ZMP
si:dkeyp-27b10.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate otogelin (OTOG) [Source:UniProtKB/TrEMBL;Acc:Q1LXP4]
Human Orthologue:
C12orf64
Human Description:
chromosome 12 open reading frame 64 [Source:HGNC Symbol;Acc:26901]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16038 | Essential Splice Site | Available for shipment | Available now |
| sa23212 | Nonsense | Available for shipment | Available now |
| sa9582 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16038
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 |
|---|---|---|---|---|---|
| ENSDART00000092804 | Essential Splice Site | 290 | 706 | 5 | 18 |
| ENSDART00000122151 | Essential Splice Site | 290 | 669 | 5 | 17 |
| ENSDART00000135822 | None | None | 510 | None | 12 |
| ENSDART00000136524 | None | None | 245 | None | 6 |
| ENSDART00000139768 | None | None | 199 | None | 4 |
| ENSDART00000140587 | Essential Splice Site | 452 | 592 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 18 (position 5322602)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 6096392 |
| GRCz11 | 18 | 6236757 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YGCCGTGGAYGTCCTGGAGGAAGGAGTCTGCTGTCCCAAGAAGWTCTGTG[G/A]TACAAAMATACAAACAYACAAATCCATCAGAAACAGGTCATCACCCAGGA
Long Flanking Sequence:
TAAAATTATTTTAACCTACTTTAATTTTACAATAAACTTTACTGACATTCAGTGTGGACAACAAAGTATGTCATTGTTCAGAGAACCTGTTTCTTACTCTGACAATAAACACTTTGAATCTTGAGTCTTAAATGCACCATGTTTTGAAGCAGTAACATCTAAACATCTGAATTTTGTAAACCATAGTCATGATACTTCAATTCCGGCAACCACAGCTGCAGTTTTTTATTTACTGTTAAATTAGCAGATTTTTTGTTGCGTTGTATGATGATGTCCTGTTATTTCAGTGTGTACGGATAACGACGGTGCACCACGGGCTCCAGGTGAGGTGTGGAACGGCTCTCTGCGCGGCTGCTGTCTCTTCCGGTGTCTGGAAAACGGTAGTGTGGTTCCTGTAGAGCCCGAGTGCAGTTATGAACCGGCTCCGCTGTGTGAGAGAGAGGGAGAATACGCCGTGGATGTCCTGGAGGAAGGAGTCTGCTGTCCCAAGAAGATCTGTG[G/A]TACAAACATACAAACACACAAATCCATCAGAAACAGGTCATCACCCAGGAACATTCGATGTACTATTTTTAATATACTATGAACTGGAAAGTACTAATCTCTAATGCTAATTCCACTTAAGCTGCGTCCCAGTTCAGAGCGTGTGTCCTTCGAAGGTCAATTGCGTAAACCTGGGACAACAAATTAAAGGGTTCATGTGGAGCTTTCATTTTTTTTTAAATGTATTTTAATACTCTGAGAACTGGTCAGAATAAGCATGTTGTTTATTTAATAAATTGCCTAATTGTTGTCTTCTTCTAACTGCTACTATTGCTGCAGTTCCTATAATAGCCACAAGGGGAGTTATGCAGTTGAAGTCAGAATTATTGGCCACCATGAATTTTTAGCCCCCCTTGTTTATTTATTTATTTATTTATTGACAGCACAGAATAATTGATTAGATATTTTTCAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAATTAGGTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23212
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 |
|---|---|---|---|---|---|
| ENSDART00000092804 | Nonsense | 297 | 706 | 6 | 18 |
| ENSDART00000122151 | Nonsense | 297 | 669 | 6 | 17 |
| ENSDART00000135822 | None | None | 510 | None | 12 |
| ENSDART00000136524 | None | None | 245 | None | 6 |
| ENSDART00000139768 | None | None | 199 | None | 4 |
| ENSDART00000140587 | Nonsense | 459 | 592 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 18 (position 5324171)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 6097961 |
| GRCz11 | 18 | 6238326 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTACTGCATGTGTGTGTATTTTTGTTCAGAATGTAACCTGACCATCTG[T/A]CAGAGTGAAGTTCCCAGCTGTGAGAATGGAGACAAGCTGGTGATCGGCTA
Long Flanking Sequence:
ATAAATTACAAAATTGGCCATTTTTTTGGCCAGCCAGGTGATTAAATGAACTGAGGAAACATAATCGTTCTCCTAACTTTACATTGCTAAATAAACATAAAAAATATAATGTGACCCCCAATCCCACCCCCCCCCCACCAGAGCTTGCTGAGGCCCCTTTGTGGTGCTGTAGACTATCAAAATAATATATATAGCTTAAAGGGGCTAATAATTTTTACATTAAAATGGTGCTTTAAAAAATTAAAAACTGCTTTTATTCTAGCCAAAATAAATCAATTAAGACTTGCTCCAGAAGAAAAAATATTATCAGACATACTGTGAAAATTTACTTGCTCTGTTAAACATCATTTGGAAAATATTTGAAAAAGACAAAATATATAATAATTTTTACTATGTATTGTTTATGTTAAAGGCATGCAAATAAAAGCTTTTATTTTTTTCATTCAATTTTTTTACTGCATGTGTGTGTATTTTTGTTCAGAATGTAACCTGACCATCTG[T/A]CAGAGTGAAGTTCCCAGCTGTGAGAATGGAGACAAGCTGGTGATCGGCTATAGCGCTCTGTCCTGCTGTCCTGAATACAGATGTGGTAAGAGCTGGTGTAATCCTTATTCTGCTGCTGTTTGCATGGTCAGTGCATGAGGCTCGCTTTTCTGATTGGTTTCTGCCAGAATGTGATCCACTGGCCTGTCAGAGCGTCCCGCCGCCGATCTGCAGAGAGGATCAGTTCCTGGTGGAGGTCAGAGGAGCACACGCCTGCTGCTACAGCTACATGTGTGGTAATTACCAAGTGGAAATACAGTACTTCAACACTACAATCTCAATGCTGATGATGCAGAAACGGACACTGAAAGAAATGATATCACAAGAAGTCTACAAATGTTTTTTTATGTTACTTTTAACTTTTTATAATCAGTTATTCAGGTTTCAACACATTTTTTAACACTTTTTGTTGCGATGTAACAACAGTGTGACAGTATACTATATTACAATCATATTTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9582
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 |
|---|---|---|---|---|---|
| ENSDART00000092804 | Nonsense | 390 | 706 | 8 | 18 |
| ENSDART00000122151 | Nonsense | 390 | 669 | 8 | 17 |
| ENSDART00000135822 | None | None | 510 | None | 12 |
| ENSDART00000136524 | None | None | 245 | None | 6 |
| ENSDART00000139768 | None | None | 199 | None | 4 |
| ENSDART00000140587 | Nonsense | 551 | 592 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 18 (position 5325367)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 6099157 |
| GRCz11 | 18 | 6239522 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAKACTGGAGAGATACTGGCTGTGGATATGAACACCACCAATCACTGCTG[T/A]CCACAGTATCATTGCGGTAGTTATAAGCACTCACTGGAMAGGACTACACA
Long Flanking Sequence:
GATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGAACGGTGGATGGATGGATGGATGGATGGATGGATGGATGGATAAATGGAACAATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATAAATGGAACAATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATAAATGGAACAATGGATGGATGGATGGATGGATAGATAAATGGAACAATGGATGGATGGATGGATGGATGGATGAATGGATGGATGGATGGATAGATAGATATTGTCATAGTTGTCATGGAACATATCTTAAACAATTATATTTATTAAACCTATTTATCCAAGTCCAAAATATTGATTATGTGTGTGGTGTTTTTACAATCCTGTGTTTCAGTGTGTGAGTCCTGCATTGAGCCCATACCAGTGTGTCAGACTGGAGAGATACTGGCTGTGGATATGAACACCACCAATCACTGCTG[T/A]CCACAGTATCATTGCGGTAGTTATAAGCACTCACTGGAAAGGACTACACATCACATCATTTACTGTTCGATGATGAAAGGAGAATCAGTGTGTGTGTGTGTGTGTGTGTTACTGTTTCAGTGTGTGATATGAGTCTGTGTCCTGAGCCCAGTGTGAGTTGTGCTCCTGGAGCTGTGCTGATAAAGAGACCCGTGCCGGACAGCTGCTGTCCAGAAACACACTGCGGTACTGACACCTTTTAGGATCTCTTTCTTTCTTTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTTTTTCTTTCCTTATTTCCTTCATTTCTTTCATTCCTTCCTGCCTTATTTTCTTCTTACCTTCCTTCATTTTTTCCTTCCTTCCTTCCTTCTTTCCTTCCTTCCTTTCTTTCTCTTTCTTTTTTTCTTTCTCTCTTTCTTTT
Associated Phenotype:
Not determined