ZMP
ephx2
Ensembl ID:
ZFIN ID:
Description:
epoxide hydrolase 2 [Source:RefSeq peptide;Acc:NP_001008642]
Human Orthologue:
EPHX2
Human Description:
epoxide hydrolase 2, cytoplasmic [Source:HGNC Symbol;Acc:3402]
Mouse Orthologue:
Ephx2
Mouse Description:
epoxide hydrolase 2, cytoplasmic Gene [Source:MGI Symbol;Acc:MGI:99500]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36296 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14928 | Nonsense | Available for shipment | Available now |
sa42857 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6457 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28783 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36296
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 |
---|---|---|---|---|---|
ENSDART00000058890 | Essential Splice Site | None | 557 | 1 | 20 |
Genomic Location (Zv9):
Chromosome 17 (position 5839879)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 5918815 |
GRCz11 | 17 | 6076045 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCTAAAGTCATAAGTGTAGCAGTGGTCTCTTCAAGCGACGCACAGCAG[G/A]TAAATAAACATACAATTTCGCCAAAATGAACTTTACTTTACTTTTCGACA
Long Flanking Sequence:
TAATTATTCATTTATTATGCATTGTTTTATGAACACGTTATTATACTGTATATGCATAGTATATATAGTAGCTTTATTTAATCAAATTGAGATTGATATTAAAAACTTTGTAGTCGCTAATTCCTATAATCTGACAAAGTTTGCGATTTATGTAACTATTGACTTTAGAGCTCTATCCACTACTAGTGAAAGGCTTTTCTTTTGAATATTAAATAGGTCCTGTTGACTTCCTCTAGCGTAATTCGTCTATTCTAATAAGCAGCGGAGGATTTGTGGATTCGTCCAATCACCATCTTTCCTCCGCCTGCCTTTCAGCCAATCAGGTACGAGTTTTCAGTGAACGTCAAGACGTGACATTAATATGTATGAGCTGTTTCCTTCGCCACACTAGAACTGGTGTTTGTAGTATTTGGGCTGGGTTTAAGAGCAGTATATTAGGAGTTTTCCTATGTGCTAAAGTCATAAGTGTAGCAGTGGTCTCTTCAAGCGACGCACAGCAG[G/A]TAAATAAACATACAATTTCGCCAAAATGAACTTTACTTTACTTTTCGACAGCGTTACGTAATGAACTTTGTCCTGCTTAACTGTGTAGTTTTGACCAACCAGAATGCCTGTCAAGCCTAAAGTATAATGTTTTCTGCTTTTGTATTTCTCTTTTTTTGCACAGTGTCAGTTTTTAAGGGATTTTCAACTAGTTTCCAATGAAGAAGGCAGTGTTGTTTAGTTTGTGGGGTGGTGTTGTTACCCCACAGATTGGTCAAGCATTTCAGAAGTTTGAGGAAACCACTGGCATTTCAAAGTATGTGTCTTACTTTCTTTTAAAACAGTATTTTATACCAATAAAAATAAATGAATGTGCTTTTTTATATTAGTTTTTTTACATCTTTTATTTAAGGAAGTCACTGACATTTGAAAGTATTAGATTTTTTTTCTTTTAGCAGTACATGACATTTTGTGTAAAAAAATAAGTAAATAAATGTGCATTATTAGTTTTTTCATCTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14928
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 |
---|---|---|---|---|---|
ENSDART00000058890 | Nonsense | 272 | 557 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 17 (position 5828862)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 5907798 |
GRCz11 | 17 | 6065028 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGTTCTCCTGTGTCATGGATTCCCTGAGAGCTGGTTTTCCWGGAGGTA[T/A]CAGGTGAGAAAYATMAAACTTTAYAGCTGATGTAACTGAAACGCAGACCT
Long Flanking Sequence:
AAGATGTTTTAATCTGTCCTATTTAGACATATGCAGATATTTAGTATATTGTGATAATGAAAATGAGGGTGACACGGTGGCTCAGTGGTTAGCACTGTGTCCTCGCTGCAAGGAGGCGACTGGTTTGAGTCCCGGCTGGGTCAGTAGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCTGTGTAGGCGTTGGATTTCTCCGGGTGCGCCGATTTCCCCCGCAGTCCAAACACAGGCGCTATAGTGTATGAGTGTAAATGAGAGTGTTTCCCAGTACTGGGTTGCAGCTGGTAGGGCATCTGCTGCGTAAAAATAAGGGACTAAGCCGAAGGAAAATGAATGAATATAGAGGAAGGCTAATAATTCAGGAGGGCTAATAATTCTGACTTCAACTGTCTGTGTTTGTAAGCCTGGTGTGAAGATCCACTATGTGGAGATGGGAGACGGTCCACCTGTTCTCCTGTGTCATGGATTCCCTGAGAGCTGGTTTTCCTGGAGGTA[T/A]CAGGTGAGAAACATCAAACTTTATAGCTGATGTAACTGAAACGCAGACCTTTGAAGATGAAGAGATTAGACTAGAAGAGCCTGGCGGATTTAGGCTTAAAGATCAGTCTGGTAAGCCACAGGTTGGTGGGTTTGAAACACCAAAAGGGTGATTCATGAGATTTCAGTAGAATATCTTTGATTGCGACCCCAGAGGATGAGTAAACCTTACATTGCATAATAAAGCAGACCTGAAGCCAGCCTGGTGAACGAGGTGGTTCTTTTTGTCTCAAAAGCTGGACATTTTTAGTTATTTGGTTAATTTTCTATTTAATTAAAAATATATGTATATATAATTCATTTTTATTTTAAACTTTCTATTAATTGCTGTATTTAAGTGACATTTAAGCACCATTATTTTGCTGGATTAGCCTGTCAGATAGTTAAAAAATAGGAATCTGTTAAAGTTTTAATTTAAATCTGTTGCCTGTTGTCATTTATTAGACAAATGACAAACTGGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42857
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058890 | Nonsense | 342 | 557 | 12 | 20 |
Genomic Location (Zv9):
Chromosome 17 (position 5811159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 5890095 |
GRCz11 | 17 | 6047325 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACTCTGGTGGGCCATGATTGGGGCGGCGTTCTGGTCTGGAACATGGCA[C/T]AGTTTCACCCTGAGAGAGTCCGGTATATTATACACTATTACAGCTGTTTA
Long Flanking Sequence:
GTCTACAGAACAAACCATCTTTATACAATAATTACCCTAACGTAGTTAACCTAATTAACCTAGTTTGGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTATTATTTAATCAATCAAATATTATTTACTGTCATCATGACAAAGATAAAAGAAATCAGTTATTAGAAATGAGTTATTAAAACTACTATGTTTATAAATGTGGTGAGAAAATCTTTTCTCTGTTAAACAGAAATTGGGGGAAAAAAAGTAAACGGGGGCTTATAATTCTGACTTGAACTGTATATATACATGTGTGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATCCTCATGTCATGTTCTTTTGTTATTCAGCTGGTTGTGGTCATTTCTGAGCTTGTGTGTTTGTGTTCCGCAGGCCATTGCTCAGGTCACTCTGGTGGGCCATGATTGGGGCGGCGTTCTGGTCTGGAACATGGCA[C/T]AGTTTCACCCTGAGAGAGTCCGGTATATTATACACTATTACAGCTGTTTAACGTATTTATATTGACTGTGTCCGATTGTTATTGTGTTTAGTGTAAAAACTGGACAAAATACATCCACCATGCTTCTATTTATTTTGTCGTAAACAAATAAATACATGCATTCATAAATTGCTTGTTTGTTTAATTGTACTTTTTGTGTCAGAATATGTTTGCATTAAGAGAGGAAAATGATTTAAAATGAAAATCATATTGAAAATCAGATTTGAACACATTAAAAGCAAAAACAAATAAAGCAATCCTAAACGGTTTATATATTATTTGAAAACTTTTTTCTTTTGATTTTGTACTTAAATATAATTTCGTTTAAATTTTTGCTGAAATATGATTTTCGTTCTGACACTTCCTTATGATATTCTGCCAGTTTAAAGGTTTTTTTTTGTCTTCAGATATTTCATTCTTCTGTGGGAGATCATTTTCCATATTAAACTTGTGAAGTGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6457
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 |
---|---|---|---|---|---|
ENSDART00000058890 | Essential Splice Site | 425 | 557 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 17 (position 5802363)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 5881299 |
GRCz11 | 17 | 6038529 |
KASP Assay ID:
554-5381.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGCAGGATGGATTTCCTAAGTTATCCCCTGCTGGAGTTTGTCAGAGAG[G/A]TAAATACATCAAACNNNNNNATTTTCAGTTTTTGATTTGTCTGCATCTTT
Long Flanking Sequence:
AGTCGTGGGCCGCATTAAATTTGTTTAATATAAATATATTAAGGCGAGGCAGTGGCGTAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTTGCTGGGTCGCTGGTTCGCTGGTGTGGATGTTGCGGCTGGAATGGCATCCGCTGCGTAAAAACTTGCCGGATAAGTTGGCGGTTCATTCCGCTTTGGCGACCCCAGATTAATAAAGGGACTAAGCTGACAAGAAAATGAATGAATGAATGAATAAATATATTAAACTACAAATATAAAGAATGATAAACCTAAAACTAAACCGACTAAAATAAGCGAAAGAGAAAAGTGATACTGCTAAAGCTTAAACTACAAATAAAATGAAACAATACAAATACAAGGTATAAGATATTAAATCTAATACTATATTACAATATTGAGTATTGTTCAAATATATACTGAGAAACTTTATTTTTATAATCTGCAGGATGGATTTCCTAAGTTATCCCCTGCTGGAGTTTGTCAGAGAG[G/A]TAAATACATCAAACTATAACATTTTCAGTTTTTGATTTGTCTGCATCTTTTACTATTGCAGATGCGCACTTTGCAATATGGATATGTTTCACTGCTGTTCAGGTTGTGATTTGCTCAGCTCTGCTGTTTCTCAGGTGGATTGTTTGTTGGGTCTCCGGATGATCCTCCGCGCAGCTCCATGCTGAGTGTGTCTGCGCTTCAGTTTTACACAGAGCAGTACAGCAAGAGCGGATTCAGGTACACCGAGAACATGAGCTCCTCGATCTGTGTGCTTTTTGTACTTCTGTCTTCACGCTGCAGAATGTTTTTTGTTGTCTTGTCATCAAGTGACTACTATTTTCTTCCAGTAGTTAAGTAATGTGTACAATGTAAAATATTCACAATAGAATTAAAAGCTTCAAAATGTCCTGAAACAATTTAGTTTCTTGTGTGTAAATAGAATAATATGCGTAATATTTAATTTAATGTTAACTTTATTAAATTTTACGTAATTTATCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28783
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058890 | Nonsense | 454 | 557 | 16 | 20 |
Genomic Location (Zv9):
Chromosome 17 (position 5802143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 5881079 |
GRCz11 | 17 | 6038309 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCAGCTCCATGCTGAGTGTGTCTGCGCTTCAGTTTTACACAGAGCAGTA[C/A]AGCAAGAGCGGATTCAGGTACACCGAGAACATGAGCTCCTCGATCTGTGT
Long Flanking Sequence:
CAAGAAAATGAATGAATGAATGAATAAATATATTAAACTACAAATATAAAGAATGATAAACCTAAAACTAAACCGACTAAAATAAGCGAAAGAGAAAAGTGATACTGCTAAAGCTTAAACTACAAATAAAATGAAACAATACAAATACAAGGTATAAGATATTAAATCTAATACTATATTACAATATTGAGTATTGTTCAAATATATACTGAGAAACTTTATTTTTATAATCTGCAGGATGGATTTCCTAAGTTATCCCCTGCTGGAGTTTGTCAGAGAGGTAAATACATCAAACTATAACATTTTCAGTTTTTGATTTGTCTGCATCTTTTACTATTGCAGATGCGCACTTTGCAATATGGATATGTTTCACTGCTGTTCAGGTTGTGATTTGCTCAGCTCTGCTGTTTCTCAGGTGGATTGTTTGTTGGGTCTCCGGATGATCCTCCGCGCAGCTCCATGCTGAGTGTGTCTGCGCTTCAGTTTTACACAGAGCAGTA[C/A]AGCAAGAGCGGATTCAGGTACACCGAGAACATGAGCTCCTCGATCTGTGTGCTTTTTGTACTTCTGTCTTCACGCTGCAGAATGTTTTTTGTTGTCTTGTCATCAAGTGACTACTATTTTCTTCCAGTAGTTAAGTAATGTGTACAATGTAAAATATTCACAATAGAATTAAAAGCTTCAAAATGTCCTGAAACAATTTAGTTTCTTGTGTGTAAATAGAATAATATGCGTAATATTTAATTTAATGTTAACTTTATTAAATTTTACGTAATTTATCAATGTATTACTTGTTAATTGAATTAACTATATGCGTATGAAAAGTGTGTATGTGTATACAGTAGGGATGTAACGGTATCAGAATTTCACGGTACGATAATACATCGGTATGAATGGGACGGTACAATATTTATTGAATAATTTACAGGAAAAACAAAACTAATGAAAAACTCGGAAAAAAAAGTGCCAAAAGTGTTTATTTACCTTAGCACTGAACATATCAA
Associated Phenotype:
Not determined