ZMP
otx2
Ensembl ID:
ZFIN ID:
Description:
Homeobox protein OTX2 [Source:UniProtKB/Swiss-Prot;Acc:Q91981]
Human Orthologues:
OTX1, OTX2
Human Descriptions:
orthodenticle homeobox 1 [Source:HGNC Symbol;Acc:8521]
orthodenticle homeobox 2 [Source:HGNC Symbol;Acc:8522]
orthodenticle homeobox 2 [Source:HGNC Symbol;Acc:8522]
Mouse Orthologues:
Otx1, Otx2
Mouse Descriptions:
orthodenticle homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:97450]
orthodenticle homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:97451]
orthodenticle homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:97451]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
hu3625 | Essential Splice Site | Available for shipment | Available now |
hu3237 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa36505 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
hu3625
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008816 | Essential Splice Site | 84 | 289 | 4 | 4 |
ENSDART00000126097 | Essential Splice Site | 84 | 289 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 17 (position 44292923)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44132601 |
GRCz11 | 17 | 44246366 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGTTAGTTCACGTCGTAAATAATAAAAACCCCTTTTTTTCAACACATC[A/C]GGTTTGGTTCAAAAACCGAAGGGCAAAGTGTCGCCAACAGCAGCAACAAC
Long Flanking Sequence:
TGTATAACATGTTGTACTGTGCCGATTCAGATATGTTAATGTGTAATATTTATAGTATTTTTTACATTTAATAATTAAATCTAAGCATGGACGTTTTTTATTAAATGACAACCTGTGATGCTTTTGTTTATTTAAAACAGCGACTCCTCGAAAGCAGAGACGAGAAAGGACAACATTTACTAGAGCGCAACTAGATGTGCTGGAGGCTTTATTCGCGAAAACACGCTACCCGGATATTTTCATGCGCGAGGAGGTGGCCTTGAAAATCAACTTGCCGGAGTCCCGTGTACAGGTACGCATCTTTCAACTCATGAGAAAGTTAAATAATTATAATAATAATAAAAGTATTGTATCTATATGAACTGAGCGATGCACTAAAATATTATCAATATCACATTTGTTTTATTTTGAGCGAAGACCAAACAGAGCATATATAAAGACCATAGTGCTGCCGTTAGTTCACGTCGTAAATAATAAAAACCCCTTTTTTTCAACACATC[A/C]GGTTTGGTTCAAAAACCGAAGGGCAAAGTGTCGCCAACAGCAGCAACAACAACAAAACGGAGGCCAGAACAAGGTGCGACCTGCCAAAAAGAAGAGCTCTCCAGCGCGGGAGGCCAGTTCTGAGAGCGGGGCGAGTGGCCAGTTCACCCCGCCCTCCAGCACTTCAGTCCCGGCCATCTCTACCACAACCGCTCCGGTGTCTATTTGGAGCCCAGCCTCTATCTCGCCGCTGTCAGACCCACTTTCTACCTCCTCCTCCTGCATGCAAAGATCCTACCCCATGACCTACACTCAAGCGTCTGGATATAGCCAGGGCTATGCTGGTTCCACTTCCTACTTTGGGGGTATGGACTGCGGCTCATACTTGACGCCCATGCACCATCAGCTGACCGGGCCGGGATCCACTTTGAGCCCCATGAGCAGCAACGCTGTCACCAGTCACCTAAATCAGTCCCCCGCGTCCCTCCCCACACAAGGTTACGGTGCCTCGGGGCTCGGCT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
hu3237
Status:
Confirmed mutation in F2 line
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008816 | Nonsense | 87 | 289 | 4 | 4 |
ENSDART00000126097 | Nonsense | 87 | 289 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 17 (position 44292912)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44132590 |
GRCz11 | 17 | 44246355 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTCGTAAATAATAAAAACCCCTTTTTTTCAACACATCAGGTTTGGTTC[A/T]AAAACCGAAGGGCAAAGTGTCGCCAACAGCAGCAACAACAACAAAACGGA
Long Flanking Sequence:
TTGTACTGTGCCGATTCAGATATGTTAATGTGTAATATTTATAGTATTTTTTACATTTAATAATTAAATCTAAGCATGGACGTTTTTTATTAAATGACAACCTGTGATGCTTTTGTTTATTTAAAACAGCGACTCCTCGAAAGCAGAGACGAGAAAGGACAACATTTACTAGAGCGCAACTAGATGTGCTGGAGGCTTTATTCGCGAAAACACGCTACCCGGATATTTTCATGCGCGAGGAGGTGGCCTTGAAAATCAACTTGCCGGAGTCCCGTGTACAGGTACGCATCTTTCAACTCATGAGAAAGTTAAATAATTATAATAATAATAAAAGTATTGTATCTATATGAACTGAGCGATGCACTAAAATATTATCAATATCACATTTGTTTTATTTTGAGCGAAGACCAAACAGAGCATATATAAAGACCATAGTGCTGCCGTTAGTTCACGTCGTAAATAATAAAAACCCCTTTTTTTCAACACATCAGGTTTGGTTC[A/T]AAAACCGAAGGGCAAAGTGTCGCCAACAGCAGCAACAACAACAAAACGGAGGCCAGAACAAGGTGCGACCTGCCAAAAAGAAGAGCTCTCCAGCGCGGGAGGCCAGTTCTGAGAGCGGGGCGAGTGGCCAGTTCACCCCGCCCTCCAGCACTTCAGTCCCGGCCATCTCTACCACAACCGCTCCGGTGTCTATTTGGAGCCCAGCCTCTATCTCGCCGCTGTCAGACCCACTTTCTACCTCCTCCTCCTGCATGCAAAGATCCTACCCCATGACCTACACTCAAGCGTCTGGATATAGCCAGGGCTATGCTGGTTCCACTTCCTACTTTGGGGGTATGGACTGCGGCTCATACTTGACGCCCATGCACCATCAGCTGACCGGGCCGGGATCCACTTTGAGCCCCATGAGCAGCAACGCTGTCACCAGTCACCTAAATCAGTCCCCCGCGTCCCTCCCCACACAAGGTTACGGTGCCTCGGGGCTCGGCTTCAACTCCACC
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa36505
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008816 | Nonsense | 100 | 289 | 4 | 4 |
ENSDART00000126097 | Nonsense | 100 | 289 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 17 (position 44292873)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44132551 |
GRCz11 | 17 | 44246316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTTTGGTTCAAAAACCGAAGGGCAAAGTGTCGCCAACAGCAGCAACAA[C/T]AACAAAACGGAGGCCAGAACAAGGTGCGACCTGCCAAAAAGAAGAGCTCT
Long Flanking Sequence:
TATAGTATTTTTTACATTTAATAATTAAATCTAAGCATGGACGTTTTTTATTAAATGACAACCTGTGATGCTTTTGTTTATTTAAAACAGCGACTCCTCGAAAGCAGAGACGAGAAAGGACAACATTTACTAGAGCGCAACTAGATGTGCTGGAGGCTTTATTCGCGAAAACACGCTACCCGGATATTTTCATGCGCGAGGAGGTGGCCTTGAAAATCAACTTGCCGGAGTCCCGTGTACAGGTACGCATCTTTCAACTCATGAGAAAGTTAAATAATTATAATAATAATAAAAGTATTGTATCTATATGAACTGAGCGATGCACTAAAATATTATCAATATCACATTTGTTTTATTTTGAGCGAAGACCAAACAGAGCATATATAAAGACCATAGTGCTGCCGTTAGTTCACGTCGTAAATAATAAAAACCCCTTTTTTTCAACACATCAGGTTTGGTTCAAAAACCGAAGGGCAAAGTGTCGCCAACAGCAGCAACAA[C/T]AACAAAACGGAGGCCAGAACAAGGTGCGACCTGCCAAAAAGAAGAGCTCTCCAGCGCGGGAGGCCAGTTCTGAGAGCGGGGCGAGTGGCCAGTTCACCCCGCCCTCCAGCACTTCAGTCCCGGCCATCTCTACCACAACCGCTCCGGTGTCTATTTGGAGCCCAGCCTCTATCTCGCCGCTGTCAGACCCACTTTCTACCTCCTCCTCCTGCATGCAAAGATCCTACCCCATGACCTACACTCAAGCGTCTGGATATAGCCAGGGCTATGCTGGTTCCACTTCCTACTTTGGGGGTATGGACTGCGGCTCATACTTGACGCCCATGCACCATCAGCTGACCGGGCCGGGATCCACTTTGAGCCCCATGAGCAGCAACGCTGTCACCAGTCACCTAAATCAGTCCCCCGCGTCCCTCCCCACACAAGGTTACGGTGCCTCGGGGCTCGGCTTCAACTCCACCGCGGATTGCTTGGATTATAAGGACCAAGCGTCCTCATGG
Associated Phenotype:
Not determined