ZMP
otof
Ensembl ID:
ZFIN ID:
Description:
Otoferlin [Source:UniProtKB/Swiss-Prot;Acc:Q5SPC5]
Human Orthologue:
OTOF
Human Description:
otoferlin [Source:HGNC Symbol;Acc:8515]
Mouse Orthologue:
Otof
Mouse Description:
otoferlin Gene [Source:MGI Symbol;Acc:MGI:1891247]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17391 | Nonsense | Available for shipment | Available now |
sa23735 | Essential Splice Site | Available for shipment | Available now |
sa23736 | Nonsense | Available for shipment | Available now |
sa18571 | Nonsense | Available for shipment | Available now |
sa43473 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17391
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008840 | Nonsense | 38 | 1837 | 2 | 43 |
ENSDART00000136255 | Nonsense | 212 | 1992 | 7 | 46 |
Genomic Location (Zv9):
Chromosome 20 (position 31189503)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 31260716 |
GRCz11 | 20 | 31163595 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCTCTTGTGTGCAGATGATGCKGCYATTCTGGATGCAGAAGATCTGGAT[C/T]GAAAAGCCATGCGTCTAGGCGGCATTCTTGACCCTGATACAATCTCACTG
Long Flanking Sequence:
AAATTTTGGACCTTATTCTTGATAACAAAAACAAATGACCAATAAAAAAGCGTGAAGCACCCAATTTGGACCATATTAAAATGAATTTGAATACTAATTTAGCAATTTTTGTTGTTATCCATGTTTTTTCTATAAAATGTACTTTTTCTTAACAAGAGAGGCTAGAAAATTGTATTAAATTGGCAAAAAAATAAAATAATAATAATCATTAGCAGCTATTAAGTATAAGTATTTGTGTCTCCATTTTTAATCATTATATGACATTCATTCATTGATATTCACTGGTTTTGATTTGTTGGTATTTTACTTTAGACATCAATTGTAAAGACTGAAGAATCATAAACTGCACATTAGACATGAAACTTTAAAAGGAACAGAAGTTGATTGCATATTATAAATATATATTTTATAAAAGAAATGGAGCCTGTTCCTTTCAAAGTTTCACTTCTGTGCTCTTGTGTGCAGATGATGCTGCCATTCTGGATGCAGAAGATCTGGAT[C/T]GAAAAGCCATGCGTCTAGGCGGCATTCTTGACCCTGATACAATCTCACTGGCCTCGGTTACTGCAGTGACCACTAATGTCTCCAACAAAAGGTCACATGTCTAATGTGCACATGCTGTATTTTTAAACCCATACACGTACACTATTCTATTTTGAAGTTTGTATGTTTGCTTCTTGAAGTTTATATGTTTGTGAAAAGGTCACAGGGAAGAAAAACCTCCTATTTATGTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTCCTTTCTAAAATTAAAGAAAGAACAGTTTGCTTTGTTTCTGATGTTGTTTCATTGACTTTTGTTTTTCATGTAATTAGTTTGATAAAAATACCTAATCAAGGTCTAGTTGACATGTTTGATTTTCCATATTTTATTGTGTGCTCGACATAATACATGCAAAATTTGATTTAAAACAACTAATCGTTTAAATTTGTGTCCTTAAGGTTGATCCTCTTGTTTTTCCAGATCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23735
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 |
---|---|---|---|---|---|
ENSDART00000008840 | Essential Splice Site | 151 | 1837 | 5 | 43 |
ENSDART00000136255 | Essential Splice Site | 325 | 1992 | 10 | 46 |
Genomic Location (Zv9):
Chromosome 20 (position 31195750)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 31266963 |
GRCz11 | 20 | 31169842 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCCACGTGCCTCCAGACGTCATGTTTGACAAAATTATAAAGATTTCAG[T/C]GAGTAGATAAAGCCACGCATCATACACTTTTACAAACCTTTAATCAAACC
Long Flanking Sequence:
GCAAGTGTACATCTCTTCTTAGCCATTTTATTAGCCCAAAATAAGTCAGGAAGGTCTTTGAGAACTTCCTTAGCTCAAATTCTCCTCTCGCCCTGCAAACACGAGGGAGTCCCGGGCTCAAGGATCTAATGAGCTCAGGGCTCTCTCCTGGGACAGCATGCCAAATAAGATTTATTATCACTCATCAGCTAAGTGTGAACTCTTAAAAAAGTTTTATTTCATAATGAACACTTTTTTTAGTCTTCTTACTTGTTTTACTTGTTTTTTTTATTTTTACTAAGCAGTGACATGCATTATAATGCCAGATCCTACATTAAATATTAGATTGTCGTAGGTGATAAACATTGCACACCCACGTACAGCAGATGATGAACAGTCTCATTAATTTCATGTCTACAGCCATTTTGATTATCTTTATCTCTCTCTCTTCAAACAGTATTTTGTCTTCGACTTCCACGTGCCTCCAGACGTCATGTTTGACAAAATTATAAAGATTTCAG[T/C]GAGTAGATAAAGCCACGCATCATACACTTTTACAAACCTTTAATCAAACCTCCATTGGAAACAGCGGATTAAGTTGTACTTTTTTTTTTGCTAAAATTAAGGTAATACATTCTAAAAACCTTCTGCGAAGCGGCACCCTCGTGGGCACCTTCAAACTAGACGTGGGGACTGTTTACACACAACCTGGTCGGTAACCATAAAAATAAGTGAGAGATGTACTGATTAAATGGGAAGATGGCTTTTATTTGTTGAATGTTTCTCACAGAACATCAGTTTCATCACAAATGGGCGATGCTGTCAGACCCTGATGACATCACGACTGGCTGCAAAGGTTATGTTAAATGTGACATCGCAGTCGTGGGAAAAGGAGACAACATCAAGACTCCACACAAGGCCAGTGAAGCAGACGAGGATGACATAGAGGGGTTAGTGTGCTGTGTTCTAATCATGTGATAATAAATTGTGCCATACTGTAGCACCAATTTTGGATTGGTGCCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23736
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008840 | Nonsense | 589 | 1837 | 14 | 43 |
ENSDART00000136255 | Nonsense | 763 | 1992 | 19 | 46 |
Genomic Location (Zv9):
Chromosome 20 (position 31206597)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 31277810 |
GRCz11 | 20 | 31180689 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAAGGTCTGAATGATGTTCAAGAGATCATAAAAACAGAGAAGGCATA[T/A]CCAGAACGAAGACTAAGAGGTGTATTAGAAGAACTTAGCACAAGCTGCAG
Long Flanking Sequence:
ATGGACAATTTAACTTACCCAATTTACCTGTAGGCTACCACATATCTTTGGACTTGTGGGGTAAACCAGAGCACCCAGAGGAAACCCACGCAAACATTGGGAGAGCATGCACTCTCTACACATAAATGCCAACTGACCCAGCCGAGCCTTAAAACAGCAACCATCTTACTGTGAGGCGATCATGCTACCCACTGCACCACCGTGACACCCTACAAAAGAAATTAGTTATTAGAAATGTGTTATTAACACTATTATGTTTAACAATTGGTTAAAAAAGTATCTATTTTAAACAGCACTTGGAAAATAAATGTAAAAAGTATAAATAAATATAAACACAAATTATACTGGCAATGTGAATTTTTAAGCAGAGAGGACTAACAATCTAATTACAAACATATATTTAGGGTTCATGAGAACACAGCTAATGTTCATGTCTTTCTTTGTAAACAGGAGGAAGGTCTGAATGATGTTCAAGAGATCATAAAAACAGAGAAGGCATA[T/A]CCAGAACGAAGACTAAGAGGTGTATTAGAAGAACTTAGCACAAGCTGCAGGTGACAAAACACAGTGAGCTAATGTGCATACAGCGCATGCAACAATCAGTAATCTCTTGACTTCTTTTCCTTATTCTCCACAATTGAAGCCGGTTTGTTACACTTGCAAACAAGGATCAGAATCTTTCTGGAAGAACCAAGCTGGACAGAGAGAGGCTGAAGTCCTGTATGAGAGAAATGGTACTCCCACACAACCCATTTAGTTTCTGCTTACACATTGAGAACTGCTGATGGGAATGTAATTTGCGTGGTTATATTGTTCACAGGAGAGTATGGGTCAGCAGGCGAAGACCATCCGCACACAAGTGAAAAGAAACACAGTTCGAGATAAACTCAAGCTAGTGTTGAATTTCCTTCAGAGGCTTCGATTCTTAGCAGACGAGGTAAAAGAAATCACCTGATCACTTCCTAGTGAACACGATCAGAATCTCAAACTTTGTGGTTGATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18571
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008840 | Nonsense | 592 | 1837 | 14 | 43 |
ENSDART00000136255 | Nonsense | 766 | 1992 | 19 | 46 |
Genomic Location (Zv9):
Chromosome 20 (position 31206604)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 31277817 |
GRCz11 | 20 | 31180696 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCTGAATGATGTTCAAGAGATCAYAAAAACAGAGAAGGCATATCCAGAA[C/T]GAAGACTWAGAGGTGTATTAGAAGAACTTAGCACAAGCTGCAGGTGACAA
Long Flanking Sequence:
ATTTAACTTACCCAATTTACCTGTAGGCTACCACATATCTTTGGACTTGTGGGGTAAACCAGAGCACCCAGAGGAAACCCACGCAAACATTGGGAGAGCATGCACTCTCTACACATAAATGCCAACTGACCCAGCCGAGCCTTAAAACAGCAACCATCTTACTGTGAGGCGATCATGCTACCCACTGCACCACCGTGACACCCTACAAAAGAAATTAGTTATTAGAAATGTGTTATTAACACTATTATGTTTAACAATTGGTTAAAAAAGTATCTATTTTAAACAGCACTTGGAAAATAAATGTAAAAAGTATAAATAAATATAAACACAAATTATACTGGCAATGTGAATTTTTAAGCAGAGAGGACTAACAATCTAATTACAAACATATATTTAGGGTTCATGAGAACACAGCTAATGTTCATGTCTTTCTTTGTAAACAGGAGGAAGGTCTGAATGATGTTCAAGAGATCATAAAAACAGAGAAGGCATATCCAGAA[C/T]GAAGACTAAGAGGTGTATTAGAAGAACTTAGCACAAGCTGCAGGTGACAAAACACAGTGAGCTAATGTGCATACAGCGCATGCAACAATCAGTAATCTCTTGACTTCTTTTCCTTATTCTCCACAATTGAAGCCGGTTTGTTACACTTGCAAACAAGGATCAGAATCTTTCTGGAAGAACCAAGCTGGACAGAGAGAGGCTGAAGTCCTGTATGAGAGAAATGGTACTCCCACACAACCCATTTAGTTTCTGCTTACACATTGAGAACTGCTGATGGGAATGTAATTTGCGTGGTTATATTGTTCACAGGAGAGTATGGGTCAGCAGGCGAAGACCATCCGCACACAAGTGAAAAGAAACACAGTTCGAGATAAACTCAAGCTAGTGTTGAATTTCCTTCAGAGGCTTCGATTCTTAGCAGACGAGGTAAAAGAAATCACCTGATCACTTCCTAGTGAACACGATCAGAATCTCAAACTTTGTGGTTGATTTTCCTCTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43473
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008840 | Nonsense | 1296 | 1837 | 33 | 43 |
ENSDART00000136255 | Nonsense | 1453 | 1992 | 36 | 46 |
Genomic Location (Zv9):
Chromosome 20 (position 31218200)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 31289413 |
GRCz11 | 20 | 31192292 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGAAATGATTTTGATATTTTGTCTTCTTATGAACCAGGGCTCCCTCTG[T/A]ATGTATAAACTACCACTGTCTGAGGAGATCACCAGAGAGGCAGGATTTGA
Long Flanking Sequence:
CATTTATTTACTGAAAAAAAACAATTAGTTGTTCTCTTTGAATAATCCTGTTACATTAAGGACTGGAGTAAAGGCTGAAAATATTCAGATTTGACATCACAGGAATAAGTTAAAGCTTAAAATATATTAAAATAGGAAACATTTAATATTTTTGAGTGTTTTTGATCAATTAATGCAATATTGAAAAGTGTCTTCCACACTTTGTAACAGAAGTATACAAGATAAAAGAACTGTAATCTGAAGAAATCCAAGCTAAAGATCTTTATCTCAGGTGTACAATAAAGAGCTGGAGAGTGAGTTCGGTAGCTTTGAGGACTGGCTTCACACCTTCAACCTGTACCGAGGAAAGGCTGGAGATGATGATGACCACAATGTGGTTGATGAGGACAGAATTGTGGGCAGATTCAAGGTAAGAATGAGTAAAACACAAAACACTGTATACATTCAAAGTGTGAAATGATTTTGATATTTTGTCTTCTTATGAACCAGGGCTCCCTCTG[T/A]ATGTATAAACTACCACTGTCTGAGGAGATCACCAGAGAGGCAGGATTTGATCCAAACATGGGCATGTTCCAGAGTATTCCTCACAATGACCCTATCAACGTTCTTGTCAGGATTTATATCATTCGAGTGAGTGTATTCAACTCCAAAGATTTAAGTTGACTTCACTTGTGTGCACACAATAACATGTGTGTTACAAAATGTAAATGTGATAATAGCAGACACTTAAACAGTACACTATACATGCTTACCATATAAGTGATGTGCAGTGCACTATATGCATATCCATTGTATGTATAAATCTGGTGTATACATTAGGGTTAAGTTGAATGTGTTTTATGCACTGTTCCTTATCTGCTAAATCTGCTTAAGAAAAATGAATCTCTACTCAGGCCACAGACCTGCATCCTGCAGATATAAATGGAAAGGCCGACCCTTATATAGTCATTAAATTGGGAAAGTCAGACATTCGAGACAAGGAGAACTACATATCCAAGCAGCTG
Associated Phenotype:
Not determined