ZMP
si:ch211-239f4.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human and mouse ecotropic viral integration site 5-like (EVI5L) [Source:Uni
Human Orthologue:
EVI5L
Human Description:
ecotropic viral integration site 5-like [Source:HGNC Symbol;Acc:30464]
Mouse Orthologue:
Evi5l
Mouse Description:
ecotropic viral integration site 5 like Gene [Source:MGI Symbol;Acc:MGI:2442167]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17572 | Nonsense | Available for shipment | Available now |
| sa32739 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa12742 | Nonsense | Available for shipment | Available now |
| sa15533 | Essential Splice Site | Available for shipment | Available now |
| sa19554 | Essential Splice Site | Available for shipment | Available now |
| sa17798 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17572
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000074683 | Nonsense | 63 | 996 | 1 | 23 |
| ENSDART00000125037 | Nonsense | 63 | 707 | 2 | 17 |
| ENSDART00000125276 | Nonsense | 50 | 387 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 1 (position 45691823)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 44535042 |
| GRCz11 | 1 | 45236345 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTCCCATGATGCCGCTCTSTCCGCCCCYGCCGCTTCCYCAGCTGACTCC[G/T]AAAACCTCAGTCCAGATGAGCTYGAGCTTYTGGCTAAACTGGARGAGCAG
Long Flanking Sequence:
CAAATTTATCTTATCTGCTTATCATATTTTCCCACCAGAAAATAATTGTGCCTTTTATTCTTTGTTTTTGCAGTCTAGAGATCAGAAAATGACACTAAAGTTGTCTCATCATAACATCTGAATGATTACTAATCAAAATCAAAAGCATACAGCCCTGCAGTACATAATCATTCTTCCTTTGTTTCCACAGATTAATGCAGGCCTAATAAAGACGTCTTCAAGAAGGCCTGTCCCTGTCCACAGCGTCCTCCTGTGAGACAGATCCTTCCAGATCTCCACATCACTTGACCTTTCTCGTCTCGGATTCTTCCATCATGTCCAGCCCAAGCAGCAGCCCAGAGAGAGAGGGGGGGATGGCAGGTTCAGTTCAGCTGGAGGACCTCAACTCGCCTGCCGGTTTAGAAATTGACCCGCCGTTTATTGGCAGCCCGGTGCTCAGTCCAGATTCCAGTTCCCATGATGCCGCTCTCTCCGCCCCTGCCGCTTCCCCAGCTGACTCC[G/T]AAAACCTCAGTCCAGATGAGCTCGAGCTTCTGGCTAAACTGGAGGAGCAGAACAGGTAGGATGAGAGCTATACATGCAGACAGATCGGAAGTGATCAGATAAAGAAACAGTTCACTCAAATATGAAAGGTCTTACACAGGGTGTCCGAGGGTCTTAAAAAGTCTAAAAATGTCTAAAAAATTTATTTTAGGCCTTAGAAACACTTAACTTCACTGAAATTTTGTCTTGTGGGTCTTAAACAATTGTAAACAGGACTTAAATTCACAAACACACTTCACATACAGTGTTTAGCTTCAGTGTAGAAGTGATTCAGCTGTTGTTTTATATTAACTATAGTTACTGTTGGCGGTTCATTCCGCTGTGGCGACTCCGGATTAATAAAGGGACTAAGCCAAAATGAATGAATAGCTACTGCCCTAAGTGTGCATAGGCATTTGAGGCATAAAAAGGGCTTTTATTATGCATCTGTTATACTTTTATTGCAATTTATAAGCTTAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32739
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 |
|---|---|---|---|---|---|
| ENSDART00000074683 | Essential Splice Site | 144 | 996 | 2 | 23 |
| ENSDART00000125037 | Essential Splice Site | 144 | 707 | 3 | 17 |
| ENSDART00000125276 | Essential Splice Site | 131 | 387 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 1 (position 45696154)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 44539373 |
| GRCz11 | 1 | 45240676 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTCAACGAGTGGGATGAGTGGAGACGAAAGAAGGACAAGCTTTTAAAG[G/T]TGATTACTTGGGCTGTCTTTAAGGGTTGAATTATATTATCGGAACATTTT
Long Flanking Sequence:
AGATGTCAGGGTGATGTTCCTCACATATTTGTAGGTCTGCGGCCTCTAAAAGATTGAAAACCCCTGCTTGGACACAGTTTTTCTCTGTTTTTTCAGAAACCATCATATATTTCTAGGATGCTTTGATGAATAAAAAGTAAAAAAAAAAAACACATGTCTTTCCTAAGAATCTTAAAGGTTTCAGTTTACTGTTGATTGATTAATTACATCTGTTCAGCCGTCTTTACAGAAACCGAAAAATCTATTTGGGTGCAGATTGTCCACTCTATCACCTGTGCACACTAATTTCCCTTTATTTTGTTGCATTCAGGTTGCTAGAAGCAGATTCCAAGTCCATGCGATCAATGAGTGGCTCTCGGAGGAACAGCGGCTCCTCTCTGGTGTCAAGCTCATCTGCCTCCTCCAACCTGTCCCAGCTGGAGGAAGACACCTGGATCCTGTGGGGACGCATTGTCAACGAGTGGGATGAGTGGAGACGAAAGAAGGACAAGCTTTTAAAG[G/T]TGATTACTTGGGCTGTCTTTAAGGGTTGAATTATATTATCGGAACATTTTGTCTTGATTTTAGCCTGATGTGGAAAAATAGACCAATGATGTGTTGATTATGAACCTGCAACAGCTTATTTGTTGGCCCAATATGCTAGTAGTAAGATTGGGTTACTAATCTAAACATTCTTGAGGTAAATTGTTACCTTTATATTAAACTTTTCATGAATGCCAACTTGAAATTGCGAATTGAAGTACAGATTGATTCAGTTTACAACACTTGTCATTAAGTTATGTACTAACTGTTACTAGTCCAGTGTGTTCAGCAGCCCTTGCAACACTAACAGCCTCCCTAGGTCCTACTGTCCACCAGTTTTATTTATATGCGGGCACTGTAAGTGTCATATCACTATTAGTTAGATTTTTTTTAATTATATATGTCATTATTTCCAAAGATACCCATATTAGTTGTTTACAAGGAAGTGATAATGGTGGCATTTTCAAAAACGTGCTTTGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12742
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000074683 | Nonsense | 185 | 996 | 3 | 23 |
| ENSDART00000125037 | Nonsense | 185 | 707 | 4 | 17 |
| ENSDART00000125276 | Nonsense | 172 | 387 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 1 (position 45698996)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 44542215 |
| GRCz11 | 1 | 45243518 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AWGCCTGTGAAGAATCARTATTCTGAACTCTKGAAGATGTCCTCGCCCTG[T/A]GAAAAACTYATACGCAGAGATATCGCCCGCACYTATCCCGAACATGACTT
Long Flanking Sequence:
CATCATGTCAACACCACAGTCTACCTGAGTATTGTTGCTGACCACGTCCATCCCTTTATGACCACAGTGTACCCATTGTCTGATGCCTACATTCAGCAGGATAACATGCCATGTCATAAAGTGCAACTTGGGTCCAACTTGGTACTTATAAGATGTACCTAATAAAGTGGCTAGTGAGTGTATATCAGCATCAGCCATTAACTAAAAGTCATTTAAATATATTAGCTTACTGGATATTCGCAAAAATCCACTATCATGCATTTATTCTGAGTCTGAATAGCTATCTGCTTACATCATTAATGCTAGCTTCAAAGATGTACAGGATCTGAAACTTGTACATTCATCTCTCTTTTTGTGCCTCACCCTCCGTTTCTGCAGGAGCTCATCAGAAAAGGCATCCCTCATCATTTCCGAGCAATCGTTTGGCAGTTGTTATGCAATGCCACTGATATGCCTGTGAAGAATCAGTATTCTGAACTCTTGAAGATGTCCTCGCCCTG[T/A]GAAAAACTCATACGCAGAGATATCGCCCGCACCTATCCCGAACATGACTTCTTCAAAGGCCAGGACAGCCTGGGACAGGAAGTGCTGTTTAATGTCATGAAGGTGAGAAAGACAGAAACGGGTCATGACAGCAAGAGAGAGCAGCACAGGACTGATAATGAGTGCACACATTATTGATTTACAAACAGAAAGAAAATTATTTATTAATTGATTTAAATTGTCATCCTTTATTTAAGCTCATGTTCTTTCAAATGCGCATTTTTATTTATATTTGCAGCATGTTAGACTAAAAATGCTGTGTTCCAAAATATATAATATATTTTAATTTCAATATATAATATATTTTATTTTAGTATATAATTATATTTTATATAATTATCATATATTAATATTTAGAAATTCAGAATTGTGTTGTTTCAACTCATTTTATATAAGTCGATTAAACAAGTATTTTTTACTTAGATTTTATTGTTATTACTTCTATTGAACAATTTAATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15533
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000074683 | Essential Splice Site | 219 | 996 | 3 | 23 |
| ENSDART00000125037 | Essential Splice Site | 219 | 707 | 4 | 17 |
| ENSDART00000125276 | Essential Splice Site | 206 | 387 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 1 (position 45699099)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 44542318 |
| GRCz11 | 1 | 45243621 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAAGGCCAGGACAGCCTGGGACAGGAAGTGCTGTTYAATGTCATGAAG[G/A]TGAGAAAGACAGAAACGGGTCATGACAGCAAGAGAGAGCAGCACAGGACW
Long Flanking Sequence:
ACATGCCATGTCATAAAGTGCAACTTGGGTCCAACTTGGTACTTATAAGATGTACCTAATAAAGTGGCTAGTGAGTGTATATCAGCATCAGCCATTAACTAAAAGTCATTTAAATATATTAGCTTACTGGATATTCGCAAAAATCCACTATCATGCATTTATTCTGAGTCTGAATAGCTATCTGCTTACATCATTAATGCTAGCTTCAAAGATGTACAGGATCTGAAACTTGTACATTCATCTCTCTTTTTGTGCCTCACCCTCCGTTTCTGCAGGAGCTCATCAGAAAAGGCATCCCTCATCATTTCCGAGCAATCGTTTGGCAGTTGTTATGCAATGCCACTGATATGCCTGTGAAGAATCAGTATTCTGAACTCTTGAAGATGTCCTCGCCCTGTGAAAAACTCATACGCAGAGATATCGCCCGCACCTATCCCGAACATGACTTCTTCAAAGGCCAGGACAGCCTGGGACAGGAAGTGCTGTTTAATGTCATGAAG[G/A]TGAGAAAGACAGAAACGGGTCATGACAGCAAGAGAGAGCAGCACAGGACTGATAATGAGTGCACACATTATTGATTTACAAACAGAAAGAAAATTATTTATTAATTGATTTAAATTGTCATCCTTTATTTAAGCTCATGTTCTTTCAAATGCGCATTTTTATTTATATTTGCAGCATGTTAGACTAAAAATGCTGTGTTCCAAAATATATAATATATTTTAATTTCAATATATAATATATTTTATTTTAGTATATAATTATATTTTATATAATTATCATATATTAATATTTAGAAATTCAGAATTGTGTTGTTTCAACTCATTTTATATAAGTCGATTAAACAAGTATTTTTTACTTAGATTTTATTGTTATTACTTCTATTGAACAATTTAATTTTTTTTCGGTGAAATAAATAAATTCTATGAAAGTTAGTTACTGTATTAAAGTAAAGTAATAACTGTTTTTACTTTTGATTTCATTTTAATGAAATATATGTAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19554
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000074683 | Essential Splice Site | 244 | 996 | 4 | 23 |
| ENSDART00000125037 | Essential Splice Site | 244 | 707 | 5 | 17 |
| ENSDART00000125276 | Essential Splice Site | 231 | 387 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 1 (position 45701896)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 44545115 |
| GRCz11 | 1 | 45246418 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTTATTGTCAGGGCAGCGCCTTCATCGTTGGATTGCTACTTATGCAGG[T/C]TTGCCTCTGCGTTTTGCTTATCATGATGAGCTAAAACAATGTCAAGAAAT
Long Flanking Sequence:
CTCTTCAAGAGTTCACACTTAGATGTTGCTTGACGCTATTGGCATGCTGTCCCAGGAGAAAACCATGAGCTCGGAGATAATTGAGCCCAGGGCTTTCGCCTGGTCGATTAGCATTAAGAAGGTCCGAGATCAGGTAGGTCTTGAGAGCTCCAACTGGTAAAAGGAGGAGATTGGGTGGAAGGGGGGATTCTTCCAAAACAAAGATAGGCAATAGGGTAAAATCTGTCTATTTATTGTAGGCTTGGATCAATCTGATTAGATTAGTGCTGATAACGGCCACGATCAATCATATCACATGCTCCTCTCGAAATTACTTAAATTGTACCATTGCTATATTCTCATACGTATGATATACAGGATGCATGATTGTTTTGTTTGTTTAATATTATTAAGTCTTTAACATGTTTGTATCTCAACCTCACAGGCTTATTCTTTGGTGGATCGTGAAGTTGGTTATTGTCAGGGCAGCGCCTTCATCGTTGGATTGCTACTTATGCAGG[T/C]TTGCCTCTGCGTTTTGCTTATCATGATGAGCTAAAACAATGTCAAGAAATGTCTCTGAGCCAAACTTTGCGTAAACCAAATTCACTATTCACCGTAGATGCCGGAGGAGGAGGCTTTCTGTGTGTTTGTCAGACTAATGCAGGAGTACAGACTTCGAGAGCTGTTTAAACCAAGCATGGCTGAGCTGGGGCTGTGTATCTACCAGTTTGAACACTTGCTACAGGTAAGAAAGACAAATATGCAGAATAATACAGGGTGATACAGGTCTGCATTAAAATGTTCTTGGAAATACAGGTGATATAAAAGTTGATACAGTCTGATATAAAAGTGTGCCATTTGCTTACAAACATTTTGTACTATTATTACAATTTAAGGGGATAATTCAAGCAAAAATGAAAGCTCTATGATTTACTCACCCTAAATTGTTCCAAACCTAGTTGAGCTTCTTTCTTCTGTTGAATTTAAAAGAAGATATTTCCAAGATGCTGGTTGATATAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17798
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 |
|---|---|---|---|---|---|
| ENSDART00000074683 | Nonsense | 356 | 996 | 7 | 23 |
| ENSDART00000125037 | Nonsense | 356 | 707 | 8 | 17 |
| ENSDART00000125276 | Nonsense | 343 | 387 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 1 (position 45704368)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 44547587 |
| GRCz11 | 1 | 45248890 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WATTTCGAGTAGGAATAGCGATATTGCAGTACAACCAGACTGACCTCATA[C/T]AGCTAGACATGGAGGGAATGTCGCAGGTKGGAGCAAAAGCATCWCTGCTA
Long Flanking Sequence:
GAGCTGAACGTACATTTCCGTTCTCAGAGTTTCCACACATCCATGTACGCCTCGTCCTGGTTCCTCACCCTCTTCCTCACCTTCCTGCCCCTGCCAATAGCTACACGTATCTTTGACATCTTTATGTACGAGGTATGGACACAAGAGACTTTATGCATATTAAAGCATCCTTGATGTGATATTTATTATTGGGTTGCAGTATGTCCTAATAATACTATGAGAAAATACTATACTATTTATTTTACTGTAAGGGAAATATAACACCTTAAAGCTTAGTGAGGGTAAGTAAAGTATTATCATGTTCAGATTTTGTGTGTATTTATCACAGATGGGTTTTCATGCTGTGTGAATACTAGAGATGTGAATATTTCAGAGAGTGTGTGTTTGTTGTAGTTGCTAGCCTGTGACTATATGAATACTGTGTGTTGTTTTCACAGGGTTTGGAAATCATATTTCGAGTAGGAATAGCGATATTGCAGTACAACCAGACTGACCTCATA[C/T]AGCTAGACATGGAGGGAATGTCGCAGGTTGGAGCAAAAGCATCTCTGCTATGTGTTTAACACATGATAACACATATAATGGCATAATTTTAACCGATGTTTGTCTCACAATCTCACCACAGCACTTTCAGAAGGTGATTCCGCATCAGTTCGATAGCTGCCCAGATAAACTTATCCTACGGGCTTATCAGGTCAAATACAATCCCAAGCGAATGAAAAAGTGAGTGATTTGGGAGTAAAACCTAAAGGGAAATTTGTTTATAATGATTTTTGTGACATATTTTGGGACATACTCTACCTGACAAAAGTCGATTGCAGTTGTAAGAGTAACAAATAATCACTTCTAGTTGGTCATTTTGAAAAGTGTCAGAAGGTAGATTTTTCCAATGAATCATCTGTTGACCTGCATCCCAATCATCACAAACACTGCAGGGAGACCTATAGGAAGCCACATGGACCCAACATTCTCATAGAAATCTGTCAATTTTGGTGAAGGAAAAA
Associated Phenotype:
Not determined