ZMP
si:ch211-107m8.2
Ensembl ID:
ZFIN ID:
Description:
inositol polyphosphate-4-phosphatase, type I-like [Source:RefSeq peptide;Acc:NP_001122019]
Human Orthologue:
INPP4A
Human Description:
inositol polyphosphate-4-phosphatase, type I, 107kDa [Source:HGNC Symbol;Acc:6074]
Mouse Orthologue:
Inpp4a
Mouse Description:
inositol polyphosphate-4-phosphatase, type I Gene [Source:MGI Symbol;Acc:MGI:1931123]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38543 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa8633 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10195 | Nonsense | Available for shipment | Available now |
sa33832 | Nonsense | Available for shipment | Available now |
sa20671 | Nonsense | Available for shipment | Available now |
sa18836 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10910 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38543
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 |
---|---|---|---|---|---|
ENSDART00000061745 | Essential Splice Site | 275 | 940 | 9 | 22 |
ENSDART00000100762 | Essential Splice Site | 266 | 917 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 14138266)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 14098228 |
GRCz11 | 6 | 14227665 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATGTCTGATGAGAGTGTCTTGACATAATTTTGTGTTGTGATGCTGGTA[G/A]GGTATCTGAGCTGGAGGAGTTGGGAGAATTATCCCCATGTTGGGAGAATC
Long Flanking Sequence:
CAATTGAACAATTGAACAGTTGAAGCTTTGCAATTAAATAATAGAACAATTGAAGCTTCGCAAAATGAAGCACATACTTGGCACACCAGGTAAACATACATTAGAATTGACTTGTTTAAAAATATTGCAATTTTTAAATTAAACATATAATCTATAAGTGCTTTTAGCTTATTATAAGTTTAAGTGTCTGCATAATATGCATTCTTTTATACTTTTTAAGGCTTTTATATATTGTTTGTTCCATAGTGGGCACTTCTAAAATGTCCAATAAGATACTAATCCCTATTATTAACTATTATTTCTTTTCAATTAACAAATGTCTTATTAAAACCTATACAAACTTGTAAAACTGATCTGAGATCAGGTATAAACTATGAAACCTGATTTGCCACTGGGGTGAAAATGAACAAACTAGTGTTTATAGATAGTTTTCTAATTTTGATCTCCACTGAATGTCTGATGAGAGTGTCTTGACATAATTTTGTGTTGTGATGCTGGTA[G/A]GGTATCTGAGCTGGAGGAGTTGGGAGAATTATCCCCATGTTGGGAGAATCTCAGGCGGCAGATTGTAACACAGTACCAGAGCATCCTTCTGTCCTATCAGGACACACGGTCAGACCTGCAGGACTACAAAGGTCAGTCTGTACTTTAAGTTTGCCGGAGGTGTTTCTGTTTTGTTATACATAAATCTCTTCAGAAGCTTCAGATATTCAGTACTTAAGCACAAGATCTATGAAAACAGAAACATATGATGAATGAGCTTCAAAGATGTTAGACTACATTAATTGTCTGTCTGGGATTTAAAGTTTGATTTAGGATTTCTAAACAAATTAGCTTTTTAAATAAAAAAGGGACGTAAATTCTAATTTTGCACTACTTTATTGCCAATAGTGAAATAGTTACTTGATCTAGCTTGATTGATATAATAATTATTATCATCAATACCTAAACTAATCACTACCCTAATAACTTTTAATAAACTGCAAATTATGAGTTTATTAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8633
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061745 | Nonsense | 527 | 940 | 13 | 22 |
ENSDART00000100762 | Nonsense | 516 | 917 | 13 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 14120225)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 14080187 |
GRCz11 | 6 | 14209624 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YGGCAGCAACAGCCGTTCATCCCTCCATGTTGATTGGCATGAGGAAGAGT[G/A]GGTAAGAAAAYWTCTCTTAKATTTTTATTTTAATTACAATATTTTAWTAM
Long Flanking Sequence:
AGACAAAACCTTCCTGGCCAAAATCCCAGGCACATAGTTTGATTGTTTTGTGTTACATAAACATGATCAAACTTTTAGATTTTCTCTATGGTGCTGTAACCTAAAGATGCTCAAGTTCTGGTACTCATGCAACTGATAGTGAACTGCCATCTGCTCATCTGCATTCTAGGGAGAGGCTTACTGATAGCTCAATTTTGAGTTGTTTTTTTTTTTTTTTTTTTTTTTTACTTGTCCCCAGCGTGGTCTTTGGCTGAAACTATAATCTGTTTTTCTCACTCACTTTCAGACTCGACAGCTAGTGACGGTGTGTGACTGTAAACTGCTGGCGTCTGCAGTGCAGGCCCTGAACGCAGCAAGACCTGAGTACATCGCCTCGAAAAACTCACCCTCGGCTGACTCAGAGCAGGTGGTGCTGAGGAACGATCAAGACACACTGCTGGCCAAATGGAGTGGCAGCAACAGCCGTTCATCCCTCCATGTTGATTGGCATGAGGAAGAGT[G/A]GGTAAGAAAACATCTCTTAGATTTTTATTTTAATTACAATATTTTATTACTGTGACAATGTAAATTAATACAATTTAAAATCGCATATTCTATTTTATTTTATTATGTTTGTATGGTTTAAAGTGAATTTAAGAACTGTTATTGCATTATTAAAGTATTATTTCCCATCCCTGAATACATACTGTACATACATACATACATACATACATACATACATACATACATACATAAACACATACATACATACATACATAGATATTTTTTGGGGACTTCCCAATAGACAAATGTATTTTTATTCTGTATAAAGTCTATATTCTATCCCCTTCCCAAGTCGTTCACAAAGTTGGGGGTATGCTCTTTATACAAATCGTGTCTTTTCTACAGGAAAAGGTGTGGGGCAATGTGGACAAGAGTCTGGAGTGTATAATCCAGCGAGTGGACAAGCTGCTGCAGAGAGAGCGTCTGCACAGCAGCAGCAGTGAGGACATGTTCCAGTCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10195
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 |
---|---|---|---|---|---|
ENSDART00000061745 | Nonsense | 668 | 940 | 17 | 22 |
ENSDART00000100762 | Nonsense | 645 | 917 | 16 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 14104945)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 14064907 |
GRCz11 | 6 | 14194344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTCATTATCAAGCTGAGAAACTGTCTCCGTGATGATGGTTTTCTAAGA[C/T]AGCTTTAYACCATYGGCCTGYTCGCTCAGTTTGAGTGTCTRTTGAGTACC
Long Flanking Sequence:
TCTGTCATCATTTTTCCTGTTAAAACTCATACAGTAAGTGTTTAAAGCAGCTTTGGACATATGCTTTTAAGCTTTCTAAGTGAATATACATTTGCATGTCAACTTAACCAGAGATAAAAATGTTCTGTTAGTCAATAATGATAAACATAAATTGTGTTAAAAGCAAAAATAGTCAATGTCTTGGGTGGATTATTGTTATTTCTATTGTTATCCACTAGTATATGCAATCTATATAGTATATGTAATCTATTAGGTTGTCCACTTATGTAGAGTTTTTAAATGCACAGGTTTTTTCCATGCAATGACAATTCATACAGAATTAGAATGACATATTGAATATGTAATTATAAATGTTTTGGGTGAACTATCCAAACCAATTTTCATTTAATTCTAACGTGTATTCTGTTTCTTATCTTTTTGTGTCTTTTAAGCTCACAGCGCTAATTTGTGGCTTCATTATCAAGCTGAGAAACTGTCTCCGTGATGATGGTTTTCTAAGA[C/T]AGCTTTACACCATCGGCCTGCTCGCTCAGTTTGAGTGTCTATTGAGTACCTACGGTAAACCTACTCTCACAAATATGCTCATTCTTTGCTCCTGAATATGCAGTATTTACTAAATTAAACCACTTATGTTATTAAAAACATATATGTAGGACATACAGTTGAAGTCAGAAATATTACCCCCTTGATATATATATATATATATATATATATATATATATATATTTCCCTATTTTCTGTTTTAACAAATTTCTAAACATAATGGTTTTAATAACTAATTTCTAATACTTTACTAGATATTTTTTCAAGAAACCAATATTCAGCTTAAAGCAGGGGTCTCAAACTGCCATTTACGGTCCACCCTCCTCCTCCCTCTGGCTGGCAACTGATGTCAAAAACATAACGACATTCGCCCCACCAAAACATATATTTTAGAACCTCGATCATTATTTTGCAGTCACATCTATCCGCTTGTGGTTTTGACCCTCCAACTAGTCGACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33832
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 |
---|---|---|---|---|---|
ENSDART00000061745 | Nonsense | 854 | 940 | 21 | 22 |
ENSDART00000100762 | Nonsense | 831 | 917 | 20 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 14098904)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 14058866 |
GRCz11 | 6 | 14188303 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATATTTGTGCCTCTACATGCTCAGATTTGCCGACGACTGAACGGAGTG[C/T]GATTCACCAGCTGCAAAAGTGCCAAGGACCGCACTGCCATGTCAGTAACC
Long Flanking Sequence:
ATTTTCAGTAATTTTACAGACTTCTCTATATATCATTTATCATAGCTTATATTCTTTTAAACTACTAAAATGTCGATAAAAGTCACTTTGTTCAACTGTAGAGTTAAATTTTCAAGATCAAAACTCAACAGAGCACGAATCAGGGTTCCGTAATGCAATTCACAACCTGAAATGAATAGAAAACACTTGTGAAACACAAAATACAGAAACTTAATTAACAGATATGTTTTACAGTATAAATGGTACACCCATTTAATTTGCAGCATATTCTGTAAGCTGAAAAAACAATCACAGCAGACAGTGAATTACTGGGTTACTTAGTTCACACATAATAACAACATACAGGTTTAAAAATATTATTATTGTTTTTATTATTATTATTATTATTATTATTCATCACAGTAACAACTGAATTGGCATATAGGAGCATGAACAAAATTGGTTTTAAATCAATATTTGTGCCTCTACATGCTCAGATTTGCCGACGACTGAACGGAGTG[C/T]GATTCACCAGCTGCAAAAGTGCCAAGGACCGCACTGCCATGTCAGTAACCCTGGAGCAGTGTCTGATCCTGCAGCACGAGCATGGCATGGCCCCGCAGGTCTTCACACAGGCCCTCGACTGCATGCGCAGGTAAGAAACCTCAACAACTGCCTGTTTATAAGCACTGCACGCTTTGGGGATGTGCCTCTTTTTTTCATTCTCATTTAAATGCATCATCCTTCATTGCTTGCTGCTTTTTGGTGTTTTAGTAGGTTTTTATTGCTCTGTGCTTCATTCAGCCTTATAAGTTTGCTCATTTGTTTACTGGTTTCGTTTGCTCCTTCATACTTCATCCTTTCATCTCCTCTCTCCACGCTCTACTAGAGACACAAATGCAAATAAATGGCTCCTGTAGAGTGTGAGGAAGCTGCTGAAACTTGGATCCGCTGATTTTGTTTTGCTTGCCAGATGTTCTGTGCTTATAAATAAGAGTTTGAACTGTCAGGTTTTGTGCCGTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20671
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 |
---|---|---|---|---|---|
ENSDART00000061745 | Nonsense | 911 | 940 | 22 | 22 |
ENSDART00000100762 | Nonsense | 888 | 917 | 21 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 14084260)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 14044222 |
GRCz11 | 6 | 14173659 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCCCAGCGAGGGCTGCCGTCGCGAGAATACCACGAAGAACGTTGGATG[T/A]CGCAAGTATGCCTTTAACTGTCTGCAGCTGAAGGCTTTTCCTAAACATTA
Long Flanking Sequence:
ATCAATTCATATGTATAAAACATTTGAAAATGCACTGTTCGAATCTCAAAAAGAGGGCAGATGGTCAAAAGTAATTATTATACAGCCGATGTAGCCTGCTAATCTTATTTCTTTCTCTTTTGTCACATTTCTGTCAAATGATTTGCTTCAGAGCTTTGACTGCATCTATGCTACCCAAAAAATGCAGGACTTTTAGTGAGCCTCTTTGCTTATAGCAATGCTGCGTTAGCATTTTCAGCTTGTTTTAGCTGTGTTATGACATTGTTTGCTTGTTTGTTTGTTTACGCTTTTTTTATTTTTGAATGGTGACTGGCTTCCGCCACCCTCATACCCTGTTCACCGATGATACTCATGCTCATTACACTGCTGAAATGTCTTTTGTGGCTGTGCTAATTTTTGCCTGTGGTTTTTCTAAACATGGCTTCATGTTCTGTTTGTTTTCACTCACTCAATCCCAGCGAGGGCTGCCGTCGCGAGAATACCACGAAGAACGTTGGATG[T/A]CGCAAGTATGCCTTTAACTGTCTGCAGCTGAAGGCTTTTCCTAAACATTACAGACCTCCTGATGGCACTTTCGGAAAAGTGGAGACTTGATGAGACTGACATGATACGGAAATATTAGTAATTATGAAGCTTCTTCAAACTAAGTACAGTAAATCTGCTCAATTTGCTCTGAAGATAATCGCATATTTACACTTCAGGCGTGCGTTTGAAGTGAAAATGCTGACTGCACTGAATTGTATCAATAGATACAGTTCTATTTCATAAGCTCAGTATCACCAAACATATTTATTACATGTAATGCTGTATTTTAGCGTATTGTAGTTCACGGTGAAGGATTTAATCACTGTCAATATTGTATTTAGCAATCTTGGCCCTTTAGAGTGCAAATAGAGGGTTTAGACCTTTATGCTGAATATAATCATGCAGTATTGACTATCTATTGCAAAGATTTGTGTTTAGTATCCTAAAGAAATAGTTCACCCAACTATGAAAAATTGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18836
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 |
---|---|---|---|---|---|
ENSDART00000061745 | Nonsense | 920 | 940 | 22 | 22 |
ENSDART00000100762 | Nonsense | 897 | 917 | 21 | 21 |
ENSDART00000061745 | Nonsense | 920 | 940 | 22 | 22 |
ENSDART00000100762 | Nonsense | 897 | 917 | 21 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 14084235)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 14044197 |
GRCz11 | 6 | 14173634 |
KASP Assay ID:
2259-7328.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAATACCACGAAGAACGTTGGATGTCGCAAGTATGCCTTTAACTGTCTG[C/T]AGCTGAAGGCTTTTCCTAAACATTACAGACCTCCTGATGGCACTTTCGGA
Long Flanking Sequence:
GAAAATGCACTGTTCGAATCTCAAAAAGAGGGCAGATGGTCAAAAGTAATTATTATACAGCCGATGTAGCCTGCTAATCTTATTTCTTTCTCTTTTGTCACATTTCTGTCAAATGATTTGCTTCAGAGCTTTGACTGCATCTATGCTACCCAAAAAATGCAGGACTTTTAGTGAGCCTCTTTGCTTATAGCAATGCTGCGTTAGCATTTTCAGCTTGTTTTAGCTGTGTTATGACATTGTTTGCTTGTTTGTTTGTTTACGCTTTTTTTATTTTTGAATGGTGACTGGCTTCCGCCACCCTCATACCCTGTTCACCGATGATACTCATGCTCATTACACTGCTGAAATGTCTTTTGTGGCTGTGCTAATTTTTGCCTGTGGTTTTTCTAAACATGGCTTCATGTTCTGTTTGTTTTCACTCACTCAATCCCAGCGAGGGCTGCCGTCGCGAGAATACCACGAAGAACGTTGGATGTCGCAAGTATGCCTTTAACTGTCTG[C/T]AGCTGAAGGCTTTTCCTAAACATTACAGACCTCCTGATGGCACTTTCGGAAAAGTGGAGACTTGATGAGACTGACATGATACGGAAATATTAGTAATTATGAAGCTTCTTCAAACTAAGTACAGTAAATCTGCTCAATTTGCTCTGAAGATAATCGCATATTTACACTTCAGGCGTGCGTTTGAAGTGAAAATGCTGACTGCACTGAATTGTATCAATAGATACAGTTCTATTTCATAAGCTCAGTATCACCAAACATATTTATTACATGTAATGCTGTATTTTAGCGTATTGTAGTTCACGGTGAAGGATTTAATCACTGTCAATATTGTATTTAGCAATCTTGGCCCTTTAGAGTGCAAATAGAGGGTTTAGACCTTTATGCTGAATATAATCATGCAGTATTGACTATCTATTGCAAAGATTTGTGTTTAGTATCCTAAAGAAATAGTTCACCCAACTATGAAAAATTGCTGGTTATTTATCCAGGTCATCTAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10910
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 |
---|---|---|---|---|---|
ENSDART00000061745 | Nonsense | 920 | 940 | 22 | 22 |
ENSDART00000100762 | Nonsense | 897 | 917 | 21 | 21 |
ENSDART00000061745 | Nonsense | 920 | 940 | 22 | 22 |
ENSDART00000100762 | Nonsense | 897 | 917 | 21 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 14084235)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 14044197 |
GRCz11 | 6 | 14173634 |
KASP Assay ID:
2259-7328.1 (used for ordering genotyping assays)
KASP Sequence:
AGAATACCACGAAGAACGTTGGATGTCGCAARTATGCCTTTAAYTGTCTG[C/T]AGCTGAAGGYTTTTCCTAAACATTACAGACCTCCYGAYGGCACTTTYGGA
Long Flanking Sequence:
GAAAATGCACTGTTCGAATCTCAAAAAGAGGGCAGATGGTCAAAAGTAATTATTATACAGCCGATGTAGCCTGCTAATCTTATTTCTTTCTCTTTTGTCACATTTCTGTCAAATGATTTGCTTCAGAGCTTTGACTGCATCTATGCTACCCAAAAAATGCAGGACTTTTAGTGAGCCTCTTTGCTTATAGCAATGCTGCGTTAGCATTTTCAGCTTGTTTTAGCTGTGTTATGACATTGTTTGCTTGTTTGTTTGTTTACGCTTTTTTTATTTTTGAATGGTGACTGGCTTCCGCCACCCTCATACCCTGTTCACCGATGATACTCATGCTCATTACACTGCTGAAATGTCTTTTGTGGCTGTGCTAATTTTTGCCTGTGGTTTTTCTAAACATGGCTTCATGTTCTGTTTGTTTTCACTCACTCAATCCCAGCGAGGGCTGCCGTCGCGAGAATACCACGAAGAACGTTGGATGTCGCAAGTATGCCTTTAACTGTCTG[C/T]AGCTGAAGGCTTTTCCTAAACATTACAGACCTCCTGATGGCACTTTCGGAAAAGTGGAGACTTGATGAGACTGACATGATACGGAAATATTAGTAATTATGAAGCTTCTTCAAACTAAGTACAGTAAATCTGCTCAATTTGCTCTGAAGATAATCGCATATTTACACTTCAGGCGTGCGTTTGAAGTGAAAATGCTGACTGCACTGAATTGTATCAATAGATACAGTTCTATTTCATAAGCTCAGTATCACCAAACATATTTATTACATGTAATGCTGTATTTTAGCGTATTGTAGTTCACGGTGAAGGATTTAATCACTGTCAATATTGTATTTAGCAATCTTGGCCCTTTAGAGTGCAAATAGAGGGTTTAGACCTTTATGCTGAATATAATCATGCAGTATTGACTATCTATTGCAAAGATTTGTGTTTAGTATCCTAAAGAAATAGTTCACCCAACTATGAAAAATTGCTGGTTATTTATCCAGGTCATCTAAGAT
Associated Phenotype:
Not determined