ZMP
xpo7
Ensembl ID:
ZFIN ID:
Description:
exportin-7 [Source:RefSeq peptide;Acc:NP_001121702]
Human Orthologue:
XPO7
Human Description:
exportin 7 [Source:HGNC Symbol;Acc:14108]
Mouse Orthologue:
Xpo7
Mouse Description:
exportin 7 Gene [Source:MGI Symbol;Acc:MGI:1929705]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9320 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa34881 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa9930 | Nonsense | Available for shipment | Available now |
| sa16794 | Nonsense | Available for shipment | Available now |
| sa38791 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9320
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000027612 | Essential Splice Site | 6 | 1087 | None | 28 |
| ENSDART00000145264 | Essential Splice Site | 6 | 1090 | None | 28 |
Genomic Location (Zv9):
Chromosome 10 (position 20104149)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 20112835 |
| GRCz11 | 10 | 20070216 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGGGAGTGAGAGGAGCATGAATGGAGCAAAATGGCGGATCATGTGCAGG[T/C]AAGTAAATTATTTTGTTTTGCTATTATGAAATKAATGAATTTTGATYCAC
Long Flanking Sequence:
AACTAATTCCATTAAATGCAGAATTTTGAAACAGTGAACATAACATTTTTACATTCAGGGTCACTGTACACATTTTTTTGACATCAAACAAGTGATGCACATTGTTTTGTGTAAAATTAGTCAGCACGTTTTTTTACTTTTACAACAGGTGCAAACATTCACCGCGTGAACACTCACAAAACATTTTCATCAGTTAATAGCCTTGATTCTCAACTTGCAAAGTTTAATCACGCTTGAAATTATAAATCCACGTGACAGCTAATATTTGAATTCGCAGTTTCACTTTAAGAAGCATGTAAACAAAGGCTCTTTTCGGCGTTATTTCGGCGGTGGACGTCCATCGTAACGGTATTCACGAAGCCTCGAGCGAACATCTGGCTTGATCAGTGCGTACGTCAATTGCGTAAATGTTCCAGTGATTGTGTGCAGATGCGCGCATGCTCATTGTCAGGGGGAGTGAGAGGAGCATGAATGGAGCAAAATGGCGGATCATGTGCAGG[T/C]AAGTAAATTATTTTGTTTTGCTATTATGAAATGAATGAATTTTGATCCACTGCAGTCTAATGGTAAATGTCGAGACTTATTTCGGCGATGCGTGCGTGTTTGTTTTAAATGCATGCTTCGCCAAACGAGAGAGCTTGACTAGCATGCTTTATTGGATGCGATTATCAAGTGTTGACTTGTGGCCTGTCATCATGTTGATTTTAACTCTGTGGTCCAAGCTAACACACAACTCTGTCGCATAAGTGAAAGTTGTTTTGAAGCAAGATGCGAAGACTATCGGTTTAAGCAGCAGGAATTGGCAGATACAGAGAGATTGTTTATTTCCCCCCCTGCACGTAACTCTATAGCGACAGTCATGTTTTACATTGTAAACAAGGCATCATCTTCATCCAAACCCTTGCTGTGCAATAACTACACACTGGCCTTATATCCACAATGCGATAGTGACTCGAAATAAGCGAGTCTTTTTTCCGAGTGAAAAGACTGCTGTTAAGCCTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34881
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 |
|---|---|---|---|---|---|
| ENSDART00000027612 | Nonsense | 10 | 1087 | 2 | 28 |
| ENSDART00000145264 | Nonsense | 10 | 1090 | 2 | 28 |
Genomic Location (Zv9):
Chromosome 10 (position 20108854)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 20117540 |
| GRCz11 | 10 | 20074921 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTAAATAGCAATGACTTTTTATTGTTTTTGTTCTTTCAGAGCCTAGCC[C/T]AGCTAGAGATCCTGTGCAAGCAGCTGTATGAGACCACAGACACCACCACA
Long Flanking Sequence:
CATAAACGTGATGTTCAATGTTGTGATTGTACAAGAAGATACAGAAGCTTTGCTGAAGTAATATTATTTGGCTTAGGGTACAACCTTAGCTTTGACGTAGCTGTTATGTCCAGGTTTGTTGAGGTAGTGTACTGTTACAGTTTCATAAGTGTTCTCAAATTTCAACTTAATCACAAGTTGTAAATGCAGCACTATCATGGTAAGTTTTTTTTTTTTTTTGACACATTCCCTCATTTATGAGAAGTGCATATGGTTTTAAAAAATAAAAATATATCAATCATAGTTATATGAATAATGATAATTTTGGGTCAAAAGTAAACCAAAATGTGAAATTTGATTACAGATGGTTAAGAAATTATCTACCAAAATACATCCTTTGAATGTTGTTTTAATGAAGTCAAAACATATTTGTATTTCTAATATAAAAAATAATGTGATGGCAACAAAGACATTTAAATAGCAATGACTTTTTATTGTTTTTGTTCTTTCAGAGCCTAGCC[C/T]AGCTAGAGATCCTGTGCAAGCAGCTGTATGAGACCACAGACACCACCACACGTCTTCAGGCCGAGAAAGCACTGGTGGAGTTCACCAACAGTCCTGACTGCCTGAGTAAATGCCAGTTGTTGCTGGAAAGAGGAAGTGTAAGACTTTAACTTTCTGAAAACTGTAGAACACAATCTCTCAAATGATCTAACCTCAACTATTTTTTCAAAAACTCCATTCTTCCCACATTATTTTGAGTTGAGTAAGTCTTTTCTGAATTGCGAACTGTGTTTTTGTTTGTTTGTTTGTTTTTCCAGTCCTCGTACTCACAGTTGTTGGCTGCGACGTGTCTCTCCAAGTTGGTGTCACGAACAAGTAACCCCCTTCCTCTGGAGCAGCGCATTGACATTCGTAAGTTTATAGAATCCGCCACAAATTCAACTTTAAAATTAGATCCCAATTTTTGAAATTGTCTAATTGATTCCTCAGGAAATTATGTTCTCAATTATCTGGCAACCCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9930
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 |
|---|---|---|---|---|---|
| ENSDART00000027612 | Nonsense | 73 | 1087 | 3 | 28 |
| ENSDART00000145264 | Nonsense | 73 | 1090 | 3 | 28 |
Genomic Location (Zv9):
Chromosome 10 (position 20109202)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 20117888 |
| GRCz11 | 10 | 20075269 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCGTACTCACAGTTGTTGGCTGCGAYGTGTCTCTCCAAGTTGGTGTCA[C/T]GAACWAGTAACCCCCTTCCTCTGGAGCAGCGCATTGAYATTCGTAAGTTT
Long Flanking Sequence:
TAAGAAATTATCTACCAAAATACATCCTTTGAATGTTGTTTTAATGAAGTCAAAACATATTTGTATTTCTAATATAAAAAATAATGTGATGGCAACAAAGACATTTAAATAGCAATGACTTTTTATTGTTTTTGTTCTTTCAGAGCCTAGCCCAGCTAGAGATCCTGTGCAAGCAGCTGTATGAGACCACAGACACCACCACACGTCTTCAGGCCGAGAAAGCACTGGTGGAGTTCACCAACAGTCCTGACTGCCTGAGTAAATGCCAGTTGTTGCTGGAAAGAGGAAGTGTAAGACTTTAACTTTCTGAAAACTGTAGAACACAATCTCTCAAATGATCTAACCTCAACTATTTTTTCAAAAACTCCATTCTTCCCACATTATTTTGAGTTGAGTAAGTCTTTTCTGAATTGCGAACTGTGTTTTTGTTTGTTTGTTTGTTTTTCCAGTCCTCGTACTCACAGTTGTTGGCTGCGACGTGTCTCTCCAAGTTGGTGTCA[C/T]GAACAAGTAACCCCCTTCCTCTGGAGCAGCGCATTGACATTCGTAAGTTTATAGAATCCGCCACAAATTCAACTTTAAAATTAGATCCCAATTTTTGAAATTGTCTAATTGATTCCTCAGGAAATTATGTTCTCAATTATCTGGCAACCCGGCCAAAGCTTGCTGCCTTCGTGACACAAGCCCTGATCCAGCTCTATGCCAGAATCACCAAACTCGGCTGGTTCGACTGCCAAAAGGAAGATTACGTCTTCAGGAATGTCATAGTTGATGTGACAAGATTTCTGCAGGTATGATTGATTATGAAAGTCTTTTGGTGAAGATAATATTCTTCATTTCAGAATTATACAATGGATGACAATTCAAATGCAATTTGGTTTCTTTTCGAGTGTTCATTCTTGTTAGATGTGAAGTGTTTGTCATCCAGACTAAAACAATTAGTCATGTTTTATTTGTCACTTGAATGAATTGCAGTTGAATCACAATTAATCACATGCACTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16794
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 |
|---|---|---|---|---|---|
| ENSDART00000027612 | Nonsense | 787 | 1087 | 22 | 28 |
| ENSDART00000145264 | Nonsense | 790 | 1090 | 22 | 28 |
Genomic Location (Zv9):
Chromosome 10 (position 20123680)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 20132366 |
| GRCz11 | 10 | 20089747 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGATYTCWGACTCACTGAATGWGTTTTTCATGAAGGTCACAGAGATTA[C/T]AGTTYGATGTGTCGTCGCCGAATGGAATCCTGCTGTTYAGGGAGACCAGC
Long Flanking Sequence:
TAATTTTATTGTTATTGCTGTTTAATTTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACAGATAAACAGATAGATGGATAGCTATATTTGCGCACTTTAACTGTTAAATAATTCTTTTAAATTAATTTTTAAAAATGTAAATGTAATAAATTAATAAAAAGTACATTATTTAAAATCTTTGCTTAATATATTGCTAATTAGAAGCAATATGGGGAAATAAATTCAGTTCAGTTGTGCTTCTTAACAGATTTTTAGATACCCTTCTTACATGCCCATCTTGCAGAGGGCAATAGAGCTGTGGTACCACGTGCCCGCCTGCACCACACCGGTCCTCAAACTCATGGCTGAGCTCGTCCACAACAGGTACGCTAATGTTACATGTCACAAATGTCGTTGAGAGCTGTGTTTTAAATGTTATGTGTGATCTCTGACTCACTGAATGTGTTTTTCATGAAGGTCACAGAGATTA[C/T]AGTTCGATGTGTCGTCGCCGAATGGAATCCTGCTGTTCAGGGAGACCAGCAAGATGATTACAACTTACGGTACATCCTTATTAATTACCCAATGCAGGGCTCGAAATTGCGACCATTTTAGTTGCATGTGCGCCGAAATTTTATCTAAGTGACCTCAAAACATAATTGGGAGCATTTGTGCAAGTGCATAAAATTAATGTCATGCGACCAGTTTTCATAGCAAAATGTTCACCACATGTGTGGAATTAGGAGGCATTCACGCATTAAGCATCTTTGCACCTAAAAACACCAAACGCAGCGCTCAGGAATGATTTAAAATAGTTGACATGTCAACTTGCTGTAGTAAACAAAGCCCGCAATGCTTGCACTGCCTTAAAGCTCTTCTTATTGGCCCGCTGTGCTAGAACAGAAAATGAATGGATTGGTTAATATCAGCTGTCAATCACTCAGTTCCCATGACCGGGAGCTACAGGTCTGGCAATGAGAGAATGAAAACAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38791
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000027612 | Nonsense | 1078 | 1087 | 28 | 28 |
| ENSDART00000145264 | Nonsense | 1081 | 1090 | 28 | 28 |
Genomic Location (Zv9):
Chromosome 10 (position 20133388)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 20142074 |
| GRCz11 | 10 | 20099455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTCAGTATTTAGAAGAGAAGTCAATGACTCCATGAAGAATTCCACATA[C/A]GGGGTAAACAGCAACGACATGATGAGCTGACATTCCATAGAGCACCAGGC
Long Flanking Sequence:
GAATGAAGACAAAACTAAACCAGTTGAATATGACTTTTACATATACATGACTGAAAACTGAATATGATCAATGTGTTACATCTGTTCTTTGATACTTGCTGACTGCTTGTAAATTCAAAACCGAATTTCCTAATGTAAAACTATGTACACTAAATTTCTGATTAATATTAGCCTCTGCATAATCCTACATTACAAGTTTTAACAACCCCCCAGAACGGCCTTTTGTTGGCTTGATGTACATCACATAACATATCTTTACTAAACTCAAACTAAGATTTTACAAGCAGTACTAGCATTTATTAAATAAACCTAACAGGCATCTGCCAATATACTCACCAATTGTTTTTTTTTATTTTCATTTGCCCCTTAGTGAGTGATAATTTTAGCACGTTTATAACTTCATCCTCAAACTCATTTTTTCTGTCTCTCTTTCACAGGTTTACACAGAATCTTTCAGTATTTAGAAGAGAAGTCAATGACTCCATGAAGAATTCCACATA[C/A]GGGGTAAACAGCAACGACATGATGAGCTGACATTCCATAGAGCACCAGGCTCCGCCCGTGTGGCCCGGCCCCTCCCTCAACTCCCACCCGCCCCCAGCCCGGCTGCTGGGGGAGCACCGCTGCGCAAGCCTGCACCTCCCGCTCCCCAGTCCCTAAAAACCCCATTACCTCTCTCCCCTCACACCTCCCCATCCCTTTTTTATATATATATATATATAAATATATATATACACATATAAATATATACATATTTTAAAGCCAGTTTCTAGAGGTCATTCTCCTTGACCATTCTCTTGTCATTTGGGGCTTGAAGTCCAAAGAGAGAGAATAGGGTACGGCTGGGGAATGGGTTTGGGGTGTGGGACCGCACCAGTGTGGACTCTATAGAATGGGCAACACACCCAAACCGCTCCGAGGGACGAAGTGGGCGCCTGTGTTTGTATGTGAGTGTGTGTGTGAGAGTGCAAGTGTGTTTGAGAGCATGTCTGTGGGAGGAAGGG
Associated Phenotype:
Not determined