ZMP
rps21
Ensembl ID:
ZFIN ID:
Description:
40S ribosomal protein S21 [Source:UniProtKB/Swiss-Prot;Acc:Q7ZUG5]
Human Orthologue:
RPS21
Human Description:
ribosomal protein S21 [Source:HGNC Symbol;Acc:10409]
Mouse Orthologue:
Rps21
Mouse Description:
ribosomal protein S21 Gene [Source:MGI Symbol;Acc:MGI:1913731]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa5976 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa9451 | Essential Splice Site | Available for shipment | Available now |
| sa13335 | Essential Splice Site | Available for shipment | Available now |
| sa37621 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa5976
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000033663 | Essential Splice Site | None | 81 | None | 6 |
| ENSDART00000139870 | None | None | 81 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 9327380)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 9285521 |
| GRCz11 | 23 | 9220491 |
KASP Assay ID:
554-3762.1 (used for ordering genotyping assays)
KASP Sequence:
ATCCGGACCCTTGCTCTTTCCTTTCCGCGTCGGCCATTTGTGTTAATCGG[T/A]AAGAACACCACGAGCTCTAGTGTTTWGTTATATTTTAACWGTTTTGAGCG
Long Flanking Sequence:
AAATGAATATGGAAATATGGAAAGAAAAGCATTAGGTTCGTTCTACTCTATAAAATCTTTTGTCTGAGGTACTGGTCTGGAATTACACATAGGTAAACTTATGAAATATAGAAAATTGCATGTAGTGTAAATCTATAGTAGCGTGCAGTTAAAATGTATTAAAATAAACATCTGAATGTGTAGTTTTTGGGTGTTTCCAAAATACACTTTGACAATTAGAAATGGTTGCTGCATGTTTTAAAAAAACCCCAAAGATTTAGCCTGAACTGGCTTGATCTGATATCCAAAATATCCCATGAATAATAAAACGTAAATGTTTTTTTCGGTAGTTTCCTATTTTAATTTTAGGGACAACATTTCACAAAATTTTATCTTTCTTCTTCTTCTTTTGTTTTGATTTGGCGGATCGCACCAGTTAAAACTTTTATCTTACATTTCCTATTTCGTCACATCCGGACCCTTGCTCTTTCCTTTCCGCGTCGGCCATTTGTGTTAATCGG[T/A]AAGAACACCACGAGCTCTAGTGTTTAGTTATATTTTAACTGTTTTGAGCGCATATTTGCCACATGTTTGGTATTGCATTTATGTACGGAACAGTTATACACAACATGTGTCGCATGTATGCTTGCTAAACCGTTTTCCGTGAGCGTATTTGTGTTAAAATGCGGCAGCAGGGCTCAGCCGCTAACGTTAAACATGTGGAGAGACGCGCTCTTTGAGGCCGCTCTCATAAAAGGAATTGATTGAAATAGTAAATTAATGAAGTTTAAATTGTAAATACACAAGTATGTGTCTACATAGAGCTAATTTAAATACAATTTGACCGGTTTCTCTGTTTACCGCAGACCGAGTTGGTTGACAGTCATCAATAAAAGCGAAGATGCAGAACGACGCTGGTGAATTCGTGGACCTGTACGTCCCTCGTAAATGGTGAGTTTACCACAAACTCGATTTTATGAATGTTTATATTAGTGATATTGTGAGTTTCACACACGGTTCTAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9451
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 |
|---|---|---|---|---|---|
| ENSDART00000033663 | Essential Splice Site | 62 | 81 | 4 | 6 |
| ENSDART00000139870 | Essential Splice Site | 62 | 81 | 3 | 5 |
| ENSDART00000033663 | Essential Splice Site | 62 | 81 | 4 | 6 |
| ENSDART00000139870 | Essential Splice Site | 62 | 81 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 9333922)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 9292063 |
| GRCz11 | 23 | 9227033 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAATGGACAGTTCAAGACCTATGCCATCTGTGGCGCCATCCGTAGAATGG[T/A]ATGTTCAGACACTCTTAAAGSTCATTCTGCTRCACAAGTACAACATGTGT
Long Flanking Sequence:
TATTTTACTTTTGTTTGACTTTAATAATCATATTCTGCCACTGTCCAAACAAATATAAATTAGTTGTCTAAATTAGTTTGAAAAGTTGTCTAATATTTGTTTAAATAATTAGAAGTTAAATATAGTTTTTTGGTACCTATTTAACTTTTGGATTTTTTTTATACAATGTCAAAAGCGTGTTGTTTTATGGTATCTATGGAGTCTTAAATTCCACAGTATAAACATATTTTGTATGTGTACTACGTATATATGATTAACAGTGTTAAGTATGATTGTTTTTTTTTTCTGCAAATGTGTTGTGTGGTATTAAAAAGGTTTTAAATTTAACTCTTAGAAACCTGCAGATACCTTGTGTTTGATTTATACATATGTCATATGCTGGATGACCGTGGAACATTATTTCATGATTTTACATGGTTTCTTCCAGGTGGACAGGGTTACAGGCAGGTTCAATGGACAGTTCAAGACCTATGCCATCTGTGGCGCCATCCGTAGAATGG[T/A]ATGTTCAGACACTCTTAAAGCTCATTCTGCTGCACAAGTACAACATGTGTAGGGAATTACAAAGGTGGTGTGGGTGTTCATATCAGTGGGGAAGCATACAAGGTGTTATTTTGAGACTTTTGCTTGATGATCCACAGGGTGAAGCTGATGACTCCCTCCTGAGGCTCGCAAAGACCGACAGCATTGTGGCCAAGTAATCTGTAAGTATGCAGCTACTTTTATCAATTCATCTGTCAGCACTAGGGCTTTCGTTCTTCTTAGCCAGCATCACTGAGCACTTTACAGACTGACATTGCAAGTCCAAACCTTTGTATTGATACGGTTAAACTTCCGGTGTAAGCTCAATGTGGCAATTTTAAATTTTGTTAGGGTCCTTTCACAGTATCGATGTTGTAATGAAATTAAAATACATTCAGTTTAATAGACTTAAGCATTCATTTATTCAAGCATAAAATGAGATGAAAGCTTGTGTAACAGCTATCGCTGTCAGGATCAGCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13335
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 |
|---|---|---|---|---|---|
| ENSDART00000033663 | Essential Splice Site | 62 | 81 | 4 | 6 |
| ENSDART00000139870 | Essential Splice Site | 62 | 81 | 3 | 5 |
| ENSDART00000033663 | Essential Splice Site | 62 | 81 | 4 | 6 |
| ENSDART00000139870 | Essential Splice Site | 62 | 81 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 9333922)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 9292063 |
| GRCz11 | 23 | 9227033 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAATGGACAGTTCAAGACCTATGCCATCTGTGGCGCCATCCGTAGAATGG[T/A]ATGTTCAGACACTCTTAAAGSTCATTCTGCTRCACAAGTACAACATGTGT
Long Flanking Sequence:
TATTTTACTTTTGTTTGACTTTAATAATCATATTCTGCCACTGTCCAAACAAATATAAATTAGTTGTCTAAATTAGTTTGAAAAGTTGTCTAATATTTGTTTAAATAATTAGAAGTTAAATATAGTTTTTTGGTACCTATTTAACTTTTGGATTTTTTTTATACAATGTCAAAAGCGTGTTGTTTTATGGTATCTATGGAGTCTTAAATTCCACAGTATAAACATATTTTGTATGTGTACTACGTATATATGATTAACAGTGTTAAGTATGATTGTTTTTTTTTTCTGCAAATGTGTTGTGTGGTATTAAAAAGGTTTTAAATTTAACTCTTAGAAACCTGCAGATACCTTGTGTTTGATTTATACATATGTCATATGCTGGATGACCGTGGAACATTATTTCATGATTTTACATGGTTTCTTCCAGGTGGACAGGGTTACAGGCAGGTTCAATGGACAGTTCAAGACCTATGCCATCTGTGGCGCCATCCGTAGAATGG[T/A]ATGTTCAGACACTCTTAAAGCTCATTCTGCTGCACAAGTACAACATGTGTAGGGAATTACAAAGGTGGTGTGGGTGTTCATATCAGTGGGGAAGCATACAAGGTGTTATTTTGAGACTTTTGCTTGATGATCCACAGGGTGAAGCTGATGACTCCCTCCTGAGGCTCGCAAAGACCGACAGCATTGTGGCCAAGTAATCTGTAAGTATGCAGCTACTTTTATCAATTCATCTGTCAGCACTAGGGCTTTCGTTCTTCTTAGCCAGCATCACTGAGCACTTTACAGACTGACATTGCAAGTCCAAACCTTTGTATTGATACGGTTAAACTTCCGGTGTAAGCTCAATGTGGCAATTTTAAATTTTGTTAGGGTCCTTTCACAGTATCGATGTTGTAATGAAATTAAAATACATTCAGTTTAATAGACTTAAGCATTCATTTATTCAAGCATAAAATGAGATGAAAGCTTGTGTAACAGCTATCGCTGTCAGGATCAGCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37621
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000033663 | Essential Splice Site | None | 81 | 5 | 6 |
| ENSDART00000139870 | Essential Splice Site | None | 81 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 9334123)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 9292264 |
| GRCz11 | 23 | 9227234 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCCCTCCTGAGGCTCGCAAAGACCGACAGCATTGTGGCCAAGTAATCT[G/A]TAAGTATGCAGCTACTTTTATCAATTCATCTGTCAGCACTAGGGCTTTCG
Long Flanking Sequence:
TCTTAAATTCCACAGTATAAACATATTTTGTATGTGTACTACGTATATATGATTAACAGTGTTAAGTATGATTGTTTTTTTTTTCTGCAAATGTGTTGTGTGGTATTAAAAAGGTTTTAAATTTAACTCTTAGAAACCTGCAGATACCTTGTGTTTGATTTATACATATGTCATATGCTGGATGACCGTGGAACATTATTTCATGATTTTACATGGTTTCTTCCAGGTGGACAGGGTTACAGGCAGGTTCAATGGACAGTTCAAGACCTATGCCATCTGTGGCGCCATCCGTAGAATGGTATGTTCAGACACTCTTAAAGCTCATTCTGCTGCACAAGTACAACATGTGTAGGGAATTACAAAGGTGGTGTGGGTGTTCATATCAGTGGGGAAGCATACAAGGTGTTATTTTGAGACTTTTGCTTGATGATCCACAGGGTGAAGCTGATGACTCCCTCCTGAGGCTCGCAAAGACCGACAGCATTGTGGCCAAGTAATCT[G/A]TAAGTATGCAGCTACTTTTATCAATTCATCTGTCAGCACTAGGGCTTTCGTTCTTCTTAGCCAGCATCACTGAGCACTTTACAGACTGACATTGCAAGTCCAAACCTTTGTATTGATACGGTTAAACTTCCGGTGTAAGCTCAATGTGGCAATTTTAAATTTTGTTAGGGTCCTTTCACAGTATCGATGTTGTAATGAAATTAAAATACATTCAGTTTAATAGACTTAAGCATTCATTTATTCAAGCATAAAATGAGATGAAAGCTTGTGTAACAGCTATCGCTGTCAGGATCAGCAGGTGAGCGCAGAAACTCTATTTAAAAAACTAGGGTAAAATAAACAATCATATTTTTAAGACATGGCGGGAGGAAATGTAATTTATTGCTGTGCTTGTCCGATCTGAGACGCACTTTATATGGTATATCAGGCGGTGAAGATCAACAATTTTATTTATTTATTTTTTTTTGAAGAAATTGGACCTTAAACATGGTATGACTGCA
Associated Phenotype:
Not determined