ZMP
inpp5ja
Ensembl ID:
ZFIN ID:
Human Orthologue:
INPP5J
Human Description:
inositol polyphosphate-5-phosphatase J [Source:HGNC Symbol;Acc:8956]
Mouse Orthologue:
Inpp5j
Mouse Description:
inositol polyphosphate 5-phosphatase J Gene [Source:MGI Symbol;Acc:MGI:2158663]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34839 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17484 | Essential Splice Site | Available for shipment | Available now |
sa34838 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34837 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30650 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34839
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 |
---|---|---|---|---|---|
ENSDART00000108588 | Nonsense | 53 | 789 | 1 | 12 |
ENSDART00000143215 | None | None | 399 | None | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 6894480)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 7907280 |
GRCz11 | 10 | 7865980 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCATCAAACTGCCAGATGGGCACAACTGGAAAGCCACCAATGTTGGAA[C/T]AGACCCCGGTGCCGCAAACAAACCCAGGCGTTAAGGAGAGAGCCAGACCA
Long Flanking Sequence:
TTTCATGTGGGGTAGTGCTGTTTTATAGGTAATCTGAGCCTTTTTTTTTTTTCCCTTTTACATTGTTCTGTGTTGTCATTATTTTTGTTGTTGTTGTGTGAGTATCTTTTGAAGAATTGTTGTTATTTCTGTATTATAGTGAAAATCCAATAAATATAATTATTAAAAAAAAAAAAATGCTGCTTTTAGTGGATGGCGTTGGGATGTTCGTTAACAGTACACTCTTTTATATTCAACACCATTTGTCATTAACTTATCAAATGTTGATTACCAGCACTAAACCTAAACTGTTCCTTTAACACCTTCATGCCTCTTTGTGTCATCCCTGCAGATAAATAAATCAAATGCAGCCCATTCAGAGCTGCTCAATGCCGGAAGGACCTGCTGGAGTCTTAGGACTCCATAAACCTCCAGTCCAAGCCCTGCTTGGAAAACCCTGCAAACTGCCCGTGTCATCAAACTGCCAGATGGGCACAACTGGAAAGCCACCAATGTTGGAA[C/T]AGACCCCGGTGCCGCAAACAAACCCAGGCGTTAAGGAGAGAGCCAGACCAGAGTCAACATCACAGTCCACAAACTACATCAGCATCAGTCGACCCAGGCCAACAGCACTGGGAACTAAAGCATCAATCAAAGTCTCAAGACCAACTGAGCCTTTACTGCAGGTTAAAGCTACAGGAATGGCCAATTTGCTGTCAATCTCCCCAACTGAATCACCATTGCCTTATTGCAACTCTCAAAAACCAACGAGCCCCACTTCTCAACTCGGATTCAATCCACCATCCATTCCACCAACACTTCCAAGCCCTCCAGCACAGCCCATCCGTGCAAACACACTAAATAACCTAATGCCCAAACCAGTCTCTAACTCAAACCCCAGCCCTCCACCTAACCCTGTTCATCAGCTGATCCAAAGTCAAGACGTACCCAATGCAGGAGACACAACTGACAAAAAACTGAACAAGGCTATCAACGAAGAGGGGGATTTCAGGTGAGACTTCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17484
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108588 | Essential Splice Site | 575 | 789 | 9 | 12 |
ENSDART00000143215 | Essential Splice Site | 346 | 399 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 6868523)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 7881323 |
GRCz11 | 10 | 7840023 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCACATGGCTTTCAGAGGARTTCATGGGACTGGGTGGGCCTGTACAAGG[T/A]AATCCATGGCATTTTCACGTAAACTACTAATCAAGTGGGTACAGGCTGTT
Long Flanking Sequence:
TGCAGTTACCAGGCTGTACCTGTTAAAAAGCTGTCTGCGGCTTTTTTTTTTTGTCTGCTCAACCACTCCCTCCTGGATTTTGTGGGAAAATCTCCTGTTTATTGCAGCCTAAAATGACTGATTTTATGACTAATTTCTGTGTTGAATTCAGTGATAGTTTTTGTATTTATTCTAGATCATAAAAGCTTTTTAATAAGTGAAAGTCAGAAAAGTCTGGTCATTTTACATTTGGTTTAAAGTGGTAAACCTAAATGTATTAAACTTGACTTTATTATGCATCTTGTTTACGGTAAATTTGTCAGATGTACAGCCAAAAGTACTGCATTAACACATTTTTGCACACTTTCTTTGTCCTGCTCAGTTTCCCTTTAAGGTGACCTTGCCATTAGTGACACTGGAAGTGGAGAAAGAATGGACCAAGTTCTCTGATGCAACAGTCAAACTCACAATGGCACATGGCTTTCAGAGGAGTTCATGGGACTGGGTGGGCCTGTACAAGG[T/A]AATCCATGGCATTTTCACGTAAACTACTAATCAAGTGGGTACAGGCTGTTAAAAATCAGATTAAGCTTTTTTTTTTACAAGGACAAATTGCACACATTATAATAATTAATCACCATGTGTTCTAACAGGTGCCATTAACTCTTTCAACTTTATTAAAGGTGTGTGTCATTTATATTCACCCAAAAATAATTGCTAAAATAAGGATCATATTCTCAGGAAACTCAAAATCGCAGTATTATTAACTTACACATTTTGCATCACCTTTTCATAAAAATACACTCTTAAAACTATTGGACAAAAATGTTTGACCAAAAACATCTCATAGAATTGAGATAAACCTTTCCGGGAAAGTTTCTTACTAGAACTATTTGCGGCTGCCCAATAAATATTATAATGTTTATATGAAACTTAATTATGTGATCTGACCAGTATCATGCTCTCTTTCACTTTCATTTACCTTACAGAAATCTATTTATGGTTGTTTTGTTGGTAATCTTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34838
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108588 | Nonsense | 657 | 789 | 12 | 12 |
ENSDART00000143215 | None | None | 399 | None | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 6860340)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 7873140 |
GRCz11 | 10 | 7831840 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCAGCACCAGCATGTCGTTCACGCTCTGATAGTTCGGATGTGAGCTCT[G/T]AAGATGACAGTACACTCGTCCTGTTGGCCCCGAGCTCACGCAGCCCCAGC
Long Flanking Sequence:
TCAAGCCAAGAGCAAAAGAAAAATATGGTTGAGTTCAAAACTGAGACCATACAAAGGTTGATTGCAGGTTAAAACAGAGGCAAGAAAAGCATTCTGACTCTAGAGCAAGACCAGAATGAACTCAATTATAGACCAAGTCTAGACCAGGAATTCCCAACCTTGATCCTAGAGGCCCTCTATGACCAAAGTTGCCCATCCCAGGTCTAGATCGAGACCAAATAAGGTTTAAGTCCAAATCTAGACCAAGACCAAAAAGGAGACAATTACAAGTCACAACAGAGACCAAAGCATGAAACCAATCTGTTAAAAAGTCAAATAGGTTTATTAACATAATTTTAGGTTTTATTTTTCTTTCACTGTACTGTTCCTGTTTAACTTGTATATATTCTTTGTCATATATTTTTGTCTCTACATATTTTTTCCCACAGGTGCAGTTGCCCATGTCCACTCCACCAGCACCAGCATGTCGTTCACGCTCTGATAGTTCGGATGTGAGCTCT[G/T]AAGATGACAGTACACTCGTCCTGTTGGCCCCGAGCTCACGCAGCCCCAGCCCTGGAAACCACAGCGGCAAACGCCACCACCACCAGAAGCGCCAGCGGAGCCGCAGTCCCGCTGTACCAGCACTTTCCGGCACGCCTCTTCCGTCCCTGCAGTCTCTCAGCCTGTGTCCTCGTCCCCGAGATGGCCCCCAAAAGACATCTTCCCCACGCCCTTCAACCAATGCCAAGAAGGAGCGTCTGGTTTCTCCGGACTCATTAACCTCACCCTCCCTCAGTCCTCTTAGTCCGAGGAGCCCAGGATCACCTGGAAATGGCATCAGTGCTCCAGAGGCTCTCGTAGCAGCCATTTTAGGAGAGCCCAGACCTGCTCAAATAGGAAAACCAGGTGATGTAATTCTATGACCTTCCTCGCTTGCGATTCATTTCTAGACTTTAGGAGATATCGCAATGCAACTACTTGAGCAAAATGGCCTGTTTCTTCAGTCGCTTTTCAGATCTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34837
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108588 | Nonsense | 680 | 789 | 12 | 12 |
ENSDART00000143215 | None | None | 399 | None | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 6860271)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 7873071 |
GRCz11 | 10 | 7831771 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGTTGGCCCCGAGCTCACGCAGCCCCAGCCCTGGAAACCACAGCGGC[A/T]AACGCCACCACCACCAGAAGCGCCAGCGGAGCCGCAGTCCCGCTGTACCA
Long Flanking Sequence:
TAAAACAGAGGCAAGAAAAGCATTCTGACTCTAGAGCAAGACCAGAATGAACTCAATTATAGACCAAGTCTAGACCAGGAATTCCCAACCTTGATCCTAGAGGCCCTCTATGACCAAAGTTGCCCATCCCAGGTCTAGATCGAGACCAAATAAGGTTTAAGTCCAAATCTAGACCAAGACCAAAAAGGAGACAATTACAAGTCACAACAGAGACCAAAGCATGAAACCAATCTGTTAAAAAGTCAAATAGGTTTATTAACATAATTTTAGGTTTTATTTTTCTTTCACTGTACTGTTCCTGTTTAACTTGTATATATTCTTTGTCATATATTTTTGTCTCTACATATTTTTTCCCACAGGTGCAGTTGCCCATGTCCACTCCACCAGCACCAGCATGTCGTTCACGCTCTGATAGTTCGGATGTGAGCTCTGAAGATGACAGTACACTCGTCCTGTTGGCCCCGAGCTCACGCAGCCCCAGCCCTGGAAACCACAGCGGC[A/T]AACGCCACCACCACCAGAAGCGCCAGCGGAGCCGCAGTCCCGCTGTACCAGCACTTTCCGGCACGCCTCTTCCGTCCCTGCAGTCTCTCAGCCTGTGTCCTCGTCCCCGAGATGGCCCCCAAAAGACATCTTCCCCACGCCCTTCAACCAATGCCAAGAAGGAGCGTCTGGTTTCTCCGGACTCATTAACCTCACCCTCCCTCAGTCCTCTTAGTCCGAGGAGCCCAGGATCACCTGGAAATGGCATCAGTGCTCCAGAGGCTCTCGTAGCAGCCATTTTAGGAGAGCCCAGACCTGCTCAAATAGGAAAACCAGGTGATGTAATTCTATGACCTTCCTCGCTTGCGATTCATTTCTAGACTTTAGGAGATATCGCAATGCAACTACTTGAGCAAAATGGCCTGTTTCTTCAGTCGCTTTTCAGATCTGCAGTTGTTCAGGGTCTCATACCTTGTTGTGCTTAATTGCTTCCCAAACCCTTCCTCTTCTTCAATGGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30650
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108588 | Nonsense | 742 | 789 | 12 | 12 |
ENSDART00000143215 | None | None | 399 | None | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 6860084)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 7872884 |
GRCz11 | 10 | 7831584 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGCCCTTCAACCAATGCCAAGAAGGAGCGTCTGGTTTCTCCGGACTCAT[T/G]AACCTCACCCTCCCTCAGTCCTCTTAGTCCGAGGAGCCCAGGATCACCTG
Long Flanking Sequence:
GAGACAATTACAAGTCACAACAGAGACCAAAGCATGAAACCAATCTGTTAAAAAGTCAAATAGGTTTATTAACATAATTTTAGGTTTTATTTTTCTTTCACTGTACTGTTCCTGTTTAACTTGTATATATTCTTTGTCATATATTTTTGTCTCTACATATTTTTTCCCACAGGTGCAGTTGCCCATGTCCACTCCACCAGCACCAGCATGTCGTTCACGCTCTGATAGTTCGGATGTGAGCTCTGAAGATGACAGTACACTCGTCCTGTTGGCCCCGAGCTCACGCAGCCCCAGCCCTGGAAACCACAGCGGCAAACGCCACCACCACCAGAAGCGCCAGCGGAGCCGCAGTCCCGCTGTACCAGCACTTTCCGGCACGCCTCTTCCGTCCCTGCAGTCTCTCAGCCTGTGTCCTCGTCCCCGAGATGGCCCCCAAAAGACATCTTCCCCACGCCCTTCAACCAATGCCAAGAAGGAGCGTCTGGTTTCTCCGGACTCAT[T/G]AACCTCACCCTCCCTCAGTCCTCTTAGTCCGAGGAGCCCAGGATCACCTGGAAATGGCATCAGTGCTCCAGAGGCTCTCGTAGCAGCCATTTTAGGAGAGCCCAGACCTGCTCAAATAGGAAAACCAGGTGATGTAATTCTATGACCTTCCTCGCTTGCGATTCATTTCTAGACTTTAGGAGATATCGCAATGCAACTACTTGAGCAAAATGGCCTGTTTCTTCAGTCGCTTTTCAGATCTGCAGTTGTTCAGGGTCTCATACCTTGTTGTGCTTAATTGCTTCCCAAACCCTTCCTCTTCTTCAATGGCTTTGCCAAAGTGGTTTATTTGTCTTTATATTTTGCATTATTTATAATAGATTGTAAATGGTGACAGTTCTACAGTGCACATCAGCCTTATAGTGCAGGACAACCTAACCCAAGGTGAAACTGTCCTGTAATCGTAGACTTCAAACAAACAGTGATGTCAGCAGTCATTTCAGCCTATACCGTAACTAGTG
Associated Phenotype:
Not determined