ZMP
skiv2l
Ensembl ID:
ZFIN ID:
Description:
helicase SKI2W [Source:RefSeq peptide;Acc:NP_001038366]
Human Orthologue:
SKIV2L
Human Description:
superkiller viralicidic activity 2-like (S. cerevisiae) [Source:HGNC Symbol;Acc:10898]
Mouse Orthologue:
Skiv2l
Mouse Description:
superkiller viralicidic activity 2-like (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1099835]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14407 | Nonsense | Available for shipment | Available now |
sa14666 | Nonsense | Available for shipment | Available now |
sa14992 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14407
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 |
---|---|---|---|---|---|
ENSDART00000089609 | Nonsense | 153 | 1249 | 5 | 29 |
ENSDART00000135607 | Nonsense | 153 | 743 | 5 | 19 |
ENSDART00000136216 | None | None | 114 | None | 2 |
The following transcripts of ENSDARG00000062206 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 27404875)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27334987 |
GRCz11 | 19 | 26919210 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAATTCAYTCTCGTTACAAAGACAGCCTGGACCTCCGTCAGAGAGTCTG[C/T]GAGGGAGCAACACAAACTAYCCATTTCTGCCAGGTACAGYACTTTGCATT
Long Flanking Sequence:
GCGGTTTGGAAGCAATCCTTATTTAGCTTTTAGTTCTCTGCCAGGACTGTTCTCTGAAGTTGCATGTGCTTTTAAACTCGCTTTTAAAGTGTAAAAAAAATTCAAAATAAAACATTTTTGAATACTAAATCACCTTTATTTTTTGAAGTATGCGATAAAATATTTCAGATTCTTATTTAATATGCTTTCTTGTTTGTTTGTTTGGTTTTTTTTAAATAAACCAAAATCAAGTGTAGTAGTGCAACAAGATTATGTTTGTTTTATTTTTTGTTTTGTAAACCAACAATGACTTTAACAGTCATTATTTAAAACAATAAAAACATGGTCAACCGTTCGGTAAAGGGGCAGTCAAAGGGTCAATATTGTATTTTTTTTAATCATGTGTTCAATATTGTTGTTGTTTTTTCCCTTTATGCCAGGTGTTGTTAGAGGACACAGGTTTGTCTGCAAAAAATTCACTCTCGTTACAAAGACAGCCTGGACCTCCGTCAGAGAGTCTG[C/T]GAGGGAGCAACACAAACTATCCATTTCTGCCAGGTACAGTACTTTGCATTCGAATGTTTTTTGTAAAAATTAATTTCTAAATGATATACTTTTTAAAATTCAGCTCTTCTTTGTATTCCCAGCTGGAATGGAAGAACTGACTTTAGAGCAGATCAAAAACAAGTCAGAGCTGGAAGAAGACATTGACTTTGAGAAAGGTTGGTTGTCTGTTTTTGTTTCATGTAAGTCCATTACCTTCTAGCTACCTTGATGGTTGTAAATGCATGTAGAAGAATAGAAGAAAAAATAACTAGGACATATAAAAGAGAAAATATTAGTCTGTCTTGTTTTTGTCAGTAGGCAGTAATTTGTGAATGTTTGTGAGAGAAAAAAATGCCGCAACAATTTGTTCCATGTCTTAGATTTGATGACAGTTCCTCCTGGGCTGAAGGCTGGTATGGACTTCAGTGACAAAGGTCTGATTTTATTGCTTCCCACACACACGTGCAGATGCACACTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14666
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 |
---|---|---|---|---|---|
ENSDART00000089609 | Nonsense | 569 | 1249 | 16 | 29 |
ENSDART00000135607 | Nonsense | 569 | 743 | 16 | 19 |
ENSDART00000136216 | None | None | 114 | None | 2 |
The following transcripts of ENSDARG00000062206 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 27396641)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27326753 |
GRCz11 | 19 | 26910976 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCTTCTGCACTGTTAGGATCGTGCGGTGTGGCARACRCTGTTAAATTA[T/A]CTGTCTCAGAGGCAGCAGACTCCAGTGGTGGCRTTYACRTTCTCTAGGAC
Long Flanking Sequence:
AAAAATTGTGTCACTGTTCCCTAGTTTAGGTGTGTAAAAGTGTGCAGTCAACATCCATAACAAATGTTATTAATAAGACATTATAAAATGGGGTTCGACGTAATTTTTTGAATATTTGGGGAAAAAAAAGAATTACGATTTTAAAAGAAAGCTAATAATTGTACCCATTGCCAGCTGTACATTATAGTTGGACTTGTTATAAATGTTTAGCTAAGGGCTGCTCAAAATGAATGTAAATACACCTTAATGAAGACTGTTTTGTTTTTCAGCTACTACGCTGCAGTGGAAGCCAAGAAGGAGCGCACTAGTAAACATGCACAGTCTTTTGGCACAAAGAACGTATCGCAGCACAACACAACAGCCAGTCAGGTCAGCATCCATCTTTGAATCTACTCTCTAACATAATACATCTCTTTTTCTAATGGCAGTGTTTTGACAGTTTTCTGCATCTTCCTTCTGCACTGTTAGGATCGTGCGGTGTGGCAAACGCTGTTAAATTA[T/A]CTGTCTCAGAGGCAGCAGACTCCAGTGGTGGCATTTACATTCTCTAGGACACGATGTGATGAAAACGCTCGCTCTTTGACCTCTCTGGACCTCACCACATCCATAGAGAAGAGCGAGATCCACTCCTTCCTGCAGAAGAGCCTGACCAGACTGAGAGGAGGAGATCGACAGCTACCACAGGTACTGTACATGGTCAACTTTTTATTGGCCAATCAGATATCTTTAAAACAAAGAAGGAAAAAGCTGAAGGCCATTTTAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAAATTGTATCATTGTATTGTGTTGTAATATAATTTTTTTTCTATGGATATACACTCACTGGCCACTATATTAGGTACATCTTTCTAGTACCAGGTTGGAGCCTCTTTTGCCTTCAGAACTGCCTTAAAGGGTTTCAGCAGGGTGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14992
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 |
---|---|---|---|---|---|
ENSDART00000089609 | Nonsense | 1155 | 1249 | 28 | 29 |
ENSDART00000135607 | None | None | 743 | None | 19 |
ENSDART00000136216 | Nonsense | 20 | 114 | 1 | 2 |
The following transcripts of ENSDARG00000062206 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 27360884)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27290996 |
GRCz11 | 19 | 26875219 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCAAGTTCTCGCTGTAGCCCAGCGTATCGGTGACCTGCAGAGGGATTG[T/A]GGGATTGCTCAGACCRCTGAAGACTTCGTGGCCCAGTTCAAGTTTGGCCT
Long Flanking Sequence:
CACATGTGGGGGGAACCGGAGCCCCCAGAGGAAATCCACACCAACATGGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGATCCAGCCTAGGCTCGAACCAGCACCCTTTTTGCTTTGAGGCGACAGTGCTACACACTGCGCTGCCTTGCTGCCATATAAATAAATAAATAAATACATATGTATGTGTTGTTTAAAATTACTTTTTTTGATTAAAAAATATTGTGACTATATTTTTTCTACTAACCGTTTCTTCCTTAATGTTGATTATTTTTGATTGTTGATTACCTTAGTAAAATCTTTACTATCACTTTGTATCATTTTAATGCATCTGAAACTATTCATTTTATGAAAAAAATAGTCTTACCGACCCCAAACTTTTGAAGTGTATATAATATTTATTTATATATACCATTTTGTCCTATTCTCTTGCTTTCCTAGGGAATCAATCAAGTTCTCGCTGTAGCCCAGCGTATCGGTGACCTGCAGAGGGATTG[T/A]GGGATTGCTCAGACCGCTGAAGACTTCGTGGCCCAGTTCAAGTTTGGCCTGACTGAGGTTGTGTACTGCTGGGCAAGAGGAATGGTAAGCATTGACCTTAAAACACAAATGAACCAACCAGTGTGTGTTCTGCCTTTTATAGTCGATTCAATTTGGTTGGTCCATGTGACATTCTACTAGCTATTATAAAATAAGACAATATTAATATTCTATCAAGAAGGCATTTTTATTAAATGCTGTATGATCTTGCAAATTCTTTTTTTATTTTTGTAATTCAGTGAAATGAATTCTTTATGATATGAATGCTTTGCATGAATTTTGAGAGTAACTTTAATTAACATGGCACAAACAGCACTTAATACACCCCTGGTCTGTTTTTATACAGATAATTGCACTACAGGACTCAATGCTGTGAATTTTTTTTATTTATTTATTCATTTTTTTTTTTTACAATACGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGCGTGTGTGTGTGT
Associated Phenotype:
Not determined