ZMP
LOC100001845
Ensembl ID:
Human Orthologues:
SLX1A, SLX1B
Human Descriptions:
SLX1 structure-specific endonuclease subunit homolog A (S. cerevisiae) [Source:HGNC Symbol;Acc:20922
SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae) [Source:HGNC Symbol;Acc:28748
SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae) [Source:HGNC Symbol;Acc:28748
Mouse Orthologue:
Giyd2
Mouse Description:
GIY-YIG domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1915220]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14819 | Nonsense | Available for shipment | Available now |
sa27082 | Nonsense | Available for shipment | Available now |
sa41067 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14819
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 |
---|---|---|---|---|---|
ENSDART00000111285 | Nonsense | 9 | 266 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 7 (position 66031299)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 59213039 |
GRCz11 | 7 | 59515469 |
KASP Assay ID:
2259-9717.1 (used for ordering genotyping assays)
KASP Sequence:
TAAAAAWAAGTTGTTTTAAACAGGATGGTTGTGGAGGTGGAGAGTTTCTA[T/A]GGTGTGTATATGTTGTACTGTACAAACCCGAAATTTAAGGGTCGAATATA
Long Flanking Sequence:
AGCTTTTTGTTTTAAGTCACGCCTCTAGACCACAATAATGGCCAATCCCTATCAAAGTACGACGTTTTGACCAATCAAAACAGAGAGCATTTGGGGTCCTTGGTAGTGTTGGCTTCTTTGAATTTGCTTGATCGAAATGTTAAAGAATTAGAAAAAAATAATTAAACTAATAAATACAGCGTCAATGTTTTATTTGTTAATAACACTGATGGCTGTAAAATATTTTATCTAATACTTTAAATCTTAATATGCGACATCCATATCAAATTATTTGCACATGCAATACCGGGGCAGCTTTCATTTGAAAAGAAAGAACCACATGACCACACCAAACGCAACAGTGGATTTTTGTTTTAACGTTAGTATTTAATAAAATGTCATATTTATTTTAAGCCAGAAGTTTTGATCAGTAGTATCACTTAAGATGAGGAACAATTTAAAGGTTCTTTGTAAAAAAAAGTTGTTTTAAACAGGATGGTTGTGGAGGTGGAGAGTTTCTA[T/A]GGTGTGTATATGTTGTACTGTACAAACCCGAAATTTAAGGGTCGAATATATATTGGCTTCACTGTGAATCCAGAGCGCCGTATCGGACAACACAACGCCGGGCGACACCGAGGAGGAGCCAAGAGAACCAGTGGCAGGGGACCTTGGTGAGACATCAGCTGATAATATTCAATTAAGTTAACTGTTATTTCTATAACGCTTTTACAATGTAGATAGTGTCAAAGCAGTTTTAACATAGAAGTTCTAGTAAACTGAAACTGTGTCAGTGTGGTTTAATTTTTTACTGCTGAAAGTCCAAACACTGAAGAGCAAATCCATCCATGCGCAGCTCCACAAGTCCAAAGCCAAACTATCAGCAGTTTTTTTTTTTTTTTTTTTACTGACGTTGTCAACATATACTTTGTTAACTTAAACAGATAAATTCAAAACTATTAAAAATATTAACAAAAACATTAAATAGTAGTAGAAATAAATATTTTTTTTAAGAAATATATAACACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27082
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111285 | Nonsense | 183 | 266 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 7 (position 66029958)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 59211698 |
GRCz11 | 7 | 59514128 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAAAATAGTTGAGACTCATCCCTATTGGAATTACTTTTTTTTTTTTTTT[G/T]AATTGTTTCAGACTGTGGATAGATTGTCTTGTTTCCACCCTTCCTGTCAA
Long Flanking Sequence:
AGCTAATTTTTAAAAAGTAAAAATTACTTTGGCTGACTAATAAATGTACTTTGGCAGACTAATAAATCTTTTCTTTCCTAGTTTGAATGGGCTTGGCAACATCCTCACATCTCTCGTCGTTTGTCCCACGTTTCCCGTCGCAGCCGTAAAGAGTCAGGTTTGCAATTTCACTGGCGTGTGGTGTCAAACATGTTGCGAGTGGCACCATGGAGTCGACTCCCTATCACTGTGCGCTGGCTAAAGCAGGAGTATCGAATGGATTTCGCCCCTGATTTACAGCCTCCACTGCACATTCCTCTAACGTTTGGCTGTGTTCGTGCAAAGAGAAAACCACAACATGTGAGCAAAGAGCAAGAGGAAAGACAGGTGGAGCTCTGTGTGTTGTGTGGGGAATTTATTAAGGTAGGTTTTAGTTTAGTTTTACTGTAGTTTTGAGGAAAAATTGCTGTCATAAAATAGTTGAGACTCATCCCTATTGGAATTACTTTTTTTTTTTTTTT[G/T]AATTGTTTCAGACTGTGGATAGATTGTCTTGTTTCCACCCTTCCTGTCAAATGGTTTGTCACCTCATTTGCTTGGCTGGACACTTTTTGAAGGCAGACCCCTTCCACCTAATTCCTGTTGAGGGAAAGTGCCCTGGATGCCATCATTCAGTGCTGTGGGGAAGTTTGATACTGTATAAAAATGCAGACTTGGAAGAAATGAACATCCCTTCATCCCAGGTCAGCTCTGACATGCACCGTAAAACATCAATAATTAGTTTAATCAATTGAAGATTTGCTTTGAATTTACTTAATTTGACATTAATGACGTTTTTTCCTCCTACCATTGGGGGTGAAAATGCATGCAAAATACGCATGGCTCTTGAAGATATTCTAAGGCCTTGTGATGTAAAGCCATAAGTCTGTGCAAAAAAGAGTACCGGTACATTACACATTATCCATTGAACTCAAAAGCATAGCCTTCAAGTCACTTTTTTTCCACAAACATTGAGACAGCCTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41067
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111285 | Essential Splice Site | 255 | 266 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 7 (position 66029738)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 59211478 |
GRCz11 | 7 | 59513908 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGTATAAAAATGCAGACTTGGAAGAAATGAACATCCCTTCATCCCAGG[T/C]CAGCTCTGACATGCACCGTAAAACATCAATAATTAGTTTAATCAATTGAA
Long Flanking Sequence:
CTATCACTGTGCGCTGGCTAAAGCAGGAGTATCGAATGGATTTCGCCCCTGATTTACAGCCTCCACTGCACATTCCTCTAACGTTTGGCTGTGTTCGTGCAAAGAGAAAACCACAACATGTGAGCAAAGAGCAAGAGGAAAGACAGGTGGAGCTCTGTGTGTTGTGTGGGGAATTTATTAAGGTAGGTTTTAGTTTAGTTTTACTGTAGTTTTGAGGAAAAATTGCTGTCATAAAATAGTTGAGACTCATCCCTATTGGAATTACTTTTTTTTTTTTTTTGAATTGTTTCAGACTGTGGATAGATTGTCTTGTTTCCACCCTTCCTGTCAAATGGTTTGTCACCTCATTTGCTTGGCTGGACACTTTTTGAAGGCAGACCCCTTCCACCTAATTCCTGTTGAGGGAAAGTGCCCTGGATGCCATCATTCAGTGCTGTGGGGAAGTTTGATACTGTATAAAAATGCAGACTTGGAAGAAATGAACATCCCTTCATCCCAGG[T/C]CAGCTCTGACATGCACCGTAAAACATCAATAATTAGTTTAATCAATTGAAGATTTGCTTTGAATTTACTTAATTTGACATTAATGACGTTTTTTCCTCCTACCATTGGGGGTGAAAATGCATGCAAAATACGCATGGCTCTTGAAGATATTCTAAGGCCTTGTGATGTAAAGCCATAAGTCTGTGCAAAAAAGAGTACCGGTACATTACACATTATCCATTGAACTCAAAAGCATAGCCTTCAAGTCACTTTTTTTCCACAAACATTGAGACAGCCTAAAAACATATATTTCAACACCTTGTTCATGTTCTTTTTTATGCATGGACTCATTGCTCATTAGTTCTTCAGTCTAACTCGGTTTGCTCAGTTCAGTGTAATGAATTATCCTCTTAAGGCCCAAGGTGTTTTTTACATGCATTTTTTATTTCTTTTTGCTATTTGGGCTAATTGGAACCTAATTAGAATAAAAATCTAAGTATCATCTTTTGATGTGATGTACT
Associated Phenotype:
Not determined