ZMP
si:dkey-177f24.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human G2 protein (G2) [Source:UniProtKB/TrEMBL;Acc:Q1LV92]
Human Orthologue:
C11orf41
Human Description:
chromosome 11 open reading frame 41 [Source:HGNC Symbol;Acc:24836]
Mouse Orthologue:
D430041D05Rik
Mouse Description:
RIKEN cDNA D430041D05 gene Gene [Source:MGI Symbol;Acc:MGI:2181743]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39204 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa9549 | Nonsense | Available for shipment | Available now |
| sa36670 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39204
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089349 | Essential Splice Site | 57 | 961 | 1 | 16 |
| ENSDART00000089615 | None | None | 126 | None | 2 |
| ENSDART00000132342 | None | None | 584 | None | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 27959587)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 28032439 |
| GRCz11 | 18 | 28010679 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTAGCAATATTCTTACTTTTATTACACAACGCGCAGGCTTCTGACGG[T/C]AAGTCGATGTTTTATTTTTATTTTTATGTTGAACCGACACTTTAAAATAC
Long Flanking Sequence:
ATGTCACAAAACTACATCTCGCTCGCATGCGGGAACACTTTTTTTTTATAAGACAGACAAAGAATTACATGCATCTCTTCTATCCTCCGCTCTCATTATGAGGGTTAAGCAGGACTGCGAGCTTTAGATAAACCAGGCCTCCCCCAAAAACTGCAGAGCTCTCTCGCGTCCCCCTTGTCGCAGTGATGGTGGACTATATGGACATTTCCACGAATGCGGCTCTCTTCTGGCACTTGGAGCGGCGTGACCACCGCACGTCCCACTGACTCGCGGATCTGAGCAGATGTCTGGTCCACTACCGACACCGGGCCACCTCCTCTGCAAACCCAAATGGCTGTTCGCGTGGCTGGGATCTGGAGAGATTTGCGCAGACTGAGCAGCAGCGTCCTGCGCTCTGGAGACTGGAGGAGAGGATGCTCGTGCACAGGGATGCGGAGCGCTAAACTCTCATCTTTAGCAATATTCTTACTTTTATTACACAACGCGCAGGCTTCTGACGG[T/C]AAGTCGATGTTTTATTTTTATTTTTATGTTGAACCGACACTTTAAAATACTGCGTTTCCACCCAAGTCTAGTAAAGATTCTTAACATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATGTATTTATTTATTTATTTATTTATTTATTTATTTATAAAGGAAATATATTTTAGTAGTATTGTTGTCATCTGTATGATGTTTATCAAGAAACTTACGTTTGTGATTTATATACTATATTTATTTTATTTTATAATAATTTTATTATTATTATTATTATTAATAATTATTATTATTACTATTATTATTATTATCATCACCATCGCTATTCATTATGTATTAAAATAAATAATGATAATTATTATTATTGTTATTATTATTATTATTATTATTATATATTTATAATATAGCCAGTCCTGCTGATTGGCATTAAAACAAACAAACAAATATATAAAATAAATAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9549
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 |
|---|---|---|---|---|---|
| ENSDART00000089349 | Nonsense | 108 | 961 | 2 | 16 |
| ENSDART00000089615 | None | None | 126 | None | 2 |
| ENSDART00000132342 | None | None | 584 | None | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 28013476)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 28086328 |
| GRCz11 | 18 | 28064568 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATCAGTAGTCCAATCAGATCCTAAAGGCTCATCAAAGAGCAGAAGGGAA[C/T]AACCTGCCTTTTCCTCTWTTCTCACACTACTTGCCAGCACAGCCCAAAAA
Long Flanking Sequence:
AAACTGCATAGTTGCAATTCAAACAACTACATACTTGAATAAAAAAGCCTCAAAAGCACATTATGTTGTCCAACCGCTGCAATATTTTTCAAACCGTTAATTGATCTGCCGTCACTCAATGTGGGTGGAGTAATACACAAAGGTAAAGAGGCTGTACGAGTGCTGTTATTGCGGAATATCACACAGCTATCAGCCAATCAGATTTGCAAACCAGACCGAACTTGTAAATAAATATACCTTTAGAGGAGATATTACATCATGGATTTTTTTTTTCTCAAAATTAACTTTGATTATAATAGGCATGTTGGACTGCTCTTGGATTTATAATTTTCTCTCTTTCTCTTTTAGATGAGTTCAGTCATGAAGCCTCTGGATCATTTCTGGAAGTGGCCTCATCACCCTCCTCTATTCATTTACTGGGCGGCTTTTTTATGACAGACAGGAATCCAGCATCAGTAGTCCAATCAGATCCTAAAGGCTCATCAAAGAGCAGAAGGGAA[C/T]AACCTGCCTTTTCCTCTTTTCTCACACTACTTGCCAGCACAGCCCAAAAAGCTCCTGAACCCCCTACAAAAGTTGCTGTGCGTGACAACGAAACCCATCAATGGCCTTTAAATGGATCTTTGGAGAGAGTGGAGTCATCATTCTCCCATCCGCCATCTCGGCTGGTCAGCAACCACTCTCACTCAGGTTTGTTTTCCAGCATGCATTTTGAGACTGTTTTTCTCACCCTGTAATACTTAAATCTTAGTTTATTAATTTCAGGATTTAGGATTATTTTATATAATTTTTATTCTGTTATTGATTACTCAACCTCATGTCATTCCAAACATTTGTTTATCTTTGCAACACAAGTTATTGGAGATAAAATCTTTCATAGACAGCAAGACATTCAAAGTCCAAAAAAGTAACCAAAAGCTTTTTCAAAACATCCCATGTCAGTTCAGCTGTAGTCATATGAAGCTCCATGAACACTTTTGTGCACCAAAAAAAATTTATAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36670
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089349 | Essential Splice Site | 565 | 961 | 9 | 16 |
| ENSDART00000089615 | None | None | 126 | None | 2 |
| ENSDART00000132342 | Essential Splice Site | 195 | 584 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 28064011)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 28136863 |
| GRCz11 | 18 | 28115103 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAGTCTTCTGTCCATGCCCATTAAAGTCCTTTTTCTCCGTGTTCTTGC[A/T]GTGATTCAGGATGTGTCAAACTCATCTCTGGAAGTGCAATACCAGAGCTT
Long Flanking Sequence:
ACATGCCTTGCCTATATATAATCCCTTTAGAGAGGGATTAATTGTCTTTTCTAATGTATTTAAAACATTCAGTATGTATTTGACATTTTTATAAACATTGAGCATTTTGATAATCACCCCTGGGAATGACATGGAAATGAATCTCACAAGGTTTATGAGCAAAAGAGGAGTCATCAACACTCTTAAGATTTACTTTTTGTGTAAACTCTGCAGGAAAATGGATCATGAGGTCCAGAATTTAGAATCATTGTCCACAGCAGTGGTTGAACTGCACATGCATCATCCTACAGAGTTTATTTCTAACTCTGATTAAACTGTACCTTTTTCTTAGTACTCTTGACTGAGTCAGCTTGATTAGATGTGTTTGATTATGGCTGGAGCTACACTATGCAGCACAGTGGATTCTGAGATTAGGGATGAGATGTGAGATTAGTAACCAAGACTTTTATTTAAAGTCTTCTGTCCATGCCCATTAAAGTCCTTTTTCTCCGTGTTCTTGC[A/T]GTGATTCAGGATGTGTCAAACTCATCTCTGGAAGTGCAATACCAGAGCTTTGCCAGTCTAATGGAGGAGCGGCTGGCTGAGCTCTTCATGGTGGCCCACCAGCAAGGCGTTCGCTTCAAACGGGCAACAACAGTGGGCAGTTACACTGTGCAGGTATTACACAATGGAGTTGCATAGTATTAAGCAAATTTGTGAACTACTGTAGATTATGTAATGAAAAAAATCTATTGGAAGTAATCAAGGTGTTTCATTGCATTCAGATGGTTAGTATCAGGCGTGTTCATGGGACAAAAAACCCAGCTGAGATGACCTACTATGTCCAGCAAAATGGGACCCCAATGCTTGGTACATCTGCAGCCAAGCTTCTGAACACAGTGGACTCACAGACCATGGCGCTTACACTGGGATACTTTGTCCAATTGCAGGCTGAAGGTCAGAATTACTCATTATTACTATTTATTTATTAGCAGATTACAGCAATGATAATTAAGTCAATTGTA
Associated Phenotype:
Not determined