ZMP
si:dkey-71b5.7
Ensembl ID:
ZFIN ID:
Human Orthologue:
OTOA
Human Description:
otoancorin [Source:HGNC Symbol;Acc:16378]
Mouse Orthologue:
Otoa
Mouse Description:
otoancorin Gene [Source:MGI Symbol;Acc:MGI:2149209]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7423 | Missense | Mutation detected in F1 DNA | Not yet available |
sa45573 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17950 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7423
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 > A
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000116114 | Missense | 695 | 1151 | 17 | 26 |
ENSDART00000145100 | Missense | 166 | 405 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 24149753)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 22154247 |
GRCz11 | 16 | 21958499 |
KASP Assay ID:
554-4078.1 (used for ordering genotyping assays)
KASP Sequence:
CCCTTTGGTGTGTGAATTAGACCCGGTYTGGATCTCCTCTCTGAACCCTG[C/A]AGCTCGCAACGCCACCCTGAAGTCTCTGGCATCCTGTCAGTACATCCAGC
Long Flanking Sequence:
GCTAGGTTTGTGTGTAACATGTAAACAGACCTTGTAAACCATGATTTTGTCTGGCCCCATAAGCCTGTGAAATGTCACATAGTTAATTTGAGTGTGTTGTGAAACTAAAATTGCTGTTTTTAAGCGTTGTTTGCCTTTTGTAGCTCAAATAAAAATTTTTGGCACAAGTTTTATGTTCGTAGGATGTTGGCAAAGGTATGTCCCCGTAAACCACCAAAAAGTCACATTGACCTCATAAACCATGTATGCCTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGCGTGTGCGTGTGCGTGTGCGTGTGCGTGTGCGTGTGCGTGTGCGTGTGCTTGTGCTTGTGTGTGTGTGTGTGTGTGTGTGTGTTTATGTGTGCGTGTGCAGAAGGGGAACCTGTCTGATCTGACAGCCGCAGAGGTCTTGACTCTCGGCCCTTTGGTGTGTGAATTAGACCCGGTCTGGATCTCCTCTCTGAACCCTG[C/A]AGCTCGCAACGCCACCCTGAAGTCTCTGGCATCCTGTCAGTACATCCAGCAACAGAACAGACAGGATCTGTTTAGACTGCTCAATGCAATCTATGGGTGAGAGCACGTGCAGATTCACACACAAATCACAGTTTCATATAGACCTCAGTATCCACATCACTGCATTTACAGGTGTTTCAGTGGTGAAGAGGCTGCAACTGAAGAGTACTTTAAAGAGCCCCTATTATGAGCTTTTGAAAATGACCTTCTATGCATGTGCAACATGCAGCTCTAAGTAAATGAAAACATCCAGCTGAGATTTAAATCTGAAAGTGCACCTTGTTTAAAAATATAGATTTTTTTAAATAAAAGATTTGACACAGAGTTGTTAAAATGATTTGTCGTTTGTCTGGATCTTTTGCCTGTTCGTATTGTCATCGACACAAAAGAAGACCAAATATGTCCTCTGCCGGATCCAGTAAAACGTGAACGCGCCTTTGCCTTTAAACCCAATAGCAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45573
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 |
---|---|---|---|---|---|
ENSDART00000116114 | Essential Splice Site | 925 | 1151 | 21 | 26 |
ENSDART00000145100 | Essential Splice Site | 396 | 405 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 24146051)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 22150545 |
GRCz11 | 16 | 21954797 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTGGACACATTGGAGATACTGGCCAACTGTAACTTTACACAGACACAG[G/A]TAATTCAAGCATAAATACATTCAGTCAATATCTTTAAAAAAAAAAAAAGT
Long Flanking Sequence:
GAGAATTCTAGGGATGTAACAGTACATATCTGAACATACGTGCTGTATGAAAATATATAATTCATAACAAATCTTGATTTTGATATTTGTTACAAATAAAAACAAAGAACAGTTTGTTAATCTTTATGGAGTTTAAAGTTTTTGTCATGCTTTGATTTGTAGTAAATGGGAAGAAATTATCATGATTGATTGCAGTTTTAACCGAGTCAGAAAAACTGTATACAGTGATCAGTTACACCACATCAAAGAGCATCAAAACAGCAATAATTCTTTAAATTCAGCAGCAGCAGCAGGATCTGAGAATATAACAGCTCATCTTCAAAGATCATGTCTATGGTGTGTTGCAGGCATGGGGTTCTGTGTCTATGTTGAATGAGTCCCTTATTTCTAATCTGGGCTGCATCTGCCAGAGCTTCAGTGCAGAAGAGCTTGGAAACCTCAGCATTGCCTCGCTGGACACATTGGAGATACTGGCCAACTGTAACTTTACACAGACACAG[G/A]TAATTCAAGCATAAATACATTCAGTCAATATCTTTAAAAAAAAAAAAAGTCTATATGAAAGGTTTTTTTTTTTTTGTAATGCCATTGTTTAAAAGATGTTAGTAAGAATTTAAAAGTGTTGATGTTAAATGTTTTTAAATGTATCAGATGTGCCAGAAAGAAAGATCTAATTCAAATAAATTTGATAAATTTGCACAAAAATAAGCTGTGGCCAAAAAAGCAGTTGTCAACATTTATATTAATAAAAAATACTTAAAACTTATTAATACTTAACAGATTAAGCAGCAAATAAGCCAGTAATAATCAAGTTAAAATCATTTTTGAAAGATTTGTGGAGCATTTGCTTGACTGCAATATTCTGAGTAGACATTTAGAACATGTTTCAGAGAATAGAATAGAATAGAATAGAATAGAATTGAATAGAATAGAATTGAATAGAATTGAATAGAATAGAATAGAAGCACATTTTTAAAATATGTTTATAAGATCTGTACACAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17950
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000116114 | Essential Splice Site | 1019 | 1151 | 23 | 26 |
ENSDART00000145100 | None | None | 405 | None | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 24144338)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 22148832 |
GRCz11 | 16 | 21953084 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGAAAACTGGACTGAAGCTCAGATCTGCATAATGGGGAACATCATTGG[T/A]GAGGAAATTTACCAGTGGATTACGCTTAAATACTTACATGTTGAAGTTTG
Long Flanking Sequence:
CCACTGCAGAGAAACCTGAAAATGTGAAAAGAATCCACTGGGAATGGAATTATCTTTACAAGATATTTTTCTAACATATATAAATCAAGCAGATAAACAAGCATAAATACTGAAAGTGGTTGATTTTGCAGCGGGCAGCAATCTGGCAGGCTTTTCAAAGAACAACTGGAATGAATGTGTTTGGTCTTGGAGAACTGGAGACAGCTGGTCTGGGACAGTTTATCTGTGGTCTACAACCTGCCCAGATTGATCTGCTCAATCCTCTCAGCTTCAGGTAGACATATTAGCACATTTAGTTTTTTCTTTTTCAATTTCCAAGTATATTTATATAGACTAACGTCTACCTCAACTGGCTTCAACAGGGAAGCAGTAGAGGCGGTGGGTCGCACATCTTGCCCACCGAACATTTTGGACCGTCTCAAGGAAAAGACAGTGGCTGTGTTTGGAAAGCCAGAAAACTGGACTGAAGCTCAGATCTGCATAATGGGGAACATCATTGG[T/A]GAGGAAATTTACCAGTGGATTACGCTTAAATACTTACATGTTGAAGTTTGAAATGTTAAAAACTGCCTGTGTCATTGAATGCCTCTCTAGCTGGTCTAAACGCTGTTGAGATGAGCCGTCTAAATCCAACCATCTTGCCTTTCATTCAGCCTTCTGCAATCCCTCTCATACCTGGGGATCGTTTGGCTGTAAGTTCACTGTCTTTTTTAAAAAATATAGCATATCTTACCTTAAGGTAGGGGTGTCAAATTCAGTTCCTGGAGGGCCGCCACCCTGCACAGTTTAGTTCCAACCCTGCTTCAACACACTTACCTGGAGGTTTAAAACAAGCTTGAAGGATTAAATTAGTTTGATCAGGTGTTTTTAATTATAGTTAAAACTAAACTCTGCAGAGCTGTGGCCCTCCAGGAACTGAGTTTGACATCTGTGCCCTAAGTTATCATCATATATACTCTGAACTAAAGTTGGTTTACTATTAAAAGTAGACCAGAAAACCAGAG
Associated Phenotype:
Not determined