ZMP
xpo1
Ensembl ID:
ZFIN ID:
Human Orthologue:
XPO1
Human Description:
exportin 1 (CRM1 homolog, yeast) [Source:HGNC Symbol;Acc:12825]
Mouse Orthologue:
Xpo1
Mouse Description:
exportin 1, CRM1 homolog (yeast) Gene [Source:MGI Symbol;Acc:MGI:2144013]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10716 | Nonsense | Available for shipment | Available now |
sa7435 | Missense | Mutation detected in F1 DNA | Not yet available |
sa42931 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7436 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10716
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 |
---|---|---|---|---|---|
ENSDART00000092188 | Nonsense | 78 | 1074 | 3 | 24 |
Genomic Location (Zv9):
Chromosome 17 (position 23801485)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23954927 |
GRCz11 | 17 | 23973328 |
KASP Assay ID:
2261-1044.1 (used for ordering genotyping assays)
KASP Sequence:
AAAGCTYGGGTCATTAATGCTTGATTTGYTCTCTTGGCATTACAGYACTA[T/A]GCTCTGCAGATTCTGGAAACAGTTATTAAAACAAGATGGAAGATTCTGCC
Long Flanking Sequence:
TAAGACAGAAAGGGATGTGGTCAGTAGTCGACCAATGAGAAAACGTATCGCTGACGTTTAAAGCATTTCAAAGAATTCTACGGTTCTTTTTGTTTTCGAACACAGTTGTTGCGTCGTTCCGGCCGGGCAGAGAAGCAAACCATTAGCTGTTTGCCATTTAATGCCTTCTTTCTTGTCTTTCACATTCTGGTGTGACACGGCCAGAAACAGCAAAACTTCTGCAGAATCTCATACAAACATTGTTTAGGATTTTGATGGGGGATTATGAATGATTTTTTTGTTCTCCTTTTTGAGTTCTTTATTACAACAATTATCACTCAAGTCAAATCTGCATGATGTTTTTTGTTTTCAATCTGAAATCAAAAAGAATATGTGGAAATGTATTAGGCAGTCAAAGTTAAGAGCAATTTTTTTTGTTTTCCTTGTGCAGCTCTGGCAGATCGGCTGGTTAAAGCTTGGGTCATTAATGCTTGATTTGTTCTCTTGGCATTACAGTACTA[T/A]GCTCTGCAGATTCTGGAAACAGTTATTAAAACAAGATGGAAGATTCTGCCCAGAAACCAGTGCGAAGGTAAGAGTGACTCACAAAAATTCCCCTCGCCACTTTGACATGAACAAGTAATTAATATCCAGTCTAAATCAATTCTTAAGTCATAAGCAGCTCAAAGGCTGGATTTGGACAAGCGAGGGATCATTGAAATGTAGAAGTCAACGTTTCCCTCTGTGACAGGCTTGACTTTACAAGACGTTTCTAGCAGGCCAAGACATTCATTAGAATCAAGTGTGTGATTGCCAAGTTGAGCTGAATTCCCTTTTTAAAAATGCATGGAAGGTCGTCTGCTCGGCTTAATGTTCATCTGTTTCCAAAAAGGATAGAGTCTCTTTTTTTAAAGCATGGCGTGAAACAAAAAATGACAAACACCTATTCATAGGCTAGTTTATTAAAAAAATAAAGCTTATTTTATGATTTAACAGTGATTTTTAGAATGATTTCAATAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7435
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 > G
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092188 | Missense | 459 | 1074 | 12 | 24 |
Genomic Location (Zv9):
Chromosome 17 (position 23804256)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23957698 |
GRCz11 | 17 | 23976099 |
KASP Assay ID:
554-4130.1 (used for ordering genotyping assays)
KASP Sequence:
GGTTCGAGAATTCAKGAAGGATACAGACTCCATTAATCTATACAAGAACA[T/G]GAGGGAGACACTTGGTGAGAACTTAGTCATTCTTCACTTTTAATGCAGAT
Long Flanking Sequence:
TCAGAGAGACTCTTATGGAGGTAATTGCACAAACTGTTGATTATGGAGAATCAGCCTTTGTGCCATTATGTTAAAGGTCTATTTGTTTTTGCATTTAGGCTCTACATTACATGTTGCTAGTGTCAGAAGTGGAGGAGACTGAGATCTTTAAGATCTGTTTGGAGTACTGGAACCACCTTGCAGCTGAACTGTACAGAGAGAGTCCTTTCTCAACGTCCACCTCTCCCCTTCTCTCAGGGAGCCAGCACTTTGATGTTCCGCCCCGCAGACAACTCTACCTGCCTGTGCTTTCTAAGGTTAGCTCACAAACACACCACTCAGAAATAATTCACCTTGGATAGCAGCACCCATAAGTGAGTGTGTCGCTGTCCTGCAGGTGCGTTTGTTGATGGTCAGCCGCATGGCCAAGCCAGAGGAAGTGCTGGTGGTGGAGAACGATCAGGGAGAGGTGGTTCGAGAATTCATGAAGGATACAGACTCCATTAATCTATACAAGAACA[T/G]GAGGGAGACACTTGGTGAGAACTTAGTCATTCTTCACTTTTAATGCAGATTTTTTGTCTAATTAACTATGCTTTATTGTTGGTTTCCATCACATTTTGAATATGTTTCTTGCTCTGTAGTCTACCTTACCCATCTGGACTATGCTGACACAGAGCGTATTATGACAGAAAAGCTTCATAATCAGGTGAACGGTACTGAGTGGTCCTGGAAGAACCTAAACACACTGTGCTGGGCCATTGGTTCCATTAGTGGAGCCATGCATGAGGAAGATGAGAAGCGGTTCCTCGTCACAGTCATAAAGGTGTGGACCTCTTTAACACATAAAACTGCTAGAGGGTACACTTTACCCATGAACAAGACTACTGTTTTGATTTGGCTAAAAGGTTTATTGTATCACTGTATTGTGCATTTGAGTCCAGAGACTATTTTTTGAAGACATTTATATTTATGATTATTTTTAATCATCAGCTATGATGCTGAAATGAGCCCAGATGCATCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42931
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092188 | Nonsense | 508 | 1074 | 13 | 24 |
Genomic Location (Zv9):
Chromosome 17 (position 23804507)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23957949 |
GRCz11 | 17 | 23976350 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCCTGGAAGAACCTAAACACACTGTGCTGGGCCATTGGTTCCATTAGT[G/T]GAGCCATGCATGAGGAAGATGAGAAGCGGTTCCTCGTCACAGTCATAAAG
Long Flanking Sequence:
GATGTTCCGCCCCGCAGACAACTCTACCTGCCTGTGCTTTCTAAGGTTAGCTCACAAACACACCACTCAGAAATAATTCACCTTGGATAGCAGCACCCATAAGTGAGTGTGTCGCTGTCCTGCAGGTGCGTTTGTTGATGGTCAGCCGCATGGCCAAGCCAGAGGAAGTGCTGGTGGTGGAGAACGATCAGGGAGAGGTGGTTCGAGAATTCATGAAGGATACAGACTCCATTAATCTATACAAGAACATGAGGGAGACACTTGGTGAGAACTTAGTCATTCTTCACTTTTAATGCAGATTTTTTGTCTAATTAACTATGCTTTATTGTTGGTTTCCATCACATTTTGAATATGTTTCTTGCTCTGTAGTCTACCTTACCCATCTGGACTATGCTGACACAGAGCGTATTATGACAGAAAAGCTTCATAATCAGGTGAACGGTACTGAGTGGTCCTGGAAGAACCTAAACACACTGTGCTGGGCCATTGGTTCCATTAGT[G/T]GAGCCATGCATGAGGAAGATGAGAAGCGGTTCCTCGTCACAGTCATAAAGGTGTGGACCTCTTTAACACATAAAACTGCTAGAGGGTACACTTTACCCATGAACAAGACTACTGTTTTGATTTGGCTAAAAGGTTTATTGTATCACTGTATTGTGCATTTGAGTCCAGAGACTATTTTTTGAAGACATTTATATTTATGATTATTTTTAATCATCAGCTATGATGCTGAAATGAGCCCAGATGCATCACTCACACCTAATGACTCCCCACCATCAGGCTCACTATAAGTAATTAATTATTTATGTTAATTTAATAATTAATTAATTATTAATATTTCTGCCTAATACCTGTTGGTCATCCATGAATTTGCACCTTTTTAACCATTGTGACTAAATCTGTGTGAGAGAAAGATGTTGCCTAGCATCGTATAAGCTAAAACTTAAGTGGCCTGAAGACAACATCAGTTTAAGTCAATGACTTGCAGACTTATTTAATCAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7436
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 > G
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092188 | Missense | 642 | 1074 | 16 | 24 |
Genomic Location (Zv9):
Chromosome 17 (position 23805823)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23959265 |
GRCz11 | 17 | 23977666 |
KASP Assay ID:
554-4131.1 (used for ordering genotyping assays)
KASP Sequence:
CACCATTTCCTGTTTTCAGGTGCACACGTTTTACGAAGCTGTTGGGTATA[T/G]GATTGGAGCGCAGACCGACCAGGCTGTGCAGGAACACCTGATAGAGAAGT
Long Flanking Sequence:
AAATAGCAGCATGTTTGATGTCATTTCAGTACACATACTCAGCAAGTTCAACATTTTTTGCTATTGTTTTAGCTATTTTAGCATTGGTTATAATACATTAAGCTGACCTTCTAATTTTAACTTAATTATAAAAGGACTGATGTAGTCATGTGGTGTTTCACTTTTTGTTTTTCTCAGAAACCCATGATGGAGTGCAGGATATGGCATGTGACACGTTCATTAAGATCGCTCAGAAGTGCAGGAGGCATTTTGTGCAGGTGCAGGTGGGGGAGGTGATGCCCTTCATTGATGAGATCCTCAACAACATCAACACCATCATCTGTGACCTGCAGCCCCAGCAGGTACCAGATAACCTCATCTGTCTCCTTTAGCCTTTTCTGACTCTGACTGTTCCACATATACCAAATATACTACTATTGAGATGCTCTTGGAAAGCAGCTGGACTTGAGTCACCATTTCCTGTTTTCAGGTGCACACGTTTTACGAAGCTGTTGGGTATA[T/G]GATTGGAGCGCAGACCGACCAGGCTGTGCAGGAACACCTGATAGAGAAGTACATGTTGTTGCCTAACCAGGTGTGGGACAGCATTATTCAGCAGGCCACAAAGGTGTGTATAGTTTCAGAAAGCAAGGTTTGTTCATTTACACCATAAAAGCTTATAGTAACAAACATGTAATTAAAATTAATAAAAAATGTGATATTCCACACTACAACTAATATAACAGCACCAGTTATCATAATTAGTTTCAGGTTATTACAGAGAGCCAATCAGAAAGCTTTTGTATTAAGCAGAACTGTGTGCTGTTTTCCCTGATTTGAAACCCATTTGTAAAACTGACTTTAAGTAAATAGTGTTGTCTTGCTGTAGAACGTGGACATTCTGAAGGACCCGGAGACAGTGAAGCAGTTGGGCAGCATCCTGAAGACCAATGTTAGAGCGTGTAAAGCAGTGGGACACCCTTTTGTCATTCAACTTGGTCGAATATACCTGGATATGCTCAACG
Associated Phenotype:
Not determined