ZMP
si:ch211-236d22.1
Ensembl ID:
ZFIN ID:
Description:
type II inositol-3,4-bisphosphate 4-phosphatase [Source:RefSeq peptide;Acc:NP_001139046]
Human Orthologue:
INPP4B
Human Description:
inositol polyphosphate-4-phosphatase, type II, 105kDa [Source:HGNC Symbol;Acc:6075]
Mouse Orthologue:
Inpp4b
Mouse Description:
inositol polyphosphate-4-phosphatase, type II Gene [Source:MGI Symbol;Acc:MGI:2158925]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19605 | Nonsense | Available for shipment | Available now |
| sa18139 | Essential Splice Site | Available for shipment | Available now |
| sa31235 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19605
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 |
|---|---|---|---|---|---|
| ENSDART00000108492 | Nonsense | 551 | 760 | 13 | 17 |
| ENSDART00000147683 | Nonsense | 618 | 827 | 16 | 20 |
The following transcripts of ENSDARG00000075201 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 53691681)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 52561252 |
| GRCz11 | 1 | 53195990 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATTGATGCTGTGTGGAAATGTGACCTGTTTTAATGGCAGAGACCGTTA[C/A]ACTGTGGAGGTGCCTCTGCCACATGATGCCTTCCAGACGCTGCCGGATGA
Long Flanking Sequence:
TGAGATATGAAAAAGTATACACAGCGCCCTCTGGTGGATTTACAAAAACTGCAAAAAAAAAATCCTCCTGGGATGTATTGGGCGCTCTCCAGAAATGTATATAGGGGTACATAATCAGAATGAGCCTGGGATGACCAAAACACCTAATTACGATTAATTAGGTGTTTTGGTCATCCCAGGCTCATTCTGATTATGTACCCCTATATACATTTCTGGAGAGCTACCAAACAGTTTTTCATCAAAGCAACAAAATGCACACTTAATCATGAAAGCATCCAACATTAATCACCAAAGCATCACAACACACAATTAACCACATAATCACAATTATTTCATAGACAATTGATCGTCTGCCAGATTTCCTTTTGGACAGTCCTAATTGCTGATATGCATGCAGTCTAAAACGAGTATCAACAGAAAAGCAGCTACTGTGTGAACCTGTGCGTGATAGTATTGATGCTGTGTGGAAATGTGACCTGTTTTAATGGCAGAGACCGTTA[C/A]ACTGTGGAGGTGCCTCTGCCACATGATGCCTTCCAGACGCTGCCGGATGAGCTGCGCCAGGGCAAGCTGCTACACGTCATCCCTGTGCTCTTCAATGTGGGCATCAACGAACAACAGACCATCGCTGAGAGGTACAGATGGTCTTTACATGTTATAGTACATAGCTCAATTAACGTCATTACGTCACCATTCGATGCTAGTTTCAAGCAATGCTAACAGTTTGTGTTCGTCATGGCATCATATGTGATTTACATTTAGTCTTTTAGCACAGAGGTTCTCAAAGTGGGGGTCAGGACCCCGAAGGGGTCGCCGGACAATGAGGGGGGCCGGGGGTGGGTGGGTTTATAATTGTCTGGTGGTTTCCAAAAATCTATTTATTTTTAAGAATTGCCATATTTTATCCATAACCTACTGAAAAGAAAAAATATTCGTTTATAGTTACTATATACTATATAGTTACTATAGTAGCTTATAGTTACTAGTTCTATTGGATTGCGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18139
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 |
|---|---|---|---|---|---|
| ENSDART00000108492 | Essential Splice Site | 665 | 760 | 15 | 17 |
| ENSDART00000147683 | Essential Splice Site | 732 | 827 | 18 | 20 |
The following transcripts of ENSDARG00000075201 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 53697716)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 52567287 |
| GRCz11 | 1 | 53202025 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGACCAAGAAGAGGAAGAACRTGGAGATATTGTGGCTTGCAGGAACGG[T/A]GAGAGTTTGAGGAGTCTGTGCAGGAANNGTGTGTGTGTGCAAGATCTTTCAC
Long Flanking Sequence:
CTTCTACAATTGCAGGATTTCGTTCTTTAGCCCTCTTTTTTATTCATGCAACACGTCCGCATGCGTCTCCTTCTCAGTGTTTAATGCTGAGCATATCGCCTCATATTTCAAGGATTCGAGTGCAGGAATTTGTTTCTCTGATATGTCAATCACGTCTGCAGAGCGTGACGGCTTCAGATGATGAATGATCCCAGCAGACGAATGCCAAACTGCATCTCAGCATGTCACATCTTGTCTTCCATCCATCTCCCTGTTTATCAGAAAAAATGTCCCTAGACTTTTTCCCATCTGATCTTTAGTACTCGTCTATACAGAGACAAAACAAGGCCTAAGCCGCAAATGCATGACATGTCAAGTGTTTCTCTCTTCTGTCTTCTGTTCAAAAGGTCTGCCGAGTTTTCAGACGCAGACGGACATTAAGGAGCTGCTGGAAACGCTCGGACAGAATGTAGTGACCAAGAAGAGGAAGAACGTGGAGATATTGTGGCTTGCAGGAACGG[T/A]GAGAGTTTGAGGAGTCTGTGCAGGAAGTGTGTGTGTGCAAGATCTTTCACAACCTCGCATTTGCAAAATGCTTGCAGGATCAGTGTGATGAATTAACATTGTCATCAAAGTTCAGAATGTTCGCTTTTTAGTCGTTTGTTTGTCCTCTGGGCATTCACGTTTGAGCAGAACATCCATCTTATTATTCTGCATGCATTAAAGCAGGGGTCTTGAACTCAAATCGGCTGGGGGATAATAATCACGGTGCTCAATTCAATTACTATTAGGGATGCACCGATACGCCAGCGATGCGGTGGCGCAGTAGGTATTGTTGTCGCCTCACAGCAAGAAGGTCACTAGGTCGATGGTTCGAACCTAGGCTCAGTTACTGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGTTCGCGTGGGTTTCCTCCGGGCGCTCCGGTTTCTCCCACAGTCCAAAGACATGCGGCACAGGTGAATTGGGTAGGCTAAATTGTCCGCAGCGTATGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31235
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 |
|---|---|---|---|---|---|
| ENSDART00000108492 | Nonsense | 667 | 760 | 16 | 17 |
| ENSDART00000147683 | Nonsense | 734 | 827 | 19 | 20 |
The following transcripts of ENSDARG00000075201 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 53704252)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 52573823 |
| GRCz11 | 1 | 53208561 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAAGAGAAAGTGTACTCAATGGTCTGTCTGTGTGTGTTGTCAGATCTG[T/A]CGACGGATGAATGGTATCCGCTTCACCAGCTGTAAAAGTGCCAAAGACCG
Long Flanking Sequence:
AAAATAAATAAAGTAAAAGTTTGGTCGGATTGGTTGGTCGGTCAGTCAGTCATTCAGTCCGTCAGCAACAGCAGCCTCTGGTGGATATACAAGAGAACTGCAGGCATGAATGGAACTCACGAGAGAAATTCAAAATCTTAAAAAGCATGCACAGCGCCCTCTGGTGGATTTGTAAAAATAAAAACTACAAAAAAAAAGTACCTTCTGGGATATATTTGGCGCTCTCAAGAAATATATATAGAGGTACGTAATCAGAATAAACCTGAGTTTAAAAAAAAATTAAAAATGAGTACTATAATTTTACTTTTAACAAAAAAATTTCATTTTCGTCAGGGTAGTAAATGCAGTTGTACAAATAGAAGTCAATGCGCCCAGTGAGCCCAATATAATCATAAAAAAGCATGATTCATTTATGCAAGGGCATGAGCTCAAACTCTAAACACCATATTGAGAAAGAGAAAGTGTACTCAATGGTCTGTCTGTGTGTGTTGTCAGATCTG[T/A]CGACGGATGAATGGTATCCGCTTCACCAGCTGTAAAAGTGCCAAAGACCGGACGTCAATGTCGGTGACGCTGGAGCAGTGCTGTCTGCTGCGGGACGAGCATCAGCTCAATAAAGACTACTTTGTGCGCGCTTTGGACTGCATGAGGAGGTAAGAGGAGTCCACATCCATCATTCCTCCAGCATGCATAAGTACATTCAACTTAAACCCTTCACTATACAAGTGCATCTGGTCAGACTGGGTTTTTCACAGATGAAAGCCATTTAAAGGGACTGTTCACCCCAAAATGACAATTTGTTTATTATTTACTCATCCTCAAGTGGTTATAAATCTTTATGAGTTTCTTTCTTCTATTGAACTCAAAAGGAGATATTTTGAATAAAGCTGAAAACCTGTAACTGCTGACTTCAATAGTAGGAAAAACAAAGGAAGTCAATGGTTACAGGTTTTGAGGAAGTTTTCAGTACATCTGAAACAGAAGAAAGAAACTTTTAATGAGTT
Associated Phenotype:
Not determined