ZMP
si:dkeyp-11g8.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5RG89]
Human Orthologue:
C1orf26
Human Description:
chromosome 1 open reading frame 26 [Source:HGNC Symbol;Acc:16785]
Mouse Orthologue:
1200016B10Rik
Mouse Description:
RIKEN cDNA 1200016B10 gene Gene [Source:MGI Symbol;Acc:MGI:1914125]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10026 | Essential Splice Site | Available for shipment | Available now |
| sa9859 | Essential Splice Site | Available for shipment | Available now |
| sa9937 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10026
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 |
|---|---|---|---|---|---|
| ENSDART00000133593 | Essential Splice Site | 226 | 537 | 6 | 13 |
| ENSDART00000133593 | Essential Splice Site | 226 | 537 | 6 | 13 |
| ENSDART00000133593 | Essential Splice Site | 226 | 537 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 34393227)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 34465740 |
| GRCz11 | 20 | 34368619 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTGTTGCCAYCCTTCTGTGTRAACRAAGCAGAGAAGCAAGGATCGCAW[G/A]ACAACAGCAATAGCATTGTGGTKGATGAACAAGAKTTGATCGAGTATGTG
Long Flanking Sequence:
ATGGGGAAAATAACTGTATATATACAGTTGAAGTAAGAATTATTAGCCCTCCTGAATTATTAGCGTTGGATTTGAGCCACTTCCATACGTAGTCCTCAACCCAGTGTAGTTTAGATATGCAGAGTCGCATCAAAATTTGTATGATTTTCAGTTCACAATGCAATTTGATAATGGTTTTATAATATTAATATAATATATTAATAAATGATGTGAACAACCAAACAAAATTGAACCAGAGCAAGATTCAAATTTCCTGTCATTGTAATTTAAAACATCACAAAATATACATTGCAGAACAAGATTACATTGCACAGGTACACAATAAAAGCTATAGATTTTTTTTTTTTTTTAAATACTGAAATAAAAGTGCTAATGTTTACAATGTTTACTTGGTCTAAAATTCAACATTTGTCAATAAAACTGAAACATCCTGACTTAAATGTAAAGCCGTTTTGTTGCCACCCTTCTGTGTGAACGAAGCAGAGAAGCAAGGATCGCAA[G/A]ACAACAGCAATAGCATTGTGGTGGATGAACAAGATTTGATCGAGTATGTGTCTTTGCTGGAGTCCTCCCTTCAGGCGGCGCTCTCTGAGGTACTAACGGAGGAGATGAAAGCAGCCTATGGAGACCTGTGGATTGAGGTATTTCTGCACCCAATGATAGTTCATTAATCTTATATGAAGCTTATATTAAAAACTGCTCTGCATTCATCTTAATACATTAGTCATATCTTGAGTAGGATTCAGGGCTCTTATTGTATTTGATGATCTTCTGCAAAGTCCTCTGTGTCCTTGCATTTGTGCATGCAGATAGTGTATGTGAAGCCTCCCTGGAGTCTGGAGGGGCTGCTGAAGTGTTTTAAGAAGCACTGGATCGCCGTCTTCGGACTCATTATCAATAGAAGCCTGCTCAGCTGTGTGGAAATGCTCAGTGACTGTCTCTGTTCAGGTGTGTATAATCCATCAAGTTCACTTAAATGGGTAGTTAATTAATGCTGGTAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9859
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 |
|---|---|---|---|---|---|
| ENSDART00000133593 | Essential Splice Site | 226 | 537 | 6 | 13 |
| ENSDART00000133593 | Essential Splice Site | 226 | 537 | 6 | 13 |
| ENSDART00000133593 | Essential Splice Site | 226 | 537 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 34393227)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 34465740 |
| GRCz11 | 20 | 34368619 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTGTTGCCAYCCTTCTGTGTRAACRAAGCAGAGAAGCAAGGATCGCAW[G/A]ACAACAGCAATAGCATTGTGGTKGATGAACAAGAKTTGATCGAGTATGTG
Long Flanking Sequence:
ATGGGGAAAATAACTGTATATATACAGTTGAAGTAAGAATTATTAGCCCTCCTGAATTATTAGCGTTGGATTTGAGCCACTTCCATACGTAGTCCTCAACCCAGTGTAGTTTAGATATGCAGAGTCGCATCAAAATTTGTATGATTTTCAGTTCACAATGCAATTTGATAATGGTTTTATAATATTAATATAATATATTAATAAATGATGTGAACAACCAAACAAAATTGAACCAGAGCAAGATTCAAATTTCCTGTCATTGTAATTTAAAACATCACAAAATATACATTGCAGAACAAGATTACATTGCACAGGTACACAATAAAAGCTATAGATTTTTTTTTTTTTTTAAATACTGAAATAAAAGTGCTAATGTTTACAATGTTTACTTGGTCTAAAATTCAACATTTGTCAATAAAACTGAAACATCCTGACTTAAATGTAAAGCCGTTTTGTTGCCACCCTTCTGTGTGAACGAAGCAGAGAAGCAAGGATCGCAA[G/A]ACAACAGCAATAGCATTGTGGTGGATGAACAAGATTTGATCGAGTATGTGTCTTTGCTGGAGTCCTCCCTTCAGGCGGCGCTCTCTGAGGTACTAACGGAGGAGATGAAAGCAGCCTATGGAGACCTGTGGATTGAGGTATTTCTGCACCCAATGATAGTTCATTAATCTTATATGAAGCTTATATTAAAAACTGCTCTGCATTCATCTTAATACATTAGTCATATCTTGAGTAGGATTCAGGGCTCTTATTGTATTTGATGATCTTCTGCAAAGTCCTCTGTGTCCTTGCATTTGTGCATGCAGATAGTGTATGTGAAGCCTCCCTGGAGTCTGGAGGGGCTGCTGAAGTGTTTTAAGAAGCACTGGATCGCCGTCTTCGGACTCATTATCAATAGAAGCCTGCTCAGCTGTGTGGAAATGCTCAGTGACTGTCTCTGTTCAGGTGTGTATAATCCATCAAGTTCACTTAAATGGGTAGTTAATTAATGCTGGTAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9937
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 |
|---|---|---|---|---|---|
| ENSDART00000133593 | Essential Splice Site | 226 | 537 | 6 | 13 |
| ENSDART00000133593 | Essential Splice Site | 226 | 537 | 6 | 13 |
| ENSDART00000133593 | Essential Splice Site | 226 | 537 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 34393227)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 34465740 |
| GRCz11 | 20 | 34368619 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTGTTGCCAYCCTTCTGTGTRAACRAAGCAGAGAAGCAAGGATCGCAW[G/A]ACAACAGCAATAGCATTGTGGTKGATGAACAAGAKTTGATCGAGTATGTG
Long Flanking Sequence:
ATGGGGAAAATAACTGTATATATACAGTTGAAGTAAGAATTATTAGCCCTCCTGAATTATTAGCGTTGGATTTGAGCCACTTCCATACGTAGTCCTCAACCCAGTGTAGTTTAGATATGCAGAGTCGCATCAAAATTTGTATGATTTTCAGTTCACAATGCAATTTGATAATGGTTTTATAATATTAATATAATATATTAATAAATGATGTGAACAACCAAACAAAATTGAACCAGAGCAAGATTCAAATTTCCTGTCATTGTAATTTAAAACATCACAAAATATACATTGCAGAACAAGATTACATTGCACAGGTACACAATAAAAGCTATAGATTTTTTTTTTTTTTTAAATACTGAAATAAAAGTGCTAATGTTTACAATGTTTACTTGGTCTAAAATTCAACATTTGTCAATAAAACTGAAACATCCTGACTTAAATGTAAAGCCGTTTTGTTGCCACCCTTCTGTGTGAACGAAGCAGAGAAGCAAGGATCGCAA[G/A]ACAACAGCAATAGCATTGTGGTGGATGAACAAGATTTGATCGAGTATGTGTCTTTGCTGGAGTCCTCCCTTCAGGCGGCGCTCTCTGAGGTACTAACGGAGGAGATGAAAGCAGCCTATGGAGACCTGTGGATTGAGGTATTTCTGCACCCAATGATAGTTCATTAATCTTATATGAAGCTTATATTAAAAACTGCTCTGCATTCATCTTAATACATTAGTCATATCTTGAGTAGGATTCAGGGCTCTTATTGTATTTGATGATCTTCTGCAAAGTCCTCTGTGTCCTTGCATTTGTGCATGCAGATAGTGTATGTGAAGCCTCCCTGGAGTCTGGAGGGGCTGCTGAAGTGTTTTAAGAAGCACTGGATCGCCGTCTTCGGACTCATTATCAATAGAAGCCTGCTCAGCTGTGTGGAAATGCTCAGTGACTGTCTCTGTTCAGGTGTGTATAATCCATCAAGTTCACTTAAATGGGTAGTTAATTAATGCTGGTAATTT
Associated Phenotype:
Not determined