ZMP
si:ch73-205c16.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
RBM10
Human Description:
RNA binding motif protein 10 [Source:HGNC Symbol;Acc:9896]
Mouse Orthologue:
Rbm10
Mouse Description:
RNA binding motif protein 10 Gene [Source:MGI Symbol;Acc:MGI:2384310]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32421 | Essential Splice Site | Available for shipment | Available now |
| sa43901 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa37584 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32421
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 |
|---|---|---|---|---|---|
| ENSDART00000111456 | Essential Splice Site | 152 | 666 | None | 20 |
| ENSDART00000133906 | None | None | 199 | None | 4 |
| ENSDART00000136805 | Essential Splice Site | 151 | 266 | None | 8 |
| ENSDART00000111456 | Essential Splice Site | 152 | 666 | None | 20 |
| ENSDART00000133906 | None | None | 199 | None | 4 |
| ENSDART00000136805 | Essential Splice Site | 151 | 266 | None | 8 |
Genomic Location (Zv9):
Chromosome 23 (position 923890)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 871030 |
| GRCz11 | 23 | 883823 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCTCAACTTAAGCTCCTCCCCCCAGCCCTCTGAGGCGGCCAATGACAG[T/C]AAGTCTTAAAGTCTGCATGAACTGTTTCGTATTGTAATTTAAGTTTCTAG
Long Flanking Sequence:
GTATATGTGTTTGTGTGTGTGTTGCTTTGTTTACGAAACAAGTGGTTCTAATTGGATTTGCATTGTAAACCTTAAATAGAAGTTAAAAAGGTATCATTTTATAAACGTTTTATTGTTTGATAGCTACTATACTCCCAAAATCATTCCGCATTATTCCACACTTTTTTTTTTTTGTTATTCTGCACAAAACACATTTATTTTTTTGATGCAAGTACATAATAGTTAAGGACACTTAATATAAAGTGGGACCAGAGTAAATGATGTGGTCATTATCATTTATGAACTGTTCCTTTAAAGTAAATAAACCCTCTCATGGCTCTTTTTCTCTTTATATCTGCAGAGGCGGAGCTGAAACTGCCTCTGGTGCCAAAGATTTTACCTCTGTGTCAGCTGAAGGACTCAACTCAGGGTTTACTGCCTCTTCCAGCCATATTCCAGACAGCCACGTCCATCCTCAACTTAAGCTCCTCCCCCCAGCCCTCTGAGGCGGCCAATGACAG[T/A]AAGTCTTAAAGTCTGCATGAACTGTTTCGTATTGTAATTTAAGTTTCTAGAGAAGCAGAATATTAAATGAGAAAAGAAGTGGGCGTGGCTTGTTTTTTCTACTGTGAGCTGATTGGGTGAAGTAAAGTAGGCGTGTCATTCAGAAAGATGGGGAAAAGTGTTTGGAGAGATTTTTACAGCCTAACAGACTCCGCCTGCTCACCATTTCTGTTTGATGTCGTACTGACAGCTGGTGGGCGTGGTTAAGTATGTTAGCCCCGCCCAATACCTCAGACAGACCTAATCTGAGGATCAAACTGAACACAAACAGTGCATGTTTAGATTTCAATTAAAGATTACAGAGGCAAACTATTGTTTTGTTCTTACTGACATGCACAGATGAACTGTTCAGCACTAAACTAGCAATGTGAGCTAACAACATCACTATAGCTAGTTTTGTTTTCATGCGTACTTTAAGCTTCATTCAGATAACACAGTTTGGTAAAACTTTACTAGAAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43901
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111456 | Essential Splice Site | 152 | 666 | None | 20 |
| ENSDART00000133906 | None | None | 199 | None | 4 |
| ENSDART00000136805 | Essential Splice Site | 151 | 266 | None | 8 |
| ENSDART00000111456 | Essential Splice Site | 152 | 666 | None | 20 |
| ENSDART00000133906 | None | None | 199 | None | 4 |
| ENSDART00000136805 | Essential Splice Site | 151 | 266 | None | 8 |
Genomic Location (Zv9):
Chromosome 23 (position 923890)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 871030 |
| GRCz11 | 23 | 883823 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCTCAACTTAAGCTCCTCCCCCCAGCCCTCTGAGGCGGCCAATGACAG[T/C]AAGTCTTAAAGTCTGCATGAACTGTTTCGTATTGTAATTTAAGTTTCTAG
Long Flanking Sequence:
GTATATGTGTTTGTGTGTGTGTTGCTTTGTTTACGAAACAAGTGGTTCTAATTGGATTTGCATTGTAAACCTTAAATAGAAGTTAAAAAGGTATCATTTTATAAACGTTTTATTGTTTGATAGCTACTATACTCCCAAAATCATTCCGCATTATTCCACACTTTTTTTTTTTTGTTATTCTGCACAAAACACATTTATTTTTTTGATGCAAGTACATAATAGTTAAGGACACTTAATATAAAGTGGGACCAGAGTAAATGATGTGGTCATTATCATTTATGAACTGTTCCTTTAAAGTAAATAAACCCTCTCATGGCTCTTTTTCTCTTTATATCTGCAGAGGCGGAGCTGAAACTGCCTCTGGTGCCAAAGATTTTACCTCTGTGTCAGCTGAAGGACTCAACTCAGGGTTTACTGCCTCTTCCAGCCATATTCCAGACAGCCACGTCCATCCTCAACTTAAGCTCCTCCCCCCAGCCCTCTGAGGCGGCCAATGACAG[T/C]AAGTCTTAAAGTCTGCATGAACTGTTTCGTATTGTAATTTAAGTTTCTAGAGAAGCAGAATATTAAATGAGAAAAGAAGTGGGCGTGGCTTGTTTTTTCTACTGTGAGCTGATTGGGTGAAGTAAAGTAGGCGTGTCATTCAGAAAGATGGGGAAAAGTGTTTGGAGAGATTTTTACAGCCTAACAGACTCCGCCTGCTCACCATTTCTGTTTGATGTCGTACTGACAGCTGGTGGGCGTGGTTAAGTATGTTAGCCCCGCCCAATACCTCAGACAGACCTAATCTGAGGATCAAACTGAACACAAACAGTGCATGTTTAGATTTCAATTAAAGATTACAGAGGCAAACTATTGTTTTGTTCTTACTGACATGCACAGATGAACTGTTCAGCACTAAACTAGCAATGTGAGCTAACAACATCACTATAGCTAGTTTTGTTTTCATGCGTACTTTAAGCTTCATTCAGATAACACAGTTTGGTAAAACTTTACTAGAAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37584
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111456 | Nonsense | 578 | 666 | 18 | 20 |
| ENSDART00000133906 | Nonsense | 159 | 199 | 4 | 4 |
| ENSDART00000136805 | None | None | 266 | None | 8 |
Genomic Location (Zv9):
Chromosome 23 (position 907270)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 854410 |
| GRCz11 | 23 | 867203 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCTCAGGCTCTGCTGGCGGGCTGCAGTGTAGAGACGGACAGCGAGGAC[G/T]AGAGCTCAGAGAAGCAGGAGCGTCTGACGGACTGGTGTAAACTGGCCTGT
Long Flanking Sequence:
ATTTCTCCCAATAATTCCTGAAATACTGATTGATCTGAGCACAGTACATGTATCCACTGTGTGATAGTCCATCCCAGATGCCTCTAAGCACAGAGAAGTTGATGGCGCTTCTGAACACTGTTAACATAGGGCTTCCGTTGTCCATACTGTCCCAACTTTTTCTGATTTTGGGTTGTGTGTATATATATTTATATTTATATATTGACTCTTCTTGTTGAATCGCTGAATACCTCCTCAATTGTAAGTCGCTTTGGACCAAAGCGTGTGCTAAACGACTAAACGTAAATGTAAAAATGCACAGAAAAACTCTTACTATGTCTAAAAAAAGGTTAAAGGTAACATAAAACAGAACACACAACAAAACAACGTCCAAGAAAAAAAAACTAAACAAAAAACATTGTTCAGTGGTCAGTGTTTTGACAGCGTGTGTGTGTGTGTTTCTCTAGAGTCCTCCTCAGGCTCTGCTGGCGGGCTGCAGTGTAGAGACGGACAGCGAGGAC[G/T]AGAGCTCAGAGAAGCAGGAGCGTCTGACGGACTGGTGTAAACTGGCCTGTCTGCTCTGCCGGAGACAGTTCCCCAGTAAAGAGGCTCTGATCCGACACCAGCAGCTGTCCGAGCTGCACAGAGTGAGTGAAGATCCTCACATCTGACCACGGGCACATCCAGCTACACTGATCTTCTGTTTCAGTGCTTGAAAAATAGCTCAGCACTTCTCAATCCTCATTCTTAACTTTGCTCTTGGTTTGTGTATGCGTTGTAGGATGTACTGAACTGATTTCACATAGGATTAATTAAACAGTATATTTCTATTGATATCTGCGTTTATTCACGTGCAGCAAAACCTGGAGCAGAAGAGATCCAGAACGACAGTGTCAAACACACAAGAGGGATCGGAAACTGAGGTGATTCAGCTTCTCTTCAACACACGACTGCTCATGATAACCCTTCCCAAAGACCAGAGGAAAGCTCGTGTGTGTGTGTGTGTTAGTGCTGGGGAAAGATGC
Associated Phenotype:
Not determined