTCGCTCGCACTGCAAGGCCATCCTGCGTGCTGCCATCCACAGCGACGCGCTCTTCCTGTCCAGCCACCTCATCATTGATTACTCCCTGCTGGTGGGCCGAGACGATTCCACAGATGAGCTAGTTGTGGGGATCATAGGTGAGAAATTATTAGGTCATTTTAAAATTCACTTTGGACTTTTAGTAGTTGTTAAAACTCTTGTATGTTTTGAAGATTATATCCGGACTTTCACTTGGGATAAAAAGCTGGAGATGGTGGTCAAATCTACTGGGATTCTTGGAGGTCAAGGTACTGTTGTGTCATCAATACTTATGATATTCTCAGACATTTTACTAATTCTTTAAACTCATGTGTCATCATCTTTCCTTCCTGACAGGTAAAATGCCCACAGT
Associated Phenotype:
Not determined