ZMP
mrpl3
Ensembl ID:
ZFIN ID:
Description:
39S ribosomal protein L3, mitochondrial [Source:RefSeq peptide;Acc:NP_956301]
Human Orthologue:
MRPL3
Human Description:
mitochondrial ribosomal protein L3 [Source:HGNC Symbol;Acc:10379]
Mouse Orthologue:
Mrpl3
Mouse Description:
mitochondrial ribosomal protein L3 Gene [Source:MGI Symbol;Acc:MGI:2137204]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa5920 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa36814 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa5920
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020928 | Nonsense | 161 | 345 | 5 | 10 |
ENSDART00000104399 | Nonsense | 135 | 319 | 6 | 11 |
ENSDART00000138823 | None | None | 137 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 18783120)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19628355 |
GRCz11 | 19 | 19201308 |
KASP Assay ID:
554-3961.1 (used for ordering genotyping assays)
KASP Sequence:
TCGGTCAAGCTATTATTTAATTTTTTTTTTTTTCAGAGGCCGGKGGGATA[T/G]TTGGAGATTTTYCAGAATGCAGGAATTCCACCCAAGCAGAAACTCACCAC
Long Flanking Sequence:
TACGGAAAATGATTATGTGAAACCTAGACAACTTGTCTCCTGTACAGCTTTTTTAAGTGCATTCTTCTGGAACTCCTCGATTGACTTTCTGTAATGGTGGAACTGTTGGTGGTAGAAAAGAAAGACTAACAGTGATGGACAGATTCTGACGGATTTTTTAAACCCCTTCAACAGTTCAGTAGAGTTTGCTATAAAAAAATAACTTTTGTCAGTGTCATTTTCCCCCATTTTTGGCAATAAGCTAGTGTGTGTGTCATCTGTCTGTATTTGACAGCTGCCACAAAGTGCTGCTTGAAGTGTAATTGTCAATTGTCCTGACCTTCAGTCCGAGCCTTCAGTCAGTCAATCAACTCCCAAAACACAGCAGAGCAGTTTGGGTTTAATGTATTCTCTTTTTCTTCACCCTTTCTATGCTTTTTAAAGATAAGTTAGAAAATCTCTTGCAGTAACTCGGTCAAGCTATTATTTAATTTTTTTTTTTTTCAGAGGCCGGTGGGATA[T/G]TTGGAGATTTTCCAGAATGCAGGAATTCCACCCAAGCAGAAACTCACCACCTTTTGTGTTACAGACAATGCTATAATCAAACCAGGTATTCTCACCTGTCAGTGTTTGTGTGTGTGTATTCTAGCCAAAATAAAGCAAACTCCAGAAAAAAAAAAAATATCAAATGAAATACTGTGAAAATTTCCTTGCTCTGTTAAACAAAATTTGAAAAAATAAAAATAAAATAAAAGCTAATAATTTTAACTTAACTATAACAGATATATAATCTGTAACAGATTAAAATCAATTTAGTTTTAATTTTGAATTTCAGTAAACACGCCCTAAGGCTAATTTATACTTCTGCGTGAAGCGCATACGTATGGTCTGGCGCAGCCTTTGCGCAGTCGCATACCCCTTGAACATAAATAATGTTGCACGTTTGCAGGTTCCCGCCTGTGAATTAGCGAGTTTTAGCTTCTTGTACTTTAAGGTAGCCTTCAGAAAAAACAAAACACCAGCAA
Associated Phenotype:
This allele has been associated with this phenotype by genetic linkage analysis and may not be causal.
See FAQs for more info.
See FAQs for more info.
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
liver ZFA:0000123 |
quality PATO:0000001 |
abnormal PATO:0000460 |
Larval:Day 5 ZFS:0000037 |
pancreas ZFA:0000140 |
absent PATO:0000462 |
abnormal PATO:0000460 |
Mutation Details
Allele Name:
sa36814
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020928 | Nonsense | 162 | 345 | 5 | 10 |
ENSDART00000104399 | Nonsense | 136 | 319 | 6 | 11 |
ENSDART00000138823 | None | None | 137 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 18783122)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19628357 |
GRCz11 | 19 | 19201310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCAAGCTATTATTTAATTTTTTTTTTTTTCAGAGGCCGGTGGGATATT[T/A]GGAGATTTTCCAGAATGCAGGAATTCCACCCAAGCAGAAACTCACCACCT
Long Flanking Sequence:
CGGAAAATGATTATGTGAAACCTAGACAACTTGTCTCCTGTACAGCTTTTTTAAGTGCATTCTTCTGGAACTCCTCGATTGACTTTCTGTAATGGTGGAACTGTTGGTGGTAGAAAAGAAAGACTAACAGTGATGGACAGATTCTGACGGATTTTTTAAACCCCTTCAACAGTTCAGTAGAGTTTGCTATAAAAAAATAACTTTTGTCAGTGTCATTTTCCCCCATTTTTGGCAATAAGCTAGTGTGTGTGTCATCTGTCTGTATTTGACAGCTGCCACAAAGTGCTGCTTGAAGTGTAATTGTCAATTGTCCTGACCTTCAGTCCGAGCCTTCAGTCAGTCAATCAACTCCCAAAACACAGCAGAGCAGTTTGGGTTTAATGTATTCTCTTTTTCTTCACCCTTTCTATGCTTTTTAAAGATAAGTTAGAAAATCTCTTGCAGTAACTCGGTCAAGCTATTATTTAATTTTTTTTTTTTTCAGAGGCCGGTGGGATATT[T/A]GGAGATTTTCCAGAATGCAGGAATTCCACCCAAGCAGAAACTCACCACCTTTTGTGTTACAGACAATGCTATAATCAAACCAGGTATTCTCACCTGTCAGTGTTTGTGTGTGTGTATTCTAGCCAAAATAAAGCAAACTCCAGAAAAAAAAAAAATATCAAATGAAATACTGTGAAAATTTCCTTGCTCTGTTAAACAAAATTTGAAAAAATAAAAATAAAATAAAAGCTAATAATTTTAACTTAACTATAACAGATATATAATCTGTAACAGATTAAAATCAATTTAGTTTTAATTTTGAATTTCAGTAAACACGCCCTAAGGCTAATTTATACTTCTGCGTGAAGCGCATACGTATGGTCTGGCGCAGCCTTTGCGCAGTCGCATACCCCTTGAACATAAATAATGTTGCACGTTTGCAGGTTCCCGCCTGTGAATTAGCGAGTTTTAGCTTCTTGTACTTTAAGGTAGCCTTCAGAAAAAACAAAACACCAGCAAAG
Associated Phenotype:
Not determined