ZMP
prmt7
Ensembl ID:
ZFIN ID:
Description:
Protein arginine N-methyltransferase 7 [Source:UniProtKB/Swiss-Prot;Acc:A2AV36]
Human Orthologue:
PRMT7
Human Description:
protein arginine methyltransferase 7 [Source:HGNC Symbol;Acc:25557]
Mouse Orthologue:
Prmt7
Mouse Description:
protein arginine N-methyltransferase 7 Gene [Source:MGI Symbol;Acc:MGI:2384879]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa552 | Essential Splice Site | F2 line generated | Not yet available |
sa44256 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38029 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa552
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000073609 | Essential Splice Site | 44 | 683 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 25 (position 14684530)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 14327453 |
GRCz11 | 25 | 14423853 |
KASP Assay ID:
554-0462.1 (used for ordering genotyping assays)
KASP Sequence:
TGTCTTTTTTAGGTCTTGTTATGCAGATATGCTCCATGATAAAGACAGAG[T/A]GAGTATGATGTCGGACACATGCTAATATTACTGCTGGATCCAAAGTAATT
Long Flanking Sequence:
GCCCGGAGAGATCATGTTGGATTTGTCTGCCTGTGAACGATTAAATATTTATTGAACGTAACAATTTTTACGCATACTTTTATTTACTTATACTGAAAAGACAATGAAGACGTTTTGCGGTCGTGCAAATCCAACAACAGGAGCGCTGGACTGGGTTGAGGAAAGCGAGGAGTATGACTATCATCAGGAGATTGCCAGGTGTGTAAAAGCGACTCATGTCACATTAGCGTAAAAACACACGAATTATTATTTAGCTGCTTATGAAAGGCTGGAATTAAATATTATTTTCAATAGCCAAACTTATGAAATGGCGCGAAAATACTTGACAGTGACTTGTTGCTGCTTAACACGTGGACGAGTAATTAACCCTTACATTTGAATTATAATGTTTATCGAATGACAGTCATGCTATATAGATCATTTAAACGTGTCCTGATATTGTGTTTTGTGTGTCTTTTTTAGGTCTTGTTATGCAGATATGCTCCATGATAAAGACAGAG[T/A]GAGTATGATGTCGGACACATGCTAATATTACTGCTGGATCCAAAGTAATTGTTCCATAAGAAGGATTAGGTCGTATGATGAATGACGTTTTGTAAAATAAGTTGAAATGTAAGAAAGAAAATCAAAATTGCTGTGAATAAATTATGATAAAAGTATTTTTAGGTGGAAAATCCCTGATTCCCAGTTATAATAAAGTCAAATGATAAGTTTACTTTTATGAAATATTGCAGTGTTTTGTATAAAGCCAAAACCTAACAAAAAGTGCTCAGGGTTAGTTTAAGTAATGTGTCGGTGCGCTTTTGGTAAGGGATTCATCTGAATAACTCGAAAAATGTGGGAAAAAATAATTGAGGTAAAGTTGATTTTATATTCACACATTCAGCCTTTCTCCTCAGAAAAGTATTCGTTGCAAATACTAAATAGTGAAATCATATCAGCAGGCAATGACTATTAATGTACAGCATTGTTCAAAGCAACATTAGCACTATTTAATTGATTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44256
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073609 | Nonsense | 215 | 683 | 6 | 17 |
Genomic Location (Zv9):
Chromosome 25 (position 14679938)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 14322861 |
GRCz11 | 25 | 14419261 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAGATGTGGACGGGCACAGACTGATGCCCCCAGGGGCAGTTCAGGAGTG[T/A]GCAGGAGCGCCATCTGTCTGTGACATCCAGCTGAGTCAGGTGCCCACAGA
Long Flanking Sequence:
CTTTTAGTTAACGACATGCTCTTACATTTCTATTCATGCTTTTTTATCCCTTCTCAATTCATTTGTGCTTTGTTTTGTGTGTTTTCCACTGTTATGTTACTTGGTTGTTTTACTTTTAAAGGGGCTATGCAAAATAAATGTGTTATTATAAGTCAACACTCCTTTCACTGTCGTCATCTTCATGTTTGATGGCTCACAATATTCATCAAAAGTCAAATAAAAATAAATAAAAAAACATTTTAGATTTGATCTTATTTTATATATTGTTGTTGATGTCTTTTTCCTGTTAATTTACTGCAGAAATGTTTTAAGCTAATATGGCAAAAACTCTGTTTAACGGCGCTGCTCTCTCTGGCACAGACAGGTTGTGAAGCAGTGCCTCATCGCGCCACAATCTATGCCCAGCTGGTGGAGTCAGACATGCTTTGGAAGTGGGCACAGATGCGGCCCATAGATGTGGACGGGCACAGACTGATGCCCCCAGGGGCAGTTCAGGAGTG[T/A]GCAGGAGCGCCATCTGTCTGTGACATCCAGCTGAGTCAGGTGCCCACAGACGCCTTCACTGCCATCAGCCCCGTCTGCACCATGTTCAGGTACACACCGTTAATCCTCTAAAAAAATCTAGATTTAATTCTTTAAAAATGTGTATGAAACCTTTGGTGATCACAGCAGGACAGTCAAATGGTCGAGCCCGATAGATCGGTTTTGTAAACAGAAAAATAAGTGGTCACAAAAGCTTTTTATAAGCTTATAGAACATATAAATTCAGTATCAGAGGTAGTTTATTATTCCCGGAGGAAAATTAAGACAGTTCCAAAAACAATTAGAGAAGGGAAGGATAAATATACAATAATAATAAATAAATGATAATACCTAAAAAAAAACAACAACAACTTATGTGTATAATAATAATTGATAATTCCAGTATATATACAAAAATCATACTATCATTTAGAATAGTGGTCCATTTGTTAAAATACAAAGTTGTGCTTGTTAACAAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38029
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073609 | Essential Splice Site | 306 | 683 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 25 (position 14676644)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 14319567 |
GRCz11 | 25 | 14415967 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTAAAAACAACTTGAATACATGTTTTTTTTGCATCATGTGATGTGCA[G/A]TGGAGGGATCACTGGATGCAGAGTGTCTACTTCCTTCCTGCAGAGGAGAA
Long Flanking Sequence:
ATGTCTTATCAAAAGCTTTATATTGAAATTTGAAGACAGCAGTAGGATTAAGAAAAATATGGAGATCACTTTATATTTCTTGTACTTATTCTTCTGTCATTCTCGGGATCTACCATTATGAGTGATAAAGATCTACCAGTTAATTGTGATTGACAGGTTGGCGACCACCACACTAAACCTACTCCTACCCGTAACCTTATATTATTTGTTATTGAAAGGTTAATTCACTCCAACATAACATTTCTGTTTTTGATTACTCACCCTCATGTCATTTCAAATACCTTTGTTGATCTTCTGAATCCAAATCAAGTTATTTTAGGTCAAGTACGAGAGCTCTCTCATCCTCCATTGAGTTCCTGAGACGTTTAAATCCAAAAACATTGTCCAAACATTCCATGTGTTCCAACTGTAATCATGTGAAGCTCCAAGAACAATTCTGTGCACCAAAAAACAGTAAAAACAACTTGAATACATGTTTTTTTTGCATCATGTGATGTGCA[G/A]TGGAGGGATCACTGGATGCAGAGTGTCTACTTCCTTCCTGCAGAGGAGAACGTGTCAGAAGGAGAAGAGCTGATGCTAATGGTCTCTCATGATGACTACAGTCTCTGGTACAGCCTTACACACAGGTACAGATGCTCTTCAGTGTGTCTTAAAAATGAACCAGAATTGACACATTCTCTGAGGAAAACCTTAATATATTTTTGACATTCTGTCTTTAAAGTGAGCAAAATGATGTCCGGGTGGCTCCGTTTCGGCCGTGCTGCACTTGTCAGGCCCACCTGGTCTGGACGAGACCTCGCTTTGGAGAACTGAATGATGAACAGAGGACTGAGAGTTACGTCAGCGCATTGCGCAGTGTGAGTTAGACTTCTTCATGAACTGTTTTATTTGTGAGCTTTACTGATGATGATTTTTTAATGGGAGCTGTTTGCGTGTATTCTTGTAGATTCTGAAACCCGACAGTGTTTGTTTATCTGTCAGTGATGGAAGCCTGCTACCTG
Associated Phenotype:
Not determined