ZMP
zgc:91897
Ensembl ID:
ZFIN ID:
Description:
importin-11 isoform 1 [Source:RefSeq peptide;Acc:NP_001153133]
Human Orthologue:
IPO11
Human Description:
importin 11 [Source:HGNC Symbol;Acc:20628]
Mouse Orthologue:
Ipo11
Mouse Description:
importin 11 Gene [Source:MGI Symbol;Acc:MGI:2442377]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa2457 | Nonsense | F2 line generated | Not yet available |
| sa34440 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2457
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000045295 | Nonsense | 108 | 975 | 4 | 29 |
| ENSDART00000133245 | None | None | 85 | None | 3 |
| ENSDART00000138268 | Nonsense | 108 | 543 | 5 | 17 |
| ENSDART00000145325 | Nonsense | 108 | 961 | 4 | 29 |
Genomic Location (Zv9):
Chromosome 8 (position 33167499)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 32310225 |
| GRCz11 | 8 | 32319457 |
KASP Assay ID:
554-3300.1 (used for ordering genotyping assays)
KASP Sequence:
GAAATCCCTGTAAACTTTTTTTTTTTCTTTTTTGAATGCAGATCGCCACA[C/T]AGATAGCAGTGCTGATCGCWAAAGTGGCACGTCTGGACTGTCCTCGGCAG
Long Flanking Sequence:
AAATTGCACAAAAAACAATCTGAGAAACTGCGATGCCGCACCGTAAAGAGAATTTAGTAAATTGTAGTTAGTAATTTGTGGTGAATATGGTTTCTTTCTGTAAACAATTTTACACTTTTATTATCAGAATGTAATATTTACTTGCTTTTAAATTTCATGTAATAAAATCAAATATGCTGGCCAAGTCTCTTCCTTCATTACAACCAAAGAAACCAAAGAGCAGTTCATTAATTTAATTGCTGCTTTAATGGTGTTAACACGTCTGCGTTTTATAGATTGTGAATTCATTAAACTAATTAAAATGGTTAATTAAAATCTCATAACCATTTAAGACATGTTTGAAAGACCTAAATGCCCACTATTCATTCCGTTCACATAAAAAAAAAAAACTATTGATAAATCTTGCTAAGTTGAATGGCTGCTATGATTTCCAGTAGCTGGTATGTTCTTGAAATCCCTGTAAACTTTTTTTTTTTCTTTTTTGAATGCAGATCGCCACA[C/T]AGATAGCAGTGCTGATCGCAAAAGTGGCACGTCTGGACTGTCCTCGGCAGTGGCCCGAGCTGATCCCTATTCTGCTGGAGTCTGTGAAGGTTCAGGACAGTCTGCAGCAGCACCGAGCTCTGCTCACCTTCTATCATGTCACCAAAACCCTGGCCTCCAAACGCCTCGCCACTGACAGGAGACTCTTTCAGGATGTGAGTCATTTTCTGCTCTGCATTCGTCTCTGCGGGTTTTAAATCTTGCATGAGGCATATTTTTGTAGGGATGATATCCAGTGCAATATTGATTCATGTGCAAATTGGTTTATTATTTAAAAAAAAAAGAGACATGAAACTGGTACAAAGTGGGAGTTTGATTTCTTGGGGCAGTGTTGAAATATGTAAAGTTTAAATATATATGTAGTTTGTAGAATATGGAATCAAAATTGTTGTGGAAATTTTAACAGAAGGTGATTAACAATTTCATTCATTCATTCGTTTTCCTATGGCTTAGTCTCTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34440
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 |
|---|---|---|---|---|---|
| ENSDART00000045295 | Nonsense | 749 | 975 | 23 | 29 |
| ENSDART00000133245 | None | None | 85 | None | 3 |
| ENSDART00000138268 | None | None | 543 | None | 17 |
| ENSDART00000145325 | Nonsense | 735 | 961 | 23 | 29 |
Genomic Location (Zv9):
Chromosome 8 (position 32973844)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 32116570 |
| GRCz11 | 8 | 32125802 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTGTGAACTCCTGAGCGACATCACCAATGAAGGCCAGGTCCAGGTTT[T/A]GAAGGTACTGTATGACTCAATCTTTCACACTCTTTCTACTCACAGCCCGA
Long Flanking Sequence:
TTACACTCTGTTGAAGTCAGTGATAAACTCACACCTGAACAATGCATGTGACTTCATTCTCCATATGAAAGGTGTCTTTATGCTGCCATCAACAAAAAAAAAACATTTAATATAAAGTGTTAAAACGTTTAAGTAGTTCAGTAGTTTTTCCTTGTGGCATTCCATTGTTATTACACATAAGATTTTTTTGTTTTATTTTTACATTTGTATTGTTTTTTTTTTACTAAAATATGGTTTAATTCCCTATCAACAGCTCCTTTAGAAACATTATTCCCAGGAAAAAACATGTCGTACTCAATACTAATTTCCCCCAACTGTTTTGTGAAATCCACATTTGCAATTTTTCTAAACTTTTGATGTAAAGAGCAGCCCTACATGCGAAACAGGAATGATTGTTTTTAATCACCTGTTCGTTTTTCTCCAGAACTATGCTGAAGCCCTCTGCAGATCTTTCTGTGAACTCCTGAGCGACATCACCAATGAAGGCCAGGTCCAGGTTT[T/A]GAAGGTACTGTATGACTCAATCTTTCACACTCTTTCTACTCACAGCCCGATCCGTCCTTCCCTGCAAGGCTCTTTTGTGCTTGTCTTCCTGGCGCTCTCTTGTGAAATGAGGTGTCCTGGCACTGCAGCAGAGTAATGACTGGAACACCCGTTCGTCAACCCTGTCGTTTTGGTTTTGACGAAGCTCAGCTATATTTCATGAAGCCCTTCTCGACATCACTTTCTTTAGCTTATGCACTCAAGCTCTTAGATCTGACAGAAGTGGTGCGCTCTTTGACACATCGATCGTTTTTTTTTCCTTCTTCTCATTTCCACACCATCAGTTAGGACAGATTTCTGCTTTGAAGATATGATGAAAGTGCTCTGCTCGGGACCCTGTTATTTTATGAACTTATTTTTTGACCGTTTTAATTAATGCATTTAGCAACGTGACCAATTGGACCTTGTAGCACCGATAATTATCTTACAGGGGTCGCGCTGCTGAAGCCTGCCTAATGTGG
Associated Phenotype:
Not determined