Busch Lab

ZMP

zgc:55877

Ensembl ID:
ENSDARG00000027169
ZFIN ID:
ZDB-GENE-040426-2023
Description:
hypothetical protein LOC406343 [Source:RefSeq peptide;Acc:NP_998235]
Human Orthologue:
KPNA7
Human Description:
karyopherin alpha 7 (importin alpha 8) [Source:HGNC Symbol;Acc:21839]
Mouse Orthologue:
Kpna7
Mouse Description:
karyopherin alpha 7 (importin alpha 8) Gene [Source:MGI Symbol;Acc:MGI:2141165]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa41661 Nonsense Mutation detected in F1 DNA Not yet available
sa38800 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa41661
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000036906 Nonsense 13 520 1 10
Genomic Location (Zv9):
Chromosome 10 (position 25842660)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 25246618
GRCz11 10 25217178
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTGAGATTCAAAATGCCTACAGAAAATCTTTCAGATAAACGCATGTCC[A/T]AGTTCAAAAATAAGGGCAAGGAGCCGACGGTGAGCTGAGCATCCATTCTC
Long Flanking Sequence:
TAAAATCAATAGATAGACAAATCAAATAGCTATTTCAGGACCAAACACATGCAGCATCTTCCCATATCACTTTTGGCCTCTAGAGGGCAACAACATACTTTTTTTATTTCACAGGAACATGTTTTAAATATTAATGTCTTTATCAAGGTTATGGTGTTAGCTCAAGTTTTAACTAAAATAATATTTTGTGATACAAAATGTGAAATACGATTTTATGTAAACCAAAGCATTCAGAAATCCTCTGGCATGAGGCGTATGCTACAAATAAATCTCACCTGATTCTAGTTGTGCTCGTCTATATAAAGCTGATTGCAACTGTTTGCGCATGTCTGTGGAGCTGTTTTGTATACAGTCTTGCGCTGTCGGCTCTGTTTTATCACTTATTGTAACGTTTGATCTTAAAATATTTTTTTCTGAAAGTTTAATAAGTGTTTTTTGTGTCAGCTACAGCACTGAGATTCAAAATGCCTACAGAAAATCTTTCAGATAAACGCATGTCC[A/T]AGTTCAAAAATAAGGGCAAGGAGCCGACGGTGAGCTGAGCATCCATTCTCACTATTTTCATCCTTTTAACTATTCAGTCTTTAATCTTTTGATATTCACACCGTATCTCCGCTTGCAGAAACTGCGTGACCGCAGAGTTGCGGAGTGTGTTGAGCTTCGAAAAGCTCAAAGGGTTGAGGGTATCATGAAGAGAAGAAATATTACATCCTTGGGAGATGAAGAACCTCTCTCACCAGAGTTTAACACGGACAATGAACAGGTGTTGACTGATTTTTTTTCTATTAATTAGACCTCTCATTATTGCAGGACTCTTACAACTTGCTGTTTTTATTAAGGTCATCTGTACAACAATTGAAGAAATTGTTGCAAACGTGAACACTGACTGCCCAGAGAAGCAGAGGAACGGTTGTCAAGCAGCAAGGTCTAGTTACAAATGTTAATTTTACTATCAATGATATCCTGGTGTGTTAAGCAAGGGTGTCCAAACTTGTTCTTGGAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38800
Status:
Mutation detected in F1 DNA
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
ENSDART00000036906 Essential Splice Site 70 520 3 10
Genomic Location (Zv9):
Chromosome 10 (position 25842325)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 25246283
GRCz11 10 25216842
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTAGACCTCTCATTATTGCAGGACTCTTACAACTTGCTGTTTTTATTAA[G/A]GTCATCTGTACAACAATTGAAGAAATTGTTGCAAACGTGAACACTGACTG
Long Flanking Sequence:
AGCTGTTTTGTATACAGTCTTGCGCTGTCGGCTCTGTTTTATCACTTATTGTAACGTTTGATCTTAAAATATTTTTTTCTGAAAGTTTAATAAGTGTTTTTTGTGTCAGCTACAGCACTGAGATTCAAAATGCCTACAGAAAATCTTTCAGATAAACGCATGTCCAAGTTCAAAAATAAGGGCAAGGAGCCGACGGTGAGCTGAGCATCCATTCTCACTATTTTCATCCTTTTAACTATTCAGTCTTTAATCTTTTGATATTCACACCGTATCTCCGCTTGCAGAAACTGCGTGACCGCAGAGTTGCGGAGTGTGTTGAGCTTCGAAAAGCTCAAAGGGTTGAGGGTATCATGAAGAGAAGAAATATTACATCCTTGGGAGATGAAGAACCTCTCTCACCAGAGTTTAACACGGACAATGAACAGGTGTTGACTGATTTTTTTTCTATTAATTAGACCTCTCATTATTGCAGGACTCTTACAACTTGCTGTTTTTATTAA[G/A]GTCATCTGTACAACAATTGAAGAAATTGTTGCAAACGTGAACACTGACTGCCCAGAGAAGCAGAGGAACGGTTGTCAAGCAGCAAGGTCTAGTTACAAATGTTAATTTTACTATCAATGATATCCTGGTGTGTTAAGCAAGGGTGTCCAAACTTGTTCTTGGAGGGTGCACCTACAGAGACAAGCTCCAGACTTATTTTAAATGTGTGATCCTGCTAATAAGTGTCTTTTGTAATGACTAAATTTACAGGATGATGTGCTGGAACTATTTGGAGCTGAAATCTGTAGGACGATGCCCTTTTAAGAAATTGGATTGAACACTTGTGTTATAATTTTCAACCTTTAGTTTGGTCCCTACAGGAAGCTGCTTTCTCGGGAAAGGAACCCTCCCCTGAAAGAGATCATTGAGGCAGGACTTCTGACCCGCTTTGTGGAGTTTCTAGGCAGGAACGATGACCCCACCCTGCAGTTTGAGGCTGCTTGGTCGCTCACTAATGTTGC
Associated Phenotype:
Not determined