ZMP
OIT3
Ensembl ID:
Description:
oncoprotein induced transcript 3 [Source:HGNC Symbol;Acc:29953]
Human Orthologue:
OIT3
Human Description:
oncoprotein induced transcript 3 [Source:HGNC Symbol;Acc:29953]
Mouse Orthologue:
Oit3
Mouse Description:
oncoprotein induced transcript 3 Gene [Source:MGI Symbol;Acc:MGI:1201782]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22205 | Nonsense | Available for shipment | Available now |
sa35408 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15373 | Essential Splice Site | Available for shipment | Available now |
sa16964 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22205
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128422 | Nonsense | 245 | 542 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 4352004)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 4568733 |
GRCz11 | 13 | 4697319 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTTAATGGAGGCTGTAGCCATGGATGCTCATCAGATGAAGACTCCTA[T/G]TACTGTCACTGTCCTTGGGGACTGATGTTGGGGGATGACAAACGGACCTG
Long Flanking Sequence:
GTTAACATTAGTTAATGCACCGAGTTAACATGAACTAACAATGAACGACTGTATTTACATTAACTAACATTAACAATTATTACACATACTGTAATAAACATATTGTTCATTGTTTTATCATGTTAGTTAATACACCAACTCAGTGTTTCCCAAACCTGTTCCTGAAGGCACACCAACAGTACACATTTTCAACCTATTTCTAATCAAACACACCTGGGCTCAACTCATAAGAACATTAGAAGAGACTTTAAAACCTGAAATGAAGGGAGACATCCAAAATATGTACTGTTGGTGTGCCTCCAGGAACAGGGTTTGGAAACTCTGCATTAACTAACATTAACTAATACAATCTTACTGTAAAGTGTTACCACGATACTCTATAGTATATGGGCAGAATTTATTTGTGTCTATGTTTTTGGTGGGTTTTGTGTAGAGACCGCAGGTTGTGACAATGTTAATGGAGGCTGTAGCCATGGATGCTCATCAGATGAAGACTCCTA[T/G]TACTGTCACTGTCCTTGGGGACTGATGTTGGGGGATGACAAACGGACCTGTCAGGGTGAGCTAAACCAATTCTTCCAGCTTTTTCCTCTCTTTCTGTCAGAGTCTGTAGACTTCACTTTGACATTGGGTTTGTTTATAGTCCCTGTGAAGTGTGATCCTAGTTCCATAGAAGTCTCGGTTCCCAAAGACCTGGTGGGAGGGCTTGAACTTTTTCTCTCGAACACTTCCTGCCGTGGCATTTCCAACGGGACTCACATTAATATCCACTTCAGTCTGAAGACTTGCGGCACTGTGGTCCAGGTAAATTATATATATATTGATGGCTCTGTGACTAAGTGTGGAATCATGGGAGTTGTAGTCCTCATAAACATATGACAGCCCTACAGAAATCATAGTGATAGATGAGCTATTCAGTCACTTCAAGATTTCAATATATATATATATATATATATATATATATATATATATATATATATATAGATCTTACTGAGAAGTAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35408
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 |
---|---|---|---|---|---|
ENSDART00000128422 | Essential Splice Site | 263 | 542 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 4351948)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 4568677 |
GRCz11 | 13 | 4697263 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACTGTCCTTGGGGACTGATGTTGGGGGATGACAAACGGACCTGTCAGG[G/A]TGAGCTAAACCAATTCTTCCAGCTTTTTCCTCTCTTTCTGTCAGAGTCTG
Long Flanking Sequence:
ACATTAACTAACATTAACAATTATTACACATACTGTAATAAACATATTGTTCATTGTTTTATCATGTTAGTTAATACACCAACTCAGTGTTTCCCAAACCTGTTCCTGAAGGCACACCAACAGTACACATTTTCAACCTATTTCTAATCAAACACACCTGGGCTCAACTCATAAGAACATTAGAAGAGACTTTAAAACCTGAAATGAAGGGAGACATCCAAAATATGTACTGTTGGTGTGCCTCCAGGAACAGGGTTTGGAAACTCTGCATTAACTAACATTAACTAATACAATCTTACTGTAAAGTGTTACCACGATACTCTATAGTATATGGGCAGAATTTATTTGTGTCTATGTTTTTGGTGGGTTTTGTGTAGAGACCGCAGGTTGTGACAATGTTAATGGAGGCTGTAGCCATGGATGCTCATCAGATGAAGACTCCTATTACTGTCACTGTCCTTGGGGACTGATGTTGGGGGATGACAAACGGACCTGTCAGG[G/A]TGAGCTAAACCAATTCTTCCAGCTTTTTCCTCTCTTTCTGTCAGAGTCTGTAGACTTCACTTTGACATTGGGTTTGTTTATAGTCCCTGTGAAGTGTGATCCTAGTTCCATAGAAGTCTCGGTTCCCAAAGACCTGGTGGGAGGGCTTGAACTTTTTCTCTCGAACACTTCCTGCCGTGGCATTTCCAACGGGACTCACATTAATATCCACTTCAGTCTGAAGACTTGCGGCACTGTGGTCCAGGTAAATTATATATATATTGATGGCTCTGTGACTAAGTGTGGAATCATGGGAGTTGTAGTCCTCATAAACATATGACAGCCCTACAGAAATCATAGTGATAGATGAGCTATTCAGTCACTTCAAGATTTCAATATATATATATATATATATATATATATATATATATATATATATATATAGATCTTACTGAGAAGTAATATTCATGCTAATCCAAATAAAATTCTAAAATTATTTTTCTTTTTATTTTGCCACATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15373
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128422 | Essential Splice Site | 488 | 542 | 7 | 8 |
ENSDART00000128422 | Essential Splice Site | 488 | 542 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 4340544)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 4557273 |
GRCz11 | 13 | 4685859 |
KASP Assay ID:
2260-5969.1 (used for ordering genotyping assays)
KASP Sequence:
CCAAACACTACCAGGTCYCAGTCTTCAAGTTCATYGGCAAGGACAACAGA[G/A]TGAGTAGGGAACAGGTKCATGCTGGGACAATTCAGCTTGTGCTTTTGTGT
Long Flanking Sequence:
TTTAGTCTGGGTTAGTTTTGGTCTAATAAAAAATCTATTAAAGTTTCTCAAAATACCAACGCGCCCGCGGTCCGCCTCAGAACACCTTCCTTTTTAGACCAGAACGCCTATGGGCGCAAAAATGAGCGCTAATGCATTTGTTATTTTAACAGCGTAGCGCAACGCCTCAAAACGACTCTTGCGCCAAGCTGAAACTAGCAAAATACTATTACCCCGTGTCTTGCACCACATTGCGCCAGGTGTATGATAGGGCCCAATAGGTCAGATAGGGGAGACATCCAAAATATGCATTGTTGGTGTGCCTCCAGAAACAGGGTTGGGAAACACTGCGCTATATGACTGGGGCTACATGTGCTGATACAAAGTGACCATTGTGCTTTAATGGCCTTACATTTGCCAGGTGCATTTCTGATGAAACGGTGCGTCAGCTTTCGGCTAAAGACGAGCTCTCCAAACACTACCAGGTCCCAGTCTTCAAGTTCATCGGCAAGGACAACAGA[G/A]TGAGTAGGGAACAGGTGCATGCTGGGACAATTCAGCTTGTGCTTTTGTGTGTGTGTGCGTGTGCGTGCATGCGTGCGTGTCTGTGCGTGCGTGCGTGTCTGTGCGTGCGTGCGTGCGCGCTAATGAGCCAGTTGTGATAAATGCATATGAAAATAAGCGAGTCGTTGACTGAATTTGTCCGTGCTGTGTTAGGAAGTGTTTCTGCATTGCCGTGTGCTCGTGTGTGGGCAGACACAAGGGGAGTCTCGCTGTACACAGGGCTGCCGAAAGCGTTTGAGAAGAGATGTCTGGATTGATCAGCACCAAGAGCAAAACATACTGTCCAGTGGGCCGATTCACATACTGCCAGATCCATGAGCCAGCATAAAGTAAACAGCGCCATCTACAGACTAACCTAACGTATTTCAACACCCAATCACAGTCTGCACTGGAAAACAAATAAGTTAATTAACAGTTTACGTATTTTGTTTTCCATTCATGTACAGTTGGGAATTGCATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16964
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128422 | Essential Splice Site | 488 | 542 | 7 | 8 |
ENSDART00000128422 | Essential Splice Site | 488 | 542 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 4340544)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 4557273 |
GRCz11 | 13 | 4685859 |
KASP Assay ID:
2260-5969.1 (used for ordering genotyping assays)
KASP Sequence:
CCAAACACTACCAGGTCYCAGTCTTCAAGTTCATYGGCAAGGACAACAGA[G/A]TGAGTAGGGAACAGGTKCATGCTGGGACAATTCAGCTTGTGCTTTTGTGT
Long Flanking Sequence:
TTTAGTCTGGGTTAGTTTTGGTCTAATAAAAAATCTATTAAAGTTTCTCAAAATACCAACGCGCCCGCGGTCCGCCTCAGAACACCTTCCTTTTTAGACCAGAACGCCTATGGGCGCAAAAATGAGCGCTAATGCATTTGTTATTTTAACAGCGTAGCGCAACGCCTCAAAACGACTCTTGCGCCAAGCTGAAACTAGCAAAATACTATTACCCCGTGTCTTGCACCACATTGCGCCAGGTGTATGATAGGGCCCAATAGGTCAGATAGGGGAGACATCCAAAATATGCATTGTTGGTGTGCCTCCAGAAACAGGGTTGGGAAACACTGCGCTATATGACTGGGGCTACATGTGCTGATACAAAGTGACCATTGTGCTTTAATGGCCTTACATTTGCCAGGTGCATTTCTGATGAAACGGTGCGTCAGCTTTCGGCTAAAGACGAGCTCTCCAAACACTACCAGGTCCCAGTCTTCAAGTTCATCGGCAAGGACAACAGA[G/A]TGAGTAGGGAACAGGTGCATGCTGGGACAATTCAGCTTGTGCTTTTGTGTGTGTGTGCGTGTGCGTGCATGCGTGCGTGTCTGTGCGTGCGTGCGTGTCTGTGCGTGCGTGCGTGCGCGCTAATGAGCCAGTTGTGATAAATGCATATGAAAATAAGCGAGTCGTTGACTGAATTTGTCCGTGCTGTGTTAGGAAGTGTTTCTGCATTGCCGTGTGCTCGTGTGTGGGCAGACACAAGGGGAGTCTCGCTGTACACAGGGCTGCCGAAAGCGTTTGAGAAGAGATGTCTGGATTGATCAGCACCAAGAGCAAAACATACTGTCCAGTGGGCCGATTCACATACTGCCAGATCCATGAGCCAGCATAAAGTAAACAGCGCCATCTACAGACTAACCTAACGTATTTCAACACCCAATCACAGTCTGCACTGGAAAACAAATAAGTTAATTAACAGTTTACGTATTTTGTTTTCCATTCATGTACAGTTGGGAATTGCATTA
Associated Phenotype:
Not determined