ZMP
si:ch211-196f5.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to mouse and human importin 4 (IPO4) [Source:UniProtKB/TrEMBL;Acc:Q5RIS6]
Human Orthologue:
IPO4
Human Description:
importin 4 [Source:HGNC Symbol;Acc:19426]
Mouse Orthologue:
Ipo4
Mouse Description:
importin 4 Gene [Source:MGI Symbol;Acc:MGI:1923001]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37841 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa17116 | Essential Splice Site | Available for shipment | Available now |
| sa44103 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa15131 | Nonsense | Available for shipment | Available now |
| sa24457 | Nonsense | Available for shipment | Available now |
| sa10254 | Nonsense | Available for shipment | Available now |
| sa14017 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37841
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 |
|---|---|---|---|---|---|
| ENSDART00000039312 | Nonsense | 124 | 1085 | 5 | 30 |
| ENSDART00000060826 | None | None | 345 | None | 8 |
Genomic Location (Zv9):
Chromosome 24 (position 12732957)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 12684594 |
| GRCz11 | 24 | 12830888 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGCATGAGACCCCGGACCGCTGGCCTGCTCTTCTTGAGTTATTAAAC[C/T]AGTCTACTAAAAGCAACAACCCACAGGATAGACAGGTAAACCCAACTACT
Long Flanking Sequence:
GTCCGCTGCAGTGATGCTCAGAATGAGAGTGAGAAAACAATGGAAGAAAATCAGTCCAGACCATAGAGAGAGGTTTGGGACTTAAACACTACAAATAAGTCTTCTAATAGTTTAATTTATATCACTGTACATTTACTATTTTGTGACCAATTTGTTTTTAATCTAACACCCTCAGTCTGAAGGCAGTGGTGCTGCAGGCTTTTCAGCAAGAAACCGAGTGAGTTTGACAGTGTAATAGTATTGTGATTAGTAAAAATATTAACCATGATACAAAGTGATTACCTATATTGACATATGCACTGTTCTCCCACGCCAGAATACTATAATATAAACATTACAGAGGAACAGATATTAGTAATAAATTATGCTTTAGGGTTTTAATCAGGCTTATGTTTTCATTTATCAGGCACACAGTTCGTCATTCTCTCTCTCAGCTGAGTGCTGTCCTGGTGAAGCATGAGACCCCGGACCGCTGGCCTGCTCTTCTTGAGTTATTAAAC[C/T]AGTCTACTAAAAGCAACAACCCACAGGATAGACAGGTAAACCCAACTACTGTCCTGCTGACATGGGACATTAATGGTATAATCAGATAAATACCATATTCATATACCATGATTTTTGCATCAAGTTTCGAAAAACACTATAGTACTATGCCTGGAATGATATTTCTAAGTGTAATTTGTTATTTACTGCAACAATTCTATCAAGTTATTTATATTTATATTAATTGTTTTATTTATAAATGAAAGTGTTTTTATTTTTTAATTAAAAGCACTTCTAGTACCTTCTAAGAATTTATTAATATGTTCTATTGTATGGTTTAAAACTATATTCACTATTTAAAATCTATATTTAGTGAAAATACCCAGGGATTTTTTTTGCTAGTTTTCACAACAATAAAAGACATGACCGCATTTACTCTTCCTCAAGCTCATTAGATTTTCTTCCTTTGTAAAACACAAAAGAAGATATTTTAAAGATTGTTGTAAAGCGATAGCCATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17116
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000039312 | Essential Splice Site | 217 | 1085 | 7 | 30 |
| ENSDART00000060826 | None | None | 345 | None | 8 |
Genomic Location (Zv9):
Chromosome 24 (position 12730914)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 12682551 |
| GRCz11 | 24 | 12828845 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAWCCCCAAACTGCTCRTTGCTCTGAAACACCTCATTCAGGCAGACCAGG[T/C]GAGGAYACTTTGATAATCTCTTGCTGTGTTYATATGGTAATGCTTCAATC
Long Flanking Sequence:
AAGGTTTGGAACAACTTTATTTTGACTAAATGATGAATAAACTACAATTCAAGGATAAGATGTCTGTAAACCAGTAAATAAGCAGTTAATATAGACATGATTTAAAATTGAAGCTGTAACAACAATATTATCATTATGCTGTCAGTTCCCACATATCTCCATTAAATTCTGTCTGTTTAGGTGGGTCTGTTATTGCTCAGCAAAGTGGTGGGATCAAACCCAGAGCCCTTTAAGCCCCACTACAAGCAACTTCTCCAGCTCTTTGGAACTGTTCTCCAAGACCTGAACAATCCTACGGCTCTCTATTACTGCATCCTCACACTTACTGCCATCACAGCCTACACCGGCACAGAGGAGATGGTCTGTACTGCTTCAACTCACTTTTGGATAAAAGAAGCCATCTAGTTCAAAAAGTTGTTTTTCTGTTTTTTAGAACTTGATGCGATCTCTGATCCCCAAACTGCTCGTTGCTCTGAAACACCTCATTCAGGCAGACCAGG[T/C]GAGGACACTTTGATAATCTCTTGCTGTGTTCATATGGTAATGCTTCAATCACTGTTTTCATTGTGCTCATCGATGATGTGCTAAACTCTGCTGGACTTGCATCACCTCATTGATCTGTTTGCCTTGAAGATTTATGTGGCTCAATGACAGTCTTTTCTTTTTATCTCATATTTTTTGTTCATTAAAGGACCAGGCTAGCGAGGCAATGGAAGTTTTTGATGAGCTGATGGAAAGTGAGGTCTCCATTGTTGTCCCACACATAGCTGAAATTGTCCGATTTTGCTTGGAGGTTTGCCTGTTCTTCCTAATCATTGAGTTCATTTGGAGAGCCATTGTGTGCTAAAGTCATTTTCTTTTAGATCAGTGCAGATGCATCACTAAGTGATTCTTTGCGTGTGAAGGCTCTATCATGTATCGCTGTTCTCATCAGACTTAAAAACAAGGTAAATCACATTCCTTCTTTTTTTTTAATGTAAATATTCATTAATCCATTTGAATCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44103
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000039312 | Nonsense | 460 | 1085 | 14 | 30 |
| ENSDART00000060826 | None | None | 345 | None | 8 |
Genomic Location (Zv9):
Chromosome 24 (position 12703996)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 12655633 |
| GRCz11 | 24 | 12801927 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCAAAATTGGACACATGACGAAGGCCTTCTATGCCTTGGAGAACTTCT[T/A]GGAGAACTTGGGTTAGAATGCATACACAAAAATCTTTTCTTCAAAAAACA
Long Flanking Sequence:
GGCTTGCTTGTCAAGTGAGAACCCATATGAGCGTAAGGGTGGTCTCATGTGTATGGCTGTGCTCGCAGAGGGCTGTGCAGATCACATACGCACCAAGTATGCTTTACTCTACAGTTATAGCAAATTTACCAAATGCATGAAAAAACATCTGATTTATTTTTCTGTTTGTGTATGTGTTTCAGGATGTTGTCATCCATGCTTCAGACAGTGTGTCGCAGCCTATCAGACAATAATCAGGTGGTCCGCAGCGCAGCACTCTTCGCCCTTGGCCAATTTTCTGAACACTTGCAGGTTAGACTAAAATATCTTTTTTCTTTCAGTGCCTTTACTGATTATTAAATATCTTGATTTGAGTGTAAGTTGGTTAATTTGTGTCTTATAGCCAGATGTTAGTAAATTCCACGCTGAGCTGATGCCATTATTACAAGGATACTTGTCTGCTGTGAATCAGACCAAAATTGGACACATGACGAAGGCCTTCTATGCCTTGGAGAACTTCT[T/A]GGAGAACTTGGGTTAGAATGCATACACAAAAATCTTTTCTTCAAAAAACATTTTTATTTTATTTTGTTTTATTTCTAAATCATTGTTGTATTTTTTGTGATTAGGACATGCTTTAAAGGTGCCATATGTTTTTGACTCTTTTAAAGCATAAAAATACCATAATATGGTTGCAGATGTTTAAGAAACATGCTGAGTGAACATTCGTGAACATCAGAAAAACAATGCTTAAGTCAGATATTCTGCTTTAAAAATGTACTTTCCATGCTGTAACGTCTGTCATGACGTTTTGGTTCTTTTAACCCCACTAATGCCAGTTTAGCACCCAAGGTTGCCTTTGTGGAAAATCGCATATTTCATTCATTCAGTCAGGAAGGCTTATAAAGTATGCATCTGTGACCGAAATGCAACCTCCAGGGGACACTAGCAGACTCCGAAATCAGACGCAGATTCAGAATTCCATGCGCGGTTGTTAGTAATTAACAAATAATATAAATGTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15131
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 |
|---|---|---|---|---|---|
| ENSDART00000039312 | Nonsense | 463 | 1085 | 14 | 30 |
| ENSDART00000060826 | None | None | 345 | None | 8 |
Genomic Location (Zv9):
Chromosome 24 (position 12703987)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 12655624 |
| GRCz11 | 24 | 12801918 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGACACATGACGAAGGCCTTCTATGCCTTGGAGAACTTCTTGGAGAACT[T/A]GGGTTAGAATGCATACACAAAAWTCTTTTCTTCAAAAAAYRTTTTTATTT
Long Flanking Sequence:
GTCAAGTGAGAACCCATATGAGCGTAAGGGTGGTCTCATGTGTATGGCTGTGCTCGCAGAGGGCTGTGCAGATCACATACGCACCAAGTATGCTTTACTCTACAGTTATAGCAAATTTACCAAATGCATGAAAAAACATCTGATTTATTTTTCTGTTTGTGTATGTGTTTCAGGATGTTGTCATCCATGCTTCAGACAGTGTGTCGCAGCCTATCAGACAATAATCAGGTGGTCCGCAGCGCAGCACTCTTCGCCCTTGGCCAATTTTCTGAACACTTGCAGGTTAGACTAAAATATCTTTTTTCTTTCAGTGCCTTTACTGATTATTAAATATCTTGATTTGAGTGTAAGTTGGTTAATTTGTGTCTTATAGCCAGATGTTAGTAAATTCCACGCTGAGCTGATGCCATTATTACAAGGATACTTGTCTGCTGTGAATCAGACCAAAATTGGACACATGACGAAGGCCTTCTATGCCTTGGAGAACTTCTTGGAGAACT[T/A]GGGTTAGAATGCATACACAAAAATCTTTTCTTCAAAAAACATTTTTATTTTATTTTGTTTTATTTCTAAATCATTGTTGTATTTTTTGTGATTAGGACATGCTTTAAAGGTGCCATATGTTTTTGACTCTTTTAAAGCATAAAAATACCATAATATGGTTGCAGATGTTTAAGAAACATGCTGAGTGAACATTCGTGAACATCAGAAAAACAATGCTTAAGTCAGATATTCTGCTTTAAAAATGTACTTTCCATGCTGTAACGTCTGTCATGACGTTTTGGTTCTTTTAACCCCACTAATGCCAGTTTAGCACCCAAGGTTGCCTTTGTGGAAAATCGCATATTTCATTCATTCAGTCAGGAAGGCTTATAAAGTATGCATCTGTGACCGAAATGCAACCTCCAGGGGACACTAGCAGACTCCGAAATCAGACGCAGATTCAGAATTCCATGCGCGGTTGTTAGTAATTAACAAATAATATAAATGTTACATTGTAACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24457
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 |
|---|---|---|---|---|---|
| ENSDART00000039312 | Nonsense | 465 | 1085 | 15 | 30 |
| ENSDART00000060826 | None | None | 345 | None | 8 |
Genomic Location (Zv9):
Chromosome 24 (position 12701276)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 12652913 |
| GRCz11 | 24 | 12799207 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGTTTCGTGACCCTTTAAATAATCACTGCTCTCTTTTTGTTATCAGGT[C/T]AAGAAATTGAGCCCTATCTTCCTTCTCTTATGGAGACCATGTTGTCAGCC
Long Flanking Sequence:
CCACACGTGAGTCTGAGCTCTCACAGAGAGAAAATGAAAACGAAACTTAACTGCAGCAAACAATAAAAGCAACACTTCACGCTTGTTTTGCCAATACAACGTGGTGTGTCTGTCGTCTAAACACTGCGACAGTAATGAATATTAATGAAGTTGCTCAAAAGAGCGTGCTGATTGGTTTGAACCAAGCCTTACTCATGAATGCATCGCACTGTAAGACGTAATAAGACACACTCTGGCACAGGCGTCCAGTCTGCACGCTGGAATACAACGCTATTATGTCATGACCGTGACGAAGCTTCAAAAATTCGTTTCAAACCGGAAGTACAAATTTGCTTGAAATAAGGCAAAAACAACCAATTTACACTTTTTAGTGAAATGTAGGTGTCCTAATAGTGTTTTTAGCAGTGTGGGACACATATATGACTGTCGACAGCTCAAAAAATGTGTTTTGGTGTTTCGTGACCCTTTAAATAATCACTGCTCTCTTTTTGTTATCAGGT[C/T]AAGAAATTGAGCCCTATCTTCCTTCTCTTATGGAGACCATGTTGTCAGCCCTTAATAATGCAGAAATCCTTAAACTGAAAGAGCTTGCTGTCAGTGCAATAGGGGCGATAGGTAATTTCCTCCTTCCGTTAATACAGCATTTCATGATATTACAGTTATGCTGAGATCTTACTTTCACAGCTAACGCCGCCACGGAGATGCTAGTGCCTTACTTTCCTCCAATTATTGACAGTCTGAAGGGATTCCTGACAGACACAAGAGAGGAGATGAGAGCTCTGCAGACACAGGCGCTGGGTAAAAACCATCTTCATACTTTGTAATTGCAAGCATTGTAAGGCATGCTTAATCTAATATAATCTAATCTTCCATCACTGCTCTTTCTCACATAGACACACTCTCTGTGTTGGCTCGAACTGTTGGGAAGGATGTGTTCAGTCCGTTGGCAGCAGAGTGTGTACAATTGGGTTTGAACCTCACTGATGCAGTGGATGATCCGGACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10254
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 |
|---|---|---|---|---|---|
| ENSDART00000039312 | Nonsense | 626 | 1085 | 19 | 30 |
| ENSDART00000060826 | None | None | 345 | None | 8 |
Genomic Location (Zv9):
Chromosome 24 (position 12697845)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 12649482 |
| GRCz11 | 24 | 12795776 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGTCATAATATTCCTGTCTATTCTATAGGCCCATTTAGATGAAGACAAA[C/T]AGTTTGTGCTCTTGGACGATGATGATGCTGATGATGGAGAAGAGGGTGAT
Long Flanking Sequence:
CAAATTATTAATTCATAAAAACAAATGACTAATATATATAAGCATTTGTCTGTTTGTGTAGTTTTTTTTTATTCATATTTACATTTTTTTAGGCATGATTTCAGTTTAAATCTAATCTTCAACTTCCATTCTTCAACCTCAAATGTTTTTTAACACTTGACAAATTGTCAGAAGTTTTTAGCATTTCCCCTTTTGGTTAAATTTGTTCATGAATAAAAAGTCTAAAAGAACCTTGCTACATCCCAACTGCAGATTGTGTTCAGCCACTCTCTTCTTCCTGTCTCTCCAGATACAGCCTATTCTCTGCTGTGTCTGAAGTGAGTCCAGACTGTCTCACACCTCACCTCACATCCATTACCACAGTGATGCAGCTTTCACTCAGATCCACAGAGGGAGTGACGGTTAGTCTGAGGCTTTTGGATCATCATCTGTACACCATCAACTTTACAGCCGTCATAATATTCCTGTCTATTCTATAGGCCCATTTAGATGAAGACAAA[C/T]AGTTTGTGCTCTTGGACGATGATGATGCTGATGATGGAGAAGAGGGTGATGCTATTTTGGATGACGAGGGCGAGACTGAGGTTGATGATCGGGATGTTGCAGGGTACGTTTCTGTCTTTCTTAACATTAGTTTTTTTCCTTATGTAAGAGACTATGTAATCAAAATTCTTTCTTCAGATTCAGTGTGGAAAATGCTTACATAGATGAGAAGGAAGATGCTTGTGATGCCTTGGGGGAAATTGCCTTCAATACTGGGTAATGAGCCTTGTTTTACATAATGCTCACACACTGACACATTTGCATTTACAAACGTGAGGCTTATTTTAGGTGTGAACATACTACTGCTTATGCTACAGAACTTTTTTTTAATTAATTTATTTTTTTTTATGCTACAGAACTAGCTTTACCATCATAATAACAAATTACTTTAAACAAAATGTCTGTGTGTGTACATGTTTGTGTCTCTGTAGACTTATGTATATACGCTGTATTGCCAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14017
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 |
|---|---|---|---|---|---|
| ENSDART00000039312 | Nonsense | 850 | 1085 | 25 | 30 |
| ENSDART00000060826 | Nonsense | 110 | 345 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 24 (position 12670275)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 12622012 |
| GRCz11 | 24 | 12768306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTGAAGGGATTCCTGCYTTAGCCTCTRCTGTACCAGCTGAAACCTTCTA[C/A]CCTCACCTCAATGACCTGCTGCCCCTAATCATGAGCAAAACTGTGAGTCT
Long Flanking Sequence:
AAAGCAAAGTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGAAGTAGTAGTACTTTTTATTGTATAAAACACTGTTTTTAGAAAACTCTCAAAAATCTGCTGGGCAGAGAATTAACATGGTTAACATGTTGTACATATCAAGCATTTTCCTGAAGCTGGAACGATTGTATAACAAATATAATATACTGTAAATGGCACTGTGATCTTCTTTTTCACTTTGTCTCACTCAGACCGTGTGCCAGGATGTGGGTGGTGATGAAGCAGATGATGACGAGCAACAGGTGTTTAAGATGATCAGTTTTTCTGATTTTGTCACAGCTCTGTGTGAGTGATGAGAGCGTGTGGAATAACTGAATGTCTGTGCGTCAGGCCGAGTTTGATGCCATGCTGCAGGAGTTTGCTGGTGAAGGGATTCCTGCCTTAGCCTCTGCTGTACCAGCTGAAACCTTCTA[C/A]CCTCACCTCAATGACCTGCTGCCCCTAATCATGAGCAAAACTGTGAGTCTATCATTCTCCTATTTAGTGATCTCTTATGAAGGTTCATAAATGAATACCAATTCACATCCAAAAACATCACAATTCAGTCACCAGCTTCTCACATAGTGTAACATGACTTTCAATTTAATGCAAAATGCAGTGCATTGTCAGAAAGCAGTTTTGGATGTATAACTGACATGAATGAAAGAGATTGAGATAAAGCTATAAAGTCAACGGGATTCTAGCACATTTTAAGAAAAATAATCAAAGTGGAGAGGAAGTTAATAAGTATTACTAGGTTCACATGGAATTTGCACGCACAGAAATCCGCAGATTTCCATAGATTTTTTGCCCATCATTAAGTCTATTTATTTACTTGTGTGCAAATTTATATTTCTTCAGTTTTAAAATGTATTTCAGTATATTATTGACTAATATAAAAATGTTAATTAGAATTATTTACAATACAGTTTTAAAGT
Associated Phenotype:
Not determined