ZMP
tnpo3
Ensembl ID:
ZFIN ID:
Description:
transportin-3 [Source:RefSeq peptide;Acc:NP_957381]
Human Orthologue:
TNPO3
Human Description:
transportin 3 [Source:HGNC Symbol;Acc:17103]
Mouse Orthologue:
Tnpo3
Mouse Description:
transportin 3 Gene [Source:MGI Symbol;Acc:MGI:1196412]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20237 | Nonsense | Available for shipment | Available now |
sa8594 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13543 | Nonsense | Available for shipment | Available now |
sa44585 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20237
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067161 | Nonsense | 44 | 923 | 2 | 23 |
ENSDART00000138201 | Nonsense | 44 | 922 | 2 | 23 |
The following transcripts of ENSDARG00000045680 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 12654158)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 13590785 |
GRCz11 | 4 | 13589634 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGACAAATGTTTCCTTTTTTTTTAAAAAATCTATCCAGATGTACGCGTG[G/A]GAAATCTCCGATCAGCTCCTGCAGCTGAAACAGGACATCGAGTCTTGTTA
Long Flanking Sequence:
TTTTTCAGGACTGTTTAATATTTGCATTATCTTCAAATTGAGATACTCGTCAAGTCATACTTTCTGTTTTAGAAAATATATATTGGCTGAATGGTTTCAAAGTATTACTTCACATTCTCTAGCTCATCTCATTTCTCATATATATGATGAGCATTCTATCCCTTTAGACTTCAATGATATGTTACACACAACATGTTCCTTCTATCTATTTGCATGTATAATATTTATCCTGGTGTGACGCATCTCATGGTGTAGTGTTTATTTTTACCTTTGATTATGCAAATTAGCTCTGGGCCAAGTTGATATTCAGTGTCTGATAGAGTGATAGCTAGTGAAATAATGCCCATTTCTTTTGATTAAATTAAATAAGCCCTTTAGGGTAAATAAACAAACACTTTAAATGTCATTGAGCCATTTTGAAATATTTAAAAAATTCTGCTTTACAAAGTGGTGACAAATGTTTCCTTTTTTTTTAAAAAATCTATCCAGATGTACGCGTG[G/A]GAAATCTCCGATCAGCTCCTGCAGCTGAAACAGGACATCGAGTCTTGTTACTTCGCAGCCCAGACGATGAAGATGAAGATCCAGACGTCGTTCTACGAGCTTCCCCCAGATTCTCACACTGCACTGAGAGATTCACTCTTATCTCACATCCAGAACCTCAAAGACCTTTCTCCCATCATCGTCACACAGGTACGTCCTACCTACTTTTGAAAATCTGTGCCAGTCATGATCGGAAATTATCGGACATGCAGTGTGGGGGGTTGACGGGGACAGTCCATCTCCACCACACACTGCACTGCTACATATTGAGAACTGTTAAGAATGTGGCGCTGGTATTCTAATGTGGTTCTCTCTCTCTCTCTCTCACCCAGCTCGCATTGGCAATCGCAGATCTGGCTCTTCAGATGGCCTCGTGGAAAGGCTGCGTTCACACCCTCATAGAAAAGTAAGAATCCTCCTTATTTTCTCCCTGGTTATGACCTACAATGGTGTTATGGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8594
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 |
---|---|---|---|---|---|
ENSDART00000067161 | Nonsense | 203 | 923 | 5 | 23 |
ENSDART00000138201 | Nonsense | 203 | 922 | 5 | 23 |
The following transcripts of ENSDARG00000045680 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 12656091)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 13592718 |
GRCz11 | 4 | 13591567 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTGTGCGGAGAAGTCTGGCCACGACGAGAAGATGCTCATCAAGGTGTWC[C/T]GATGTTTGGGGAGCTGGTTTAATTTAGGAGTGCTGGACAACAATTTCATG
Long Flanking Sequence:
TAATTTGCAAGGACTATTAATATGTAACTTTTTTTTTTAATTGGTAAATGTATTTTTTATAGCAGTATTTTGTGTGAAAATATGTATGTAGTCTTTTTGTTTTCGTTTATGTACTTTGGGACAAGCGTTTTAATTATATTTGCGGTATATTAATCTGCATTTTAGTGTTCTGCCAAGTCAAGTTATAACTTACACCTTGAAAACTATCACTGGACAGTTTTTAAATTTGGACATCTTTGTTAACCGAGGCATAGTTTTTATGATGGTTCATATCTCTGTGTGTGTCCTCATCAGTTGTTGCTGTTATTTTGCTTGCACTTCTCCTCTGTTCTATTCTCTCATTCTCTTCATGCAAATCATATCTGCGGTTATATGGTGTATGAACATTCATTTAAATGAGTTGACTGTGATCTGACTGTGGGTATTTCACTTATCTCTGTGATCAGGTGACGTGTGCGGAGAAGTCTGGCCACGACGAGAAGATGCTCATCAAGGTGTTC[C/T]GATGTTTGGGGAGCTGGTTTAATTTAGGAGTGCTGGACAACAATTTCATGGCAAACAATCAACTGCTGATGATTCTCTTCCAAGTGCTGGTAAGATGGAGTCAGATAGTCACTTTATTTTCCCACTTTTTCTTACTTTTATTTTAAAAATGTTTTTTCCCCACTCGTCATTGAAGCAGAGGGATGAGACGTCTACAAACCTGCATGAGGCAGCATCAGACTGCGTATGCTCAGCATTGTATGCAATCGAGAATGTGGCCATTCACCTGCCGCTGGCCATGCAGCTCTTCCAGGGAGTCCTTACTTTAGAAACAGCCTACCACATGGCCGTGGCCCGAGAAGACCTCGACAAGTATGTATGGCTCTGCTTGTGAATAATATAAAGGGTTCATCGAATTTCTGTAATATTCTGGAAAAGGTATATTCCAGACGTTGGAAGTCAGGGAATTTTTAGGTATTTTATTTATAATTTATTTTAGTCATGGAATATCGGGAGTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13543
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 |
---|---|---|---|---|---|
ENSDART00000067161 | Nonsense | 530 | 923 | 12 | 23 |
ENSDART00000138201 | Nonsense | 529 | 922 | 12 | 23 |
The following transcripts of ENSDARG00000045680 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 12660347)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 13596974 |
GRCz11 | 4 | 13595823 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGTTGGCCTCTGCRGCAGCTAAAGCCATCCATAACATCTGCTCGGTGTG[T/A]CGAGACCACATGGCGCAGCACTTCCAGGGCCTGCTGGACATCGCCCGCTC
Long Flanking Sequence:
TTATTTGTATTATCAAAGAAAAAGGATTTTCATACAAAGTTGTAAATTTGATCTGGATTTGTCATGAAATAGCCAGAGAAGCTGATAGCTATCTCTCTATCTTCCTCTCTCTGCATGTAAACAAACCTAAATCTCCAGTTTGTTGACGTATAAACATTAAATTGAGCATTTATCAAACATCATTTTGAGATGATAATCTCAAAATCATTTTGAGAGATAATCGTATTGTGATGATTAGCCTCATCTACAGTAGTCAACATCCAAAGTGAGTCAAAAATGTTTTTCAAAATTGTCCTAGGTCAAGAATGGGTGTTGTTTAATAGTTTAAGAACAACTTTCATCAAATGTGATGATTTACTTCAAATGTTGATTACTATATATACTCATAATGTCTGTTTTGGGTTTGCAGATACTGTTTTGAACTTCCTGATGAAGGGTTTACGGGAAAAGCCGTTGGCCTCTGCGGCAGCTAAAGCCATCCATAACATCTGCTCGGTGTG[T/A]CGAGACCACATGGCGCAGCACTTCCAGGGCCTGCTGGACATCGCCCGCTCTCTCGACTCATTTGCCCTGTCAACAGACGCCGCCGTTGGCTTGCTCAAAGGTATCAGGAAAGGGTCTTTAAAAAGTTACTTTTCCCCTTCACTATTCTGCGGTTTGCAGAAGGTACACACTTCTCCTCTAGCGCTTGACCCTTTTCTGTTGTTCTTAGTCATGCCCTTGTTGTATGGCTGGTTTGGTTTAAGAGGTGTGATTGGTTTACTTAGGTACAGCGCTGGTTTTGGCCCGTCTCCCGCTGGAGAAGATTGCGGAGTGTCTGAACGATCTGTGCGCAGTTCAAGTCATGGCACTTAAGAAGGTTAGATATATGCTGTCTGTGGACTGTATGACTCTCTGGGTGTTTAATGCTGGAAAATAATGTGTTGTTTTGGTGTGCAGCTGCTGGCTCAGGACTCCAGTAGTGGGAAGTCGTCAGACCCTACTGTATGGCTGGACAGACTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44585
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067161 | Essential Splice Site | 904 | 923 | 22 | 23 |
ENSDART00000138201 | Essential Splice Site | 903 | 922 | 22 | 23 |
The following transcripts of ENSDARG00000045680 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 12666624)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 13603251 |
GRCz11 | 4 | 13602100 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGAAATGTGATGATAATTTTCTGCCTTTCTGTAAATCTGTCACCATA[G/A]TGCAGAGGAATGTAAACAGGTTTGTTGGGCCATAAGAGAGTTTACCAGGC
Long Flanking Sequence:
TGCCGTCACAATGACTCTTCAAAGCACACCAGACGCATTAGGATGCATTCATCGCAATTACATTACACTCCCAAACAAAATGGCCATGATTAAAAGAGCTGTTGTCCACAATTAAAAGTAATACGGGACTCATCAGTGTAGATTACAGGCAGCATTTGTATCTTGGCCTATTGCAAGTTAGTGCACGTTCAGATTACTCTGTGGTTTACTCTACACAACAAGCCTAAACAAGCACCAATAACCAGTCGTCCAGGAGGGTGAAGTATGTCGTTCCTCTGCAAGTCTTGACCTGAGATGCCAAATACAAACTCTTATAGTGAGTGCAGGATGAGTCATAGACTTGCGTGGAAAGTCCAACCCACGCCAAAATGACTGATTTATTGCTCGCGCATGCTTATGGCGTGCTCGCGAGTTGATTTTAAAATAGCAGGCCATCTTGTTGTTTAGTTCTGTTGAAATGTGATGATAATTTTCTGCCTTTCTGTAAATCTGTCACCATA[G/A]TGCAGAGGAATGTAAACAGGTTTGTTGGGCCATAAGAGAGTTTACCAGGCTGTACCGATAGCTGTCTTCTACCTGCTGATGCTGCAAGACCAGGTGAGAGAGAGAGAGGAAAATGAAACAATTTGTCAGTGTATTGTGCATAACATTGAATGTGTCTTTTCTATGTTTATTCAAATTAGGGCTGCACAATATACTGTTTCGGCATTGACATCGCAATATGTGCATCACCAATCGCGAGATACTCGATGAGTCTGAATAATGTTCACCAGGAGCTTCAGAATTGATTTAATTACTGCATTTATATAGAAATGTATACGATTTATCCCCCCCCAAAAAGTTTTTCTTTATTTTTCAATATTTTTCTAGTCCAAATATTCACATTTTAGAGCAAAAACAAGATTATTTGACTTAATTTAGCTTGTTTTAAGGAAAAACTCTTAATTTTGCCTAATTTCCAAAGTTGAAAACAAAACTATTTGACTTGATCTAAGAATTTTTAG
Associated Phenotype:
Not determined