xpo7

Ensembl ID:
ENSDARG00000005540
ZFIN ID:
ZDB-GENE-060628-2
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 5 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa9320 Essential Splice Site Mutation detected in F1 DNA During 2016
sa34881 Nonsense Mutation detected in F1 DNA During 2016
sa9930 Nonsense Available for shipment Available now
sa16794 Nonsense Available for shipment Available now
sa38791 Nonsense Mutation detected in F1 DNA During 2016

Mutation Details

Allele Name:
sa9320
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
T > C
Consequence:
Essential Splice Site
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
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GGGGGAGTGAGAGGAGCATGAATGGAGCAAAATGGCGGATCATGTGCAGG[T/C]AAGTAAATTATTTTGTTTTGCTATTATGAAATKAATGAATTTTGATYCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34881
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
C > T
Consequence:
Nonsense
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
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ATTTAAATAGCAATGACTTTTTATTGTTTTTGTTCTTTCAGAGCCTAGCC[C/T]AGCTAGAGATCCTGTGCAAGCAGCTGTATGAGACCACAGACACCACCACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9930
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
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
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CCTCGTACTCACAGTTGTTGGCTGCGAYGTGTCTCTCCAAGTTGGTGTCA[C/T]GAACWAGTAACCCCCTTCCTCTGGAGCAGCGCATTGAYATTCGTAAGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16794
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
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
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TGTGATYTCWGACTCACTGAATGWGTTTTTCATGAAGGTCACAGAGATTA[C/T]AGTTYGATGTGTCGTCGCCGAATGGAATCCTGCTGTTYAGGGAGACCAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38791
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
C > A
Consequence:
Nonsense
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
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CTTTCAGTATTTAGAAGAGAAGTCAATGACTCCATGAAGAATTCCACATA[C/A]GGGGTAAACAGCAACGACATGATGAGCTGACATTCCATAGAGCACCAGGC
Associated Phenotype:
Not determined

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