ZMP
MRVI1
Ensembl ID:
Description:
murine retrovirus integration site 1 homolog [Source:HGNC Symbol;Acc:7237]
Human Orthologues:
MRVI1, MRVI1
Human Descriptions:
murine retrovirus integration site 1 homolog [Source:HGNC Symbol;Acc:7237]
murine retrovirus integration site 1 homolog [Source:HGNC Symbol;Acc:7237]
murine retrovirus integration site 1 homolog [Source:HGNC Symbol;Acc:7237]
Mouse Orthologue:
Mrvi1
Mouse Description:
MRV integration site 1 Gene [Source:MGI Symbol;Acc:MGI:1338023]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41071 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa6087 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41071
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114427 | Essential Splice Site | 600 | 820 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 68693653)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 66571674 |
| GRCz11 | 7 | 66795322 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAAGGTGTTCCACGCTCATCAAGATCCATGTCTATGCAAATGGGAAAG[G/A]TAGGCCAATATCCCAGGAAAAACCTTATATTATAGGTTATGTACACATTT
Long Flanking Sequence:
CTTAGAGACTAATGCTAACGTTGCTTATATGACAGTGCACATGGAAAAGTTGCTGTGTCATGTGACCTGATTAGCGTTACAGGTTTTTTAGTAGAAGGTAATACATACATGTTAATCATTTTCATTTCATTATTTTTGAAATGGAGATGCACTTTACACATTGAGTTCCGCATATGCTGATTTGTATGGTAACGCTTTGACAGGAAAAGAGAATGAACAAGGCCACGGAGGTGATGATGCAGTATGTGGAGAATCTGAAACGGACGTATGAGAAGGATCACGCGGAGCTGATGGAGTTTAAGAAGCTCGCCAACCAAAACTCCAACCGCTGCTATGGGGGCTCAATGGACACTGGAGGTAAAAGAAACATGTTTTCAAGCCATCATCGAGTGCTTCAAAAGATTCCCTCCTCCCTAATGTGTGCATGTTTATGTTCATTTTTTATTTCAGATGAAGGTGTTCCACGCTCATCAAGATCCATGTCTATGCAAATGGGAAAG[G/A]TAGGCCAATATCCCAGGAAAAACCTTATATTATAGGTTATGTACACATTTACACTGCACATACATTATGTACTGTTTTTTACAAATTTACTGTAAAAATAAGAAGGCAGCTGTGGTTACCAGAACTTTAGAATTAAAATACGGTAGAAACAATTAAAGAATTTTCAAAATTTTACAGTAAACTACCGTATTTCATTAATTTATAGTATTGCACACCAGTGTTTAAGAGTACTAACACTACCCATCGTATATAAATAGGAAACATACTTTTAACAAAGTTACAGATTTTTACTGTATTATTTTATATTATTTTACCATTAATATTACATTTTTTTACAGTTTATGTAAACTGTTAAAAATATCCATGACATTTATGTGGGTAAAAAAGGTCTCTGTCGTTGCAGGAAATTTAGCAGTAAAAATATGGGATAAACCGTAAACTTTTTAGTATCAATTTACAGTAAACTTGAGGAAACATATTGTTACGGTGAGATTGAGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6087
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114427 | Essential Splice Site | 662 | 820 | 18 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 68702098)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 66580119 |
| GRCz11 | 7 | 66803767 |
KASP Assay ID:
554-3688.1 (used for ordering genotyping assays)
KASP Sequence:
TTTNTTTTATTGCTCCATCCCTGTCTCTTCTTTCCTATGTGAAACAAAGC[A/G]GTGGAAACCCTCTGACGGAACAGGAAAGTGAAGCAACGCCAACCAAAGTT
Long Flanking Sequence:
CCCGAGCATCTCTCACGATAGCCCCGGGCCATCGGGCAGTCCTTATTGTTGAGCCCTGGAAGATGTAGGTGACTTTTTTTCTTCAGTATAAGATTCCTAGATGAATCCACGGTCCTTGGGGATTCATACAATAGCAGTGAATGAAGGTTTGTTTGTTTTTTTTAGATAAAAAATAAACCCATACAAACGAGTTCAGTAGCCATGTTCTCAGTTCTCTTTAAGTTGATCATGTCATATTGATATCAGAAAGTTGGGGCGACAGTTAATGGGTTACAAGACCTCCAGAAGGACATGTTTAAACATTTCAAGTTTCACCATGTGCACCATGTTTCTTTCCCTGGTATTCAAGTCTCTCCATTAGGCCGAAGGTTATTGTTGTTACTACCCATGGATGGTTAATAAACACAGAGAGATGGTTTTGATAGATCACACATATCTGCGTAATGGCAGTTTCTTTTATTGCTCCATCCCTGTCTCTTCTTTCCTATGTGAAACAAAGC[A/G]GTGGAAACCCTCTGACGGAACAGGAAAGTGAAGCAACGCCAACCAAAGTTGTGTGCAGTCCAGAGAAGGTTACAGAAGAGATCAAAGCCAAGATTGAAGAAGAAGCGTATAATAAAGGGTAACACCCTTGGCACTACACTCAATCTGTGTGACCCCCCGCTCACAAAACAATAGCAGTTCAGATGATTAGATAGAGATCACACAGTTGCATAATTGCAAAACATTCTCAGCAAGTGGTGGCATTTTTATCACTTGTTTTGCAAACTATATAACCATACTTGAAAAATATTAGGGACCAGTTACCTAATTTTCTGATTAGTTGTTGAAAAATAATGTGATGTATAATGGGGTTGTAAAAAACTCATGGTGCATTTTAAATATGTTTTCATATGCACAAAGTAATATTTTTTTTTTTTTAAAAAGGTCAGTAAATGTATTATGTCTGGGGGTAAAAATGACCAATACATGTTTTGTGTATATTTAGTTAGTTTAAATATTTA
Associated Phenotype:
Not determined