ZMP
rsad2
Ensembl ID:
ZFIN ID:
Description:
Radical S-adenosyl methionine domain-containing protein 2 [Source:UniProtKB/Swiss-Prot;Acc:Q5RH95]
Human Orthologue:
RSAD2
Human Description:
radical S-adenosyl methionine domain containing 2 [Source:HGNC Symbol;Acc:30908]
Mouse Orthologue:
Rsad2
Mouse Description:
radical S-adenosyl methionine domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1929628]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13259 | Nonsense | Available for shipment | Available now |
sa19183 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13885 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13259
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 |
---|---|---|---|---|---|
ENSDART00000019617 | Nonsense | 43 | 359 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 35528317)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 35413241 |
GRCz11 | 17 | 35361187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGCGCTGTTGAGATGGCTCTCCATGCAGGTTTCTGGCGCACATGTGCAA[C/T]AAACTCCTGCTAGAAAGATCAGCCGCCCAGAGAGTCGCAMCAGTAAACAG
Long Flanking Sequence:
CAAAGCCTATAATAAAAATAATAATAATAATAATAATGATCGTTTTTGTTGTTATATTGTTGTTGTTGGCTATTTCACTGTTCAGAATGCTGAGACAAACCAAATATTGTAAATTCATATAATCATAAGCCTATAATATTATAAATGGCCTGCATGCTTTATGGGAGCGGCAGCCTATAATGAAAATTAAATGCATCAGGTGTCTATAAGAGAAATGAAACTCGTGCATAACAGCTGATAGTGTTTATCTTTCGTTTTCCGTCCCCCCGAGCAAGAAAAGAAACTGATCAGAGTGGCAACTTGACACTGCCCGGCCCCGTCCCGTATAAAAGAGGCGTGTGTTCTCCGGGCTTCAGAATCGACACATCTTCATCATGGTGACATCAAACCAACTTGGCTTTGCTAGACTGTTGATGCAGCTTTGTGTAAAGAACGTTCAAAGTTTCTTTTTAGCGCTGTTGAGATGGCTCTCCATGCAGGTTTCTGGCGCACATGTGCAA[C/T]AAACTCCTGCTAGAAAGATCAGCCGCCCAGAGAGTCGCACCAGTAAACAGAAAGAGGGATCCAGAGCTCCGTTCACAACTCCAAGCAGTGTAAACTACCATTTCACCCGGCAGTGCAATTACAAATGCGGCTTTTGTTTCCACACCGCGAAGACTTCTTTCGTCTTGCCTATTGAAGAAGCAAAGCGAGGCTTAAGACTGCTGAAAGAAGCAGGTAAACAACTTGTCTCTTAAAAGTGCAGGTGATTAGGGTACAACAAGTCAAATTAATATTAAGATAACCTATACGTTATAATTATAGCCATTTCCCCATGCAGCTGAATGATTACATTATGATTTGCAAACTCTTTCAAGCTTTTTTGAATAGCCAATGCAAATAAGGTGCTAATTTGCATACACTACTTTTATTATTTTTAATTTACGTAATCCAAAACATATGGATTAGGCGAAGTCAGGTTAAAAACTTTAATGTTAACATTGATGTTTTCTTCTTTTTTTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19183
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019617 | Nonsense | 105 | 359 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 35528131)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 35413055 |
GRCz11 | 17 | 35361001 |
KASP Assay ID:
2261-1338.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTCCACACCGCGAAGACTTCTTTCGTCTTGCCTATTGAAGAAGCAAAG[C/T]GAGGCTTAAGACTGCTGAAAGAAGCAGGTAAACAACTTGTCTCTTAAAAG
Long Flanking Sequence:
TTAAATGCATCAGGTGTCTATAAGAGAAATGAAACTCGTGCATAACAGCTGATAGTGTTTATCTTTCGTTTTCCGTCCCCCCGAGCAAGAAAAGAAACTGATCAGAGTGGCAACTTGACACTGCCCGGCCCCGTCCCGTATAAAAGAGGCGTGTGTTCTCCGGGCTTCAGAATCGACACATCTTCATCATGGTGACATCAAACCAACTTGGCTTTGCTAGACTGTTGATGCAGCTTTGTGTAAAGAACGTTCAAAGTTTCTTTTTAGCGCTGTTGAGATGGCTCTCCATGCAGGTTTCTGGCGCACATGTGCAACAAACTCCTGCTAGAAAGATCAGCCGCCCAGAGAGTCGCACCAGTAAACAGAAAGAGGGATCCAGAGCTCCGTTCACAACTCCAAGCAGTGTAAACTACCATTTCACCCGGCAGTGCAATTACAAATGCGGCTTTTGTTTCCACACCGCGAAGACTTCTTTCGTCTTGCCTATTGAAGAAGCAAAG[C/T]GAGGCTTAAGACTGCTGAAAGAAGCAGGTAAACAACTTGTCTCTTAAAAGTGCAGGTGATTAGGGTACAACAAGTCAAATTAATATTAAGATAACCTATACGTTATAATTATAGCCATTTCCCCATGCAGCTGAATGATTACATTATGATTTGCAAACTCTTTCAAGCTTTTTTGAATAGCCAATGCAAATAAGGTGCTAATTTGCATACACTACTTTTATTATTTTTAATTTACGTAATCCAAAACATATGGATTAGGCGAAGTCAGGTTAAAAACTTTAATGTTAACATTGATGTTTTCTTCTTTTTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTGACATAGTGCCATATATCAGGCAAATTCTGTGCATAATAATGTTTACTTTATTGTACTTTTTGTTTAAGTATTTAAACATTTTATTATACAGGAATGGAAAAAATAAACTTTTCTGGAGGAGAACCCTTCGTTCATCAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13885
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019617 | Essential Splice Site | 168 | 359 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 35527517)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 35412441 |
GRCz11 | 17 | 35360387 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTGTTAGTAACGGCAGTCTGATCAGAGAAAGCTGGTTCCAGAAATACGG[T/A]AAGAATCTTTCATGGCCAGCAGAGGGCGGCAGAAGTTACTTGCAAACTTY
Long Flanking Sequence:
GCCATTTCCCCATGCAGCTGAATGATTACATTATGATTTGCAAACTCTTTCAAGCTTTTTTGAATAGCCAATGCAAATAAGGTGCTAATTTGCATACACTACTTTTATTATTTTTAATTTACGTAATCCAAAACATATGGATTAGGCGAAGTCAGGTTAAAAACTTTAATGTTAACATTGATGTTTTCTTCTTTTTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTGACATAGTGCCATATATCAGGCAAATTCTGTGCATAATAATGTTTACTTTATTGTACTTTTTGTTTAAGTATTTAAACATTTTATTATACAGGAATGGAAAAAATAAACTTTTCTGGAGGAGAACCCTTCGTTCATCAGAAAGGCAGTTTTCTGGGAGAGCTGGTGCTGTACTGTAAGCAGGAGCTGCAGCTGCCGAGTGTCAGCATTGTTAGTAACGGCAGTCTGATCAGAGAAAGCTGGTTCCAGAAATACGG[T/A]AAGAATCTTTCATGGCCAGCAGAGGGCGGCAGAAGTTACTTGCAAACTTTTAACACAATTCACCCCATTGTAGTTCATAACAGTGTTTAGCTAGCTTCACAAAATAGTTAGATCTGCTTAAAAAAAATTAATAAGCTCCATTTAATAGCCGAATTTAAGAATTTGTTGTCATTTGAGATAAGCATTGCATTGTACTGTCAATTCCCTTATGAAAAATGAACAAAGCATTATATAGTTAACGTATAGTAACCATGTTTTTAGCAAATTAATTGCCTTTTGAATTACATCATACATCATGATTTTTTTTATACAATTCATATTTAATTTAATCTTATTTAGATTTTTATGTCTTTCCTTTAAACATTTTCACAGAAACTGGTCAACATTTAAACCTCTCTAAAATGTTTGTATTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
Associated Phenotype:
Not determined