ZMP
nvl
Ensembl ID:
ZFIN ID:
Description:
nuclear valosin-containing protein-like [Source:RefSeq peptide;Acc:NP_998649]
Human Orthologue:
NVL
Human Description:
nuclear VCP-like [Source:HGNC Symbol;Acc:8070]
Mouse Orthologue:
Nvl
Mouse Description:
nuclear VCP-like Gene [Source:MGI Symbol;Acc:MGI:1914709]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa42107 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa42106 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42107
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000038315 | Essential Splice Site | 316 | 796 | 10 | 23 |
The following transcripts of ENSDARG00000025605 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 396714)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 394697 |
| GRCz11 | 13 | 524988 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCAGGAGAGTCTGAGCAGAAGCTGCGGGAGCTGTTCGAGCAGGCCATC[G/T]TAAGAGAAACACACAACACATTTACAGCGCTACATTCATTCAGTTCAACT
Long Flanking Sequence:
CTCTCTCTCTCGCTGTGACTTTCTCAACTCAAGTCTATTGATTGGCTCGACAAATGTTGCGAATGTTTTGCCAAAGCATTTAGAAAGTTTACATTGAAAAGTACATGCATGTATAATAATAAAGAAACATAGTAAACAGTAAATAAAAAAAAGATATATATATATATATAATTAAATGAAAAAGCATAAATAATATATCATATATATATATATATAAAAAATAAAAATATCAATAGATATCAGAATAAACTACATTTAACAATCAACATTCTATTATAAAACAGTAGTAAAACAATATTACTCGGTATATTTACAATGCTTTATTACTAATAATCTCTTATAATAATTCCCTCTCTGTCTGTCTGTCTGTCTGTGTGTGTGTGTGTGTGTGTGTGTAGGAGACCGCTCTGCCGCTGCTGAAGATCTCTGCTCCAGAGCTGGTGTCTGGAGTGTCAGGAGAGTCTGAGCAGAAGCTGCGGGAGCTGTTCGAGCAGGCCATC[G/T]TAAGAGAAACACACAACACATTTACAGCGCTACATTCATTCAGTTCAACTCAACTAAAGTGTACTAGTCACAATAATCATGGCTTCAGATCAGCTTCACATGAGCTGCACATCAATACATCACAGTCACCGTCTGAAAAGGGAAGGAGTTGTGTGGAGGATTGGCAGTATATCAGCGTAATTCACCTGCAGTTATACAGTGTCTTTCCAAAACAAGTCATATTTACATGCAGGGGTAATAATAATGATGCTGCTGGGTCATTTACATCCTCTCTGGGCTGATTTTGAGTCTTAATTTGGCCACAATGTCTCTGTGTGTCAGCAGATGTGATGATTCTTGCTGACAAATCTGACTTTGACACACATTTTGGGAAAATGCTTTGAATATTTTCAAGAACTCCTCAACACACTGTTCAGACGGACTCCGCTTTGGTGATGTTGCTGCTGTTTTGCTACATTAACTTCCATTATAATCACTTTTATTGACTGTAAAGCCGTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42106
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000038315 | Nonsense | 482 | 796 | 14 | 23 |
The following transcripts of ENSDARG00000025605 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 393923)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 391906 |
| GRCz11 | 13 | 522197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGCTCTGGCTCGTCTGCTGGATCTCCTGAAGAGCAGTGTTTCTCTGAGT[G/T]AGGATCAGCTGGCGGCTCTCTGCGTCCTCATGTCAGACTTCAGCTCTTCA
Long Flanking Sequence:
CTATACTGTACACTACTGTACTATACCCTATTATACTATGCACTACTAAATCATACTATACTATACCACATACTACTATAATCTGCCCTATTATACTAAACTATGCTCTACTGTACTTTACTATACTGTACTTTGCTGTGCTGTTCTACACTATATCCTACTATACTAAACAACGCTCTACTATACCATACTATACAATGCTAGACTATATCCTGCTACCATGTACTATACTATAAGATACAACAGCTGGTGTGAAGTGTGTAAATGTGTGTAAATAGGTAATTTGTCACACTTGTAAAGCACTGTAAAAGTTTGCAAGTGCATCTGCAGACGGCTTGTAGCTGTAACTGTAAGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCATCAGTGGTGTTCCTAACAGCAGCTTGTTTCCCTGTCAGACATTAGCTCTGGCTCGTCTGCTGGATCTCCTGAAGAGCAGTGTTTCTCTGAGT[G/T]AGGATCAGCTGGCGGCTCTCTGCGTCCTCATGTCAGACTTCAGCTCTTCACTAGTCAGAGTCCAGCCGTCCGCTAAGCGTGAGGGGTTCGCCACGGTGCCGGACGTCACCTGGGCGGATGTAGGAGCGCTGCAGGACGTCCGTGAGGAGCTCCACATGGCCATCATGGTACAGCTGCACTGCAGATATTCACACTACTGCCGTCCAGCAGGATCTTACTCTACCTCTGTCTGTGCTGCTGATAAACTCCATGCATCTCCAGCAGATTCTGTGCCGGTGGAGGAAACTGCACCCGGTTTGACCAGCTGTAGACAAAGTCATGTTCAATTTCCAAAACATTTATCGAGAGCGTATACAGCAGTTTATTATTTAATGAGTAATAATTACAGCAGACAGTATTTTTAATCAGTTTATTGCATGTGTGTATGGATATATACACGGTAGTCAACATTCATAGTGGATCATCACCAACCTTCACCAGAACTGTCCTATATCTACTGT
Associated Phenotype:
Not determined