ZMP
etv5a
Ensembl ID:
ZFIN ID:
Description:
ETS translocation variant 5 [Source:RefSeq peptide;Acc:NP_001119933]
Human Orthologue:
ETV5
Human Description:
ets variant 5 [Source:HGNC Symbol;Acc:3494]
Mouse Orthologue:
Etv5
Mouse Description:
ets variant gene 5 Gene [Source:MGI Symbol;Acc:MGI:1096867]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa279 | Nonsense | F2 line generated | Not yet available |
| sa41407 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa16031 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa279
Status:
F2 line generated
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101770 | Nonsense | 20 | 522 | 3 | 13 |
| ENSDART00000126015 | Nonsense | 20 | 524 | 3 | 13 |
| ENSDART00000139434 | Nonsense | 19 | 97 | 3 | 6 |
| ENSDART00000145005 | Nonsense | 19 | 180 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 23667593)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 22823379 |
| GRCz11 | 9 | 22634248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTAAAACTGGGTGACACTAACCAACGTGTTTTTCCATAGCAGAAGTCAT[T/A]GCAAGTGGAGGAACCATATAACAGACCAGTTAATGACAGAAAGAGAAAGT
Long Flanking Sequence:
CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTTCTGTGTGTGTCTGTTTTTACACATACGGTCTGTCAGGCGGGATGTTGTGATGGGTAACAGAGAGAGAAGAGGGAGGATGAATAGACAGGATCAGATGGATCTGAGGGTTTTGTCAGACTGTACGCAGGGTTTGGTTTTTTGATGTGGGACACACTTGACTGTCCAGTAGATGCTTTGCCTGATTCATCTCTCTTTTCTTTTTAGAGAGAACAGAAGACCCAAAGAGGACGTTACAGCTATCGCTTTTAAGCGAAGATCCTATTCTGGGAGCCTCTTTGAAGACCCAGGTGACATGGACGGATTTTATGACCAGCAAGTTCCATTTATGGTCCCACCTAATGTAAGTATATTTCTTCATTTGCATGAATCTAGCATTTCTAAAGGAGGTTTATTTGTCAGCTTTAAAACTGGGTGACACTAACCAACGTGTTTTTCCATAGCAGAAGTCAT[T/A]GCAAGTGGAGGAACCATATAACAGACCAGTTAATGACAGAAAGAGAAAGTTAGTGGAGACTGAACTTGCTCAGGATACAGAGGGTAAATTCAGCCTAATGAATGTGACTAATGGATGTTTAACAGATGGATCTGATTATTGTGATGCATTAACAGTGAGAGAGTGTGCTCAAATTAGCTTGATTTATGCTGTGATTGTTGAAGGTTGCCTTTCATTGATCAAATTCTTGGATCACAGTGGCTTTTCTTGCACTCAAACAGTCTTGTCTTTGCCTGTCATCTGCAGAACTTTTCCAGGACCTCAGCCAGCTGCAGGAGATCTGGATTGCAGAAGGTTTGTGGCATACTTTGGTTCCATGCATGTAATTTTTGCTTTGTCATGCAGCTGGCATTAATATTCCAAGCTCATGTATGCATGTGAAACATATAATTCCTAAGTGATGCACTTCATCCCAGCTGCTGTTTATTTTTCATGACCGGAGCCATTTCATTTAGTTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41407
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101770 | Essential Splice Site | 48 | 522 | None | 13 |
| ENSDART00000126015 | Essential Splice Site | 48 | 524 | None | 13 |
| ENSDART00000139434 | Essential Splice Site | 47 | 97 | None | 6 |
| ENSDART00000145005 | Essential Splice Site | 47 | 180 | None | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 23667678)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 22823464 |
| GRCz11 | 9 | 22634333 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAGAAAGAGAAAGTTAGTGGAGACTGAACTTGCTCAGGATACAGAGGG[T/A]AAATTCAGCCTAATGAATGTGACTAATGGATGTTTAACAGATGGATCTGA
Long Flanking Sequence:
GGCGGGATGTTGTGATGGGTAACAGAGAGAGAAGAGGGAGGATGAATAGACAGGATCAGATGGATCTGAGGGTTTTGTCAGACTGTACGCAGGGTTTGGTTTTTTGATGTGGGACACACTTGACTGTCCAGTAGATGCTTTGCCTGATTCATCTCTCTTTTCTTTTTAGAGAGAACAGAAGACCCAAAGAGGACGTTACAGCTATCGCTTTTAAGCGAAGATCCTATTCTGGGAGCCTCTTTGAAGACCCAGGTGACATGGACGGATTTTATGACCAGCAAGTTCCATTTATGGTCCCACCTAATGTAAGTATATTTCTTCATTTGCATGAATCTAGCATTTCTAAAGGAGGTTTATTTGTCAGCTTTAAAACTGGGTGACACTAACCAACGTGTTTTTCCATAGCAGAAGTCATTGCAAGTGGAGGAACCATATAACAGACCAGTTAATGACAGAAAGAGAAAGTTAGTGGAGACTGAACTTGCTCAGGATACAGAGGG[T/A]AAATTCAGCCTAATGAATGTGACTAATGGATGTTTAACAGATGGATCTGATTATTGTGATGCATTAACAGTGAGAGAGTGTGCTCAAATTAGCTTGATTTATGCTGTGATTGTTGAAGGTTGCCTTTCATTGATCAAATTCTTGGATCACAGTGGCTTTTCTTGCACTCAAACAGTCTTGTCTTTGCCTGTCATCTGCAGAACTTTTCCAGGACCTCAGCCAGCTGCAGGAGATCTGGATTGCAGAAGGTTTGTGGCATACTTTGGTTCCATGCATGTAATTTTTGCTTTGTCATGCAGCTGGCATTAATATTCCAAGCTCATGTATGCATGTGAAACATATAATTCCTAAGTGATGCACTTCATCCCAGCTGCTGTTTATTTTTCATGACCGGAGCCATTTCATTTAGTTTGTTGCACCAGCCTTGCGGCAGAGTCCAAAAAGTTGGCACTAAGATGGCTGTTCTTTTTTAGACGAAGGAAAAATACAGAAATAAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16031
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 |
|---|---|---|---|---|---|
| ENSDART00000101770 | Nonsense | 442 | 522 | 12 | 13 |
| ENSDART00000126015 | Nonsense | 442 | 524 | 12 | 13 |
| ENSDART00000139434 | None | None | 97 | None | 6 |
| ENSDART00000145005 | None | None | 180 | None | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 23680454)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 22836240 |
| GRCz11 | 9 | 22647109 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATGAACTAYGACAAGCTGAGTCGCTCACTGCGCTACTACTATGAGAAG[G/T]GAATCATGCAGAAGGTAAAGRCAGGTTCACCTTTTCCTKTACTTCGCACT
Long Flanking Sequence:
AGTGCCGACAATGTGATGTAATACTATCTTTTGTAACCTTTACCATAATCCCAGATGGTCAAATTCATCCTTTATAAATGTTGCTTTGCCATAATATGTTGAGAGCGTAACAGAAAAGTAGAGGCTTGACTTGGCAAGCGGATATGTCAGCAAACACTTTGTCATCGTATTATTAGCAGCTTCTTTAAAAAGCCCTTTATTACATTAACCATGTATAGAGCATTCATTAAAATACTCCTCAGAAAAACCCTGGAGTGTTTCTGAGAGACTTTTAAACTCATGCGACTTGAAATAAAATTAATCTGTTAATAAAGAATTAAAAACAGCCACGGTGGCTCCCTACACATGTAATTCTTTATTCCGAAATATTTTTGGGTATACTAAGCAATGTCAATTATCTTGTGTGTTATCAGGTGGCTCGACGCTGGGGCATCCAGAAGAACAGACCCGCCATGAACTACGACAAGCTGAGTCGCTCACTGCGCTACTACTATGAGAAG[G/T]GAATCATGCAGAAGGTAAAGGCAGGTTCACCTTTTCCTGTACTTCGCACTCCACTCACAACGACCGTAGTTGCTCAAACTTTCCTTCAATCCTCTAAAAATCTCTCTCGTTCCTTTTCAGGTTGCCGGCGAGAGGTACGTCTACAAATTTGTGTGCGATCCTGAAGCGCTCTTCTCCATGGCCTTCCCAGACAACCAGAGGCCCAATCTCAAAGCAGACCCTGACGGCCTGCCCACTGTGGATGATGACACACTTCCATTGGCACATTATGACGACGGGTCCTCGTATTTAGTTGACGGTGGCGAGCAGTGTGTTTCTGGGATGCCTTTCCCTGATGGTTACGTGTACTGAACTCGAACACATCTGTCCCATTGCCTCGACTCCTTTTGAACTGTTGCCCACTTCCAGATTAACCCTCCCAATCATGAAAGAAGAACGAGGAGAAATCTGCGCCACCTTTTCTATGACGAGAAAGGTGTCAAGGAGGTGAGGAAAGCAGG
Associated Phenotype:
Not determined