ZMP
si:ch211-244p18.3
Ensembl ID:
ZFIN ID:
Description:
INO80 complex homolog 1 [Source:RefSeq peptide;Acc:NP_001038584]
Human Orthologue:
INO80
Human Description:
INO80 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:26956]
Mouse Orthologue:
Ino80
Mouse Description:
INO80 homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1915392]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43459 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa765 | Essential Splice Site | F2 line generated | Not yet available |
sa15927 | Essential Splice Site | Available for shipment | Available now |
sa23725 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43459
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103333 | None | None | 277 | None | 7 |
ENSDART00000103336 | None | None | 1555 | None | 35 |
ENSDART00000127757 | Essential Splice Site | 268 | 270 | 8 | 8 |
ENSDART00000128806 | None | None | 1552 | None | 36 |
Genomic Location (Zv9):
Chromosome 20 (position 28371143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 28442446 |
GRCz11 | 20 | 28341536 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATTCTTCAACTGTAATGACTCTAATTTTAACCATTTTATTTTATTTCA[G/T]AAAAATAAATAACAGTTTCATGTCTTTATTAATCCTGCCATCTAAATTTA
Long Flanking Sequence:
AGATTTTTTAAAAGTTTGGGCTGAGATTATTTTTAAAAGAAGTCTCTTTTATTTATTGAAGTTGCAATTATTTATAATTTGTAGTATTTCTTTTTTCTGTTACGTTTAAAAAATATTTTGAGTTTTTAAAAAAATATACATAACTTACATAATCTCTCATACAGTAAGAGACTTACAGATCTTGCTCAAGTTTTGTAATTTTTTTCCAAACAACAACAATTATAAACGGTAAAACATGGAGAGCTGCAAATCCTTTGGATGATTGCCTTTAAAGAAGAAAAGATGTATATTTATACACCTAATATTAAATGAAAAAGTTACAACTCAAGAAAAATTGGGACATGTTGGTAAAATATACTCAATCCATTTACTCCAAATTAGAAAAAGTATTCAGTCTGTGTTCTCAATGAAAAGATTTTCTAAGACATATATAATGTGCACTCTATCAATCTATTCTTCAACTGTAATGACTCTAATTTTAACCATTTTATTTTATTTCA[G/T]AAAAATAAATAACAGTTTCATGTCTTTATTAATCCTGCCATCTAAATTTATATTGCCTAAATATAAAGATTTACAAGGGAAAGCAATCTCTACTTCAAAAATTGTATTTAAATGTATTTTAATCTCTTTCAGTATGAGGTTAATTTCTGACAATGCCAAAAGTACATGATGGTGATTGGGGCCACTTTTCACCCACTGTAGCATATTTTAAAATAGATTCATGTGAGAAAAAACATAATTGCTTAGAAATCCTTCTAATATGCTGAATATAAAGAAACAACTTGAATTATTTTATTTTAATAGGTATGTGTTTGAGTAAAATATTAGGTATAGTTCACCCAACAATAAGGATTCTATCATCATTTTCTCACACTTGTTACAAAACTTTACGAGATGAAGTAAAACTAAGTTTCTTTCTTCTGTTGAACTCAGATAATTAAATATTTTGAAACATGTAAACATTGACTAAAATATTTCCTATTAATTAAGTCAATGTTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa765
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000103333 | None | None | 277 | None | 7 |
ENSDART00000103336 | Essential Splice Site | 435 | 1555 | 9 | 35 |
ENSDART00000127757 | None | None | 270 | None | 8 |
ENSDART00000128806 | Essential Splice Site | 433 | 1552 | 10 | 36 |
Genomic Location (Zv9):
Chromosome 20 (position 28369683)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 28440986 |
GRCz11 | 20 | 28340076 |
KASP Assay ID:
554-0671.1 (used for ordering genotyping assays)
KASP Sequence:
ATCGACATCGGTGGAGGAGTCATGGTCAACGTCAGCCAGGAGGACTATGG[T/C]GAGGGCTTTTTTTACTGTTTATGAATGATTATTCACGGAAATGGGTATTT
Long Flanking Sequence:
GTTTATGCTTGTACACTTGTCCAGTTGGCCCACCAGTGTATGCGTGAGGTCCGGAGGGCTGCCATCCAGGCACAGAAGAACTGCAAAGAGACTTTACCACGAGCTCGTCGCCTCACCAAAGAGATGCTGCTGTACTGGAAGAAGTACGAAAAGGTGGAAAAGGAGCACCGTAAACGTGCCGAGAAAGAGGCTCTCGAGCAACGCAAACTCGATGAGGAGATGCGGGAGGTATCAAAATACATACAGTAAAAAAAGCATTACTTTGAGAATCACTTTCTGAAACAGCTGTTCCCTGTGCGTTAGGCTAAGCGTCAGCAGAGGAAGCTGAACTTTCTGATCACACAGACGGAGCTGTACGCTCACTTTATGGGTGGCAAGCAGAACGCTGGAGGAGACTGTACACAAGAGGAGATCCTGCGCAAGTTGGAGGACAATAGCTCCCAGCGGCAGATCGACATCGGTGGAGGAGTCATGGTCAACGTCAGCCAGGAGGACTATGG[T/C]GAGGGCTTTTTTTACTGTTTATGAATGATTATTCACGGAAATGGGTATTTAGGGTTCAAATAGTCATGGACAACATGGAAAAGTCATGGAATTTTGACATGGCATTTTCAATGCCTGGAAAAGTTTTGGAAAAACAGAAAAACCCACAAAGTTTTGGAAAAGTCATGGAAAACAGATATCTGTATACTTAAATATAGGTTAGTTGTCTTAAACTTTTTCTGTCTTTGGCCAATCACTTACTCTCACATTATTAGTGCAGTGTAAGCATTATCTAAATAAATTTTACATAGAAAAAAAATTTGCATCACAGTGGCGCAGTGGGTAGCACAATCGCCTCACAGCAAGAAGGTCACTGGTTTGAGCCTCAGCTGGGTCAGTTGGTATTTCTGTGTAGAGTTTGCATGTTCTCCCGGTGTTTGCGTGGGTTTCCTCTGGGTGCTCCAGTTTCCCTCACAGTCCAAAGACATGCTCTATAGGTGAATTGGGTAATCTAAAATTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15927
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103333 | None | None | 277 | None | 7 |
ENSDART00000103336 | Essential Splice Site | 435 | 1555 | 9 | 35 |
ENSDART00000127757 | None | None | 270 | None | 8 |
ENSDART00000128806 | Essential Splice Site | 433 | 1552 | 10 | 36 |
Genomic Location (Zv9):
Chromosome 20 (position 28369683)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 28440986 |
GRCz11 | 20 | 28340076 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCGACATCGGTGGAGGAGTCATGGTCAACGTCAGCCAGGAGGACTATGG[T/C]GAGGGYTTTTTTTACTGTYTATGAATGATTATTCACGGAAATGGRTATTT
Long Flanking Sequence:
GTTTATGCTTGTACACTTGTCCAGTTGGCCCACCAGTGTATGCGTGAGGTCCGGAGGGCTGCCATCCAGGCACAGAAGAACTGCAAAGAGACTTTACCACGAGCTCGTCGCCTCACCAAAGAGATGCTGCTGTACTGGAAGAAGTACGAAAAGGTGGAAAAGGAGCACCGTAAACGTGCCGAGAAAGAGGCTCTCGAGCAACGCAAACTCGATGAGGAGATGCGGGAGGTATCAAAATACATACAGTAAAAAAAGCATTACTTTGAGAATCACTTTCTGAAACAGCTGTTCCCTGTGCGTTAGGCTAAGCGTCAGCAGAGGAAGCTGAACTTTCTGATCACACAGACGGAGCTGTACGCTCACTTTATGGGTGGCAAGCAGAACGCTGGAGGAGACTGTACACAAGAGGAGATCCTGCGCAAGTTGGAGGACAATAGCTCCCAGCGGCAGATCGACATCGGTGGAGGAGTCATGGTCAACGTCAGCCAGGAGGACTATGG[T/C]GAGGGCTTTTTTTACTGTTTATGAATGATTATTCACGGAAATGGGTATTTAGGGTTCAAATAGTCATGGACAACATGGAAAAGTCATGGAATTTTGACATGGCATTTTCAATGCCTGGAAAAGTTTTGGAAAAACAGAAAAACCCACAAAGTTTTGGAAAAGTCATGGAAAACAGATATCTGTATACTTAAATATAGGTTAGTTGTCTTAAACTTTTTCTGTCTTTGGCCAATCACTTACTCTCACATTATTAGTGCAGTGTAAGCATTATCTAAATAAATTTTACATAGAAAAAAAATTTGCATCACAGTGGCGCAGTGGGTAGCACAATCGCCTCACAGCAAGAAGGTCACTGGTTTGAGCCTCAGCTGGGTCAGTTGGTATTTCTGTGTAGAGTTTGCATGTTCTCCCGGTGTTTGCGTGGGTTTCCTCTGGGTGCTCCAGTTTCCCTCACAGTCCAAAGACATGCTCTATAGGTGAATTGGGTAATCTAAAATTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23725
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 |
---|---|---|---|---|---|
ENSDART00000103333 | None | None | 277 | None | 7 |
ENSDART00000103336 | Nonsense | 1033 | 1555 | 25 | 35 |
ENSDART00000127757 | None | None | 270 | None | 8 |
ENSDART00000128806 | Nonsense | 1030 | 1552 | 26 | 36 |
Genomic Location (Zv9):
Chromosome 20 (position 28340550)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 28411853 |
GRCz11 | 20 | 28310943 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTAGGTGACTTCAGTACCCCTGGAACGCTACTGTGCAGATCGCAGCGCC[G/T]AGTATGAATGGAGGTTAATGCGTGACGGGGGGAGTCTCATTGCTAAGCAG
Long Flanking Sequence:
GAGATAAGAATGAAAGGAAGATAATATCATCCGCTTGTCAGCACGCCATAAAATTGTCCATAATGCTGAAAGAGGGATAATGCAAGAGGTAGAGGGAGAGGAAAAAAAAGAAACATGCAGTGGAAGGGATTGTGAGTGGTGTGAATCACTACAGGAAATGGTCATCTGTTACTCAAAGGCCTGTTAGCGCTGTTAGCACCGCTGACCTCTGCCACGCTTTCCTGCCAGAGCGGCGGGGTTCGGACAAAATGTCAGAAAGACAGGGTTGTGTGTGTGTGTGCGCACGTTCGGCAACTGGAAATGATTCTTCTCTTCCTAGAGGTGCAATTTGTTTGGCGTTTCTTAGCAACAGAAAGAGTGGACAGGGAAATAGATGTCAATTATCTGGAGGATTGACAATTTAATATTGTAAACAGCCTCTGAGGTGTTGAATAATGGCTTTTCTTATTCCCTAGGTGACTTCAGTACCCCTGGAACGCTACTGTGCAGATCGCAGCGCC[G/T]AGTATGAATGGAGGTTAATGCGTGACGGGGGGAGTCTCATTGCTAAGCAGTGCTTCCTGTACGGATCCCCCGAGCTGGCATGTGCTTGGGCTCAACGCTCTCAGTCTTTCCTCCCACCAAACCCAGGGGGCGTCATGGCCCTGCAGCAGAGGCACGGCTGGTCCTTTATAAGGATTCCAGGTGGGTGAATTCCTGGGTGGGAGCTAGCGTGCGTTTGTGTTTGTTTATGCTTGCCCGTGTGTAAATGTGGTGGAGAGGTACTTGATTTTTTCCAAGACGTTTGTATCCGGGTATTGTCCTTGAAAAGACATTTTTACTTAAGACAAAGCACTTTCTCACGTTCATTGGTTTGTTCATATGAGTCTCGAATGTCTCCAAGGGAAGTCTCGATTTGATTAAAATTTATAATGCCATGAATGGCGACAACTCCCTCTCTTAATGTGTGGGCACATAATGATGGGTACACACCACATTATTTCAGGCTCCATTTCATTGTTTGG
Associated Phenotype:
Not determined