Busch Lab

ZMP

OTOA (2 of 2)

Ensembl ID:
ENSDARG00000088059
Description:
otoancorin [Source:HGNC Symbol;Acc:16378]
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 3 alleles of this gene:

Allele Name Consequence Status Availability
sa11090 Nonsense Available for shipment Available now
sa12733 Nonsense Available for shipment Available now
sa7598 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa11090
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124820 Nonsense 30 1020 1 8
Genomic Location (Zv9):
Chromosome 7 (position 32733257)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 31127597
GRCz11 7 31398747
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAATCATAAYGTGAGTTGGTCTTTTGGACAGTCACTTCTGGATTTGTTTT[T/A]GGCTCCTGCAKATCCTTCTTGCAGTTTCACAAGTCTKGAATGCCAAGCKA
Long Flanking Sequence:
TTGAGGCTCATAAATAATCATAAATGTCCTCATGCTGCAGGTATTTGGAGGTTCCTGAAGGTGCAGCTGATGTGGAGCGAGGGGTTTGCGTCTTTAATGATATACAACAGTTTGCGGTTATTGAAAATTAAGAATGATTAAAAAATCCATATGAAACAGTCCCCTAAAAGTGACGTTACATCTTTAGTGTCAGGCTCAGACGCAATTTGCACTCTCACTACAAGCGTACCGCGCCAAAGCCCAAGTGCTTTGGCACACCTTTTCCAACCGGGCCAGGGCTGGCCAACTGAACTGCGCCTGACCCCGATTCCAAGCACTCACACTACTCAAACGAATCTGGAAATGTGCCTGGGCACGGTTTGACTAGCATAGTGTAAGTGCGCCCTAATTTACTATTTTGTCTATTTATTTCATGTCTTGTGTTTTTTGTGTGTGTGTGTTCAGGGGTATGAATCATAACGTGAGTTGGTCTTTTGGACAGTCACTTCTGGATTTGTTTT[T/A]GGCTCCTGCATATCCTTCTTGCAGTTTCACAAGTCTTGAATGCCAAGCGACAAGCAGCATCCAGTATATTCGTACTGGCACAACCTTAGTGGACATTTCGACTTCTAGTCTCACTTGTGATCAACAAAACTTCAACCAGCTCAATGAAACCCTTTGTGCATCAGTTTTATTGACAGCATCTCAGGAATCAAACACCCTTTATCAGATGTGTCAAGTGCTGAGCACGTTGTCTCGAACAGAAGTGGCCAATGTCTGGAGGAACATGTGTCGCATGGTCCAGAACATCACCTTACCTCTCATGGAGTCCTGCAGCGATCCTGCCACTGTAAAGTTAAGTCGTAGTGCACGGTCCACTCTGAGCCTCAACGAACTCCTCTGTGACTATAAGAATTGGACTGTGACTGGTTCTGTGGACCCTGCTCTGGTCACAATGTGCAGTGAAAACGATCGTGAGACATTCATCCTATCTGTGTGTAACAGTGCTGAAACCATGCAAGTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12733
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124820 Nonsense 76 1020 1 8
Genomic Location (Zv9):
Chromosome 7 (position 32733394)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 31127734
GRCz11 7 31398884
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGTGGACATTTCGACTTCTAGTCTCACTTGTGATCAACAAAACTTCAAC[C/T]AGCTCAATGAMACCCTTTGTGCATCAGTTTTATTGACAGCATCTCAGGAA
Long Flanking Sequence:
TTAAAAAATCCATATGAAACAGTCCCCTAAAAGTGACGTTACATCTTTAGTGTCAGGCTCAGACGCAATTTGCACTCTCACTACAAGCGTACCGCGCCAAAGCCCAAGTGCTTTGGCACACCTTTTCCAACCGGGCCAGGGCTGGCCAACTGAACTGCGCCTGACCCCGATTCCAAGCACTCACACTACTCAAACGAATCTGGAAATGTGCCTGGGCACGGTTTGACTAGCATAGTGTAAGTGCGCCCTAATTTACTATTTTGTCTATTTATTTCATGTCTTGTGTTTTTTGTGTGTGTGTGTTCAGGGGTATGAATCATAACGTGAGTTGGTCTTTTGGACAGTCACTTCTGGATTTGTTTTTGGCTCCTGCATATCCTTCTTGCAGTTTCACAAGTCTTGAATGCCAAGCGACAAGCAGCATCCAGTATATTCGTACTGGCACAACCTTAGTGGACATTTCGACTTCTAGTCTCACTTGTGATCAACAAAACTTCAAC[C/T]AGCTCAATGAAACCCTTTGTGCATCAGTTTTATTGACAGCATCTCAGGAATCAAACACCCTTTATCAGATGTGTCAAGTGCTGAGCACGTTGTCTCGAACAGAAGTGGCCAATGTCTGGAGGAACATGTGTCGCATGGTCCAGAACATCACCTTACCTCTCATGGAGTCCTGCAGCGATCCTGCCACTGTAAAGTTAAGTCGTAGTGCACGGTCCACTCTGAGCCTCAACGAACTCCTCTGTGACTATAAGAATTGGACTGTGACTGGTTCTGTGGACCCTGCTCTGGTCACAATGTGCAGTGAAAACGATCGTGAGACATTCATCCTATCTGTGTGTAACAGTGCTGAAACCATGCAAGTGCTGATCAGACAGCCCAGCAATGCCTGGGTGTGGGAATTCTGTGCAAACATATCCGACATATACATTGTGAGCCTGTATTGTTCATATGACAGGTGGACTGTTGAAAACCTTGACCCGTCGATTGTGACGTACTGTTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7598
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124820 Missense 474 1020 1 8
Genomic Location (Zv9):
Chromosome 7 (position 32734588)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 31128928
GRCz11 7 31400078
KASP Assay ID:
554-4255.1 (used for ordering genotyping assays)
KASP Sequence:
ACACTGAAAACTTCACTCGGAATGTATGTGTCAATGCTACAGTTCTGMAG[A/T]ATTTGCTGGCCAATTTAGACAACACCTGGTTGTTGGAACAATGCTCAAAC
Long Flanking Sequence:
CTGAACAGATCGCTCTGTGTATCCAAAATGATGAGATTCGATTTGTTAACGTTGTGTGTGTTAACCAAACATTCGTCACTGTACTTGGGATGAGCATTGATACTGCTTGGGTGCACCAATATTGTACTTACTCTTTCAACAACCCCCCCACGTCTACACCGACAGTGAATACTGAAATGAGGTGTGACTATAACAATTGGATGAACATGTCTGTGGATCCGACAGTAGTCACTCTGTGCTGGCAGAACGACCAGATCGGCTTCCATAAGAACATCTGCTGCAATGTCCGCCTATATGAGAAGTTGTTTCTACATCCTGAAAACCAATGGCTGATTAGAGTGTGCTCTGATAATAACACTGCGAATGTGTTGTTGCAGGTTTGCACCTATTCAGACTGGAGCCAGCCTACTATTGTAGACATGACTGACCTTGCTTTCTGCGCTGATTATGACACTGAAAACTTCACTCGGAATGTATGTGTCAATGCTACAGTTCTGCAG[A/T]ATTTGCTGGCCAATTTAGACAACACCTGGTTGTTGGAACAATGCTCAAACTTGACCTCATCTTACCCAGGTATTGTACCTGGGAAAGAGGGGGGACTCATAGGCTTCCGACCAGCTGAGCAATGTCAGTACTCCAGTTGGGATTTGGTGCTCCCGGACCCTGCTCTCCTCGCTCTTTGCTGGGACTATGACCAAGTCAACTTTGTCTTTTCTGTCTGCTCTGACTCTTCCTTGCTCTCCCACATCACTCAAGAGCCCTCCAACCTGTGGGTCGGCACTCTCTGTGTCACATACACACCTCCGCCTGTCTCCAGTGGAAATGGGAGCAATGCCACAACTCCCCAGTCTTGTCCAATAAGGGACTTGGCTAAGAAGCTAAACTGGACATGCAGCATAGACTTCAGTGTTGTCTGCCAACCAGGTGCCAGTCAAGCACAGGGTCTTCGGATGTTGTTGCGCTGCGGGATAGAAATGATCCAACCTCGCTTGGAGAAACTGATG
Associated Phenotype:
Not determined