ZMP
rbm19
Ensembl ID:
ZFIN ID:
Description:
probable RNA-binding protein 19 [Source:RefSeq peptide;Acc:NP_944597]
Human Orthologue:
RBM19
Human Description:
RNA binding motif protein 19 [Source:HGNC Symbol;Acc:29098]
Mouse Orthologue:
Rbm19
Mouse Description:
RNA binding motif protein 19 Gene [Source:MGI Symbol;Acc:MGI:1921361]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26817 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20801 | Nonsense | Available for shipment | Available now |
sa33947 | Essential Splice Site | Available for shipment | Available now |
sa40776 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa26817
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 |
---|---|---|---|---|---|
ENSDART00000062459 | Nonsense | 205 | 927 | 5 | 25 |
ENSDART00000130336 | Nonsense | 205 | 927 | 5 | 24 |
ENSDART00000131073 | Nonsense | 98 | 275 | 6 | 12 |
Genomic Location (Zv9):
Chromosome 6 (position 45803626)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45864560 |
GRCz11 | 6 | 45866442 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGAGGAATCAAGTGATGACGGCGAGGATGCTGCAGATGAAGAGGACAAA[C/T]AAGGTGCAATATTTAATTTAACAAATTTTAGCACTGATTACGATGTGCAT
Long Flanking Sequence:
GAGCACTTACAATAAATGTGATTGCAAACTATAAAGTAAGATCTGATGTTTGCCATTTATTTTCTTTAGAGTAGTTTATAACTGAATTTATTGTAAAATATGCATTACAAATAAATCATTCTGAATTTATGCTCTTGCTCCACAGAAGCCGAAGAAGATTTTAAATGTTCTGGGAGATGTAAGTTTGCTTTTTTGTTTTGTGTCAACACAGTTCATACAAAATCGATGAACTTGCTGACATTCTATGAAATGTTGTTTGTAATTCCCAGCTTGAAAAAGATGAGAGCTTCCAGGAGTTTCTGGCAGTGCACCAGAAACGTGGACAGGTTCCCACATGGGCCAATGACACTGTGGAAGCGACTGCTGTTAGACCTGAAATGGAGAAGAAGAAAGAGAAGAAGCAGAAAGCGGCTGTTGAAGATGATTACCTGAACTTTGACTCTGATGAATCGGAGGAATCAAGTGATGACGGCGAGGATGCTGCAGATGAAGAGGACAAA[C/T]AAGGTGCAATATTTAATTTAACAAATTTTAGCACTGATTACGATGTGCATTAACTCTTTGACTGCCCCTCTACCAAATAGTTGGCCATGTTTTTACTGTTTTAAATAATGTCTGTTAAAGTCATTTAAAGAATGGTTGTTTTAAATAATGACTTACACGCATTGTTGGTTTACAAAAAAAAAAAAAATCAAGCAAACATCCTGTTGCACTATTGCACTATATTACTATACTTGATTTCTTTTTTTTTTTTTTTACAATAAAATCAAAATCATGTTAAATGAGAATCTGATTGAGGTGATTTAGTATTCAAAAGCGTTTTATTTTGAATATTTAAAAAAATAAATTACTCTTACACTTCATATTTTCAGATTTTTCATAGTATGTGTATTGAGTGCGGTACTTTTACCATAAACCGACATATCAACCATTTGGTAGTAGGGATGCAACGATTAACCGATTTCCCTATTAACCGCGATTTAATTCATCACGGTTAAATAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20801
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062459 | Nonsense | 357 | 927 | 10 | 25 |
ENSDART00000130336 | Nonsense | 357 | 927 | 10 | 24 |
ENSDART00000131073 | Nonsense | 250 | 275 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 6 (position 45798052)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45858986 |
GRCz11 | 6 | 45860868 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTAGTTCCCGTTTGTTCATTATCTGTGTGAACCCACAGGAGGGCGCTA[C/A]ATTGAGGTTTTCAGAGCCAACAACTTTAAAAACGACAGGCGTTCTGCAAA
Long Flanking Sequence:
GCAGTAATGTGCACCTTATGTAAAGCTGCTTTGTAACAATAATTATTGTGAAAATACAAATAAACTTAAATTAAATTGAATGTATTTTATTTTGACCACAGCAACAAGTGAAAGAGTTTATGATGCCTTTGAAACCCGTTGCCATTCGATTCGCTAAGAACAGTGACGGCCGCAACTCGGGTAAGAGCATCTGCTTTTTTTCTGCCTGTTGATGGGTTGAAGATGTCAAGCTGCTGCAGATTGATTGATGTTGTATTTCCTGCAATAAGGTTACGTGTATGTGGACCTACGATCAGAGGCAGAGGTCGAGAGAGCCCTGCGCCTTGACAAGGACTACATGGGTGAGCACCTTTTCACTCTTTCTGATAAGTTCAGTACAGTGATGATTTTTCTTTGCTTCTGACATTTTTTACAGGTTTAATCTAATTTGAAAACAAGTATGGTACATGAAACTAGTTCCCGTTTGTTCATTATCTGTGTGAACCCACAGGAGGGCGCTA[C/A]ATTGAGGTTTTCAGAGCCAACAACTTTAAAAACGACAGGCGTTCTGCAAAAAGAAGCGAGATGGAAAAGAATTTTGTGCGCGAGCTGAAGGACGACGAGGAAGAGGAGGATGTTGCAGAATCTGGACGACTTTTCATTAGAAACATGCCCTACACGTGCACTGAGGAGGATCTGAAAGAAGTATTTAGCAAACACGGTTAGTCGCAGACACATGATAAATATTGTTATAAACAACAAGTGGATGACACAAAATACAGGTGTAAACAGAGTATGTTGAGCTTGTCTTCCAGTGGTAGTCAAAAACACTTTTTGTCTGGATTAGTTTTGTAATGTAGACTCATGTCAGGGAGTCCGCAGTGTCTTAAAAGGTCTTACATTTCAAAAACTAAATCTTAGGCTTTGAAAAGTAATGGATTCACTGAAATATTGTGTTGTAGGTCTCAAATAATTTAATAAAGTCTTAATTTTCATATGTCCATGTGAATTTATCCGATCAGTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33947
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062459 | Essential Splice Site | 720 | 927 | 17 | 25 |
ENSDART00000130336 | Essential Splice Site | 720 | 927 | 17 | 24 |
ENSDART00000131073 | None | None | 275 | None | 12 |
Genomic Location (Zv9):
Chromosome 6 (position 45791671)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45852605 |
GRCz11 | 6 | 45854487 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCATTAAGAACTTGAACTTTATCACCTCAGAAGAAACATTACAGAAGG[T/C]AAACTAAAAACACACACACACACACACACACACACACACACACACACACA
Long Flanking Sequence:
TTGTATTTCTCTTTCTAGTTTCAACATGTCCCTTTGTATCTTGAATGGGCTCCTGTCGCTGTCTTTACAACTCCCTCAGCACCTAGACCAGGTAATACTTTAATTCTGATTCAGCCATCTGCTGTAATTTAACAATCAATTCAATGTTAGGTGACTATGATGAGTTTTCATTTGTTGTCCCTTTTTTTCTCATTAATAATAAGTAATAATAATAAAACTATTCTAGAGTACATCCCAATCTGTGTTTCTGTGATTTATTTTTCTTATATTTGTTCTGTGTTGTCTCAATCTGTGTTTCTGTGTTAGTTCTTTGTGTTATTCTCTGATTCTGTTTTTCCTCCCAGAGCCTCAAACCAAAGAGAAATCTGCTGTGAAAAATGATTCAGTCCAAAATGAAGAAGAAGAGGAGGAAGAGGAAGAAGATGACCAGATTTTACCTGGCTCGACTCTCTTCATTAAGAACTTGAACTTTATCACCTCAGAAGAAACATTACAGAAGG[T/C]AAACTAAAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAAACACACACAAGCATATGCTTGAGCAGCAAAGCGGTTGTGGTTTAGGGATTTGCAGTGGAAACCTGAGAGGCCTTCTTGTTTTGCTGATCACAGGAGACTCATTTAAGATGCATATTAGTTCTAGGTGTAAACATGTGTTGTGTGATCAGATCACCCGAAACGGATGTTCATAACAGGTGTAAACATGGCCCGTGTCTCACCATATGGCTTTCATTGCATTCTTTTGACAGACGTTTTCTAAATGCGGCGTGGTGAAAAGCTGCACGATATCAAAGAAAAGAGATAAAGCAGGTTTGTTTTCTCCGAAATGCATATTTACTGTATTGATATTCATCTGTGCGCTTGTTAGTTTTCTCATTTCTCCGTCTCGTTTCAGTCGCTGTGTGAATCTCACCCTGATCTCTTTGTGTGTGTGTGTGTGTGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40776
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062459 | Nonsense | 796 | 927 | 21 | 25 |
ENSDART00000130336 | Nonsense | 796 | 927 | 21 | 24 |
ENSDART00000131073 | None | None | 275 | None | 12 |
Genomic Location (Zv9):
Chromosome 6 (position 45788200)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45849134 |
GRCz11 | 6 | 45851016 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCCTTATGTTGTTTTTGTAGGTCAGGTGTGGCACAGGCCAAGAGGAAA[A/T]AGCAAACCGCCAGGAAACAGACGACCTCTAAGATCTTGGTGCGAAACATC
Long Flanking Sequence:
GCTTTAGACCATGCGCTTAGATCGATAAAGTAAAGCCCGTTGTTATGTTCAAGAAACCATTTTGGATTGTTTTGAGTTTTCTGATATCGTCCTGCTACAATTGGCCATAACAAGATAATCAAGGTATGGACATTGTGAGGAACAATACTCTCAAACTTGGCACAAACCTGACCCATTGATGCAAAGCAGCATGGTTCCATGAATTTTTTTATTTTTTTACATCAAATTCCGACCCTATGATCTAATAACACAGTAGAGGTTAAGACTCATCAGACCAGGCAATCTTTTTTTTTTTATCTTATATTGTTTATTTTTTTATATATAGTAATAGGCATAGTAAAGTATGAGTAAGTTTACATTTTTGGGTCAACACTTCTTTCCTAGTTGCCCCGTGACATTCATTAATGTCATTTAAATGTGGCACCGGTCACATGTATGAGTGAAAAACGTGTTCCTTATGTTGTTTTTGTAGGTCAGGTGTGGCACAGGCCAAGAGGAAA[A/T]AGCAAACCGCCAGGAAACAGACGACCTCTAAGATCTTGGTGCGAAACATCCCTTTCCAGGCCACAGTCAAAGAGCTGAGAGAACTCTTCTGGTAAACATCCTTTCACATTTTAATGTTTCATGCCATATTATTCCAACAAGTGTGGAATTTCTAGCATGTATATGGTACCTTAACAATATTCGTATGCAATAGCATTTTTAATACCAGAGAGAAAATATTGCATTAGCATGAAGTAAAATTAAAATGTTTTCACGTCTTCATTTTTTTTAGACGTGAAGGTTTGAATGGTTTGAATGGTTAAGATGTTCACTTGCATTGCCAAAATTTAACCATTGTTTGAAAGTTGTTTGCATCGTTGTTTAAAGCAACGTCAATGCTAACTTAGAGTTGCAGGCAAAAATATTAGATTATTAGAAAATTATTTGAAATTTGAATTCTTCAAATATTTCCAGGGTGATGTGTAACAGAGCAAAGACATTTTCACTATTCCTATTATATA
Associated Phenotype:
Not determined