Busch Lab

ZMP

prmt8b

Ensembl ID:
ENSDARG00000045760
ZFIN ID:
ZDB-GENE-030131-7791
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.
Availability:
Order Allele From ZIRC
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.
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