ZMP
wu:fd99c08
Ensembl ID:
ZFIN ID:
Human Orthologue:
RBM16
Human Description:
RNA binding motif protein 16 [Source:HGNC Symbol;Acc:20959]
Mouse Orthologue:
Rbm16
Mouse Description:
RNA binding motif protein 16 Gene [Source:MGI Symbol;Acc:MGI:1925212]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43004 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31015 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43004
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 |
---|---|---|---|---|---|
ENSDART00000112675 | Essential Splice Site | 409 | 1286 | 11 | 20 |
ENSDART00000112675 | Essential Splice Site | 409 | 1286 | 11 | 20 |
Genomic Location (Zv9):
Chromosome 17 (position 49167214)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 48854025 |
GRCz11 | 17 | 49011028 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAAACCAGCAGCACCCGTTCAAGGACGCGCTCAAGATCCCGCTCTAG[G/A]TTGGTGCGCCAATGTCTGTAAAAGGCTCTTTCCATTTTTTTAGCCACAAG
Long Flanking Sequence:
GCCTTGTAATTGACACGTGGTATAATGGATTATGATGGTGTTGAATTTCTATTAATGTAATGTAAATGTAAATGTAATGTAATGTGTATTTAATGTGTATTTAATGCACCATTTATTTGGACAGTCTATGAGCATGGAGAGCCAGGACGCTATTTTTGGCACTGAAAATTCTGCCCCATCTGGCCAGAGCAGCGCCCCGTCACAGCACCAAGTTCAAGAATCAAAAATGGATGATTCCATGGACAACCAACAACAGGTAAGATCTGATATCAGAGATTACTTTAGAGGAAAAGCCTGTGTTATGCATTGGCAGTAGTTTGAAGGTGGTGTCTCACTTACGCATTGATAAATGGATTGTTGAAATGCCCTTTCCATGTGTGTTTTTTGCAGGACATGGATATTGATGAGGGACAGGATGTGGTCGATGAGGAGCTCTTTGAGACGGATGAGAAGAAAACCAGCAGCACCCGTTCAAGGACGCGCTCAAGATCCCGCTCTAG[G/A]TTGGTGCGCCAATGTCTGTAAAAGGCTCTTTCCATTTTTTTAGCCACAAGATAAGATAGCTGATAAGATTGCACTGTATCTCCAGGTCACCTAAGAGGAGGAGGTCAAGATCACGCTCTGGGTCTCGGAAGCGGAAACACAGAAAACGCTCAAGGTCTCGGTCAAGGGACCGAAAGAGGAAGTCCTCCCGTTCTTATTCCAGTGAGCGAAGAGCACGGGAGAGAGAAAAAGACCGGCAGAAAAAAGGGCTTCCTCCAATCCGCTCGAGGGTTCTCAGTGGTAGGAACACATCTACTTTCTTTCGTTACCAATTTGTAAGGGCAACATTGTGTTTCAGTGATGTCACTGCTGTTTAAACTTTTTTTTTTTACTAGTAAAAGGAATTGATGACTTTTATATTGTTTGATATAGGCAGTAATCCACAAATGTGAACCCTTGCTAGAGCACTTTAAGAGTTACTGAGTTCTTGCCAAGGTCTTCAATGAAATCACATCAGTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31015
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 |
---|---|---|---|---|---|
ENSDART00000112675 | Essential Splice Site | 409 | 1286 | 11 | 20 |
ENSDART00000112675 | Essential Splice Site | 409 | 1286 | 11 | 20 |
Genomic Location (Zv9):
Chromosome 17 (position 49167214)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 48854025 |
GRCz11 | 17 | 49011028 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAAACCAGCAGCACCCGTTCAAGGACGCGCTCAAGATCCCGCTCTAG[G/A]TTGGTGCGCCAATGTCTGTAAAAGGCTCTTTCCATTTTTTTAGCCACAAG
Long Flanking Sequence:
GCCTTGTAATTGACACGTGGTATAATGGATTATGATGGTGTTGAATTTCTATTAATGTAATGTAAATGTAAATGTAATGTAATGTGTATTTAATGTGTATTTAATGCACCATTTATTTGGACAGTCTATGAGCATGGAGAGCCAGGACGCTATTTTTGGCACTGAAAATTCTGCCCCATCTGGCCAGAGCAGCGCCCCGTCACAGCACCAAGTTCAAGAATCAAAAATGGATGATTCCATGGACAACCAACAACAGGTAAGATCTGATATCAGAGATTACTTTAGAGGAAAAGCCTGTGTTATGCATTGGCAGTAGTTTGAAGGTGGTGTCTCACTTACGCATTGATAAATGGATTGTTGAAATGCCCTTTCCATGTGTGTTTTTTGCAGGACATGGATATTGATGAGGGACAGGATGTGGTCGATGAGGAGCTCTTTGAGACGGATGAGAAGAAAACCAGCAGCACCCGTTCAAGGACGCGCTCAAGATCCCGCTCTAG[G/A]TTGGTGCGCCAATGTCTGTAAAAGGCTCTTTCCATTTTTTTAGCCACAAGATAAGATAGCTGATAAGATTGCACTGTATCTCCAGGTCACCTAAGAGGAGGAGGTCAAGATCACGCTCTGGGTCTCGGAAGCGGAAACACAGAAAACGCTCAAGGTCTCGGTCAAGGGACCGAAAGAGGAAGTCCTCCCGTTCTTATTCCAGTGAGCGAAGAGCACGGGAGAGAGAAAAAGACCGGCAGAAAAAAGGGCTTCCTCCAATCCGCTCGAGGGTTCTCAGTGGTAGGAACACATCTACTTTCTTTCGTTACCAATTTGTAAGGGCAACATTGTGTTTCAGTGATGTCACTGCTGTTTAAACTTTTTTTTTTTACTAGTAAAAGGAATTGATGACTTTTATATTGTTTGATATAGGCAGTAATCCACAAATGTGAACCCTTGCTAGAGCACTTTAAGAGTTACTGAGTTCTTGCCAAGGTCTTCAATGAAATCACATCAGTAAC
Associated Phenotype:
Not determined