ZMP
rnasen
Ensembl ID:
ZFIN ID:
Description:
ribonuclease 3 [Source:RefSeq peptide;Acc:NP_001103942]
Human Orthologue:
DROSHA
Human Description:
drosha, ribonuclease type III [Source:HGNC Symbol;Acc:17904]
Mouse Orthologue:
Rnasen
Mouse Description:
ribonuclease III, nuclear Gene [Source:MGI Symbol;Acc:MGI:1261425]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa191 | Nonsense | Available for shipment | Available now |
sa13985 | Nonsense | Available for shipment | Available now |
sa31863 | Nonsense | Available for shipment | Available now |
sa35230 | Essential Splice Site | Available for shipment | Available now |
sa17917 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa191
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089017 | Nonsense | 142 | 1289 | 2 | 31 |
The following transcripts of ENSDARG00000055563 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 14455396)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13311049 |
GRCz11 | 12 | 13349352 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCACCCACTATGCCCTACCCTCCAACATACCCTATGAGCTACCCTCCA[C/T]AACCCCAGCTTCCCCCTCCACCCAGCTTCAACCCAGCTTATGGTCAGCCT
Long Flanking Sequence:
ACCCCAGTTTTAATGTCTTTTAAAGAATATTTCTGTTTATGTCTATATATTTTTTTACATCTATAGCTTTCTTAAAGATGTCTTTCCATGCTGGCCGTGGATGCCCGAGGGGTAGACTACCCGCTCCGGGTCAAATATATCATCCTGCTTCCCCACGATATCACTACGACCCTTCCGCTGCTCCCGGACCTGTCTATAACCCCCAGGGCGGCAGCAGCTACATGCCACCTCATCCTGACTTCATGTCGTTCCACTTCCCTCCACCATCACAGGCTTCCAACACCCTGCCTCAGTGCCCCATACGTCCACCAGTCTTCACAGAACCACCCCCTTTTCCACCACCTCCTCCTCACAGCTCAGATGGCTCGACTCCAATGCCGATTCAGAACTCTTATCCTTACATGATGCCCAATATCCCCCCTCCACCCCTGCCACCTATGCCACCCTCAGTTCCACCCACTATGCCCTACCCTCCAACATACCCTATGAGCTACCCTCCA[C/T]AACCCCAGCTTCCCCCTCCACCCAGCTTCAACCCAGCTTATGGTCAGCCTAGTGGTTCCTTCAAGCCTGAACGTTCCCGTCCACCACTTCACTACAAGACGGATTCCTGTTCTCGTTCCCCTGAGAGACTTCGGCACCATGATGATCACCGGCACAGGGGTCACAGTTATAGCGAATATGGAAGCAGACACAACCGAGAGTTTGGAGGAGAGAAGCGGGACAGGGGGTGTAGTTCAGAACGGAGGCGTTCAGACAGTCCTCGGCGGTGTAAATCCGACTATGACCGAGGACGTGTGTCATCGAGACACCGCAGCAGGTAATGTGCTTCACCTCTCATTTTTCTCATTTTTTATTGATACAGAATGATGTTGCTTGTATTTGGGTCATCTGATAATTCACTTGCACTTAAGATTCCTCTTAAAGAATGCTATAAGGCATATTTAAGGATGCTCAAATAAGTTTATCTTATTCAATCTGCTGCATTTGAGCCTTTTTAAGTG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa13985
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089017 | Nonsense | 698 | 1289 | 13 | 31 |
The following transcripts of ENSDARG00000055563 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 14467625)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13323278 |
GRCz11 | 12 | 13361581 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTTCAACTCCAGTGTCATTACTTTCCCMATAATTGTGCAWTTTGGTATM[C/T]GACCTGCTCAGCTTAGCTACGCTGGAGACCCGCAGTAAGTGTGACCGCAT
Long Flanking Sequence:
CAGGGGTTCAGAGAAGAATCCCAAAACATTTGCCCCTTTCACACGTACAAACTTTTTCGTAAAAATGCAAATACATTGCCATAAAGTGATCATGTGTAAACAGGCATTTAAAAATACAGAAAACAGATAGAGTTTCCTGTACAACACAAGTTTTTGTTTTACAAAGTTTAAAATCCAACCCTCAATCCAACTGTTAAAATAGTGCTGTTAGATGACATATGACAAGGCAGTCAATGACATACAAACAACCGACAACCTTGACAATTTAAAAACAGGCTTTAGAAGTTCATATGTTACCCTTACAAATCTGTTTCCCAGTGGAGAAAGCAATGGCTATTTTTCCCTTGAGGATGCCCACTGTTCTAGTGCTGTCATGTCATCAAAATATGTGTGTGCCTATATTTACACAGAAACCCAGCTCTGTGAGAATCGACCAGTTGGACCGTGAGCAGTTCAACTCCAGTGTCATTACTTTCCCCATAATTGTGCATTTTGGTATC[C/T]GACCTGCTCAGCTTAGCTACGCTGGAGACCCGCAGTAAGTGTGACCGCATTTACCATTTCTATTCTTGTATGCTTGCTTAAGAAACATCTAATGAGTTTTCTGCAGTGGTTCTTATAATTAGGGATATGAGTCTAAACTAATTTCATTTGCAATTGTGTCTAATTGTGTCTAATTGTGGAGGGAGTTTTCATCTTCTGAGCTTTTTCAAGAGGCTGAAAACAATGGATCATTAGCTGCTATTGTTTGTATGAACAGAACTCTTATTTTATGAAATTGCAGTTCTTGTGAGGATGCAACTTTATTGTGCTGTATCAGTTTCCATTCTAGTTTTTGATTAATAGATAGGTCTTTATTAATATTTTGATAATGATTGTAATGTTCTTCTGCTGCTATCACATATTCTTGTTACGATTAATTGCTGAAGCGTGTTTAAAAATAATTTTTAAAGTTCAAATCAATTTGTCTTTATTTCTATAGCACTTTTGCGATGTAGATTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31863
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089017 | Nonsense | 792 | 1289 | 16 | 31 |
The following transcripts of ENSDARG00000055563 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 14472788)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13328441 |
GRCz11 | 12 | 13366744 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTGCAGCACGCTATGATGCTTCCTGTTCTCACCCATCACATCCGCTA[T/A]CACCAGTGCCTGATGCATTTGGATAAGCTGATTGGTTACATGTTTAAGGA
Long Flanking Sequence:
TGAAATGTTAAGTTAGGTAATGACTTTCATGGTGCTACATGTGCTGGGGTATGAGTTACAAAGGTACTTTATTTCACATTATTGTTTCTTTAAAAAGTCCTTCTGCTAATCTGCTGTTCGTGAAAGCATGGGAACCCTGATACATTGTTCTAATGGTTCTGATTTACAGGAAGCTCTCCAGAAGATCAGGCAGAAGAATACGATGAGAAGGGAGGTCACAGTGGAACTCAGCAGTCAGGGTTTCTGGAAGACTGGCATTCGTTCTGACGTCTGCCAGGTACATGAACATACACTCATTCAATGCATATATTTCAAGAATAGTCTAATCTGCTGCCTTAGGTATTGTGTATGTTGAGCTTTAGTCTAAACCAACACAACCTGGCTTATCATTTTGTAAAGCACAAGTGGTTCACCACAATTTTATCTTCTGTAAAGCAGCGGATTTGATCTTTTTTGCAGCACGCTATGATGCTTCCTGTTCTCACCCATCACATCCGCTA[T/A]CACCAGTGCCTGATGCATTTGGATAAGCTGATTGGTTACATGTTTAAGGAACGATGCTTGCTGCAGGTAACACAGACTAAGTAAATCAGAGAAAAAGTCACAGTAAACAAAAAGCAACTCTCCCAGCTATCAGTGAATTATCTCATGTTGAAAGCCACTGTGGTACTGCATAATGTAAATCATGATCTGTGTGGGTTATTTATGGGGCAATCCGATGAGATTAAAGGTACGTCTCTGTTCCGTTGAACATGATGACATCTGCACTGTACCGCATTGATCCAAATCAGTATTTTAGATTTTAAGGATTTCTATAAGCAAATGTGCTACAAAATAATGAAAAATTTTGCATTAGGAAGATATAAAAACACAGGCAGAGCTGTGATAAAATGAAATGCTATTGGTTGTTTTTTTTTTTTTTTAATTGCTGAAGCTATTATATGTCCTGCCTAGTCTTCGGTTAAGATTGTCAAATAAAAATTGCAAATTTCAAAGCGCTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35230
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 |
---|---|---|---|---|---|
ENSDART00000089017 | Essential Splice Site | 861 | 1289 | 17 | 31 |
The following transcripts of ENSDARG00000055563 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 14473698)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13329351 |
GRCz11 | 12 | 13367654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAAATATGGAGACCGGAAAGTGCATCATATGTACATGAGGAAAAAAGG[T/C]TAGCAAATATTCTTGTAAATGTATGTTAGAAAATGTTTTTAATGTAAGTT
Long Flanking Sequence:
TTTTTTTTTTAATTGCTGAAGCTATTATATGTCCTGCCTAGTCTTCGGTTAAGATTGTCAAATAAAAATTGCAAATTTCAAAGCGCTTGATGACTTTTAGAAAGAGCAGCTAAACACCAGTTAAAATGATCATGAGATATTAAATGTTATATTTTTATAGCTTCTATTTAGGAATCAATTAAAAAAAAATGCTCAAACAACTAACTTGAGAAATATGCTTCACTTTAAAAGTAGAAGATATCATCAACGGTAAAAATCTAAATTGAAAACGGTATTATTTTTAGTTGTGTGCTGTTAAATGTTCATATTTTTTTACTTCTATACCATTTAATTCTTGCTTTGTGTTTCTTACTTCTTCAGTTGGCAATGACTCACCCCAGTCATCATCTTAATTTTGGGATGAATCCTGACCATGCTCGCAACTCTTTGTCCAACTGTGGGATACGCCAGCCAAAATATGGAGACCGGAAAGTGCATCATATGTACATGAGGAAAAAAGG[T/C]TAGCAAATATTCTTGTAAATGTATGTTAGAAAATGTTTTTAATGTAAGTTGTGTATTTTACCGACTGATTTGTCTCTTTATCATAAGGAATTAACACCTTGATCAATATAATGTCACGACTGGGCCAGGATGACCCATCACCTTCCAGGTTTGTGGTTTGTCATTATATTAATGAGGTCATTTGGTTGTGACTTGGAACATTTAGTGCCATATGTACAAAATTAAGCAAATTATTGTAAGAACGCAATCTTATAACAGCAGAACTTCCTCTCACTTTTACTACACACTCTCCGTGTTTCTCCTGCTAACAGCAACTATTATAGCTGCTAAGTGCATAGAATTCTGCAGAATTTTAGCCTGTGATTGAATGTAGTTACTTGTGTAAATGTGTGTAAATTTATTTAAAATGTTCAATTGATTTATTTACAAAATTATTTAGTATTTTCTGTCTTACAATAGATATGTTTTATGAGAGACTTGCTCTGCAAATACAGATAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17917
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089017 | Nonsense | 1279 | 1289 | 31 | 31 |
The following transcripts of ENSDARG00000055563 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 14495599)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13351252 |
GRCz11 | 12 | 13389555 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTCATCGAAAGAAAGTACCGTCAAGAACTGAAGGAGATGAGAAGAGAG[C/T]GAGAGAGACAGGAGAGAGATAGTGATKAAGGATAGAACAGCAGAAAGTGG
Long Flanking Sequence:
TTCCCCCTGGCGACGTAGTTGCAAACTGCGGTTATACCTAAAAACATGTTCTTACTCCTTTAGTGGGGCCGCAGTAATGATCTTTAAAGTGTCAGCCACTGTATATGGAAACCGTTTGTCTCAAAGTTCATTACTTGCATAGTGAAGCCCATAATTACCCTTGAATTTCATTTCATAAAACTTTAAGCAAGTTTATATACTTATTCAATGCTGTGTGTGTCTTTGTGTAATTGGCAGTAAGTACTGCTGACTCGAGTGCATACAAGTAAAACTTTAAAAAGACGATTGCAATCCACTGAAATGTTTAGTTTTTTTTATCTCCCCAAATATGGAAGTAATGCTTTGATGAAGCAGCCATTATAGTCCTAAAGTTTATGAAAGTCTTTTTCTATATCCTGATCTTTTCCTCACCCTCTACAGATAACTTTCCTCAGATGGCTCATCAGAAACGCTTCATCGAAAGAAAGTACCGTCAAGAACTGAAGGAGATGAGAAGAGAG[C/T]GAGAGAGACAGGAGAGAGATAGTGATGAAGGATAGAACAGCAGAAAGTGGAGAAGGAAAAGCATTTCTTAGGTAGAGTTGCAGGGAGTAAGTCAGACAACAGCAGGCAGAGGAAAGCAAGTATGTTTTAATTTTGTTGTTTTGTTGTTCTGTGTATAAATCTGTGTTTGTTTAATCAATTCATATTAATAAGGTTTTAAAAGATTAAAATTTACATTAACTAACCATCAGTTTTTGGTGTATATGTGTTGTTATGGTTTTGGTCATTGGCTTTTTTATGCACCTATTATTCAAAACAATGCCTTGGTATTTCCTTTTCTGTTTGGTTAAAATTACAAAATAATTTCAAAATGAGAAGCAATAATGTGCTTGTATGAAAGCAGGGCACATTTGAATAAAAAGAATGTGTGTGTTTGGTGTATACGTCAATAATAAAAAACTAAACTAATGTTGATTTACTTGCACAAGCAAACAATTAGAGATAAACATTTGTTATTTATT
Associated Phenotype:
Not determined