ZMP
zgc:100970
Ensembl ID:
ZFIN ID:
Description:
28S ribosomal protein S27, mitochondrial [Source:RefSeq peptide;Acc:NP_001003778]
Human Orthologue:
MRPS27
Human Description:
mitochondrial ribosomal protein S27 [Source:HGNC Symbol;Acc:14512]
Mouse Orthologue:
Mrps27
Mouse Description:
mitochondrial ribosomal protein S27 Gene [Source:MGI Symbol;Acc:MGI:1919064]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12506 | Splice Site, Nonsense | Available for shipment | Available now |
sa535 | Essential Splice Site | Confirmed mutation in F2 line | Not yet available |
Mutation Details
Allele Name:
sa12506
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 > G
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092773 | Splice Site, Nonsense | 94 | 398 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 983013)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 871532 |
GRCz11 | 8 | 937275 |
KASP Assay ID:
2260-0004.1 (used for ordering genotyping assays)
KASP Sequence:
GATAAYATATCATCCAGAGATGAAGTGGATCAAGCAGAATATTACCTGTA[T/G]AAGTGAGTATCTTGGCTTTATTTTAATGTTTTGTTCAGGTGTTGGTKTGT
Long Flanking Sequence:
GCTGTAATCACTGCCAGAGGTGCATCAACAAAAACTCTTTTTTCACATTGTCATCATGGGGTATTGTGCGTAGAATGTTGAGGAAATCAATTAATTGAATCCATTTTGGAATAAGGCTGTAACATAAACAAACATGGAAAAAGTAAAGCGCTATTATTACTTTCTGGATGCACTATATATGTCACTTCAGGATTTATTTATTGATAGATTTTTGCATTTTTTCTTAAAACTTCTGGCATTATTTGTTTGATTTTTTGTGTTTTGCTGTGAAAATACACAAAAATCATGGAATTATACATTTTTTCTTGTTTCTTTTTAGACTATTGTTCCAGTATCATGCAGCCCTAATTTTAATAATTTTATTCTATATAATGAAATTAGAATGCCTCTGCTGTTTTCCTCAGTATTTGTGTTGAACGTACATATGCACACATTTATGTTCAGTTCATAGATAATATATCATCCAGAGATGAAGTGGATCAAGCAGAATATTACCTGTA[T/G]AAGTGAGTATCTTGGCTTTATTTTAATGTTTTGTTCAGGTGTTGGTGTGTTTGTGCTGTGAGTGTGTTTGTGCGTTCAGGTTTCGTCACAGTCCAAACTGCTGGTTTCTCCGGGATTGGACCGTTCACAGCTGGATTCGACAGTGTCTTAAATACGGAGCCAGAGATAAAGCTCTTTACACGCTGAAGAACAAGGTCTGAATTTCATTTTAACATGAAATTTTAATTGTTATTTATTTTATGTTATTATTATTATTATTATTATTTCTTCTTCTTCTTCTTCTTATTTATTCTATGTTTAATTTTTAATTGTATTTATTATTTTTATTATTATTATTACTCTATTTTTTGTTTGTCATTTTATTACTATTTTATTATATTTTTTTTTTGAAAAAATTATTGTTGTTTTATTATTATTATTATTTTATTTTTGTATTATTATTATTTATTATTATTTATTCTGTTTTTGAAATGAATTTATTATTTTTTTATTTAATATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa535
Status:
Confirmed mutation in F2 line
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 |
---|---|---|---|---|---|
ENSDART00000092773 | Essential Splice Site | 280 | 398 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 986437)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 868108 |
GRCz11 | 8 | 933851 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGCCGTGAGTTCAGACTTCACAGGCGTGCAGATCTCCGAGGACGCGG[T/C]GAGTGTGTGTTCATCACAAGAAGGATAGATGACCATAATGAGCCCTAAAC
Long Flanking Sequence:
CAGGCTATACAAGTACTTTTACATGAGACTGAGGAATGTTGTGCAGGATATTGTGCAAAAGAGGTATTTAAGGTTTAACATTGTGCACGAGTTATTTAAGGTGTAGCAAGCAGTGCAATTTGAATGTGGTACATTTATATTACATAAACATCGCTTTCCTTATTGAGTCCTTGTAAGATGGAGTTTAGATAAAGTGTCAGGTGCATAAGAGAGCAGAGTGTTTCTACAGGTGGTTTGTCAAGCCCACTCACCTGAATACAGCACTTTTCTAGTGGTTTTTAGATACTTTAATTAAAAAAAATGGTACATATCGTGCCTTCAATCTCAATGCTGTGGATGCATGTGTGTGTGCGCAGGTAAAGTGGAGTTCTCCAGAGGGATCCACGCTGTGTTTCATGAGATGCCGCTGATCTGGAGCTCTGGTTATCTGCGCCGCGCTGTCGCCGTCCTGCAGGCCGTGAGTTCAGACTTCACAGGCGTGCAGATCTCCGAGGACGCGG[T/C]GAGTGTGTGTTCATCACAAGAAGGATAGATGACCATAATGAGCCCTAAACATCTGTCAGAGTTATCAGAGAGTCCACTTCAATGATGCTTCTGTAGTTTAAGATCACAGGACAGAAATACGGTTTCCAGAGAATTATGATTTAACAGATGAGAAACTTCTGTGAACGCCTCAAAATAACACACTGCTGATGCGAATGGGATTTAATAATAATAATAATAATCGAATAATGAGGATGATAATATAGAGTGGAGGAACTATGACGTCACTTTGTAGGCTAATCGGCTGCTAGCATAAAACTGGTTCCCTCGTGAAAATCCCTATAGGATTTTCCCATAGGCTTTTCGAAGATTGCGAATAATAAGCTCTGTGATCAAACACTGTTCATTACACTTACACGTTTTGTCCAGCCGGATAATCCTCACACGAAAATACAACTTTGAGCACTTTTGGATCTTAAATGCAAACGCAAGAGTTGAAAAGCTAACATTAGGCTATTAAC
Associated Phenotype:
Not determined