ZMP
zgc:110006
Ensembl ID:
ZFIN ID:
Description:
Protein EURL homolog [Source:UniProtKB/Swiss-Prot;Acc:Q503Y8]
Human Orthologue:
C21orf91
Human Description:
chromosome 21 open reading frame 91 [Source:HGNC Symbol;Acc:16459]
Mouse Orthologue:
D16Ertd472e
Mouse Description:
DNA segment, Chr 16, ERATO Doi 472, expressed Gene [Source:MGI Symbol;Acc:MGI:1196400]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21778 | Essential Splice Site | Available for shipment | Available now |
| sa31790 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21778
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000049633 | Essential Splice Site | 223 | 277 | 5 | 5 |
| ENSDART00000125529 | Essential Splice Site | 223 | 277 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 10 (position 36083491)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 35116193 |
| GRCz11 | 10 | 35060053 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTATTCAGTATTGAAGTTTGAAGCTGTTGAACTGTTGTGTGTCCCTCA[G/T]ATGTGTTCGAGGAGCTCTCTGTGGTCGTTCAGGAGAAAGACTCTCTCTCG
Long Flanking Sequence:
GCACTTAAGGATGAGTAAATCAGTTTTGGGTGAACCATCCCTTTACGTTTTGATACAGATTACCCAGTATTTCCAGCTGGAGATCCATACAATCAATCCCAGTTTATTTTTGTAAAATGTGTTTTTATTATTTTACCTAAATGTGTGTCATAGCTAAATGATTTAAAGCAAAAGTTCACTCAAAAATTAAATGTCATAATTTTCTTACCTCTTTTTTTTCTGTTAAGTGCAAAAGAAGGTAATTGAAGTTTGTTATAAACCGGTAACTATTAACTTCCATAGCATTAAGTCAATTGTGATCAGTTTGAAAGCACTTGAGGGTGAGTAACTGATGCCAGAATGTTCAATTTTGGGTAATCAGTCACTTTTTAATGAACATTATCATAATATTTTGACACAAATCCCCAATATTACCAGCTGGAGATTCAAACAGTCAATCCCAAATTCCCAACGTATTCAGTATTGAAGTTTGAAGCTGTTGAACTGTTGTGTGTCCCTCA[G/T]ATGTGTTCGAGGAGCTCTCTGTGGTCGTTCAGGAGAAAGACTCTCTCTCGTCAGAGCTTCATGTTCGACACATCGCCATCGAGCAGCTCTTCAAAAACTGCGCCAAGCTGCCCTGGCTACAGATAGGCAGAGCGGGCGTCAAAGCTGCAAACAACCCAGTGGAATAACAGATCTTCAGGTCCCACGAAAAAAAAAAAGACCAGAACCAAACCACAGACTTCCTCAGAAGCTCAAAGCTCAGACGGGAGACGCACAGGTGTCTAAAGTCACCAGAATGGTGGATTTTCAGTAGTAAAAGTACTGGATTTGTCCAAAGTGTTACTATGCAGAACGACAGACGTGTTTTTAATACATTTCCGTTGCTTTTATTTTATTTTTTGGACTGCTCACCTCACTGTTTACTCACTGCACTTGATCACGGGTGGTTCGTAGACTTGGATGAGCTTGACAGTGACATTCAGGCTTGCCGATTGTTTGTTGCCGTGGAAACTGTTGCTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31790
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 |
|---|---|---|---|---|---|
| ENSDART00000049633 | Nonsense | 263 | 277 | 5 | 5 |
| ENSDART00000125529 | Nonsense | 263 | 277 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 10 (position 36083371)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 35116073 |
| GRCz11 | 10 | 35059933 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATCGCCATCGAGCAGCTCTTCAAAAACTGCGCCAAGCTGCCCTGGCTA[C/T]AGATAGGCAGAGCGGGCGTCAAAGCTGCAAACAACCCAGTGGAATAACAG
Long Flanking Sequence:
GTTTTTATTATTTTACCTAAATGTGTGTCATAGCTAAATGATTTAAAGCAAAAGTTCACTCAAAAATTAAATGTCATAATTTTCTTACCTCTTTTTTTTCTGTTAAGTGCAAAAGAAGGTAATTGAAGTTTGTTATAAACCGGTAACTATTAACTTCCATAGCATTAAGTCAATTGTGATCAGTTTGAAAGCACTTGAGGGTGAGTAACTGATGCCAGAATGTTCAATTTTGGGTAATCAGTCACTTTTTAATGAACATTATCATAATATTTTGACACAAATCCCCAATATTACCAGCTGGAGATTCAAACAGTCAATCCCAAATTCCCAACGTATTCAGTATTGAAGTTTGAAGCTGTTGAACTGTTGTGTGTCCCTCAGATGTGTTCGAGGAGCTCTCTGTGGTCGTTCAGGAGAAAGACTCTCTCTCGTCAGAGCTTCATGTTCGACACATCGCCATCGAGCAGCTCTTCAAAAACTGCGCCAAGCTGCCCTGGCTA[C/T]AGATAGGCAGAGCGGGCGTCAAAGCTGCAAACAACCCAGTGGAATAACAGATCTTCAGGTCCCACGAAAAAAAAAAAGACCAGAACCAAACCACAGACTTCCTCAGAAGCTCAAAGCTCAGACGGGAGACGCACAGGTGTCTAAAGTCACCAGAATGGTGGATTTTCAGTAGTAAAAGTACTGGATTTGTCCAAAGTGTTACTATGCAGAACGACAGACGTGTTTTTAATACATTTCCGTTGCTTTTATTTTATTTTTTGGACTGCTCACCTCACTGTTTACTCACTGCACTTGATCACGGGTGGTTCGTAGACTTGGATGAGCTTGACAGTGACATTCAGGCTTGCCGATTGTTTGTTGCCGTGGAAACTGTTGCTTGGTTTACGGTTGTCTCCTCCCTCAGCTCATTGCAGTGGAACTGGTTAGTGATGCTGGATATTGCATTATTATTTCTCCTGTTATGCAGAAGCTTTAGTAGTTTACATTTCTTTGGTTCTGTC
Associated Phenotype:
Not determined