ZMP
zgc:158331
Ensembl ID:
ZFIN ID:
Description:
inositol polyphosphate multikinase [Source:RefSeq peptide;Acc:NP_001073533]
Human Orthologue:
IPMK
Human Description:
inositol polyphosphate multikinase [Source:HGNC Symbol;Acc:20739]
Mouse Orthologue:
Ipmk
Mouse Description:
inositol polyphosphate multikinase Gene [Source:MGI Symbol;Acc:MGI:1916968]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27886 | Missense | Mutation detected in F1 DNA | Not yet available |
sa5850 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6234 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa27886
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000048866 | Missense | 54 | 372 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 7906506)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 7201092 |
GRCz11 | 12 | 7234595 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGTGCCGCTCTCTCACCAGGTGGCCGGACACAAGTATGGCGTTGATAAA[G/A]TGGGTCAGTACACCTTTCATGTCATTCATTTTCATTCTGTTATTCAAAAA
Long Flanking Sequence:
GAATCGTTTGCAGGACGGCGAGTTCCCGTGCGATATGACTAACTCCGCCAGTATATCGTGTCGATCTTTGTCCTCTGCTCGTTCCGTATCTGCCATCTCCTACCAATTACCGCGGGCGGAGTGTAAACATCTCTGAAGCCAGGAAGTGGGATGTGGCCCAGGTGAAAAGCTCGTTATATGGTCGCGAGCGTGGGCGCCGTGACTGATGGCACGCGATCGGGCACACGCACATCAGGATGACGCGTCGAGGCTGTGCGGTCAATATGTGATTTTGTGCGCGGACAGCGGTCTAGAGAATTAAAGAGCCCTTGCAGAAAAGTCTCTGTCAGCTCGGCATCATAATGGACTCGTCCGTGGCGCTGGGGAGGCTGGAGCTCGCGTGCCCGCGCTCGGTTGTGACCCGCGGCTCGTGTTTACCGGAGGGCGCGCAGAGCTCTCACCTGAACGGCTGCGTGCCGCTCTCTCACCAGGTGGCCGGACACAAGTATGGCGTTGATAAA[G/A]TGGGTCAGTACACCTTTCATGTCATTCATTTTCATTCTGTTATTCAAAAAGCGGGCCTGGTTGTCACAGTTATAATTCTAGTGAGATTTAAAGGGGTAGTTCACTCCAAAATGAAATATACTTACTTTTGAATGCCTCCAAACCTGTTTGAGTTTCTTTCTTTTTTTAGCAGATATTATAAAAATGTTCATACTTAAACGATATTGTCAAGAAAGCTGAAAACTATTGACATCCATAATAAGACAAACAAATACGAAAATCAATGGTTACAAGTTTTCAGCTTTCTTCAGAGTATCTTATTTTATGTTTAACAAATAAAAGAATCTCAAACAGGTTTGGATCAAGTATAAGTACATTTAGAGATGATTCTTTTACGATTTTTTTATTTGTCATATAAATGGCTATATAATATATATAACCAACCTATGAAATAAGTCACATCCACTCCATGAATGATGCAATTATTTATAAAGTGCAGATGTAAACACAGGGATGAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5850
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 |
---|---|---|---|---|---|
ENSDART00000048866 | Nonsense | 273 | 372 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 7871459)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 7166045 |
GRCz11 | 12 | 7199548 |
KASP Assay ID:
554-3698.1 (used for ordering genotyping assays)
KASP Sequence:
CCGGATCCCAGAGCCTTCCGGAAAGCCYGATCAAACCTGAGAYCTGCGAG[C/T]AGAACAACAACATCTCCACCATGTACTCCCTGCACAAGAAAAGCTGCGTC
Long Flanking Sequence:
ATCTAAAACGCTTTTAGTGTCAGGTATTTGGAGTTTGAGAACATGCAAACTCCACACAGAAATGCCAACTGGCCCAGCTGGGGCTCAAACCAGCAACCTTCTGGCTGTGAGACAACGGTGCTAACCACTGTGCCACTGTGTCCCATTAATAACTTAATTCCTCGAGTAATTTTTTGCGTGTACTAGTGTAATTTTGTCCTGAACTGCATGCAGATAGCTGGTCTGAATTAGTGGTCTCAGTATAGAGCTTTAAATGATATTACAAGCACCATCCTCATCCCGCAGGTCTATCCAAGTTCTTCTACAATGGTGAAACTCTCCGCAAAGACGCCATCACTGCCAGCATCCTCAAAGTCCAGAAGATCCTACAATGGTTCGAAGGCCAGAGTCGGTTCAACTTTTATGCAAGCTCTCTTCTCTTCGTGTACGAGGGCGTCTGCGCGCCAAATCCCGGATCCCAGAGCCTTCCGGAAAGCCCGATCAAACCTGAGACCTGCGAG[C/T]AGAACAACAACATCTCCACCATGTACTCCCTGCACAAGAAAAGCTGCGTCCGGAGCCACTACCAAACCAATCAGGACAACGGCGTCTGGAGCTCCTCGCAGCAGCCCAACGGAAACTGCAGCCTGGCAAGACTGGAAGAGGAGCAAAAAGAGACCAAAAATGAAGCAGCAGCGGACACGGTTAGTGACGTGGAGGTTAAGATGATCGACTTTGCACATGTCTTCCCTAGTGACGTTCCCGACCAGGGATACATCTACGGCCTGAAGAACCTCCTGAAGGTCCTACATCAGATTCTGGAGTGAAGGTATGGGTGGTCTTGGTTGTGTCTGTTTATCCGCCTCTCTCTAAATCTGCACTACCTACAGCGTCAGTGGAGTAACCTGTTTGTAATCCATCGTCTACAATGTATGTGCTTTAGTCTTTTAAAAGCTTTGTACAGTTTGTTATGATATCTTACTCAGGTAAATGAATCTATAGTGCTTGTACGTTTATCCCGACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6234
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 |
---|---|---|---|---|---|
ENSDART00000048866 | Nonsense | 297 | 372 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 7871387)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 7165973 |
GRCz11 | 12 | 7199476 |
KASP Assay ID:
554-4315.1 (used for ordering genotyping assays)
KASP Sequence:
TGTACTCCCTGCACAAGAAAAGCTGCGTCCGGAGCCACTACCAAACCAAT[C/T]AGGACAACGGCGTCTGGAGCTCCTCGCARCAGCCCAACGGAAACTGCAGC
Long Flanking Sequence:
CCCAGCTGGGGCTCAAACCAGCAACCTTCTGGCTGTGAGACAACGGTGCTAACCACTGTGCCACTGTGTCCCATTAATAACTTAATTCCTCGAGTAATTTTTTGCGTGTACTAGTGTAATTTTGTCCTGAACTGCATGCAGATAGCTGGTCTGAATTAGTGGTCTCAGTATAGAGCTTTAAATGATATTACAAGCACCATCCTCATCCCGCAGGTCTATCCAAGTTCTTCTACAATGGTGAAACTCTCCGCAAAGACGCCATCACTGCCAGCATCCTCAAAGTCCAGAAGATCCTACAATGGTTCGAAGGCCAGAGTCGGTTCAACTTTTATGCAAGCTCTCTTCTCTTCGTGTACGAGGGCGTCTGCGCGCCAAATCCCGGATCCCAGAGCCTTCCGGAAAGCCCGATCAAACCTGAGACCTGCGAGCAGAACAACAACATCTCCACCATGTACTCCCTGCACAAGAAAAGCTGCGTCCGGAGCCACTACCAAACCAAT[C/T]AGGACAACGGCGTCTGGAGCTCCTCGCAGCAGCCCAACGGAAACTGCAGCCTGGCAAGACTGGAAGAGGAGCAAAAAGAGACCAAAAATGAAGCAGCAGCGGACACGGTTAGTGACGTGGAGGTTAAGATGATCGACTTTGCACATGTCTTCCCTAGTGACGTTCCCGACCAGGGATACATCTACGGCCTGAAGAACCTCCTGAAGGTCCTACATCAGATTCTGGAGTGAAGGTATGGGTGGTCTTGGTTGTGTCTGTTTATCCGCCTCTCTCTAAATCTGCACTACCTACAGCGTCAGTGGAGTAACCTGTTTGTAATCCATCGTCTACAATGTATGTGCTTTAGTCTTTTAAAAGCTTTGTACAGTTTGTTATGATATCTTACTCAGGTAAATGAATCTATAGTGCTTGTACGTTTATCCCGACTAAAGAAGAATATCGAAACACTCTAATGATATTATGCCTCAGATGTTACAGAGCAGTTCCTGTTTCCAGAGCCA
Associated Phenotype:
Not determined