ZMP
prmt8b
Ensembl ID:
ZFIN ID:
Description:
Protein arginine N-methyltransferase 8-B [Source:UniProtKB/Swiss-Prot;Acc:Q5RGQ2]
Human Orthologue:
PRMT8
Human Description:
protein arginine methyltransferase 8 [Source:HGNC Symbol;Acc:5188]
Mouse Orthologue:
Prmt8
Mouse Description:
protein arginine N-methyltransferase 8 Gene [Source:MGI Symbol;Acc:MGI:3043083]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20225 | Essential Splice Site | Available for shipment | Available now |
sa40239 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20225
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059489 | Essential Splice Site | 23 | 419 | 1 | 10 |
ENSDART00000067266 | None | None | 334 | None | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 10229574)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11166201 |
GRCz11 | 4 | 11165050 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCGGTGTCTGCTCCTGCGGAGAAAGATGGCGGAGGCGGAGAGCACGGAG[G/T]TAAGTCAAAGACTCCTTAAGCCATGGTTTAAACATCAATGCACGTATAAA
Long Flanking Sequence:
CGACAAGGATTTCAAAAATCAGATAACAGAGGATCACCATGGCAAGCTTAAATGAAACATGCATCTGATCTGTCCAAGCACAGGTAACGCGGAGATGCGCAGCGCCAGGTGATGTGGATGCTGAAGCGGCGCGGATCAACTGGTCTCCAAGTGGCGCTCAGAACCTCCGGTAGAACTTTTTACACGATGGGTTTTCATTATAGGAGTAGGAATAGTGAAGTTCGAGGACTATCTGCTAAGTCTTTATGACAATTTCCCTATTAGTCTCTTTTTAGGCATTTACTGTTTATTAAACGCTTTGCAAATTAACAAATGGCTCGTTTCAAAGCGCACACCGAGTATTGCCTATTGCAGCGCGTTTTGAAACTTTTCTAGGAGATTTAGCGAGAACACTTGCCCTCATCGAGTTAATCCGGATCCCGTTGGCTCGTATGGGACTGAGGCACTCATCGCGGTGTCTGCTCCTGCGGAGAAAGATGGCGGAGGCGGAGAGCACGGAG[G/T]TAAGTCAAAGACTCCTTAAGCCATGGTTTAAACATCAATGCACGTATAAAAATTGACATGTACCATTGCAAATCGCGTGTGAATCGTTTTAGTATCTTATTAATGCGTAAATACGTGCATAATGACACGTTGATTTGGAGGTCATACAAATCAGTGCCCGGGATGTGTATGACTATGCAGACTAAACACCAGTGCGGCAGAGCAGGAAAACAAGTCCTGGCGAGATCAAACACCGCGTCCAACGTCAAAATGCAGAGCTCATATTAATATTTAGGATGCAGACAAGTTGAATGAAGATTAAGAAGACATATAATGATAGATGTTAATGGAAACCTAAAAGACAACAAATTAGCCTGATTCTGTAGCTATAAGTCGATAAAGTTACTCGTGTGCTGGTTAAAAAACACTCAGTTCCTCTTATATGTGTTCTGTTGGGTCACCGGCTGAGCGCTGTCCTTGGTGCTGCAGTATTTTGCCCCCCTCCCCGGCTAATTAGCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40239
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059489 | Essential Splice Site | 263 | 419 | 6 | 10 |
ENSDART00000067266 | Essential Splice Site | 178 | 334 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 10218777)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11155404 |
GRCz11 | 4 | 11154253 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGTGGTTGCCATTGAAGATCGACAGTACAAAGACTTCAAAATTCACTG[T/A]AAGCACAAACACACACACAGACACACAAGCACATATACACACACTTATAA
Long Flanking Sequence:
ATAACAAATATAAATACATAATAATATTTTTTCAAATTAGTTTTGAATTTGTAAAAAAATTGGATAATAATAGATTATTTTAAATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATGACCTCATATATTTATATGAATAATAAAACATTAAATATTTAAAATATTTAAGATAACAAAGTAGATCATTGTCTAATAATAATTATAAATTATCAAAAAAAAATGTAAAAGTAGTTTTAAATAAAATATATAAATCATTTAAAAACAATCATTATATGTAATTATTATTAATCATATTTATATCATAATAACTTAAAATGATTGGATTTTTTAACTTGAACTTCTATTTTTCTTTTTTAGAAACCTGGTGGTTTCATGTTTCCAGACAGAGCGACATTATATGTGGTTGCCATTGAAGATCGACAGTACAAAGACTTCAAAATTCACTG[T/A]AAGCACAAACACACACACAGACACACAAGCACATATACACACACTTATAAACCATTTAATAATATATCTCCTTACTATTCCCTAATATATTTTTTTCTGAATCCCTTGCATTTATTTATCCTACAAATAAGAAATTAAGAAAAAAAAAAAAAAAACTCCTGTTGAATTTTATCACTCCCCCGCAGCAAAAGCTTTTCTTTTCTCCATCCCCTCCACTGCCTCCTTCTAGTTTTTGGATGGAAGAGTGAGATTCGTTTCGGCCGAATGTAATCAAATGCTGCCAGACACAGAGGAGGCACAAGTCTATTTTAGGTCCAAATGAAGGCGACCAGACACAGCCAAGACAGATTTTTCAACCTTTCAAGCCCATTTTCCATCTGAAATATCTTCAAATGTGCTTTCAGGGTGGGAAAACGTCTATGGATTTGACATGACGTGCATCCGAAATGTTGCCATGATGGAGCCCCTGGTGGACATAGTAGATCCTAAACAAGTCGTTA
Associated Phenotype:
Not determined