ZMP
evx2
Ensembl ID:
ZFIN ID:
Description:
homeobox even-skipped homolog protein 2 [Source:RefSeq peptide;Acc:NP_571307]
Human Orthologue:
EVX2
Human Description:
even-skipped homeobox 2 [Source:HGNC Symbol;Acc:3507]
Mouse Orthologue:
Evx2
Mouse Description:
even skipped homeotic gene 2 homolog Gene [Source:MGI Symbol;Acc:MGI:95462]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41335 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa140 | Nonsense | Confirmed mutation in F2 line | Not yet available |
Mutation Details
Allele Name:
sa41335
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000082329 | Essential Splice Site | 135 | 418 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 1994266)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 2002670 |
| GRCz11 | 9 | 2003467 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCGTTCCCCGGGCAGCATCAGCCAACACAAGGAGAACAACAATAAAGG[T/G]AAAGAAATTGCGTGAAAAGGCGTTTTTTTTTCAATTTGTTTATGTCGATA
Long Flanking Sequence:
TATTTAGAGGCGGCAGCTGAGCTGAATGCGGATTAGATCCGCCACCAGTCATCGGAGCACCAGCCCTGGGACTTTGGATTTTTTCTGCACGACTTCATGATGGAGAGGATAAGAAAAGAAATGATTCTGATGGAAAGGGGACTACACAGTCCAGTGGCAGGGAAGAGGCTCTCCAACCTCACCGACTCGGCCGGGAACGCGGTGCTCGAGGCCCTGGAAAATTCCCAGCACGCAGGTCGCCTCAGCCCGAGAATAACTTCCGCCTCGCTGCATGGGGATATTCCCACCAAAGGCAAGTTCGAGATCGACAGCTTATTTGGGAACCACCACAACGACAACACTTCCTCAACAGAAGTGTCGTCCTCCGAAAGCCGGAAGAAAATAAACCTGTATCCTGAAGTTTCTCCTGACTCCGACATGAACAGCGATGTGGAAGTGGGCTGCCCGTCTCATCGTTCCCCGGGCAGCATCAGCCAACACAAGGAGAACAACAATAAAGG[T/G]AAAGAAATTGCGTGAAAAGGCGTTTTTTTTTCAATTTGTTTATGTCGATATTTATTTTTTAAAGATAACTGCTTTAGAATTTGGTTTATATTAATGGTTTAAATGTGCTTAGTATTTATTTTTTTTATTGTGTGTTCAGTAATATTTTAGTGTTGCATTTTTCCTAATGTCTGAGTGCTAGCATGTCGATGCATTTATCGAAATAAATTGTCTGTCGTTGCATTATGTAGTGTACACATTTAGCGTTTTAAAAAAAATATATATGCAAACGTTTGCATTTAATTGTGTATATGTAATTGCATTTTATTTTTTCCTTTAGATCTTTCGTTTATTCAAAATATTTTACACTGAATCTCTGAGTAAAAAAAATGTAATGCGATCCCAAAACGTTCCCGTTTAATTTAACTTATTTTACAAATGCATGATTTTCTTTGTTCATTATTTTAATGTTCAAATTAATGTGTTTTTTACCTCAAAATATATTTGTAAAATATTTATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa140
Status:
Confirmed mutation in F2 line
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000082329 | Nonsense | 168 | 418 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 1994899)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 2003303 |
| GRCz11 | 9 | 2004100 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCGAATCTTAACGGTAATTCCATGGGAAACAGCAGCTCGAGCTCGGAC[C/T]AGGTGAGGAGGTACCGGACTGCTTTTACCCGAGAGCAGATTGGAAGACTG
Long Flanking Sequence:
TGTTCAGTAATATTTTAGTGTTGCATTTTTCCTAATGTCTGAGTGCTAGCATGTCGATGCATTTATCGAAATAAATTGTCTGTCGTTGCATTATGTAGTGTACACATTTAGCGTTTTAAAAAAAATATATATGCAAACGTTTGCATTTAATTGTGTATATGTAATTGCATTTTATTTTTTCCTTTAGATCTTTCGTTTATTCAAAATATTTTACACTGAATCTCTGAGTAAAAAAAATGTAATGCGATCCCAAAACGTTCCCGTTTAATTTAACTTATTTTACAAATGCATGATTTTCTTTGTTCATTATTTTAATGTTCAAATTAATGTGTTTTTTACCTCAAAATATATTTGTAAAATATTTATACATTTGAATTGTATCTCTTTCGTTATCCGATTTAGGTTTCTCGGACAGCAATTCAGGAGGCTCCAATACAAGTTCATCCTCTCTATCGAATCTTAACGGTAATTCCATGGGAAACAGCAGCTCGAGCTCGGAC[C/T]AGGTGAGGAGGTACCGGACTGCTTTTACCCGAGAGCAGATTGGAAGACTGGAGAAAGAATTTTACAGGGAAAACTACGTCTCGAGACCCAGGAGATGTGAATTAGCCGCAGCATTAAACCTGCCCGAAACAACAATAAAGGTAATGCTCTGATTTTGTTCACCAGGATATAATTTGTACCTGCTAATTTATAATGTTTAGCAAACAAATATTAACTGGTTACATGCTCTAGCACTATAAATTCACGCATTTAAATGCCCATTGCCAAATCTAAAATAATAATCCATTCTGTTATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAGAATATTTCTATATAGTGGACATAAATAATGCAGGGATGTAGCTAAAGCACTGTGTAATACAGACAATTTTATTTTGTCTGATGCAGAACCCCGTCTTTTTCATCTGAGCTCTCCTAAGATATTAAAATTAGTTGCATTTGCAAAACTATT
Associated Phenotype:
Not determined