ZMP
ipo7
Ensembl ID:
ZFIN ID:
Description:
importin-7 [Source:RefSeq peptide;Acc:NP_957199]
Human Orthologue:
IPO7
Human Description:
importin 7 [Source:HGNC Symbol;Acc:9852]
Mouse Orthologue:
Ipo7
Mouse Description:
importin 7 Gene [Source:MGI Symbol;Acc:MGI:2152414]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31613 | Nonsense | Available for shipment | Available now |
| sa21124 | Nonsense | Available for shipment | Available now |
| sa7608 | Missense | Mutation detected in F1 DNA | Not yet available |
| sa34228 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31613
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 |
|---|---|---|---|---|---|
| ENSDART00000051879 | Nonsense | 113 | 347 | 4 | 9 |
| ENSDART00000108471 | Nonsense | 113 | 1039 | 4 | 25 |
| ENSDART00000113602 | Nonsense | 113 | 772 | 4 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 66999986)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 64914970 |
| GRCz11 | 7 | 65138998 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTTTTTCCCTCCTCTCTTCTCTTTCCTAGAGTGCAACTCACAACTTG[C/A]ATTCACCACATGATTAAGCACGACTACCCCGGTAGATGGACAGCTATAGT
Long Flanking Sequence:
TATCATAGCTAGTTAAATCAGTAGATCTTATTACCTTTATAAAACTTTTTACCTGATTAATACCTTTTCACACTTGCTAAGTGCATTTTACAGTTCACGAATCTATTTCAGTCGCAAATGAAAAGCATGCACTGTGTACAATGTAGCTGCATATATATGCTAATATTTCAGTCAGCACACAGCCTTTGAGTCCAAATTCGACTGTTATCTCAGACCTCTGTCTTTGTCATTCAGGTGTGATCTATTTGAAGAACATGGTGACACAGTTCTGGACTGAGGGAGATAACGCAAACACTGAAGCGCCTACCAGCACCATCCCAGAAACGGACAGGCAGTTCATTCGAGATAACATCGTGGAGGCCATCATCCAATCCCCAGAGCGCATCAGGTAACACAAACCGGTGCAAGCACATGCGGGAATGCAGGATCTATTTCTTTTCTAACATTGCTTCTTTTTTTCCCTCCTCTCTTCTCTTTCCTAGAGTGCAACTCACAACTTG[C/A]ATTCACCACATGATTAAGCACGACTACCCCGGTAGATGGACAGCTATAGTGGACAAGATTGGCTTGTATCTGCAGTCTGATAACAGTTCCTACTGGCTGGGCATCCTGCTGTGCCTCTACCAGCTGGTGAAGAATTACGAGTAAGAGAACTGTGAAGCGCTCGCAGGTTGATTTGTGAATGGTTTAGAGAAAGCAGGATTTGGCAGACAGCGTCTCATTTGATATTTTACTGTCGATACGTTCGCTCGCTTTCTGTTAGATCTGCATTCATTAATTTAGAAATAGCAAAGGTGTCAATGTGATGATGATAACAGAGTAGCAGGGTTAAAAGGCAAACGGAAATCCTTATTTTAATATATTTTTTGCCACTGGTCATCATTACATAATGGTGAGATGCTTATTCAGTGGCTAGCGCTGATCATTAAAGATGCTTTCATAACCACAACAACAACAAACATTGATTATGTCAAGGCTTCTTCTGGAATCAAATGTTCTTGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21124
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 |
|---|---|---|---|---|---|
| ENSDART00000051879 | Nonsense | 135 | 347 | 4 | 9 |
| ENSDART00000108471 | Nonsense | 135 | 1039 | 4 | 25 |
| ENSDART00000113602 | Nonsense | 135 | 772 | 4 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 67000051)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 64915035 |
| GRCz11 | 7 | 65139063 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGCACGACTACCCCGGTAGATGGACAGCTATAGTGGACAAGATTGGCT[T/A]GTATCTGCAGTCTGATAACAGTTCCTACTGGCTGGGCATCCTGCTGTGCC
Long Flanking Sequence:
TTTCACACTTGCTAAGTGCATTTTACAGTTCACGAATCTATTTCAGTCGCAAATGAAAAGCATGCACTGTGTACAATGTAGCTGCATATATATGCTAATATTTCAGTCAGCACACAGCCTTTGAGTCCAAATTCGACTGTTATCTCAGACCTCTGTCTTTGTCATTCAGGTGTGATCTATTTGAAGAACATGGTGACACAGTTCTGGACTGAGGGAGATAACGCAAACACTGAAGCGCCTACCAGCACCATCCCAGAAACGGACAGGCAGTTCATTCGAGATAACATCGTGGAGGCCATCATCCAATCCCCAGAGCGCATCAGGTAACACAAACCGGTGCAAGCACATGCGGGAATGCAGGATCTATTTCTTTTCTAACATTGCTTCTTTTTTTCCCTCCTCTCTTCTCTTTCCTAGAGTGCAACTCACAACTTGCATTCACCACATGATTAAGCACGACTACCCCGGTAGATGGACAGCTATAGTGGACAAGATTGGCT[T/A]GTATCTGCAGTCTGATAACAGTTCCTACTGGCTGGGCATCCTGCTGTGCCTCTACCAGCTGGTGAAGAATTACGAGTAAGAGAACTGTGAAGCGCTCGCAGGTTGATTTGTGAATGGTTTAGAGAAAGCAGGATTTGGCAGACAGCGTCTCATTTGATATTTTACTGTCGATACGTTCGCTCGCTTTCTGTTAGATCTGCATTCATTAATTTAGAAATAGCAAAGGTGTCAATGTGATGATGATAACAGAGTAGCAGGGTTAAAAGGCAAACGGAAATCCTTATTTTAATATATTTTTTGCCACTGGTCATCATTACATAATGGTGAGATGCTTATTCAGTGGCTAGCGCTGATCATTAAAGATGCTTTCATAACCACAACAACAACAAACATTGATTATGTCAAGGCTTCTTCTGGAATCAAATGTTCTTGTTGCAATTGATTGCTGAAGCTTTGATTATGATAAATGATAAATGGGGTTATCATGGTATTCACCTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7608
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:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051879 | None | None | 347 | None | 9 |
| ENSDART00000108471 | Missense | 960 | 1039 | 23 | 25 |
| ENSDART00000113602 | Missense | 693 | 772 | 17 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 67030820)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 64945804 |
| GRCz11 | 7 | 65169832 |
KASP Assay ID:
554-4068.1 (used for ordering genotyping assays)
KASP Sequence:
TGGAGGGTTACACRACCTTAGTGGACGATGAAGACAACCTCGTAGATGAA[T/A]ACCAGATCTTCAAAGCCATAATGCAGAGTATGGGTTGTTTTATGTGCAGT
Long Flanking Sequence:
GGCGGGTCAGCTCCTTCCTGCCGCCATCCTCCTGTTTAACGGCCTGAAGAGAGCCTACGCCTGCAGGGCTGAACACGAGAACGATGAAGACGATGATGAAGAAGACGGGGAGGAGGAAGAAGAGAACGGTAAATGACTTATTTTATACTGCCGTTTCCTGCTGTTTTAAGGTAACATTATAAAGGGATAGTTCACCTTAATTTAAAAGTGAGTCAACTCCCTTAAATAAAGGAGGACAAGGAATTTTGTGACCTAAACACTTACCAAAATGTAAAAATTGAAATTAATAGTGATTTTACCCTTTCATTTTGTGCCTTGCAGCCGAGTTAGGCAGTGATGAAGATGACATAGACGATGAAGGTCAGGAATACCTGGAAATGCTTGCTAAACAAGCAGGCGAGGATGGTGATGATGAAGACTGGGAGGAAGACGACGCAGAGGAAACCGCTCTGGAGGGTTACACGACCTTAGTGGACGATGAAGACAACCTCGTAGATGAA[T/A]ACCAGATCTTCAAAGCCATAATGCAGAGTATGGGTTGTTTTATGTGCAGTGTAATAGACGAGTACTTGTAGCTCGTTTTGTTTGCTAACAGGCTCTGCTTTGTTCTGTAGATGTCCAGGCTCGCGACCCCGCATGGTACCAGGCGATTACACATTGTCTCGACGAGGAACAAAGAAAACAGCTTCAGGATATCGCAACGCTTGCAGATCAGCGGCGGGCAGCACATGGTGAGGCTAAATGCTGTTAAATAAAAGCTGAATAAATGACTGTGCAGTTTCTTTCCTTCTGAATCCCCAAGGACCACATGCTCTCTCAGTTTTAAAGCTTAGAAAGTGCATAAAATAACTCGATAACTTTTAAACTGCATTTAAAAGGTTGTAAAGGGTTAGTTCACCCAAAATTGAAAAACATACTCATGTTGTTCCACCTTCTGTCATCTTCAGAACACAAATTCAGATGTTTTACCGCATGGTTTTTGGTTTGTTTGACCGATCTATGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34228
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051879 | None | None | 347 | None | 9 |
| ENSDART00000108471 | Nonsense | 1013 | 1039 | 25 | 25 |
| ENSDART00000113602 | Nonsense | 746 | 772 | 19 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 67033398)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 64948382 |
| GRCz11 | 7 | 65172410 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATGTGCTTATTTTCCCTTTATTTTATGTTTTTAGAATCAAAGATGATC[G/T]AGAAACACGGAGGATACAAGTTCACAGCACCCGTGGTGCCATCCAGTTTC
Long Flanking Sequence:
GGGAAGAGAATGAATTACATATTTAAGCAGCATGTGTTTTGTTTTAGGTCTGTGCCTCTGTTTTATGTATTGCACGGTTTCACAAAGTCATTGTTTTTTTTTCCACTTAATATTTTGATAAATATACAGTCTATTTTAAATGACCAGCTACCCAAGATCATGCGTTTCTACTGTGTGTGGATCATGATTGTTGCCTCTAATATGAATTCACTAGATGCAGCTTGTGATGAAACAAATTACATTTTGCTTTCATAAGAATTTGATTTCTAGTAAAGACAAACATGGGGAGAAAAATGGAAATTGGTATCAAATTGGTTGGTTATCTAGTAAGAAAATTGGAATCAGTCATGAAGAACAGTCGAGCATTAAAATGTATCTGAAACATGCTTTTATACTGTGAAAAAGGTTTCACCAACTCGGTATACTGCCTAAAATGCTACCTGTTTTGATAGATGTGCTTATTTTCCCTTTATTTTATGTTTTTAGAATCAAAGATGATC[G/T]AGAAACACGGAGGATACAAGTTCACAGCACCCGTGGTGCCATCCAGTTTCAATTTTGGTGGCAGCGCCCCTGGGATGAATTGAGTCCTCTCTTTTCCTTCCCCTTTCTAACTGTGACTGAATGTAGTGAAATGAAAACACTTGTGTTGCTCCCTGAAGTAGTGGTTCCAGAACTGGTTCTTCTCTCTCACTCTTCAACTCTTGACTATCAAATTTGAACAGCACCAGAAGATGTGGGAAGGTGACCAAACGCAACCAATGCCTGGGAAAACAAACCAAGAACTTGAACGCTAAGCAAAGTGGGGGAAGAAATAAAGCTCTGAACAATGTTGTCTTATGGAATCCAAAAGTTAGAGGAATACCATAACGGCAGTTCCCACACACATACTAACGGGGGCTGAAGAATTGAAATTGAGACATACCGTCAAAATCATTGTCACTGTATGGGCCAAAGGGCCTTCTCAAGATTATACCTCTGGCAGTAGTGTCAACATTTTTCTT
Associated Phenotype:
Not determined