ZMP
mavs
Ensembl ID:
ZFIN ID:
Description:
mitochondrial antiviral signaling [Source:RefSeq peptide;Acc:NP_001074053]
Human Orthologue:
MAVS
Human Description:
mitochondrial antiviral signaling protein [Source:HGNC Symbol;Acc:29233]
Mouse Orthologue:
Mavs
Mouse Description:
mitochondrial antiviral signaling protein Gene [Source:MGI Symbol;Acc:MGI:2444773]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22252 | Nonsense | Available for shipment | Available now |
| sa42165 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22252
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 |
|---|---|---|---|---|---|
| ENSDART00000086281 | Nonsense | 34 | 364 | 3 | 6 |
| ENSDART00000129045 | Nonsense | 34 | 585 | 3 | 6 |
| ENSDART00000134421 | Nonsense | 34 | 220 | 3 | 5 |
| ENSDART00000140714 | Nonsense | 18 | 348 | 1 | 4 |
| ENSDART00000142240 | Nonsense | 34 | 240 | 1 | 3 |
The following transcripts of ENSDARG00000069733 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 15144776)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 15059809 |
| GRCz11 | 13 | 15190801 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGTCGTTTTGCAACAGATATCAAAGTAAGAGAGATCTTACCTTATCTG[C/T]AATGCCTCACAATCTCTGATCGGGTAAGTGGATTCAAATTTAACCACAAA
Long Flanking Sequence:
TAAAGTGACATTAAATGTTTAACTAGGTTAATTAGGTTAACTAGGCAGGTTAGGGTAATTAGGCAAGTTATTGTATAACGATGGTTTGTTCTGTAGACTATTGTTAATAATATATATAGTTTAATGGGGCTAATAATTTTGACCTTAAAATGGCTTTAAAAAAATGTAAAACTGCTTTTATTTTAGACAAAATAAAACAAAAAGACTTTCTCAAGAAGAAAAAAAAAATTATCAAACATACTGTGAAAATTTTCTTGCTCTGTTAAACATCATTTGGGAAATATAAAAAAAATAATAAAGGGGGGCTAATAATTCTGACTTCAACTGATATTATTGTTTTTTCTAAGAAAATCACTAAATAAAACTAATTTTCATTCTTTCCCTCTTGTTGAGAGTGAAAAATGTCACTGACACGTGAGCAATTTTATAACAAGGGAATTAGGCCGTATATGGGTCGTTTTGCAACAGATATCAAAGTAAGAGAGATCTTACCTTATCTG[C/T]AATGCCTCACAATCTCTGATCGGGTAAGTGGATTCAAATTTAACCACAAATAATATCAAAATTATACCCAGATATGCAACAATAAAAAAGCTCAATTCAAATTATTTACTAACTATACTGTTGCAGGAAGAGATCGAAGCCAAGAAAGAACAATATGGAAACTACAATGCTGTGCAGACACTTCTGGACAATCTGCGCAGGCGAGAGAACTGGATTGATGAATTCATCACTGCTCTGCGGAAGTGTGAACTTGGAAGTCTGGCTAATGAGATGAGCGACATTTATGACAGGATCAGGGGGATCACAAGTAAGAGCTTACTTGTGTTTAAAGTCTGGGTGAAATCAAAATAGACAAAAATTACTTTGTTAGCTCATATTGCTCTTCTTGAGTTAAACAATGGCCCGTGCAGGTTATTTCTGAGAAAAAAAAAATTTAATCTTTAACCAAAATCTGAGAATTTGCTTTTGCTCTGGAATGATATTAATTCTCTGATGATGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42165
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086281 | Nonsense | 258 | 364 | 5 | 6 |
| ENSDART00000129045 | Nonsense | 258 | 585 | 5 | 6 |
| ENSDART00000134421 | None | None | 220 | None | 5 |
| ENSDART00000140714 | Nonsense | 242 | 348 | 3 | 4 |
| ENSDART00000142240 | None | None | 240 | None | 3 |
The following transcripts of ENSDARG00000069733 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 15148557)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 15063590 |
| GRCz11 | 13 | 15194582 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTGCTGGTGAATCTCCCATCTCCACCTCATGTACTCAAGCGTCCATCT[C/A]AAACACTTCTCAAATCCAATTGACAAGGCCTTGCTCGACCACCCAGAGCT
Long Flanking Sequence:
TTATGACTTTTCCCTTTATTTTTTGTCTATAGGTGGACCCAAACCTACAGATACTCTAGCTCCTTCTTTAACTGGAGCCACAGCAACCGTTACAACGGCAACAGTTCACACTGTCCCACCTACTACTCTTCCTCTGCTAATGCCACCTGCAGGAGATGCCCCAGTACATTCAACTGCCCCTTGCAAACAAGCAACACAGGAACCGTCTCCTGATTCTGTTCTTCAAGTTGCAGAGACACAGCAGGTGGAGCAAGTTTCTCCTCCAGCTCCGGCACCTACACCTGAACCAGTTCCCCAAACTGAAATCACACCACAAGTTATAGCACCTTCCCAAGCAGCTCCTGACATGTCCTCACCAATTAATTTAAAAGTCTTAACACACACTGGAGAAGCTGTTACCATAACACCTGTTTCTAGAGCACTAGATAGCCTTGGCTTTACAATCACCTCATCTGCTGGTGAATCTCCCATCTCCACCTCATGTACTCAAGCGTCCATCT[C/A]AAACACTTCTCAAATCCAATTGACAAGGCCTTGCTCGACCACCCAGAGCTCAGGGAATATACAGGTGCCAAAAAAAGAAGTCAAAGACTTGGACACTTCTGAGAAGTTCCCGGTCCAAGACACTAATCTCCCATTGCGACAGGAAAGAACATTTCAGGGGCCTGAAGAGACTTCCGACCCAATTGCAAATGAGGTAATAATCAACTCAAAGCACTTCACTGTTTTTCTGTGAAAAAATTGGGACAGAAGGGGTTGTCACATCAAAGATATTTAATGTAATTCCTGTAAGTATTGTCAAAAATAAGCATGTACCACAGGAACAGGGAATGGATTTAGTTCAATTTAGTAGAATTTAGTAGAATCAATCTAAAGGGGCCATTCACACAAAGTGGGTCTTTGCATCTAAAAAGGTGTGGCACAGCGCTCAGTTGGCAAATAAAACAATTCTTATGACTATTTGCAACTGTAAAAAGAAACGTGCAATGCTTGCTCCGCCTCTG
Associated Phenotype:
Not determined