ZMP
tnfrsf19
Ensembl ID:
ZFIN ID:
Description:
tumor necrosis factor receptor superfamily member 19 [Source:RefSeq peptide;Acc:NP_001038369]
Human Orthologue:
TNFRSF19
Human Description:
tumor necrosis factor receptor superfamily, member 19 [Source:HGNC Symbol;Acc:11915]
Mouse Orthologue:
Tnfrsf19
Mouse Description:
tumor necrosis factor receptor superfamily, member 19 Gene [Source:MGI Symbol;Acc:MGI:1352474]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa742 | Nonsense | Available for shipment | Available now |
sa6139 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa742
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061351 | Nonsense | 306 | 356 | 9 | 10 |
ENSDART00000143880 | None | None | 120 | None | 4 |
ENSDART00000061351 | Nonsense | 306 | 356 | 9 | 10 |
ENSDART00000143880 | None | None | 120 | None | 4 |
Genomic Location (Zv9):
Chromosome 15 (position 8316567)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 8266074 |
GRCz11 | 15 | 8242145 |
KASP Assay ID:
554-3658.1 (used for ordering genotyping assays)
KASP Sequence:
AGACTGATATGGCYTGTGCTCCTGATGAAGTCTGGCCRCTCGTTCAGTCC[A/T]GMAGAACCACAGACAGTCTCCAGACCAACCAGAGGTGCTCCTCAWGTGAA
Long Flanking Sequence:
ATTTAGAGCATTGTGAAATGTGGTATCAGATGGATGTGTGGTTTGTTTGTATGTGTTTGCAGGTGGCGTTCAGCTGGTGTCGTCTGTGTGTTGTGAGGATGTCTGGAGTCAAAACAGAAGACGAGATGCTCCAGCCTTTCACTCACACTGCAGAATCTCTGACAATGGGTCAGTTACACTCACGCACACACGCACGCACGCACGCACGCACGCACGCACACACACACACACAATGTGTAATAATACAAATTATTTTAATAACATTACGATATATCAATCAGTACAATCACTGTCATTTTAAGTAAATAAATAATACCTAAAAATAAAAATATGCCCAAAGACATTTAAATGATAACCTAATATCAGTGATGTGTATTATTGTTGTGCAATGGAGACTGAAGGTTCTTGTGGTTGCGTCCAGCAGGCTGACGAACGAGTCGGTGGGCAGTCAGACTGATATGGCCTGTGCTCCTGATGAAGTCTGGCCGCTCGTTCAGTCC[A/T]GAAGAACCACAGACAGTCTCCAGACCAACCAGAGGTGCTCCTCATGTGAAGAGGATGAGGAAGAAGTGCAGATCTCAGATCAGCGAACTGCAGAGGAGCCTGAGGATGCCTCACACAAACCACTAATACAGCAGACCACTGACACTGAAGGTCAGCAAACATCAGAGCTCTATAATCATTGATAGCGATTATTAATCGGGTTATTAAGCGGTGTGTTTTTGTGCTGCTGTCTTATATACAGCTTTGGAAGGGTTACTTTTAAAATGTATTCCCATAAAGTTACTTTTTTAATGAAGTAATTTATATTCAGTAACTTAATCCAAGCTAAAATATATGAAAGTAATGTAATCAGATTACTTTTGGATACTTTTTTTTAATGTAATCAGATTACTTTTGGATACTTTTTTTTAAATGTAATCAGATTACTTTTGGATACTTTTTAAAATGTAATCAGATTACTTCTGGATTCTCTTTTTAATGTAATCGGATTACTTTTGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6139
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061351 | Nonsense | 306 | 356 | 9 | 10 |
ENSDART00000143880 | None | None | 120 | None | 4 |
ENSDART00000061351 | Nonsense | 306 | 356 | 9 | 10 |
ENSDART00000143880 | None | None | 120 | None | 4 |
Genomic Location (Zv9):
Chromosome 15 (position 8316567)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 8266074 |
GRCz11 | 15 | 8242145 |
KASP Assay ID:
554-3658.1 (used for ordering genotyping assays)
KASP Sequence:
AGACTGATATGGCYTGTGCTCCTGATGAAGTCTGGCCRCTCGTTCAGTCC[A/T]GMAGAACCACAGACAGTCTCCAGACCAACCAGAGGTGCTCCTCAWGTGAA
Long Flanking Sequence:
ATTTAGAGCATTGTGAAATGTGGTATCAGATGGATGTGTGGTTTGTTTGTATGTGTTTGCAGGTGGCGTTCAGCTGGTGTCGTCTGTGTGTTGTGAGGATGTCTGGAGTCAAAACAGAAGACGAGATGCTCCAGCCTTTCACTCACACTGCAGAATCTCTGACAATGGGTCAGTTACACTCACGCACACACGCACGCACGCACGCACGCACGCACGCACACACACACACACAATGTGTAATAATACAAATTATTTTAATAACATTACGATATATCAATCAGTACAATCACTGTCATTTTAAGTAAATAAATAATACCTAAAAATAAAAATATGCCCAAAGACATTTAAATGATAACCTAATATCAGTGATGTGTATTATTGTTGTGCAATGGAGACTGAAGGTTCTTGTGGTTGCGTCCAGCAGGCTGACGAACGAGTCGGTGGGCAGTCAGACTGATATGGCCTGTGCTCCTGATGAAGTCTGGCCGCTCGTTCAGTCC[A/T]GAAGAACCACAGACAGTCTCCAGACCAACCAGAGGTGCTCCTCATGTGAAGAGGATGAGGAAGAAGTGCAGATCTCAGATCAGCGAACTGCAGAGGAGCCTGAGGATGCCTCACACAAACCACTAATACAGCAGACCACTGACACTGAAGGTCAGCAAACATCAGAGCTCTATAATCATTGATAGCGATTATTAATCGGGTTATTAAGCGGTGTGTTTTTGTGCTGCTGTCTTATATACAGCTTTGGAAGGGTTACTTTTAAAATGTATTCCCATAAAGTTACTTTTTTAATGAAGTAATTTATATTCAGTAACTTAATCCAAGCTAAAATATATGAAAGTAATGTAATCAGATTACTTTTGGATACTTTTTTTTAATGTAATCAGATTACTTTTGGATACTTTTTTTTAAATGTAATCAGATTACTTTTGGATACTTTTTAAAATGTAATCAGATTACTTCTGGATTCTCTTTTTAATGTAATCGGATTACTTTTGGAT
Associated Phenotype:
Not determined