ZMP
si:ch211-241e15.2
Ensembl ID:
ZFIN ID:
Description:
RNA-binding protein 47 [Source:RefSeq peptide;Acc:NP_001108158]
Human Orthologue:
RBM47
Human Description:
RNA binding motif protein 47 [Source:HGNC Symbol;Acc:30358]
Mouse Orthologue:
Rbm47
Mouse Description:
RNA binding motif protein 47 Gene [Source:MGI Symbol;Acc:MGI:2384294]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13150 | Essential Splice Site | Available for shipment | Available now |
sa38255 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13150
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089070 | Essential Splice Site | 387 | 601 | 2 | 5 |
ENSDART00000135552 | Essential Splice Site | 387 | 600 | 4 | 7 |
The following transcripts of ENSDARG00000061985 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 18107914)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 18673082 |
GRCz11 | 1 | 19366019 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTATCCATACAACACACTCATCGGACCCAACCGAGACTACTTCATTAAAG[G/A]TTGGAGAACTCATTATCTCTCTTTAATATATCAGATTGAACAAATGTGAT
Long Flanking Sequence:
TGTGTGTTTGTCTTTATGTTCGTTTCTGCAGCTCTGGGGTCACCAGATTGCAGTCGACTGGGCCGAACCTGAGATTGACGTGGACGAGGATGTGATGGAAACAGTGAAGATCCTGTATGTGCGGAACCTGATGATCGAGACCAGCGAGGAGATTCTGCGCCAAACCTTCGGCCAGTTCAACCCTGGCTGTGTGGAGCGTGTTAAAAAAATCCGAGACTACGCCTTTGTTCACTTTGCCAGTCGAGACGATGCTGTGGTTGCAATGGACAACCTGAACGGCACAGAGATCGAAGGTTCCCGTATAGAAGTGACCCTGGCCAAGCCTGTGGATAAAGAGCAATACACCCGCTATCAGAAAGCATCGAAGGGAACAGCAGCTGCCACAACTGTCGAAAGCACCCAACAAAGTTATGTGTATCAGTGTGATCCATACACACTGGCCTATTATGGCTATCCATACAACACACTCATCGGACCCAACCGAGACTACTTCATTAAAG[G/A]TTGGAGAACTCATTATCTCTCTTTAATATATCAGATTGAACAAATGTGATTCTTTCTTTAAAAAAATTATATTAATAACCATTTGGCAAATCAGATACATCATGTTTGTATGTGATTTTTGTTGGTGACCTTGTCTGTAATGCTACTGAATATAGGTGGGAGACTAGATTGTTTTCCAACTATCTTTTGCTTAGCATTCGTATTTACTGCACACACATAATCAGACTCGATCTGTACAAAAAAATGAAGGGCATGCATTACAGTTTATGTTATGATATCCTCTTTAACCCAGAGCTTTCAATCTTTTCAAAAAGTGCTTCTCAACTGGTGGCTAAAATATTGCTAAAAACATTTGCCTTGAAAATGTGTTTATATGTCACAGTTCTGACCTTTTGTCTCAGAATTACACCATAAGATTTAGATATTAAGGCAGCAGTGCAGAATCTACACTAATAGTAAGAAAAGTCAGATTTGGCAAATATAAACCCACATTGATACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38255
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089070 | Nonsense | 418 | 601 | 3 | 5 |
ENSDART00000135552 | Nonsense | 417 | 600 | 5 | 7 |
The following transcripts of ENSDARG00000061985 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 18105887)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 18671055 |
GRCz11 | 1 | 19363992 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGGGCCCAGGGCCCCGCGGCTCATACCTTGGTGGCTATTCAGCTGGC[C/T]GAGGCATTTACAGCCGCTACCATGAAGGAAAGACCAAATTGCCGGACAAA
Long Flanking Sequence:
TGGGTTTGTAACAACTGAGATCATGCTCCTTTTTCAAATTGACCAACGAGTTGTGATTGCAAATGCTCATCCATTATCTGATTAAATGAAAACTTTATCTTTACTTTTAATTCCAACATTACTCAAACACCACCGCTCCCATCTCAAAGAACAGAAGCAAATTAATAGAGGATTAAGACACATTCACACTGGCAGCAATTTGAATATACTGATGAGTAATACTGCCTAAATACTGCTTTATTTATAGCCACTCCCACATCCTCAATCCTAAAACTATAAAACAGAAAGGTGACACAGAAGCTAATGACTTTTTATGCTCTCAAACAATGAGGTGACTAGTATTTATATATAATTAGGTTGCTCCTTGCGGCACTGTGCCTGAACAGCACGTCCTTTCATTTGTATCTCAAGCAGGTACTGTAAGAGGCCGTGGTCGTGCCGGGGCCAGTAGCAGGGGCCCAGGGCCCCGCGGCTCATACCTTGGTGGCTATTCAGCTGGC[C/T]GAGGCATTTACAGCCGCTACCATGAAGGAAAGACCAAATTGCCGGACAAACCTTACGAGATCATGTCTAATCTAGAGTTGGCAGCTGTGAACCCAGTGGGCATCAAGCCTGGCACAAGTCAGTGTGAAAATTAAAGCACATACATACTGAATTTCATTTAGTTGTGCTCTACTCCATTCAGTGGAGGCAGAATATAGAAACTTTGTTTTGGGGGGTGAAATTCTATTTATTACTGACATTTAAACCTCATTATAGTCTTAGATTTGGCTTCTACTTAAAAATAAAAACACTCAAGGATACTGGAGATCAGGGCTGGAACTATAAATCAGTGTTTTGTGATTCATGGGTTGATTTTTGGAATACATCGTGATTCTCTCTCTCGATTCAGAGCCGTTTTTAACAGCAGATTGCGCTTTAGGCTAGTTTTTCATCATACACTAAGTAGATTTATGATTTAAGTTTTAAGTAGGTTTTTCAATGATTGATGTAAACACAGATCA
Associated Phenotype:
Not determined