ZMP
rpl3
Ensembl ID:
ZFIN ID:
Description:
60S ribosomal protein L3 [Source:RefSeq peptide;Acc:NP_001001590]
Human Orthologues:
AC096766.1, RPL3
Human Description:
ribosomal protein L3 [Source:HGNC Symbol;Acc:10332]
Mouse Orthologues:
Gm5879, Rpl3
Mouse Descriptions:
predicted gene 5879 Gene [Source:MGI Symbol;Acc:MGI:3647624]
ribosomal protein L3 Gene [Source:MGI Symbol;Acc:MGI:1351605]
ribosomal protein L3 Gene [Source:MGI Symbol;Acc:MGI:1351605]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20025 | Essential Splice Site | Available for shipment | Available now |
| sa16344 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20025
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000011251 | Essential Splice Site | 283 | 403 | 6 | 9 |
| ENSDART00000138327 | Essential Splice Site | 135 | 188 | 3 | 4 |
The following transcripts of ENSDARG00000003599 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 30019526)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 29737565 |
| GRCz11 | 3 | 29868407 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTGCTGGACAGAAGGGCTACCACCACCGCACAGAAATCAACAAAAAGG[T/A]AATGCTTCAGAAAGTCACTCAAATGTTCATGGCATACGTTTGTGGACGTT
Long Flanking Sequence:
ACCATCTCCGATAAGGTTGACTGGGCCAGAGAGAAGCTTGAGCAGTCCATTCCCATCGCTAATGTCTTCTCTCAGGATGAGATGATTGACGTTATTGGTGTTACCAAGGGACATGGATGCAAGGGTAGGTGGACTGCTTTCTCTTTTCCCGCTTTTGAAGTGTTTACTTTAGCGTCGTGCATGTAATGATGAAAAACATGGATTAACCGCGTCAGGCATGGCGCCCGAAACGCATGAGGAAATTTCCCATGCTGCCTTCCTTCTGACAGCACACTTGCCCTTTTTTAGAAGCAAATGCAAACTTGAATACTTTTCTGATCAAAGATGTGTTTCTGTAGGTGTGACTAGCCGTTGGCACACAAAGAAGCTGCCCCGCAAGACCCATCGTGGTCTGCGTAAGGTGGCTTGTATTGGAGCCTGGCATCCTGCCCGTGTGGCTTTCTCTGTGGCTCGTGCTGGACAGAAGGGCTACCACCACCGCACAGAAATCAACAAAAAGG[T/A]AATGCTTCAGAAAGTCACTCAAATGTTCATGGCATACGTTTGTGGACGTTTTGTTGCAGTCTTGCCTCATGCATGCTTTTGTTCACCTTTAGATCTACAAGATTGGTGTGGGCTATCATAACAAGGACGGAAAACTTGTCAAGAACAACGCCTCTACTGATTATGATCTGTCCAACAAGAGCATCAACCCTCTGGTGAGTGTGCTGTTGTCTCCCTATTGTGAATTTGATAAATTGTTTATATGCATGCATTAATACTGATGCCTTTTTATTTTAGGGTGGCTTTGTGCATTATGGTGAGGTGACGAATGACTTCCTCATGCTGAAAGGCTGTGTGGTCGGAACCAAGAAGAGGGTTTTGACTCTGCGCAAATCTCTACTGGTCCAGACCAGCCGTCGTGCTCAGGAGAAGATCGACCTGAAGTTCATCGACACCACCTCCAAGTTTGGTCATGGACGTTTCCAGACCATCGAAGAGAAGAAGAACTTCATGGTGAGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16344
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000011251 | None | None | 403 | None | 9 |
| ENSDART00000138327 | Nonsense | 174 | 188 | 4 | 4 |
The following transcripts of ENSDARG00000003599 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 30019318)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 29737357 |
| GRCz11 | 3 | 29868199 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATTATGATCTGTCCAACAAGAGCAWMAACCCTCTGGTGAGTGTGCTGT[T/A]GTCTCCCTATTGTGAATTTGATAAATTNNGTTTATATGCATGCATTAWTACT
Long Flanking Sequence:
GCGTCAGGCATGGCGCCCGAAACGCATGAGGAAATTTCCCATGCTGCCTTCCTTCTGACAGCACACTTGCCCTTTTTTAGAAGCAAATGCAAACTTGAATACTTTTCTGATCAAAGATGTGTTTCTGTAGGTGTGACTAGCCGTTGGCACACAAAGAAGCTGCCCCGCAAGACCCATCGTGGTCTGCGTAAGGTGGCTTGTATTGGAGCCTGGCATCCTGCCCGTGTGGCTTTCTCTGTGGCTCGTGCTGGACAGAAGGGCTACCACCACCGCACAGAAATCAACAAAAAGGTAATGCTTCAGAAAGTCACTCAAATGTTCATGGCATACGTTTGTGGACGTTTTGTTGCAGTCTTGCCTCATGCATGCTTTTGTTCACCTTTAGATCTACAAGATTGGTGTGGGCTATCATAACAAGGACGGAAAACTTGTCAAGAACAACGCCTCTACTGATTATGATCTGTCCAACAAGAGCATCAACCCTCTGGTGAGTGTGCTGT[T/A]GTCTCCCTATTGTGAATTTGATAAATTGTTTATATGCATGCATTAATACTGATGCCTTTTTATTTTAGGGTGGCTTTGTGCATTATGGTGAGGTGACGAATGACTTCCTCATGCTGAAAGGCTGTGTGGTCGGAACCAAGAAGAGGGTTTTGACTCTGCGCAAATCTCTACTGGTCCAGACCAGCCGTCGTGCTCAGGAGAAGATCGACCTGAAGTTCATCGACACCACCTCCAAGTTTGGTCATGGACGTTTCCAGACCATCGAAGAGAAGAAGAACTTCATGGTGAGTGGATGAGTGCTTAGGTCACAGGACATGTGCAGAGAAGCCATTGTGTCTCTTATCGCAAACAGACAAACCCTGAACGTATTGGTTAATTAAACCGAGTTCAGTGAGTGCATAGCTGCTGCTTGGAGTAATGTCTGAAGTTTAAATTGGTAGCATTAAGCCTCCGGTCGCGTAGAGGTTATGGGCCTCTTGTGTGACGCTGCATTTACTTGG
Associated Phenotype:
Not determined