ZMP

prmt3

Ensembl ID:

ENSDARG00000019791

ZFIN ID:

ZDB-GENE-041105-1

Description:

protein arginine N-methyltransferase 3 [Source:RefSeq peptide;Acc:NP_001017655]

Human Orthologue:

PRMT3

Human Description:

protein arginine methyltransferase 3 [Source:HGNC Symbol;Acc:30163]

Mouse Orthologue:

Prmt3

Mouse Description:

protein arginine N-methyltransferase 3 Gene [Source:MGI Symbol;Acc:MGI:1919224]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa8397	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa16602	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa8397

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000013409	Essential Splice Site	312	512	10	16
ENSDART00000147140	Essential Splice Site	64	226	2	6

Genomic Location (Zv9):

Chromosome 7 (position 17909461)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	16882250
GRCz11	7	17134223

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AATTGACCTTCCAGTAGAGAAAGTGGACATCATCATTTCAGAGTGGATGG[T/C]AAGTGGATGATTGTTAATATGSWAATATGTTAAAATGCTTCCCTWAGAGA

Long Flanking Sequence:

AATGTGAAGCAGGGCTGAACTGTTTAATTGAATTTAATTTAGTAAATTTAATTAATGACTCTTCACTTTCCTTCAGCTTATTCCCTTCTCCACCATGAAATGTTAACTGCCTAAATATAACCAATATATTAATCAGATTTTGTTCATTTTAATTAAATACTTTGTTGATTTTAGCTAGACACAATTATGTTCATTGAATGCCATTAACAGGTACAACCATTTAATTTTAATGATGGTAAAAATAATTGTTAAAAACGATTAATACATTCTTTAAATTTACTATGCGCACTGTTAGTACATGCTAGCTAATTGTATCAAATGCAATCATTCTGTAAAGTGCTAATGAGTATACTAATGTGTGATGCTGCTGTTTTAAAATGTACTTGCATCTATGTCTAGATCAAATAATCTTGAAGACACCATCACACTGATCAAGGGCCGGATCGAGGAAATTGACCTTCCAGTAGAGAAAGTGGACATCATCATTTCAGAGTGGATGG[T/C]AAGTGGATGATTGTTAATATGGAAATATGTTAAAATGCTTCCCTTAGAGAAAAAAAATGCATTGAACATACAATTATTTTGCAACAAAATGCCCTGCTCATTAAAGCATAATGGCCAGCTTTGCCTTAAAGCTCTGCATTCACAGCAATTACAGTTGGTTTTTACCCAAAATCAGGCATAAAGGAAGTAAATGTGTCAGCAAATTTCTTTTCTGCCCAGTCATTTCCCTTTTCAGAACCTGCTCAGGGGTTGGCAGATGAAAAAGCTGAAATGTATTGTTGATTGATACTAGATATATTGCGGGCATAATTCATAATGGCATAACTTTCATGCTCATTTAAGAAGCCAAACAACACTCCTCATTTATTTAGACATGACTGATGATGAATATGTGAAGGTTTAAGAGATGCACGTTCATTTGCACATCAATTTATCTTGGCTGAAAGTAGAATTTTACTGAATGTGGTTAAAATTTGTTACAGTTTTTTATGTTATTTTAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa16602

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
Order Allele From EZRC

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000013409	Essential Splice Site	339	512	11	16
ENSDART00000147140	Essential Splice Site	91	226	3	6

Genomic Location (Zv9):

Chromosome 7 (position 17936661)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	16909450
GRCz11	7	17161423

KASP Assay ID:

2259-8573.1 (used for ordering genotyping assays)

KASP Sequence:

GACTCTGTGCTCTACGCCAGAGACCGCTACCTTGCAGACGATGGTTTAGG[T/C]AAGCCAAATGCACAAATTACAGCATTTTTTTACACTCCTWTTCTGAGTTT

Long Flanking Sequence:

ATTGGAAATAATGAACTTGCACAAACTCTAGAAAAGACGGGTTTGTGGATGGCCACCAAGAGACTGTCGTCATTTGCGATCTCCAGCAGTTGATCTTTTTGCACAGACATGGTGGATTCGCCTGATCGGATTGAGGATCGGGAAAGGTCCATGAGCTGGAATTCGAGCTCGGGATGCCCCAAACTATGTTGCAAAATATGTCGGCGCACTAACCACTGGGATATCATGCCAACTGTGTGTATTTTATTTGTTTATCCAAACAATTTAAGTCTTATTATTGTTTAGAGAATTGAAAAAAAGAATAAAAGTTTTTAAAAATGCTGTAAAATGTGATTCATTGCCACAATATTATGTGTAATAACAATATTACAGTATGTAAGCATCTGTTTGTGTTTTAAACAGTTTATTGTTGTTTTTCAGGGCTACTTCTTGCTGTTTGAGTCAATGCTGGACTCTGTGCTCTACGCCAGAGACCGCTACCTTGCAGACGATGGTTTAGG[T/C]AAGCCAAATGCACAAATTACAGCATTTTTTTACACTCCTATTCTGAGTTTGGAAGAATCTGAGAGGCCCTTGAACTGAGCTTCCAATTGGTTTTATACTTATGGAGCACAATGAGCCCGTTCTTTACAGTGGGCTTTTATTTTCATGGTCTATCAAGCAGACTTCATTTATTTTAATAGGGGGAGTTCATACAGAGCGAATCAGGGCTGTCCAGAGCAATGAAAGATGAGTCGGCGTGTGTGTTTGTTTCCTCTGCAGGGACATTACACAGGCATTATCATGAAAATATTGAACATCATCCCCTTTACCTTGACCATCAGCAATAAAATATGGAGCAGAGTTAGTGTGTTGGGATTCAGTGGTGCTGATATCTAATTGGCTTATTTAAAAATTTTCATATTTGATTGAACCATCCCTTTTACGGATAGCGCTCACTTTTGTATTTAAATAGTTTTTTGTAAATTTCAAGTGTTTTTAGATTTCATATGTTTTTGCTCCTT

Associated Phenotype:

Not determined